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Possible Association Between Zika Virus Infection and Microcephaly - Brazil, 2015.
MMWR Morb Mortal Wkly Rep. 2016 Jan 29;65(3):59-62. doi: 10.15585/mmwr.mm6503e2.
MMWR Morb Mortal Wkly Rep. 2016.
PMID: 26820244
Free article.
Epidemiology of rare diseases in Brazil: protocol of the Brazilian Rare Diseases Network (RARAS-BRDN).
Félix TM, de Oliveira BM, Artifon M, Carvalho I, Bernardi FA, Schwartz IVD, Saute JA, Ferraz VEF, Acosta AX, Sorte NB, Alves D; RARAS Network group.
Félix TM, et al.
Orphanet J Rare Dis. 2022 Feb 24;17(1):84. doi: 10.1186/s13023-022-02254-4.
Orphanet J Rare Dis. 2022.
PMID: 35209917
Free PMC article.
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Mutations, clinical findings and survival estimates in South American patients with X-linked adrenoleukodystrophy.
Pereira Fdos S, Matte U, Habekost CT, de Castilhos RM, El Husny AS, Lourenço CM, Vianna-Morgante AM, Giuliani L, Galera MF, Honjo R, Kim CA, Politei J, Vargas CR, Jardim LB.
Pereira Fdos S, et al. Among authors: el husny as.
PLoS One. 2012;7(3):e34195. doi: 10.1371/journal.pone.0034195. Epub 2012 Mar 29.
PLoS One. 2012.
PMID: 22479560
Free PMC article.
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Clinicogenetic lessons from 370 patients with autosomal recessive limb-girdle muscular dystrophy.
Winckler PB, da Silva AMS, Coimbra-Neto AR, Carvalho E, Cavalcanti EBU, Sobreira CFR, Marrone CD, Machado-Costa MC, Carvalho AAS, Feio RHF, Rodrigues CL, Gonçalves MVM, Tenório RB, Mendonça RH, Cotta A, Paim JFO, Costa E Silva C, de Aquino Cruz C, Bená MI, Betancur DFA, El Husny AS, de Souza ICN, Duarte RCB, Reed UC, Chaves MLF, Zanoteli E, França MC Jr, Saute JA.
Winckler PB, et al. Among authors: el husny as.
Clin Genet. 2019 Oct;96(4):341-353. doi: 10.1111/cge.13597. Epub 2019 Jul 15.
Clin Genet. 2019.
PMID: 31268554
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Comprehensive analysis of germline mutations in northern Brazil: a panel of 16 genes for hereditary cancer-predisposing syndrome investigation.
Vidal AF, Ferraz RS, El-Husny A, Silva CS, Vinasco-Sandoval T, Magalhães L, Raiol-Moraes M, Barra WF, Pereira CLBL, de Assumpção PP, de Brito LM, Vialle RA, Santos S, Ribeiro-Dos-Santos Â, Ribeiro-Dos-Santos AM.
Vidal AF, et al.
BMC Cancer. 2021 Apr 7;21(1):363. doi: 10.1186/s12885-021-08089-9.
BMC Cancer. 2021.
PMID: 33827469
Free PMC article.
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CDH1 mutations in gastric cancer patients from northern Brazil identified by Next- Generation Sequencing (NGS).
El-Husny A, Raiol-Moraes M, Amador M, Ribeiro-Dos-Santos AM, Montagnini A, Barbosa S, Silva A, Assumpção P, Ishak G, Santos S, Pinto P, Cruz A, Ribeiro-Dos-Santos Â.
El-Husny A, et al.
Genet Mol Biol. 2016 May 13;39(2):189-98. doi: 10.1590/1678-4685-GMB-2014-0342.
Genet Mol Biol. 2016.
PMID: 27192129
Free PMC article.
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A novel nonsense mutation of the KAL1 gene (p.Trp204*) in Kallmann syndrome.
El Husny AS, Raiol-Moraes M, Fernandes-Caldato MC, Ribeiro-Dos-Santos A.
El Husny AS, et al.
Appl Clin Genet. 2014 Sep 30;7:177-82. doi: 10.2147/TACG.S64280. eCollection 2014.
Appl Clin Genet. 2014.
PMID: 25328414
Free PMC article.
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DDX58(RIG-I)-related disease is associated with tissue-specific interferon pathway activation.
Prasov L, Bohnsack BL, El Husny AS, Tsoi LC, Guan B, Kahlenberg JM, Almeida E, Wang H, Cowen EW, De Jesus AA, Jani P, Billi AC, Moroi SE, Wasikowski R, Almeida I, Almeida LN, Kok F, Garnai SJ, Mian SI, Chen MY, Warner BM, Ferreira CR, Goldbach-Mansky R, Hur S, Brooks BP, Richards JE, Hufnagel RB, Gudjonsson JE.
Prasov L, et al. Among authors: el husny as.
J Med Genet. 2022 Mar;59(3):294-304. doi: 10.1136/jmedgenet-2020-107447. Epub 2021 Jan 25.
J Med Genet. 2022.
PMID: 33495304
Free PMC article.
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