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Page 1
Building a National Policy for Rare Disease in Brazil.
Félix TM, Oliveira BM, Horovitz DDG. Félix TM, et al. Among authors: horovitz ddg. J Community Genet. 2024 Sep 26. doi: 10.1007/s12687-024-00732-9. Online ahead of print. J Community Genet. 2024. PMID: 39325316 Review.
The cost of genetic diagnosis of suspected hereditary pediatric cataracts with whole-exome sequencing from a middle-income country perspective: a mixed costing analysis.
Neves LM, Pinto M, Zin OA, Cunha DP, Agonigi BNS, Motta FL, Gomes LHF, Horovitz DDG, Almeida DC Jr, Malacarne J, Guida L, Braga A, Carvalho AB, Pereira E, Rodrigues APS, Sallum JMF, Zin AA, Vasconcelos ZFM. Neves LM, et al. Among authors: horovitz ddg. J Community Genet. 2024 Jun;15(3):235-247. doi: 10.1007/s12687-024-00708-9. Epub 2024 May 10. J Community Genet. 2024. PMID: 38730191 Free PMC article.
Genotypic-Phenotypic Correlations of Hereditary Hyperferritinemia-Cataract Syndrome: Case Series of Three Brazilian Families.
Zin OA, Neves LM, Cunha DP, Motta FL, Agonigi BNS, Horovitz DDG, Almeida DC Jr, Malacarne J, Rodrigues APS, Carvalho AB, Rivello CA, Espariz R, Zin AA, Sallum JMF, Vasconcelos ZFM. Zin OA, et al. Among authors: horovitz ddg. Int J Mol Sci. 2023 Jul 25;24(15):11876. doi: 10.3390/ijms241511876. Int J Mol Sci. 2023. PMID: 37569253 Free PMC article.
Venous anomalies in hypoplastic posterior fossa: unsolved questions.
Protzenko T, Bellas A, Ribeiro CMC, Gonzalez SMC, Horovitz DDG. Protzenko T, et al. Among authors: horovitz ddg. Childs Nerv Syst. 2021 Oct;37(10):3177-3187. doi: 10.1007/s00381-021-05315-4. Epub 2021 Aug 18. Childs Nerv Syst. 2021. PMID: 34406451 Review.
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: horovitz ddg. Genes (Basel). 2021 Jul 13;12(7):1069. doi: 10.3390/genes12071069. Genes (Basel). 2021. PMID: 34356085 Free PMC article.
55 results