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Page 1
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: gomes lhf. Genes (Basel). 2021 Jul 13;12(7):1069. doi: 10.3390/genes12071069. Genes (Basel). 2021. PMID: 34356085 Free PMC article.
Molecular alterations in the extracellular matrix in the brains of newborns with congenital Zika syndrome.
Aguiar RS, Pohl F, Morais GL, Nogueira FCS, Carvalho JB, Guida L, Arge LWP, Melo A, Moreira MEL, Cunha DP, Gomes L, Portari EA, Velasquez E, Melani RD, Pezzuto P, de Castro FL, Geddes VEV, Gerber AL, Azevedo GS, Schamber-Reis BL, Gonçalves AL, Junqueira-de-Azevedo I, Nishiyama MY Jr, Ho PL, Schanoski AS, Schuch V, Tanuri A, Chimelli L, Vasconcelos ZFM, Domont GB, Vasconcelos ATR, Nakaya HI. Aguiar RS, et al. Sci Signal. 2020 Jun 9;13(635):eaay6736. doi: 10.1126/scisignal.aay6736. Sci Signal. 2020. PMID: 32518143 Clinical Trial.
Whole-exome sequencing reveals insights into genetic susceptibility to Congenital Zika Syndrome.
Borda V, da Silva Francisco Junior R, Carvalho JB, Morais GL, Duque Rossi Á, Pezzuto P, Azevedo GS, Schamber-Reis BL, Portari EA, Melo A, Moreira MEL, Guida LC, Cunha DP, Gomes L, Vasconcelos ZFM, Faucz FR, Tanuri A, Stratakis CA, Aguiar RS, Cardoso CC, Vasconcelos ATR. Borda V, et al. PLoS Negl Trop Dis. 2021 Jun 14;15(6):e0009507. doi: 10.1371/journal.pntd.0009507. eCollection 2021 Jun. PLoS Negl Trop Dis. 2021. PMID: 34125832 Free PMC article.
Congenital Zika Syndrome Is Associated With Interferon Alfa Receptor 1.
Azamor T, Cunha DP, da Silva AMV, Bezerra OCL, Ribeiro-Alves M, Calvo TL, Kehdy FSG, Manta FSN, Pinto TGT, Ferreira LP, Portari EA, Guida LDC, Gomes L, Moreira MEL, de Carvalho EF, Cardoso CC, Muller M, Ano Bom APD, Neves PCDC, Vasconcelos Z, Moraes MO. Azamor T, et al. Front Immunol. 2021 Nov 25;12:764746. doi: 10.3389/fimmu.2021.764746. eCollection 2021. Front Immunol. 2021. PMID: 34899713 Free PMC article.
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: gomes lhf. 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.
Decidual production of interferon lambda in response to ZIKV persistence: Clinical evidence and in vitro modelling.
Azamor T, Cunha DP, Nobre Pires KS, Lira Tanabe EL, Melgaço JG, Vieira da Silva AM, Ribeiro-Alves M, Calvo TL, Tubarão LN, da Silva J, Fernandes CB, Fonseca de Souza A, Torrentes de Carvalho A, Avvad-Portari E, da Cunha Guida L, Gomes L, Lopes Moreira ME, Dinis Ano Bom AP, Cristina da Costa Neves P, Missailidis S, Vasconcelos Z, Borbely AU, Moraes MO. Azamor T, et al. Heliyon. 2024 May 3;10(9):e30613. doi: 10.1016/j.heliyon.2024.e30613. eCollection 2024 May 15. Heliyon. 2024. PMID: 38737240 Free PMC article.
26 results