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Hypoglycemia in CDG patients due to PMM2 mutations: Follow up on hyperinsulinemic patients.
Moravej, Hossein; Altassan, Ruqaiah; Jaeken, Jaak; Enns, Gregory M; Ellaway, Carolyn; Balasubramaniam, Shanti; De Lonlay, Pascale; Coman, David; Mercimek-Andrews, Saadet; Witters, Peter; Morava, Eva.
Afiliação
  • Moravej H; Neonatal Research Center Shiraz University of Medical Sciences Shiraz Iran.
  • Altassan R; Department of Pediatric Endocrinology School of Medicine, Shiraz University of Medical Sciences Shiraz Iran.
  • Jaeken J; Medical Genetic Department McGill University Health Center Montreal Québec Canada.
  • Enns GM; Center for Metabolic Diseases University Hospital Gasthuisberg Leuven Belgium.
  • Ellaway C; Biochemical Genetics Program Stanford University Stanford California.
  • Balasubramaniam S; Genetic Metabolic Disorders Service Sydney Children's Hospital Network Sydney New South Wales Australia.
  • De Lonlay P; Disciplines of Genetic Medicine & Child and Adolescent Health Sydney University Sydney New South Wales Australia.
  • Coman D; Western Sydney Genetics Program The Children's Hospital at Westmead Sydney New South Wales Australia.
  • Mercimek-Andrews S; Discipline of Genetic Medicine Sydney Medical School, University of Sydney Sydney New South Wales Australia.
  • Witters P; Reference Center for Metabolic Diseases Hospital Necker, University Paris V Paris France.
  • Morava E; Department of Metabolic Medicine The Lady Cilento Children's Hospital Brisbane Queensland Australia.
JIMD Rep ; 51(1): 76-81, 2020 Jan.
Article em En | MEDLINE | ID: mdl-32071842

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Idioma: En Ano de publicação: 2020 Tipo de documento: Article