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Genetic testing in inherited endocrine disorders: joint position paper of the European reference network on rare endocrine conditions (Endo-ERN).
Eggermann, Thomas; Elbracht, Miriam; Kurth, Ingo; Juul, Anders; Johannsen, Trine Holm; Netchine, Irène; Mastorakos, George; Johannsson, Gudmundur; Musholt, Thomas J; Zenker, Martin; Prawitt, Dirk; Pereira, Alberto M; Hiort, Olaf.
Afiliação
  • Eggermann T; Institute of Human Genetics, Medical Faculty, RWTH Aachen, Pauwelsstr. 30, 52074, Aachen, Germany. teggermann@ukaachen.de.
  • Elbracht M; Institute of Human Genetics, Medical Faculty, RWTH Aachen, Pauwelsstr. 30, 52074, Aachen, Germany.
  • Kurth I; Institute of Human Genetics, Medical Faculty, RWTH Aachen, Pauwelsstr. 30, 52074, Aachen, Germany.
  • Juul A; Department of Growth and Reproduction, Rigshospitalet, University Hospital of Copenhagen, Copenhagen, Denmark.
  • Johannsen TH; International Center for Research and Research Training in Endocrine Disruption of Male Reproduction and Child Health (EDMaRC), Rigshospitalet, University of Copenhagen, Copenhagen, Denmark.
  • Netchine I; Department of Growth and Reproduction, Rigshospitalet, University Hospital of Copenhagen, Copenhagen, Denmark.
  • Mastorakos G; International Center for Research and Research Training in Endocrine Disruption of Male Reproduction and Child Health (EDMaRC), Rigshospitalet, University of Copenhagen, Copenhagen, Denmark.
  • Johannsson G; INSERM, Centre de Recherche Saint-Antoine, Sorbonne Université, UFR Médecine, AP-HP, Hôpital Armand Trousseau-Explorations Fonctionnelles Endocriniennes, Paris, France.
  • Musholt TJ; Unit of Endocrinology, Diabetes Mellitus and Metabolism, ARETAIEION Hospital, Faculty of Medicine, National and Kapodistrian University of Athens, Athens, Greece.
  • Zenker M; Department of Internal Medicine and Clinical Nutrition, Institute of Medicine, Sahlgrenska Academy, University of Gothenburg and Department of Endocrinology at Sahlgrenska University Hospital, Gothenburg, Sweden.
  • Prawitt D; Section of Endocrine Surgery, Department of General, Visceral and Transplantation Surgery, Johannes Gutenberg University Medical Center, Mainz, Germany.
  • Pereira AM; Institute of Human Genetics, Otto-von-Guericke-Universität Magdeburg, Magdeburg, Germany.
  • Hiort O; Center for Pediatrics and Adolescent Medicine, Johannes Gutenberg University Medical Center, Mainz, Germany.
Orphanet J Rare Dis ; 15(1): 144, 2020 06 08.
Article em En | MEDLINE | ID: mdl-32513286
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Testes Genéticos / Doenças do Sistema Endócrino Tipo de estudo: Diagnostic_studies / Prognostic_studies / Screening_studies Limite: Humans Idioma: En Revista: Orphanet J Rare Dis Ano de publicação: 2020 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Testes Genéticos / Doenças do Sistema Endócrino Tipo de estudo: Diagnostic_studies / Prognostic_studies / Screening_studies Limite: Humans Idioma: En Revista: Orphanet J Rare Dis Ano de publicação: 2020 Tipo de documento: Article