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Long-term follow-up in a Chinese child with congenital lipoid adrenal hyperplasia due to a StAR gene mutation.
Zhao, Xiu; Su, Zhe; Liu, Xia; Song, Jianming; Gan, Yungen; Wen, Pengqiang; Li, Shoulin; Wang, Li; Pan, Lili.
Afiliação
  • Zhao X; Department of Endocrinology, Shenzhen Children's Hospital, 7019# Yitian Road, Futian District, Shenzhen, 518038, Guangdong Province, China.
  • Su Z; Department of Endocrinology, Shenzhen Children's Hospital, 7019# Yitian Road, Futian District, Shenzhen, 518038, Guangdong Province, China. su_zhe@126.com.
  • Liu X; Department of Endocrinology, Shenzhen Children's Hospital, 7019# Yitian Road, Futian District, Shenzhen, 518038, Guangdong Province, China.
  • Song J; Pathology Department, Shenzhen Children's Hospital, Shenzhen, 518038, China.
  • Gan Y; Radiology Department, Shenzhen Children's Hospital, Shenzhen, 518038, China.
  • Wen P; Pediatrics Research Institute, Shenzhen Children's Hospital, Shenzhen, 518038, China.
  • Li S; Department of Urology, Shenzhen Children's Hospital, Shenzhen, 518038, China.
  • Wang L; Department of Endocrinology, Shenzhen Children's Hospital, 7019# Yitian Road, Futian District, Shenzhen, 518038, Guangdong Province, China.
  • Pan L; Department of Endocrinology, Shenzhen Children's Hospital, 7019# Yitian Road, Futian District, Shenzhen, 518038, Guangdong Province, China.
BMC Endocr Disord ; 18(1): 78, 2018 Nov 06.
Article em En | MEDLINE | ID: mdl-30400872

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fosfoproteínas / Hiperplasia Suprarrenal Congênita / Povo Asiático / Transtorno 46,XY do Desenvolvimento Sexual / Mutação Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Child / Child, preschool / Female / Humans / Infant Idioma: En Revista: BMC Endocr Disord Ano de publicação: 2018 Tipo de documento: Article País de afiliação: China

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fosfoproteínas / Hiperplasia Suprarrenal Congênita / Povo Asiático / Transtorno 46,XY do Desenvolvimento Sexual / Mutação Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Child / Child, preschool / Female / Humans / Infant Idioma: En Revista: BMC Endocr Disord Ano de publicação: 2018 Tipo de documento: Article País de afiliação: China