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Primary adrenal insufficiency in a patient with biallelic QRSL1 mutations.
Dursun, Fatma; Genc, Hulya Maras; Mine Yilmaz, Ayse; Tas, Ibrahim; Eser, Metin; Pehlivanoglu, Cemile; Yilmaz, Betul Karademir; Guran, Tulay.
  • Dursun F; Umraniye Training and Research Hospital, Department of Pediatric Endocrinology and Diabetes.
  • Genc HM; Umraniye Training and Research Hospital, Department of Pediatric Neurology, University of Health Sciences, Istanbul, Turkey.
  • Mine Yilmaz A; School of Medicine, Department of Biochemistry, Genetic and Metabolic Diseases Research and Investigation Center, Marmara University, Istanbul, Turkey.
  • Tas I; Umraniye Training and Research Hospital, Department of Pediatric Nutrition and Metabolism.
  • Eser M; Umraniye Training and Research Hospital, Department of Medical Genetics.
  • Pehlivanoglu C; Umraniye Training and Research Hospital, Department of Pediatric Nephrology, University of Health Sciences, Istanbul, Turkey.
  • Yilmaz BK; School of Medicine, Department of Biochemistry, Genetic and Metabolic Diseases Research and Investigation Center, Marmara University, Istanbul, Turkey.
  • Guran T; School of Medicine, Department of Pediatric Endocrinology and Diabetes, Marmara University, Istanbul, Turkey.
Eur J Endocrinol ; 187(3): K27-K32, 2022 Sep 01.
Article en En | MEDLINE | ID: mdl-35894854
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Enfermedad de Addison / Insuficiencia Suprarrenal / Hiperplasia Suprarrenal Congénita Tipo de estudio: Prognostic_studies Límite: Child / Humans / Male Idioma: En Año: 2022 Tipo del documento: Article
Texto completo
Imprimir
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PubMed Links
Search on Google

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Enfermedad de Addison / Insuficiencia Suprarrenal / Hiperplasia Suprarrenal Congénita Tipo de estudio: Prognostic_studies Límite: Child / Humans / Male Idioma: En Año: 2022 Tipo del documento: Article