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When is it best to discontinue diazoxide in children with persistent hyperinsulinaemic hypoglycaemia and negative genetics for KATP channel gene variants?
Güemes, Maria; Kostopoulou, Eirini; AlYahyaei, Mouza; Gilbert, Clare; Shah, Pratik.
Afiliação
  • Güemes M; Department of Paediatric Endocrinology, Great Ormond Street Hospital for Children NHS Foundation Trust, London, UK.
  • Kostopoulou E; Department of Developmental Endocrinology Research Group, Clinical and Molecular Genetics Unit, Institute of Child Health, University College London, London, UK.
  • AlYahyaei M; Department of Paediatric Endocrinology, Hospital Infantil Universitario Niño Jesús, Madrid, Spain.
  • Gilbert C; Department of Paediatric Endocrinology, Great Ormond Street Hospital for Children NHS Foundation Trust, London, UK.
  • Shah P; Division of Paediatric Endocrinology and Diabetes, Department of Paediatrics, School of Medicine, University of Patras, Patras, Greece.
Clin Endocrinol (Oxf) ; 96(2): 107-113, 2022 02.
Article em En | MEDLINE | ID: mdl-34370339
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Hiperinsulinismo Congênito / Diazóxido Idioma: En Ano de publicação: 2022 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Hiperinsulinismo Congênito / Diazóxido Idioma: En Ano de publicação: 2022 Tipo de documento: Article