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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.
The phenotypic spectrum of congenital Zika syndrome.
Del Campo M, Feitosa IM, Ribeiro EM, Horovitz DD, Pessoa AL, França GV, García-Alix A, Doriqui MJ, Wanderley HY, Sanseverino MV, Neri JI, Pina-Neto JM, Santos ES, Verçosa I, Cernach MC, Medeiros PF, Kerbage SC, Silva AA, van der Linden V, Martelli CM, Cordeiro MT, Dhalia R, Vianna FS, Victora CG, Cavalcanti DP, Schuler-Faccini L; Zika Embryopathy Task Force-Brazilian Society of Medical Genetics ZETF-SBGM.
Del Campo M, et al. Among authors: wanderley hy.
Am J Med Genet A. 2017 Apr;173(4):841-857. doi: 10.1002/ajmg.a.38170.
Am J Med Genet A. 2017.
PMID: 28328129
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CBS mutations are good predictors for B6-responsiveness: A study based on the analysis of 35 Brazilian Classical Homocystinuria patients.
Poloni S, Sperb-Ludwig F, Borsatto T, Weber Hoss G, Doriqui MJR, Embiruçu EK, Boa-Sorte N, Marques C, Kim CA, Fischinger Moura de Souza C, Rocha H, Ribeiro M, Steiner CE, Moreno CA, Bernardi P, Valadares E, Artigalas O, Carvalho G, Wanderley HYC, Kugele J, Walter M, Gallego-Villar L, Blom HJ, Schwartz IVD.
Poloni S, et al. Among authors: wanderley hyc.
Mol Genet Genomic Med. 2018 Mar;6(2):160-170. doi: 10.1002/mgg3.342. Epub 2018 Jan 20.
Mol Genet Genomic Med. 2018.
PMID: 29352562
Free PMC article.
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Spinocerebellar ataxias in 114 Brazilian families: clinical and molecular findings.
Trott A, Jardim LB, Ludwig HT, Saute JA, Artigalás O, Kieling C, Wanderley HY, Rieder CR, Monte TL, Socal M, Alonso I, Ferro A, Carvalho T, do Céu Moreira M, Mendonça P, Ferreirinha F, Silveira I, Sequeiros J, Giugliani R, Saraiva-Pereira ML.
Trott A, et al. Among authors: wanderley hy.
Clin Genet. 2006 Aug;70(2):173-6. doi: 10.1111/j.1399-0004.2006.00656.x.
Clin Genet. 2006.
PMID: 16879203
No abstract available.
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Oxidative stress is induced in female carriers of X-linked adrenoleukodystrophy.
Deon M, Sitta A, Barschak AG, Coelho DM, Terroso T, Schmitt GO, Wanderley HY, Jardim LB, Giugliani R, Wajner M, Vargas CR.
Deon M, et al. Among authors: wanderley hy.
J Neurol Sci. 2008 Mar 15;266(1-2):79-83. doi: 10.1016/j.jns.2007.08.043. Epub 2007 Oct 2.
J Neurol Sci. 2008.
PMID: 17915255
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Spinocerebellar ataxias in Brazil--frequencies and modulating effects of related genes.
de Castilhos RM, Furtado GV, Gheno TC, Schaeffer P, Russo A, Barsottini O, Pedroso JL, Salarini DZ, Vargas FR, de Lima MA, Godeiro C, Santana-da-Silva LC, Toralles MB, Santos S, van der Linden H Jr, Wanderley HY, de Medeiros PF, Pereira ET, Ribeiro E, Saraiva-Pereira ML, Jardim LB; Rede Neurogenetica.
de Castilhos RM, et al. Among authors: wanderley hy.
Cerebellum. 2014 Feb;13(1):17-28. doi: 10.1007/s12311-013-0510-y.
Cerebellum. 2014.
PMID: 23943520
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Report of a patient with a trisomy of chromosome region 20q11.2-->20q12 and characterization with FISH.
Wanderley HY, Schrander-Stumpel CT, Visser MO, Van Maanen-Op Het Roodt EA, Loneus WH, Engelen JJ.
Wanderley HY, et al.
Genet Couns. 2005;16(3):277-82.
Genet Couns. 2005.
PMID: 16259325
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