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Complicated Gitelman syndrome and autoimmune thyroid disease: a case report with a new homozygous mutation in the SLC12A3 gene and literature review.
Zhou, Haiyang; Liang, Xinhuan; Qing, Yingfen; Meng, Bihui; Zhou, Jia; Huang, Song; Lu, Shurong; Huang, Zhenxing; Yang, Haiyan; Ma, Yan; Luo, Zuojie.
Afiliação
  • Zhou H; The Department of Endocrinology, The First Affiliated Hospital of Guangxi Medical University, Nanning, 530021, China.
  • Liang X; The Department of Endocrinology, The First Affiliated Hospital of Guangxi Medical University, Nanning, 530021, China.
  • Qing Y; The Department of Endocrinology, The First Affiliated Hospital of Guangxi Medical University, Nanning, 530021, China.
  • Meng B; The Department of Endocrinology, The First Affiliated Hospital of Guangxi Medical University, Nanning, 530021, China.
  • Zhou J; The Department of Endocrinology, The First Affiliated Hospital of Guangxi Medical University, Nanning, 530021, China.
  • Huang S; The Department of Endocrinology, The First Affiliated Hospital of Guangxi Medical University, Nanning, 530021, China.
  • Lu S; The Department of Endocrinology, The First Affiliated Hospital of Guangxi Medical University, Nanning, 530021, China.
  • Huang Z; The Department of Endocrinology, The First Affiliated Hospital of Guangxi Medical University, Nanning, 530021, China.
  • Yang H; The Department of Endocrinology, The First Affiliated Hospital of Guangxi Medical University, Nanning, 530021, China.
  • Ma Y; The Department of Endocrinology, The First Affiliated Hospital of Guangxi Medical University, Nanning, 530021, China. luoma628@163.com.
  • Luo Z; The Department of Endocrinology, The First Affiliated Hospital of Guangxi Medical University, Nanning, 530021, China. zhouhaiyang4000@163.com.
BMC Endocr Disord ; 18(1): 82, 2018 Nov 08.
Article em En | MEDLINE | ID: mdl-30409157
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doença de Graves / Síndrome de Gitelman / Mutação Tipo de estudo: Systematic_reviews Limite: Humans / Male / Middle aged Idioma: En Revista: BMC Endocr Disord Ano de publicação: 2018 Tipo de documento: Article País de afiliação: China País de publicação: Reino Unido
Texto completo
Adicionar na Minha BVS
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doença de Graves / Síndrome de Gitelman / Mutação Tipo de estudo: Systematic_reviews Limite: Humans / Male / Middle aged Idioma: En Revista: BMC Endocr Disord Ano de publicação: 2018 Tipo de documento: Article País de afiliação: China País de publicação: Reino Unido