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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2008 5
2009 7
2012 4
2013 3
2014 2
2015 2
2016 2
2017 5
2018 5
2019 5
2020 6
2021 4
2022 1
2023 3
2024 0

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47 results

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Page 1
Macular dystrophies associated with Stargardt-like phenotypes.
Amaral RAS, Zin OA, Salles MV, Motta FL, Sallum JMF. Amaral RAS, et al. Among authors: motta fl. Arq Bras Oftalmol. 2023 Mar 24:S0004-27492023005002303. doi: 10.5935/0004-2749.2021-0415. Online ahead of print. Arq Bras Oftalmol. 2023. PMID: 36995812 Free article.
TUBGCP4 - associated microcephaly and chorioretinopathy.
Da Palma MM, Motta FL, Takitani GEDS, Salles MV, Lima LH, Ferraz Sallum JM. Da Palma MM, et al. Among authors: motta fl. Ophthalmic Genet. 2020 Apr;41(2):189-193. doi: 10.1080/13816810.2020.1747084. Epub 2020 Apr 9. Ophthalmic Genet. 2020. PMID: 32270730
Retinal dystrophies and variants in PRPH2.
Palma MMD, Martin D, Salles MV, Motta FLT, Abujamra S, Sallum JMF. Palma MMD, et al. Among authors: motta flt. Arq Bras Oftalmol. 2019 Mar-Apr;82(2):158-160. doi: 10.5935/0004-2749.20190033. Arq Bras Oftalmol. 2019. PMID: 30726412 Free article.
Retinitis Pigmentosa Due to Rp1 Biallelic Variants.
Silva RS, Salles MV, Motta FL, Sallum JMF. Silva RS, et al. Among authors: motta fl. Sci Rep. 2020 Jan 31;10(1):1603. doi: 10.1038/s41598-020-58243-9. Sci Rep. 2020. PMID: 32005865 Free PMC article.
Novel Mutation in CRYBB3 Causing Pediatric Cataract and Microphthalmia.
Zin OA, Neves LM, Motta FL, Horovitz DDG, Guida L, Gomes LHF, Cunha DP, Rodrigues APS, Zin AA, Sallum JMF, Vasconcelos ZFM. Zin OA, et al. Among authors: motta fl. Genes (Basel). 2021 Jul 13;12(7):1069. doi: 10.3390/genes12071069. Genes (Basel). 2021. PMID: 34356085 Free PMC article.
47 results