Intra-family phenotype variations in familial neuromyelitis optica spectrum disorders.

Lee, Jun-Jun; Tsai, Meng-Han; Lien, Chia-Yi; Huang, Yu-Ju; Chang, Wen-Neng

Lee, Jun-Jun; Tsai, Meng-Han; Lien, Chia-Yi; Huang, Yu-Ju; Chang, Wen-Neng.

Afiliação

Lee JJ; Department of Neurology, Kaohsiung Chang Gung Memorial Hospital and Chang Gung University, College of Medicine, Kaohsiung, Taiwan; Department of Information Management, National Sun Yat-sen University, Kaohsiung, Taiwan.
Tsai MH; Department of Neurology, Kaohsiung Chang Gung Memorial Hospital and Chang Gung University, College of Medicine, Kaohsiung, Taiwan.
Lien CY; Department of Neurology, Kaohsiung Chang Gung Memorial Hospital and Chang Gung University, College of Medicine, Kaohsiung, Taiwan.
Huang YJ; Department of Neurology, Kaohsiung Chang Gung Memorial Hospital and Chang Gung University, College of Medicine, Kaohsiung, Taiwan.
Chang WN; Department of Neurology, Kaohsiung Chang Gung Memorial Hospital and Chang Gung University, College of Medicine, Kaohsiung, Taiwan. Electronic address: cwenneng@ms19.hinet.net.

Mult Scler Relat Disord ; 30: 57-62, 2019 May.

Article em En | MEDLINE | ID: mdl-30738281

Assuntos

Antígenos HLA-D/genética; Neuromielite Óptica/diagnóstico por imagem; Neuromielite Óptica/genética; Neuromielite Óptica/fisiopatologia; Adulto; Idoso; Feminino; Humanos; Pessoa de Meia-Idade; Linhagem; Fenótipo; Adulto Jovem

Palavras-chave

AQP4 gene; Familial; HLA genotype; NMO spectrum disorder; Phenptype variation

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Antígenos HLA-D / Neuromielite Óptica Tipo de estudo: Prognostic_studies Limite: Adult / Aged / Female / Humans / Middle aged Idioma: En Revista: Mult Scler Relat Disord Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Taiwan País de publicação: Holanda

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