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Congenital lymphedema as a rare and first symptom of tuberous sclerosis complex.
Klinner, Jürgen; Krüger, Marcus; Brunet, Theresa; Makowski, Christine; Riedhammer, Korbinian M; Mollweide, Andreas; Wagner, Matias; Hoefele, Julia.
Afiliação
  • Klinner J; Institute of Human Genetics, Klinikum rechts der Isar, Technical University of Munich, School of Medicine, Munich, Germany.
  • Krüger M; Department for Paediatric Adolescent Medicine and Neonatology, Munich Clinic, Schwabing Hospital and Technical University of Munich, School of Medicine, Munich, Germany.
  • Brunet T; Institute of Human Genetics, Klinikum rechts der Isar, Technical University of Munich, School of Medicine, Munich, Germany.
  • Makowski C; Department for Paediatric Adolescent Medicine and Neonatology, Munich Clinic, Schwabing Hospital and Technical University of Munich, School of Medicine, Munich, Germany.
  • Riedhammer KM; Institute of Human Genetics, Klinikum rechts der Isar, Technical University of Munich, School of Medicine, Munich, Germany; Department of Nephrology, Klinikum rechts der Isar, Technical University of Munich, Munich, Germany.
  • Mollweide A; Department for Paediatric Adolescent Medicine and Neonatology, Munich Clinic, Schwabing Hospital and Technical University of Munich, School of Medicine, Munich, Germany.
  • Wagner M; Institute of Human Genetics, Klinikum rechts der Isar, Technical University of Munich, School of Medicine, Munich, Germany; Institute of Neurogenomics, Helmholtz Zentrum Munich, Neuherberg, Germany.
  • Hoefele J; Institute of Human Genetics, Klinikum rechts der Isar, Technical University of Munich, School of Medicine, Munich, Germany. Electronic address: julia.hoefele@tum.de.
Gene ; 753: 144815, 2020 Aug 30.
Article em En | MEDLINE | ID: mdl-32479982
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Esclerose Tuberosa / Linfedema Tipo de estudo: Diagnostic_studies / Prognostic_studies / Screening_studies Limite: Female / Humans / Infant Idioma: En Revista: Gene Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Alemanha País de publicação: Holanda
Texto completo
Adicionar na Minha BVS
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Esclerose Tuberosa / Linfedema Tipo de estudo: Diagnostic_studies / Prognostic_studies / Screening_studies Limite: Female / Humans / Infant Idioma: En Revista: Gene Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Alemanha País de publicação: Holanda