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Year Number of Results
2004 1
2017 1
2020 3
2021 3
2022 2
2023 3
2024 1

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12 results

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Page 1
ATP8A2-Related Disorder: Beyond Cerebellar Ataxia.
Alves Corazza L, Lopes Braga V, Yoshinaga Tonholo Silva T, Moura Rezende Filho F, Ferraz Sallum JM, Graziani Povoas Barsottini O, Pedroso JL. Alves Corazza L, et al. Among authors: ferraz sallum jm. Mov Disord Clin Pract. 2023 Jun 30;10(8):1215-1216. doi: 10.1002/mdc3.13820. eCollection 2023 Aug. Mov Disord Clin Pract. 2023. PMID: 37635783 No abstract available.
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: ferraz sallum jm. Ophthalmic Genet. 2020 Apr;41(2):189-193. doi: 10.1080/13816810.2020.1747084. Epub 2020 Apr 9. Ophthalmic Genet. 2020. PMID: 32270730
TRANSPLANTATION OF SUBRETINAL STEM CELL-DERIVED RETINAL PIGMENT EPITHELIUM FOR STARGARDT DISEASE: A Phase I Clinical Trial.
Brant Fernandes RA, Lojudice FH, Zago Ribeiro L, Santos da Cruz NF, Polizelli MU, Cristovam PC, Innocenti F, Morimoto L, Magalhães O Jr, Ferraz Sallum JM, Penha FM, Sogayar MC, Belfort R Jr, Maia M. Brant Fernandes RA, et al. Among authors: ferraz sallum jm. Retina. 2023 Feb 1;43(2):263-274. doi: 10.1097/IAE.0000000000003655. Retina. 2023. PMID: 36223778 Clinical Trial.
Expanding the clinical phenotype in patients with disease causing variants associated with atypical Usher syndrome.
Igelman AD, Ku C, da Palma MM, Georgiou M, Schiff ER, Lam BL, Sankila EM, Ahn J, Pyers L, Vincent A, Ferraz Sallum JM, Zein WM, Oh JK, Maldonado RS, Ryu J, Tsang SH, Gorin MB, Webster AR, Michaelides M, Yang P, Pennesi ME. Igelman AD, et al. Among authors: ferraz sallum jm. Ophthalmic Genet. 2021 Dec;42(6):664-673. doi: 10.1080/13816810.2021.1946704. Epub 2021 Jul 5. Ophthalmic Genet. 2021. PMID: 34223797 Free PMC article.
Association of Sex With Frequent and Mild ABCA4 Alleles in Stargardt Disease.
Runhart EH, Khan M, Cornelis SS, Roosing S, Del Pozo-Valero M, Lamey TM, Liskova P, Roberts L, Stöhr H, Klaver CCW, Hoyng CB, Cremers FPM, Dhaenens CM; Disease Consortium Study Group. Runhart EH, et al. JAMA Ophthalmol. 2020 Oct 1;138(10):1035-1042. doi: 10.1001/jamaophthalmol.2020.2990. JAMA Ophthalmol. 2020. PMID: 32815999 Free PMC article.
Clinical and Genetic Characterization of RDH12-Retinal Dystrophy in a South American Cohort.
Daich Varela M, Moya R, Azevedo Souza Amaral R, Schlottmann PG, Álvarez Mendiara A, Francone A, Guazi Resende R, Capalbo L, Gelvez N, López G, Morales-Acevedo AM, Ossa RH, Arno G, Michaelides M, Tamayo ML, Ferraz Sallum JM. Daich Varela M, et al. Among authors: ferraz sallum jm. Ophthalmol Retina. 2024 Feb;8(2):163-173. doi: 10.1016/j.oret.2023.09.007. Epub 2023 Sep 13. Ophthalmol Retina. 2024. PMID: 37714431 Free article.
PROM1 gene variations in Brazilian patients with macular dystrophy.
Salles MV, Motta FL, Dias da Silva E, Varela Lima Teixeira P, Antunes Costa K, Filippelli-Silva R, Martin R, Pesquero JB, Ferraz Sallum JM. Salles MV, et al. Among authors: ferraz sallum jm. Ophthalmic Genet. 2017 Jan-Feb;38(1):39-42. doi: 10.1080/13816810.2016.1275022. Epub 2017 Jan 17. Ophthalmic Genet. 2017. PMID: 28095140
12 results