 |
Previous Article | Next Article 
The Journal of Neuroscience, May 15, 1998, 18(10):3943-3954
Retrograde Amnesia for Facts and Events: Findings from Four
New Cases
Jonathan M.
Reed1 and
Larry R.
Squire1, 2, 3
Departments of 1 Psychiatry and
2 Neurosciences, University of California, San Diego, La
Jolla, California 92093, and 3 Veterans Affairs Medical
Center, San Diego, California 92161
 |
ABSTRACT |
Two patients with presumed hippocampal formation lesions and two
patients with more extensive temporal lobe damage, all of whom became
amnesic in a known year, were given tests of anterograde and retrograde
memory function. The two patients with hippocampal formation lesions
had moderately severe anterograde amnesia and limited retrograde
amnesia for facts and events that affected, at most, the decade
preceding the onset of amnesia. Content analysis could not distinguish
the autobiographical recollections of the patients from the
recollections of control subjects. The two patients with more extensive
temporal lobe damage had severe anterograde amnesia and extensive
retrograde memory loss for both facts and events. The results suggest
that whether retrograde amnesia is temporally limited or very extensive
depends on whether the damage is restricted to the hippocampal
formation or also involves additional temporal cortex.
Key words:
retrograde amnesia; anterograde amnesia; hippocampal
formation; medial temporal lobe; autobiographical memory; fact
memory
 |
INTRODUCTION |
Retrograde amnesia (RA) refers to
loss of memory for information acquired before the onset of amnesia.
The condition is commonly observed after medial temporal lobe or
diencephalic pathology, and it has fascinated psychologists,
biologists, and clinicians for over 100 years (Ribot, 1881 ). An
understanding of RA should have considerable implications for
understanding the organization of normal memory as well as the function
of the damaged brain structures. Yet the facts themselves are not
agreed on. For example, RA has been described as typically extensive
and ungraded, affecting recent and very remote memories alike (Sanders
and Warrington, 1971 ; Warrington, 1996 ). Alternatively, RA has been
described as usually temporally graded, sparing remote memory
(Marslen-Wilson and Teuber, 1975 ; Squire and Alvarez, 1995 ). With
respect to what kind of memory impairment occurs, RA sometimes has been
described as affecting both fact (semantic) memory and autobiographical (episodic) memory similarly (Verfaellie et al., 1995 ; Rempel-Clower et
al., 1996 ). Alternatively, RA has been described as affecting autobiographical memory across a patient's entire lifetime and affecting fact memory to a much lesser degree (Nadel and Moscovitch, 1997 ).
There are several reasons why these issues have been slow to resolve. A
major factor is that, even when quantitative neuropsychological testing
is performed, adequate neuropathological information about the patients
is not always available. Yet anatomical data could be fundamental to
understanding similarities and differences in the behavioral findings.
In some instances, useful anatomical information has been obtained from
magnetic resonance imaging (MRI), although the amount of available
detail varies greatly across studies. Neurohistological data from
postmortem examination, in conjunction with quantitative
neuropsychological data about RA, are available for only four patients
with lesions restricted bilaterally to the medial temporal lobe [R.B.,
Zola-Morgan et al. (1986) ; G.D., W.H., and L.M., Rempel-Clower et al.
(1996) ]. In a few other cases of medial temporal lobe lesions,
detailed neurohistological information is presented, but only clinical impressions are available about the RA (Victor et al., 1961 ; Penfield and Mathieson, 1974 ; Victor and Agamanolis, 1990 ).
Another major difficulty is that the study of past memory in amnesic
patients relies necessarily on retrospective methods and imperfect
tests. For tests of factual knowledge (e.g., public events tests),
individuals vary widely in how much they know about the subject matter,
independent of the influence of amnesia. For tests of autobiographical
knowledge, it is often not possible to verify the accuracy of the
recollections, and there are also difficult issues concerning how best
to score the content of what is remembered.
The available data suggest that RA can vary considerably in its
severity from temporally limited RA covering up to a few years to more
extensive, ungraded RA involving all of the decades covered by the
tests (Squire, 1992 ; Hodges, 1994 ; Schmidtke and Vollmer, 1997 ). Many
questions remain, however, about what kind of retrograde impairment is
most typical in amnesia and what specific neuropathology is associated
with the various presentations of RA. It also remains unclear whether
autobiographical memory usually is affected to the same degree as fact
memory or whether autobiographical memory usually is affected much more
severely than fact memory.
We have assessed RA in four patients, three of whom had detailed MRI
examinations to characterize the lesions. One has damage limited to the
hippocampal formation, a second was not eligible for MRI but is
presumed to have hippocampal formation damage based on etiology, and
two others have hippocampal formation damage together with amygdala
damage and additional temporal cortical damage. All of the patients
were assessed with a number of anterograde and retrograde memory tests,
including tests of factual knowledge and tests of autobiographical
memory. The findings support the idea that damage to the hippocampal
formation produces limited RA and that additional temporal cortical
damage is needed to produce severe and extensive RA. Fact knowledge and
autobiographical memory were affected similarly overall.
 |
MATERIALS AND METHODS |
Subjects
Amnesic patients. Four amnesic patients were studied,
three men (A.B., E.P., and G.T.) and one woman (L.J.) (Tables
1, 2). Two
patients (A.B. and L.J.) have damage apparently limited to the
hippocampal formation. Patient A.B. became amnesic after a cardiac
arrest in 1976. A physician friend and his wife, a nurse, were with
A.B. at the time of his arrest and were able to administer resuscitation (CPR) immediately. He arrived at the hospital within 30 min, at which time he was in ventricular fibrillation and having generalized seizures. After treatment, he was breathing spontaneously and maintaining good levels of blood oxygen with minimal
supplementation. Seizure activity ceased after the second hospital day,
but he remained comatose for the next 8 d. Neurological
examination in 1978 indicated mildly impaired cerebellar function, but
examinations in 1987 and 1998 found no cerebellar or Parkinsonian
signs. On the basis of these findings and the etiology of his amnesia,
A.B. is presumed to have circumscribed hippocampal formation damage. This cannot be confirmed with MRI, however, because he wears a pacemaker.
For patient L.J., MRI (Squire et al., 1990 ) identified that the
hippocampal region (subtended by the fimbria, dentate gyrus, hippocampus proper, and subiculum) was reduced in size (left side, 0.37 cm2; right side, 0.42 cm2; six
control subjects averaged 0.56 cm2 on the left and
0.63 cm2 on the right) (Fig.
1A). Likewise, the size
of the hippocampal formation was reduced when its area was calculated
as a percentage of the size of the temporal lobe (left side, 3.23%;
right side, 3.38%; six controls averaged 5.02% on the left and 5.34%
on the right). L.J. became amnesic with no known precipitating event during a 6 month period that began in late 1988. Her memory impairment has remained stable since that time. Both A.B. and L.J. have moderately severe and clinically significant amnesia. Neither is capable of
independent living.

View larger version (100K):
[in this window]
[in a new window]
|
Figure 1.
Magnetic resonance images for three
of the four amnesic patients. For L.J.
(A), a coronal T-1 weighted image is shown
through the midlevel of the hippocampal formation. The area of her
hippocampal formation bilaterally is 66% of the area calculated for
six control subjects and well outside the control range. For E.P.
(B), an axial T-2 weighted image through the
temporal lobe shows the extent of bilateral medial temporal lobe
damage, which extends caudally from the temporal pole and damages
bilaterally the perirhinal cortex, the entorhinal cortex, the
parahippocampal cortex, the amygdaloid complex, and the hippocampal
region (CA fields, dentate gyrus, and subicular complex). The lesion
extends laterally to include the fusiform gyrus at some levels, and
small foci of damage are apparent in the right medial and dorsal
frontal cortex. Finally, reduced volume of the insular cortex and
inferotemporal gyrus is apparent bilaterally, although it is unclear
how abnormal a finding this is or what implications it has for
neuropathology. For G.T. (C), an axial T-2
weighted image through the temporal lobe shows the damage extending
through the anterior 7.0 cm of his left temporal lobe and through the
anterior 5.0 cm of his right temporal lobe. The lesion includes
bilaterally the amygdaloid complex, hippocampus, entorhinal,
perirhinal, and parahippocampal cortices as well as the inferior,
middle, and superior temporal gyri. There is also bilateral damage in
the insular cortex, medial and orbital frontal cortex, and cingulate
gyrus. Asterisks in A indicate the
position of the hippocampus on each side.
|
|
Two other patients developed profound amnesia after herpes simplex
encephalitis (E.P. in 1992 and G.T. in 1990). Both patients have large,
radiologically confirmed, bilateral lesions of the temporal lobe that
include the hippocampal formation (Squire and Knowlton, 1995 ; Hamann et
al., 1996 ). E.P.'s damage is primarily medial temporal but also
involves the laterally adjacent fusiform gyrus at some levels. G.T.'s
damage is more extensive and involves much of the temporal lobe
bilaterally (Fig. 1B,C).
Neuropsychological data for the four patients are presented in Tables 1
and 2 and in Figure 2. Note that all four
patients exhibit amnesia despite obtaining intelligence scores within
the normal range. Note also that the two postencephalitic patients who
have more extensive lesions also have more severe anterograde memory
impairment.

View larger version (27K):
[in this window]
[in a new window]
|
Figure 2.
The Rey-Osterrieth figure. Patients were asked to
copy the figure illustrated in the small box to the
bottom left and, 5-10 min later, to reproduce it from
memory. The copy (top) and the reproduction
(bottom) are shown from left to
right for the four patients and for a representative
control subject (CON). Neither E.P. nor G.T.
recalled copying the figure. Encouraged to draw whatever came to mind,
patient E.P. declined to try and G.T. produced a drawing of a horse's
head.
|
|
Control subjects. Two groups of control subjects were
recruited from volunteers and employees at the San Diego Veterans
Affairs Medical Center. One group consisted of nine individuals, five matched to patient A.B. and four to L.J. As a group they averaged 62.3 years of age and 15.9 years of education. They scored 22.4 and 52.6, respectively, on the Information and Vocabulary subscales of the
Wechsler Adult Intelligence Scale-Revised (WAIS-R) (22 and 57.5 for
the patients).
Four additional individuals with a mean of 11.5 years of education
served as controls for the postencephalitic patients, E.P. and G.T.
Because the two patients differ by 14 years in age, these control
subjects were selected to match the older patient (E.P., age 74 years)
with respect to age (mean, 73 years). By matching the age of this group
to the older patient, we expected to obtain a conservative measure of
normal memory performance.
Retrograde memory tests
New vocabulary (recall and recognition). Subjects
completed a vocabulary test involving 82 words that had entered into
common English usage between 1955 and 1989 (1955-1959,
n = 12; 1960-1969, n = 24; 1970-1979,
n = 24; 1980-1989, n = 22) (Verfaellie
et al., 1996 ). Twelve additional common words (e.g., tuxedo, moron)
were included to assess baseline vocabulary ability. A recall test was
given first in which each word (e.g., zilch) was presented, and the
subjects were asked to provide a definition. Responses were scored as
either "correct" or "incorrect." Immediately after recall,
subjects completed a four-alternative multiple choice form of the same
test (e.g., zilch: to destroy or eliminate; a stain; a filmy residue;
zero or nothing).
Public events (recall and recognition). The test consisted
of 145 questions about public events that had occurred from 1940 through 1995 (1940s, n = 19; 1950s, n = 17; 1960s, n = 24; 1970s, n = 27;
1980s, n = 30; 1990s, n = 28) (Squire,
1975 ; Squire et al., 1989 ). The test was administered first in a recall
format (e.g., Who killed John Lennon?), and immediately afterward in a
four-alternative multiple choice format (John Hinkley, Sara Jane Moore,
David Roth, Mark Chapman).
Famous faces (recall and recognition). Subjects were asked
to identify 141 photographs of famous people who came into the news in
one of the decades from 1940 to 1995 (1940s, n = 24;
1950s, n = 27; 1960s, n = 27; 1970s,
n = 27; 1980s, n = 24; 1990s,
n = 12) (Albert et al., 1979 ; Squire et al., 1989 ). The
test was administered first in a recall format in which subjects were
presented with each photograph and asked to name the person (e.g.,
Marilyn Monroe). After the recall test was completed, the subjects were shown each unrecalled photograph and asked either a yes or no question
[e.g., Is this person's name Marilyn Monroe? (One-half of the time,
the name that was presented was correct.)] or a three-alternative multiple choice question (e.g., Which of the following is the name of
this person? Gwen Verdon, Brigitte Bardot, or Marilyn Monroe). The
recognition score was based on the number of items that were recalled
correctly plus the items that were recognized correctly. Note that
chance performance on the recognition test was 41.6% (the average of
50% and 33.3%).
Famous names completion and famous names recognition. For
the completion test, the subjects were given a list of 65 items, each
consisting of a first name together with the first few letters of a
last name (e.g., Alfred Hitch _____ ). In each case
they attempted to complete the item to form the name of a famous
person. All of the correct completions corresponded to names of faces that had appeared on the Famous Faces test (1940s, n = 11; 1950s, n = 13; 1960s, n = 11;
1970s, n = 13; 1980s, n = 11; 1990s,
n = 6). For the recognition test, 70 test items were
constructed, each consisting of three names (e.g., Joseph Silva, Jimmy
Hoffa, Willie Turman). Subjects circled the name that they thought was the name of a famous person. The correct answers for the recognition test also corresponded to the names of faces from the Famous Faces test
(1940s, n = 12; 1950s, n = 13; 1960s,
n = 13; 1970s, n = 14; 1980s,
n = 12; 1990s, n = 6). There was no
overlap in the items used for the completion test and the recognition
test. The Famous Names tests were administered from 1 to 12 weeks after subjects had completed the Famous Faces test.
Autobiographical memory interview (AMI). The AMI (Kopelman
et al., 1989 ) is a structured interview that asks subjects to provide detailed information concerning three periods of their lives (i.e., Childhood, Early Adult Life, and Recent Life). Within each of these
periods memory was tested for both personal semantic knowledge (e.g.,
What was your home address while attending high school?) and
autobiographical memory (e.g., Describe an incident that occurred while
you were attending elementary school.). The portion of the test that
assessed personal semantic knowledge consisted of 41 items (Childhood,
n = 12; Early Adult Life, n = 16;
Recent Life, n = 13), and the maximal possible score
for each time period was 21. The portion of the test that assessed
autobiographical memory consisted of nine items (three per time
period), and the maximum score was 9 for each time period (maximum 3 points per item, 0-3 scoring scale). For each amnesic patient, the
accuracy of all responses was established in interviews with at least
two family members whose combined familiarity with the patient spanned
virtually his/her entire lifetime. Responses were assigned a zero score if any family member identified it as inaccurate.
Word association test of autobiographical memory. A set of
48 common nouns (e.g., dog, water, school) was used to elicit
autobiographical memories, using methods described previously (Crovitz
and Schiffman, 1974 ; MacKinnon and Squire, 1989 ). The words were read
aloud one at a time, and the subjects were asked to recollect an
autobiographical episode that could be associated with each word. When
a subject failed to provide a memory that was clearly specific to time
and place, probes were given to elicit the fullest possible response. Probing was done in two ways: (1) encouragement was given to be more
specific about an already stated memory, and (2) if a subject could not
produce any episode, concrete possibilities were suggested to help the
subject recall one. When subjects reported a memory that they had
already described in response to a previous cue word, they were asked
to recollect a different memory. Finally, when a subject did describe a
specific incident, he or she was asked to estimate its date.
Twenty-four cue words were used to assess the remote time period, and
12 cue words each were used to assess the recent and middle time
periods. The years defining each time period were determined
individually for each subject. For the amnesic patients, the years of
their life before they became amnesic were partitioned into three
approximately equal-sized time periods (Recent, Middle, Remote). Only
four control subjects were tested (those matched to E.P. and G.T.), and
their Recent, Middle, and Remote time periods were defined as three
equal-sized periods covering their entire lives.
For each subject the testing required 4-10 sessions, each lasting
1-2.5 hr. An index card displaying the first and last year of the time
period of interest was in the subject's view at all times. The first
36 of the 48 cue words were used to probe all three periods. Four words
were used to probe one time period, then four more were used to probe
another time period, and so on until each of the three time periods had
been probed with 12 cue words each. All subjects were tested with the
same order of words and the same order of time periods. The final 12 cue words were used to probe only the Remote time period. Testing
sessions were tape recorded for later scoring by two independent
raters. The correlation between their scores was 0.94. Recollections
were rated on a 0-3 scale, as described previously (Zola-Morgan et al., 1983 ), and the average of the two raters' scores was used as the
score for the response to each cue word. For each amnesic patient the
accuracy of all responses was established in interviews with at least
two family members whose combined familiarity with the patient spanned
virtually his/her entire lifetime.
Information and vocabulary subscales and Boston Naming Test.
To evaluate the possible impact on our Remote memory tests of anomia and pervasive loss of general knowledge, we administered the
Information and Vocabulary subscales of the WAIS-R NI (WAIS-R as a
Neuropsychological Instrument; Kaplan et al., 1991 ). These subscales
are identical in the WAIS-R and the WAIS-R NI except that the WAIS-R NI
includes multiple choice (recognition) versions of all of the test
items. Finally, we administered the Boston Naming Test both in its
standard format (Kaplan et al., 1983 ) and in a four-alternative
multiple choice format. All testing was done in 1996.
Data analysis. Because the patients all became amnesic in a
known year, it was possible to assess each patient's anterograde and
retrograde memory function separately and then average together the
scores from appropriate time periods to obtain group means (Table
3). Test items from the decade (L.J.,
E.P., and G.T.) or three decades (A.B.) after the onset of their
amnesia were taken to measure anterograde amnesia. RA was estimated by
using test items that covered either the three decades (A.B. and L.J.) or the four decades (E.P. and G.T.) preceding the onset of amnesia. Scores from items that assessed anterograde memory function for each
patient were averaged together, and scores from items that assessed
retrograde memory function for each patient were averaged together. The
test scores of control subjects (five matched to A.B., four matched to
L.J., and four matched to E.P. and G.T.) were assigned to anterograde
and retrograde time periods in the same manner as the scores of the
patients to whom they were matched.
Given the small number of patients that we have studied, it should be
noted that the statistical methods we have used necessarily have low
power. Because of this limitation, we occasionally have pointed out
certain qualitative features of the data. Thus, it will be important to
confirm these findings with additional patients as they become
available.
 |
RESULTS |
Patients with hippocampal formation lesions
The mean scores of A.B. and L.J., the two patients with
hippocampal formation lesions, and their controls on eight tests are presented in Figure 3. On the New
Vocabulary recall test, the patients performed well on the baseline
items (patients, 91.7% correct; controls, 91.7% correct). On the
recognition version, each patient missed one item, and the control
subjects made no errors. The data from the two New Vocabulary tests in
Figure 3 were submitted to a 2 (group) × 3 (time period) ANOVA, and
the data from the other six tests in Figure 3 were submitted to a 2 (group) × 4 (time period) ANOVA. There was an interaction of group × time period for the Famous Faces recognition test, with F(3,27) = 2.97 and p < 0.05, but there were no other significant findings, with F
values < 2.3 and p values > 0.10. Individual t tests at each time period of each test also revealed no
significant group differences, with t values < 2.0 and
p values > 0.07. Nevertheless, on six of the eight
tests the amnesic patients performed numerically more poorly than the
control subjects for the period after they became amnesic, reflecting
their anterograde memory impairment. In contrast, for the period before
they became amnesic, they performed similarly overall to the control
subjects except on the Public Events Recognition test.

View larger version (26K):
[in this window]
[in a new window]
|
Figure 3.
Performance of two amnesic patients (A.B. and
L.J.) with lesions of the hippocampal formation (  ) and
nine control subjects (  ) on tests of fact knowledge.
Anterograde amnesia (AA) was measured by performance on
test items covering the period from 1970 to 1995 (for A.B.) and from
1990 to 1995 (for L.J.). Retrograde amnesia (RA) was measured by
performance on test items covering the period from 1940 to 1969 (for
A.B.) and from 1960 to 1989 (for L.J.). For their control
subjects, test items were assigned to AA and RA time periods in the
same way, i.e., the data for five subjects were partitioned to match
A.B., and the data for four subjects were partitioned to match
L.J. Performance on tests of recall is presented on the
left, and performance on recognition tests is presented
on the right. Chance levels of performance on the
recognition tests were 25%, 25%, 41.2%, and 33.3% for the New
Vocabulary, Public Events, Famous Faces, and Famous Names tests,
respectively.
|
|
To examine this pattern in the data further, we calculated each
subject's median percentage correct score across all eight tests. Then
the mean of these median scores was calculated for each group (Fig.
4). A 2 (group) × 4 (time period) ANOVA
revealed no group effect (F(1,9) = 2.27;
p > 0.15) but did reveal an interaction that
approached statistical significance (F(3,27) = 2.6; p = 0.07). Further analysis of these data
indicated that the amnesic patients were impaired significantly on
items from their period of anterograde amnesia, with t(9) = 2.28 and p < 0.05. Both patients exhibited low scores
for this time period (A.B., 71.7%; L.J., 72.5%). In contrast, they
performed about as well as control subjects on items from the three
time periods before they became amnesic, with t values < 1.2 and p values > 0.10 (A.B., 84.0%; L.J.,
78.7%). This absence of measurable RA should be interpreted
cautiously. For the period 1-10 years before amnesia, the mean score
for the two patients was numerically below the control mean on five of the eight tests. It is therefore possible that some RA was present. If
so, it was temporally limited and spanned <10 years.

View larger version (14K):
[in this window]
[in a new window]
|
Figure 4.
Performance of the two patients (A.B. and L.J.)
with hippocampal formation lesions (  ) and their controls
(  ) on all eight tests of fact knowledge listed in Figure 3. The
scores are group means that are based on each subject's median score
for the eight tests.
|
|
Performance on the AMI is shown in Figure
5. For the items assessing personal
semantic knowledge, A.B. and L.J. scored overall approximately as well
as control subjects. Note that 11 of the 13 items from the Recent Life
time period inquired about the period of anterograde amnesia. A 2 (group) × 3 (time period) ANOVA revealed no significant effects, with
F values < 1.1 and p values > 0.10. Examination of the individual data indicated that the patients generally performed well within the normal range at each of the three
time periods. The single exception was that A.B. scored just below the
lowest-scoring control subject on items from the Recent Life time
period. All of L.J.'s responses could be verified as accurate by
family members. Patient A.B. provided inaccurate responses to two items
from the Recent Life time period, and his score was adjusted from 19 to
17 points. His other responses were verified as accurate.

View larger version (20K):
[in this window]
[in a new window]
|
Figure 5.
Performance of two amnesic patients with lesions
of the hippocampal formation (open bars) and control
subjects (filled bars; n = 9)
on the Autobiographical Memory Interview (AMI). Scores for items that
assessed memory for Personal Semantic knowledge (maximum, 21) are
presented on the left, and scores for items that
assessed Autobiographical Memory (maximum, 9) are presented on the
right. Eleven of the 13 test items from the Recent time
period assessed memory for information that patients could have
acquired only subsequent to the onset of their amnesia. Accordingly,
these scores reflect primarily anterograde amnesia. The scores from the
other two time periods reflect retrograde memory function. Error bars
indicate the SEM for control subjects. Individual scores for each
patient are identified by their initials.
|
|
For autobiographical memory, A.B. and L.J. performed poorly for the
Recent Life time period and well for the two earlier time periods. In
the case of autobiographical memory, all three items from the Recent
Life time period inquired about the period of anterograde amnesia. A 2 (group) × 3 (time period) ANOVA revealed no significant effects, with
F values < 1.7 and p values > 0.10. However, separate comparisons indicated that performance was impaired for the Recent Life time period, t(9) = 2.43 and
p < 0.04, with both patients scoring below all but one
control subject. Performance was intact for the other two time periods,
with t values < 1.0. All of A.B.'s responses and all
but one of L.J.'s responses were verified as accurate. That one
response, from her Early Adult time period, could not be classified as
accurate or inaccurate by her family.
Performance on the word association test of autobiographical memory is
shown in Figure 6A.
Each recollection was scored by using the 0-3 scale. The amnesic
patients provided well formed episodic memories (scores 2.5) in
response to most of the 48 cue words (A.B. and L.J. each provided 40;
the four controls averaged 39.5 episodic memories). For patient A.B.,
25 of these 40 memories were verified as accurate by family members.
The remaining 15 memories could not be identified as accurate or
inaccurate. For patient L.J., all autobiographical memories were
verified as accurate by family members. In the analyses that follow, we
included all of the patients' recollections, except those identified
as inaccurate. When we also excluded recollections that could not be
identified as either accurate or inaccurate, the results were the
same.

View larger version (23K):
[in this window]
[in a new window]
|
Figure 6.
Performance of the two amnesic patients with
lesions limited to the hippocampal formation (open bars)
and four control subjects (shaded bars) on the word
association test of autobiographical memory. A, Mean
episodic memory scores for the three premorbid time periods that
assessed retrograde amnesia (based on 12 cue words each for the Recent
Life and Middle periods and based on 24 cue words for the Remote
period). B, The mean number of prompts provided by the
experimenter before the initiation of a well formed autobiographical
recollection that scored 2.5 points. C, The mean time
between the presentation of a cue word and the initiation of a well
formed autobiographical recollection. Filled circles
show the scores of each subject.
|
|
A 2 (group) × 3 (retrograde time period) ANOVA revealed no significant
effects; all F values were < 0.8 (Fig.
6A). Examination of the individual data indicated
that the patients generally performed well within the normal range. The
single exception was that A.B. scored below the lowest-scoring control
subject for the Recent Life retrograde time period (mean, 2.58 for
A.B.; mean, 2.75 for the lowest-scoring control subject). It is also of
interest that, of the 10 recollections that he successfully produced
from the Recent Life retrograde time period (maximum, 12), nine of them were from the earliest three years of that period, 10-13 years before
he became amnesic. Thus, A.B. exhibited evidence of ~10 years of RA
for autobiographical memory.
For each well formed autobiographical memory (scores 2.5), we also
counted the number of prompts required before obtaining a successful
episodic narrative (Fig. 6B). Patient A.B. required more prompts than control subjects for the Recent Life (mean, 5.1 for
A.B.; mean, 1.1 for controls) and the Middle (mean, 4.4 for A.B.; mean,
1.1 for controls) retrograde time periods but was within the range of
controls for the Remote time period. Patient L.J. required more prompts
than did the controls for the Middle retrograde time period (mean, 4.2 for L.J.; mean, 1.1 for controls) but was within the range of controls
for the Recent Life and Remote time periods.
We next calculated the time that elapsed between the presentation of a
cue word and the initiation of an episodic narrative (Fig.
6C). Compared with control subjects, patient A.B. was slower to initiate episodic narratives for all time periods. Patient L.J.
performed similarly to control subjects but was a little slower than
control subjects for the Middle time period. A.B.'s marked slowness in
producing well formed recollections is in accord with our experience
over the years. He is generally slow at motor and cognitive tasks.
Thus, slowness is a feature of his behavior since the onset of his
amnesia; it does not reflect a specific problem retrieving
autobiographical memories.
To assess the autobiographical recollections qualitatively, we scored
the content of each memory on the basis of previously described methods
(Johnson et al., 1988 , 1997 ) (Fig. 7).
Each well formed autobiographical memory (a score of 2.5) was scored for the amount of detail that subjects provided in 10 different categories (people, places, actions, objects, spatial, emotional, temporal, sensory-perceptual, cognitive, and factual/background). The
frequency with which each memory included details about each of these
characteristics was rated on a seven-point scale (1 = minimal
detail; 7 = maximal detail). In previous studies such rating
procedures have distinguished between memory for real and imagined
events (Johnson et al., 1988 ) and between genuine and confabulated
memories (Johnson et al., 1997 ).

View larger version (25K):
[in this window]
[in a new window]
|
Figure 7.
Mean ratings of the amount of detail provided in
each autobiographical recollection by patients with lesions limited to
the hippocampal formation (A.B., shaded bars; L.J.,
open bars) and four control subjects
(filled bars). Each memory was rated according to
the frequency with which subjects included details related to 10 memory
characteristics, using 7 point scales (1 = minimal detail; 7 = maximal detail). Sens/Perc, Sensory-perceptual
detail; Fact/Back, factual context and background
information. Error bars indicate the SEM for control subjects.
|
|
A 2 (group) × 3 (retrograde time period) × 10 (memory characteristic)
ANOVA revealed a significant effect of memory characteristic, with
F(9,36) = 35.46 and p < 0.001, indicating that there was a pattern to the content of the
recollections. Subjects provided the most amount of detail regarding
people, places, and actions and the least amount of detail concerning
cognitive, spatial, and sensory-perceptual aspects of their memories.
No other effects were significant, with F values < 1.8 and p values > 0.10. Thus, the amnesic patients
exhibited the same pattern as the control subjects. Indeed, the amnesic
patients scored within the range of the control subjects on all 10 memory characteristics.
In summary, A.B. and L.J. exhibited anterograde memory impairment but
limited RA. Significant RA for facts could not be detected, and if
retrograde memory loss is present, it appears to be temporally limited
and covers <10 years. A.B. exhibited RA for autobiographical episodes
covering approximately the decade before the onset of his amnesia. L.J.
did not exhibit detectable RA for autobiographical episodes.
Patients with postencephalitic amnesia
The mean scores of the two postencephalitic patients and
their controls on eight tests are presented in Figure
8. The patients were impaired on both the
recall and the recognition versions of the baseline items from the New
Vocabulary test (41.7% and 62.5% correct for the patients; 95.9% and
95.8% correct for the controls; p values < 0.05).
Thus, these two patients were impaired in accessing word meanings.

View larger version (30K):
[in this window]
[in a new window]
|
Figure 8.
Performance of two postencephalitic amnesic
patients (  ) and four control subjects (  ) on tests of
retrograde memory for semantic knowledge. Anterograde amnesia
(AA) was measured by performance on test items covering
the period from 1990 to 1995. RA was measured by performance on test
items covering the period from 1950 to 1989. The New Vocabulary tests
did not include items from the period of anterograde amnesia for
patients E.P. and G.T. Performance on tests of recall is presented on
the left, and performance on recognition tests is
presented on the right. Chance levels of performance on
the recognition tests were 25%, 25%, 41.2%, and 33.3% for the New
Vocabulary, Public Events, Famous Faces, and Famous Names tests,
respectively.
|
|
The data from the New Vocabulary tests in Figure 8 were submitted to a
2 (group) × 4 (time period) ANOVA, and the data from the other six
tests in Figure 8 were submitted to a 2 (group) × 5 (time period)
ANOVA. The patients were impaired severely on every test (F
values > 12.0; p values < 0.03). Significant
group × time period interactions were obtained for the New
Vocabulary recognition test (F(3,12) = 19.4;
p < 0.001) and for the Famous Names Completion test
(F(4,16) = 6.18; p < 0.01). On
five of the eight tests (Public Events Recall and Recognition, Famous
Faces Recall and Recognition, and Famous Names Recognition), the
patients performed at floor levels across all time periods. When they
performed above floor levels, their retrograde memory impairment for
knowledge of events and people was similar to their memory impairment
for general semantic knowledge (i.e., word meanings).
Performance also was examined by calculating the average performance
across the eight tests (Fig. 9), using
the same method that was used for the patients with hippocampal
formation lesions. The patients were severely impaired
(F(1,4) = 119.3; p < 0.001), and there was no interaction of group × time period
(F(4,16) = 2.18; p > 0.11).
Separate comparisons between groups revealed impaired performance at
every time period, with t values > 5.7 and
p values < 0.005.

View larger version (15K):
[in this window]
[in a new window]
|
Figure 9.
Performance of the two postencephalitic amnesic
patients (  ) and their controls (  ) on all eight tests of
RA shown in Figure 6. The scores are group means that are based on each
subject's median score for the eight tests.
|
|
Performance on the AMI is shown in Figure 10. With one exception, all
of E.P.'s and G.T.'s responses could be verified by family members.
The exception was one of E.P.'s autobiographical memories from the
Childhood period. Because the two patients performed differently, their
scores are considered separately. The very poor performance of E.P. and
G.T. (for both personal semantic memory and autobiographical memory) on
items from the Recent Life time period is consistent with their severe
anterograde memory impairment. They either gave no response or they
responded inaccurately, or more commonly they provided information
appropriate to earlier time periods. For the Early Adult Life period,
personal semantic memory was impaired, and the patients each scored
>13 SD below the control subjects. For autobiographical memory,
E.P.'s score for Early Adult Life was at the lower end of the range of
control subjects, and G.T. received no points at all. For the Childhood period, E.P.'s performance was normal for both personal semantic memory and autobiographical memory (Table
4). Indeed, he scored nearly as high as
the highest-scoring control subject for both tests. In contrast, G.T.
was severely impaired on both tests. For personal semantic information,
G.T.'s score (5 points) was lower than the score of the lowest-scoring
control subject (8 points). For autobiographical memory, G.T. received
no points for the Childhood period. Thus, E.P. demonstrated sparing of
both personal semantic and autobiographical memory from his childhood, whereas G.T. exhibited severe RA across all time periods tested.
A similar pattern of RA for autobiographical events was found with the
word association test of autobiographical memory. In response to the 48 cue words, patient E.P. provided only 24 episodic autobiographical
memories (ones that scored 2.5). Four of these were identified as
inaccurate by family members. Of the remaining 20 memories, 15 were
verified as accurate (0 from the Recent Life period, 3 from the Middle
period, and 12 from the Remote period). The remaining five memories
could not be identified by family members as either accurate or
inaccurate.
Patient G.T. provided 18 episodic autobiographical memories, but 10 of
these were identified as inaccurate. Of the remaining eight memories,
four were identified as accurate (all from the Remote period). The
remaining four (two each from the Middle and Remote periods) could not
be identified as either accurate or inaccurate.
The scores obtained by E.P. and G.T. on the word association test of
autobiographical memory were similar to their scores on the
autobiographical portion of the AMI. Patient E.P. performed poorly for
the Recent Life and Middle retrograde time periods (scores were 0.8 and
1.7, respectively; compare with Fig. 6A). For the
Remote retrograde time period, however, E.P.'s score (2.3) was within
2 SD of the control score (mean, 2.7; SD = 0.3). Patient G.T.
performed poorly in each retrograde time period (1.2, 1.5, and 1.5 for
the Recent Life, Middle, and Remote time periods, respectively).
For the Remote retrograde time period in which E.P. performed
relatively well, the number of prompts required before initiating his
recollections (mean, 2.0) was within the range of control subjects
(1.1-4.2). In addition, the time needed to initiate his recollections
(2.5 min) was within the range of control subjects (1.6-5.2 min).
Finally, E.P.'s 16 memories from the Remote time period were scored
for detail according to the same 10 memory characteristics used to
evaluate the other patients. E.P. scored within the range of control
subjects on all 10 characteristics.
In summary, both E.P. and G.T. exhibited severe and extensive RA for
both facts and events. E.P. was able to recall facts and events from
his early life (Fig. 10).

View larger version (15K):
[in this window]
[in a new window]
|
Figure 10.
Performance of two postencephalitic amnesic
patients (open bars) and control subjects
(filled bars; n = 4) on the
Autobiographical Memory Interview (AMI). Scores for items that assessed
memory for Personal Semantic knowledge (maximum, 21 for each time
period) are presented on the left, and scores for items
that assessed memory for Autobiographical Memory (maximum, 9 for each
time period) are presented on the right. Test items
associated with the Recent time period assessed memory for information
that could have been acquired only subsequent to the onset of amnesia.
The scores from the other two periods reflect retrograde memory
function. For the control subjects, error bars indicate the SEM. The
performance of each patient is shown separately.
|
|
Other neuropsychological tests
Figure 11 shows performance on the
Information and Vocabulary subscales of the WAIS-R NI and on the Boston
Naming Test. The two patients with hippocampal formation lesions
performed identically to the controls on all of the tests (t
values < 1.0; p values > 0.39). The
postencephalitic patients performed differently. E.P.'s scores were
within the normal range for both forms of the Information test, but
G.T. scored >2 SD below control subjects on both forms. E.P. and G.T.
also were impaired on both forms of the Vocabulary test, scoring >3 SD
below the control subjects. This finding is consistent with their
impaired baseline performance on the New Vocabulary tests. Finally,
E.P. and G.T. both scored >5 SD below control subjects on the two
forms of the Boston Naming Test. G.T. was more impaired than E.P. on
these tests, presumably because his lesion includes much of the
temporal lobe, whereas E.P.'s lesion does not extend as far
laterally.

View larger version (19K):
[in this window]
[in a new window]
|
Figure 11.
Mean scores of all 13 control subjects
(filled bars), two amnesic patients with lesions
of the hippocampal formation (A.B. and L.J.), and two postencephalitic
amnesic patients (E.P. and G.T.) on the Information subtest of the
Wechsler Adult Intelligence Scale-Revised as a Neuropsychological
Instrument (WAIS-R NI), the Vocabulary subtest of the WAIS-R NI, and
the Boston Naming Test. Each patient's score is identified by his or
her initials. Performance on the recall version of each
test is presented on the left side of each panel, and
performance on a recognition form of the same test is presented on the
right side. The maximum possible scores for the
Information subtest, the Vocabulary subtest, and the Boston Naming Test
are 29, 70, and 60, respectively. For the control subjects, error bars
indicate the SEM.
|
|
 |
DISCUSSION |
Patients with hippocampal formation lesions
Patients A.B. and L.J. exhibited a discontinuity between premorbid
and postmorbid memory. They were impaired at remembering facts and
events from the period after they became amnesic but were much better
at remembering facts and events from the period before they became
amnesic (see Figs. 3, 4, 5, 6). These findings indicate that the brain
structures damaged in these two patients are important for establishing
new memories about facts and events but are less involved in
recollecting memories that already were established several years
earlier. This distinction between establishing new memories and
recollecting old ones depends on having assessed the postmorbid and
premorbid time periods with the same type of test item, as we did in
the current study.
Fact learning after hippocampal formation lesions
Several studies have documented impaired learning of new facts and
vocabulary words in amnesic patients with medial temporal lobe lesions
(Marslen-Wilson and Teuber, 1975 ; Schacter et al., 1984 ; Glisky et al.,
1986 ; Shimamura and Squire, 1987 ; Gabrieli et al., 1988 ; Hamann and
Squire, 1995 ). Other studies have reported that patients with medial
temporal lobe lesions, in addition to their anterograde amnesia, also
have difficulty recollecting factual information from the period before
the onset of their amnesia (Corkin, 1984 ; Beatty et al., 1987 ; Salmon
et al., 1988 ; Kopelman et al., 1989 ; Squire et al., 1989 ; Kartsounis et
al., 1995 ; Rempel-Clower et al., 1996 ; Schmidtke and Vollmer,
1997 ).
The findings for A.B. and L.J. are consistent with previous reports in
showing deficient acquisition of new factual knowledge about
vocabulary, famous people, and public events. These two patients,
together with the patient described by Kartsounis and colleagues
(1995) , appear to be the only instances in which this point has been
established for patients with lesions thought to be limited to the
hippocampal formation. One other report described three children who
sustained hippocampal damage early in life, who nevertheless attended
mainstream schools and by the ages of 12-19 had acquired levels of
factual knowledge in the low-average to average range (Vargha-Khadem et
al., 1997 ). Because the rate of factual learning that occurred during
childhood is unknown, the findings for these three individuals do not
contradict the generalization that new fact learning is impaired by
hippocampal pathology. Nevertheless, this report and others (Corkin,
1984 ; Glisky et al., 1986 ; Hamann and Squire, 1995 ) emphasize the point that repetition, day after day and across multiple learning
opportunities, in the fullness of time can provide amnesic patients
with a considerable fund of factual knowledge. The present finding that
A.B. and L.J. possess deficient factual knowledge about the years since
the onset of their amnesia shows that factual knowledge does not accrue inevitably to normal levels in the face of hippocampal pathology.
Event memory after hippocampal formation lesions
For patients with circumscribed medial temporal lobe lesions,
several studies have reported RA for autobiographical material (Kopelman et al., 1989 ; MacKinnon and Squire, 1989 ; Victor and Agamanolis, 1990 ; Kartsounis et al., 1995 ; Rempel-Clower et al., 1996 ;
Schmidtke and Vollmer, 1997 ). Some of these studies report a general
difficulty in producing autobiographical recollections, and others
describe impairments that are limited to the recent postmorbid period.
One difficulty with this literature is that it has not been possible in
many cases to determine the extent of the lesion or the likelihood that
some damage has occurred outside the medial temporal lobe (especially
in cortex adjacent to the medial temporal lobe). Another difficulty
lies simply in the problem of how to estimate the severity and extent
of memory loss for personal events. There are few standardized tests
available, and often the recollections cannot be validated. Finally,
assessing the quality of autobiographical recollections is beset by the additional problem that anterograde amnesia may impede the
reconstruction of a past memory. That is, to the extent that
recollecting the past requires an amnesic patient to hold material in
working memory while engaging in strategic search, the task of
reconstruction might itself depend on anterograde memory function.
In view of these difficulties, the key to understanding similarities
and differences in how RA presents itself lies in obtaining as much
information as possible about the underlying neuropathology. During the
past 15 years four amnesic patients with hippocampal formation lesions
came to autopsy, and their brains were examined in considerable
neurohistological detail (Zola-Morgan et al., 1986 ; Rempel-Clower et
al., 1996 ). All of the patients had been evaluated formally with
respect to anterograde and RA, using many of the same tests that were
given to patients A.B. and L.J. Two of the patients (R.B. and G.D.)
proved to have bilateral lesions limited to the CA1 field of the
hippocampus, and they had a moderate level of anterograde amnesia and
RA limited to perhaps a few years at the most. The other two patients
(L.M. and W.H.) had lesions involving all of the hippocampal cell
fields, the dentate gyrus, and some cell loss in the entorhinal cortex
(as well as subicular damage for W.H.). L.M. had moderate anterograde
amnesia and an estimated 15 years of RA. W.H. had severe
anterograde amnesia and as many as 25 years of RA. The findings for
A.B. and L.J. would appear to place them intermediate in severity
between R.B. and G.D. on the one hand, and L.M. and W.H. on the
other.
In the context of these findings, it is useful to consider another
patient who had abnormal MRI signals in the CA1 and CA2 fields after a
seizure and who was poor at producing autobiographical recollections
from virtually every period of his adult life (Kartsounis et al.,
1995 ). Considering that this patient had a history of heavy drinking,
pulmonary disease, and a history of cerebral ischemia and seizures, it
seems unlikely that his damage could be limited to the CA fields of the
hippocampus. Postmortem histological analysis will be important in this
case to determine the areas of damage.
Although histological information is not available for the two patients
reported here (A.B. and L.J.), it is noteworthy that they also were
capable of accurate autobiographical recollections. Moreover, the
recollections of these two patients exhibited the same pattern of
characteristics as the recollections of control subjects (see Fig. 7).
These findings count against the suggestion that the hippocampal
formation is needed to retrieve autobiographical memories throughout
life (Nadel and Moscovitch, 1997 ). The available data would appear to
favor an earlier idea (Cohen and Squire, 1981 ), recently articulated by
Verfaellie and colleagues (1995) : "... learning of any kind,
whether it be episodic or semantic, may be more impaired in amnesia
when information was acquired recently rather than remotely" (p
451).
Patients with postencephalitic amnesia
The findings for these two patients are similar in some respects
to previous reports of extensive, "flat" gradients of RA in
postencephalitic amnesia [patient S.S., Cermak and O'Connor (1983) ;
patient D.R.B., Damasio et al. (1985) ; and patient R.F.R., Warrington
and McCarthy (1988) ]. Extensive remote memory impairment also has been
described after temporal lobectomy (Barr et al., 1990 ; Warrington and
Duchen, 1992 ) or temporal lobe infarction (Schnider et al., 1994 ). In
virtually all of these cases, as well as in patient G.T., there is
evidence of lateral temporal cortical damage in addition to medial
temporal lobe pathology. A common interpretation of extensive, ungraded
RA is that damage has occurred to knowledge stores, thereby affecting
the ability to recollect information regardless of when it was learned
(Kapur, 1993 ; Kapur et al., 1996 ).
E.P.'s RA was not so severe as G.T.'s. His RA was severe and
extensive, but unlike G.T., E.P. was capable of considerable recall
from his early life. Thus, unlike other patients with postencephalitic amnesia (e.g., patients D.R.B., S.S., and R.F.R.) who are described as
incapable of episodic remembering, E.P.'s narrative episodes from his
early life contained the same kind of detail and structure as the
narrative episodes recalled by our control subjects (Table 4).
Inevitably, the question arises whether the narratives produced by
severely amnesic patients are true remembrances or whether they are
drawn from a collection of a few over-rehearsed stories (cf. Cermak and
O'Connor, 1983 ). In view of the fact that even recollections from
healthy individuals often have this character, it is unclear how to
decide the point. E.P. does appear to be capable of autobiographical
remembering, although we recognize that methods might yet be devised to
show that his recollections are somehow impoverished or imperfect, in
comparison with those of healthy persons.
E.P.'s severe and extensive RA is likely attributable to the fact that
his lesion includes the medial temporal cortex (perirhinal and
parahippocampal cortices), not just the hippocampal formation, and it
also extends laterally from the medial temporal lobe to include the
fusiform gyrus at some levels. At the same time, E.P.'s residual
capacity for very remote memory is probably attributable to the fact
that his lesion did not extend as far into lateral temporal cortex as
the lesion in G.T. or other patients with pervasive impairments of
episodic remembering. Thus, it is possible that damage in addition to
the hippocampal formation that includes medial temporal cortex and
fusiform gyrus is sufficient to cause severe and extensive RA. Such
damage appears to spare both episodic and semantic remembering of facts
and events from early life so long as the damage does not include more
lateral temporal cortex.
It is also worth noting that both E.P. and G.T. performed differently
on the Famous Name Completion test and the Famous Names Recognition
test than the postencephalitic patient R.F.R. (Warrington and McCarthy,
1988 ). R.F.R. exhibited no deficit at all when tests about famous
persons were redesigned to assess simple familiarity for names or name
completion ability. E.P. and G.T., as well as two patients studied
previously (patient W.I. and patient D.R.B.; Squire et al., 1990 ),
improved their performance when the tests were administered in the
revised format, but they remained distinctly impaired. The revised test
was rather easy for R.F.R., and ceiling effects might have obscured an
impairment. Alternatively, the neuropathology responsible for R.F.R.'s
impairment may prove to be different in some important way from that of
the other four patients who have been given these tests.
In summary, the findings suggest that RA can be quite limited or very
extensive, depending on whether the damage is restricted to the
hippocampal formation or also involves additional temporal cortex. At
the same time, it must be emphasized that the number of patients with
medial temporal lobe lesions or even larger temporal lobe lesions who
have been studied carefully with respect to RA is small, and an even
smaller number of patients have been studied postmortem to obtain
neurohistological data about the extent of the lesion.
 |
FOOTNOTES |
Received Dec. 18, 1997; revised Feb. 26, 1998; accepted March 4, 1998.
This research was supported by the Medical Research Service of the
Department of Veterans Affairs, National Institute of Mental Health
Grant MH24600, and National Institutes of Health Grant T32 AG00216. We
thank Joyce Zouzounis, James Moore, Nicole Champagne, Lisa Stefanacci,
and Stuart Zola for assistance.
Correspondence should be addressed to Dr. Larry R. Squire, Veterans
Affairs Medical Center 116A, 3350 La Jolla Village Drive, San Diego, CA
92161.
 |
REFERENCES |
-
Albert MS,
Butters N,
Levin J
(1979)
Temporal gradients in the retrograde amnesia of patients with alcoholic Korsakoff's disease.
Arch Neurol
36:211-216[Abstract].
-
Barr WB,
Goldberg E,
Wasserstein J,
Novelly RA
(1990)
Retrograde amnesia following unilateral temporal lobectomy.
Neuropsychologia
28:243-256[ISI][Medline].
-
Beatty WW,
Salmon DP,
Bernstein N,
Butters N
(1987)
Remote memories in a patient with amnesia due to hypoxia.
Psychol Med
17:657-665[ISI][Medline].
-
Cermak LS,
O'Connor M
(1983)
The anterograde and retrograde retrieval ability of a patient with amnesia due to encephalitis.
Neuropsychologia
19:213-224.
-
Cohen N,
Squire LR
(1981)
Retrograde amnesia and remote memory impairment.
Neuropsychologia
119:337-356.
-
Corkin S
(1984)
Lasting consequences of bilateral medial temporal lobectomy: clinical course and experimental findings in H.M.
Semin Neurol
4:249-259[ISI].
-
Crovitz HF,
Schiffman H
(1974)
Frequency of episodic memories as a function of their age.
Bull Psychonom Soc
4:517-518.[ISI]
-
Damasio AR,
Eslinger PJ,
Damasio H,
Van Hoesen GW,
Cornell S
(1985)
Multimodal amnesic syndrome following bilateral temporal and basal forebrain damage.
Arch Neurol
42:252-259[Abstract].
-
Gabrieli J,
Cohen N,
Corkin S
(1988)
The impaired learning of semantic knowledge following bilateral medial temporal-lobe resection. Special issue: single-case studies in amnesia: theoretical advances.
Brain Cogn
7:157-177[ISI][Medline].
-
Glisky EL,
Schacter DL,
Tulving E
(1986)
Computer learning by memory-impaired patients: acquisition and retention of complex knowledge.
Neuropsychologia
24:313-328[ISI][Medline].
-
Hamann SB,
Squire LR
(1995)
On the acquisition of new declarative knowledge in amnesia.
Behav Neurosci
109:1027-1044[ISI][Medline].
-
Hamann SB,
Squire LR,
Stefanacci L,
Adolphs R,
Damasio H,
Damasio A
(1996)
Intact perception of facial emotion despite bilateral amygdala lesions.
Nature
379:497[Medline].
-
Hodges JR
(1994)
Retrograde amnesia.
In: Handbook of memory disorders (Baddeley A,
Wilson BA,
Watts F,
eds), pp 81-107. New York: Wiley.
-
Johnson MK,
Foley MA,
Suengas AG,
Raye CL
(1988)
Phenomenal characteristics of memories for perceived and imagined autobiographical events.
J Exp Psychol Gen
117:371-376[ISI][Medline].
-
Johnson MK,
O'Connor M,
Cantor J
(1997)
Confabulation, memory deficits, and frontal dysfunction.
Brain Cogn
4:189-206.
-
Kaplan EF,
Goodglass H,
Weintraub S
(1983)
In: The Boston naming test. Philadelphia: Febiger.
-
Kaplan EF,
Fein D,
Morris R,
Delis D
(1991)
In: WAIS-R as a neuropsychological instrument. New York: Psychological Corporation.
-
Kapur N
(1993)
Focal retrograde amnesia in neurological disease: a critical review.
Cortex
29:217-234[ISI][Medline].
-
Kapur N,
Scholey K,
Moore E,
Barker S,
Brice J,
Thompson S,
Shiel A,
Carr R,
Abbot P,
Fleming J
(1996)
Long-term retention deficits in two cases of disproportionate retrograde amnesia.
J Cogn Neurosci
8:416-434.
-
Kartsounis LD,
Rudge P,
Stevens JM
(1995)
Bilateral lesions of CA1 and CA2 fields of the hippocampus are sufficient to cause a severe amnesic syndrome in humans.
J Neurol Neurosurg Psychiatry
59:95-98[Abstract].
-
Kopelman MD,
Wilson BA,
Baddeley AD
(1989)
The autobiographical memory interview: a new assessment of autobiographical and personal semantic memory in amnesic patients.
J Clin Exp Neuropsychol
5:724-744.
-
Kritchevsky M,
Squire LR,
Zouzounis JA
(1988)
Transient global amnesia: characterization of anterograde and retrograde amnesia.
Neurology
38:213-219[Abstract/Free Full Text].
-
MacKinnon D,
Squire LR
(1989)
Autobiographical memory in amnesia.
Psychobiology
17:247-256.
-
Marslen-Wilson WD,
Teuber HL
(1975)
Memory for remote events in anterograde amnesia: recognition of public figures from news photographs.
Neuropsychologia
13:353-364[ISI][Medline].
-
Nadel L,
Moscovitch M
(1997)
Memory consolidation, retrograde amnesia, and the hippocampal complex.
Curr Opin Neurobiol
7:217-227[ISI][Medline].
-
Osterrieth PA
(1944)
Le test de copie d'une figure complexe [The test of copying a complex figure].
Arch Psychol
30:206-356.
-
Penfield W,
Mathieson G
(1974)
Memory: autopsy findings and comments on the role of hippocampus in experiential recall.
Arch Neurol
31:145-154[ISI][Medline].
-
Rempel-Clower N,
Zola SM,
Squire LR,
Amaral DG
(1996)
Three cases of e
|