Your browser doesn't support javascript.
loading
European lipodystrophy registry: background and structure.
von Schnurbein, Julia; Adams, Claire; Akinci, Baris; Ceccarini, Giovanni; D'Apice, Maria Rosaria; Gambineri, Alessandra; Hennekam, Raoul C M; Jeru, Isabelle; Lattanzi, Giovanna; Miehle, Konstanze; Nagel, Gabriele; Novelli, Giuseppe; Santini, Ferruccio; Santos Silva, Ermelinda; Savage, David B; Sbraccia, Paolo; Schaaf, Jannik; Sorkina, Ekaterina; Tanteles, George; Vantyghem, Marie-Christine; Vatier, Camille; Vigouroux, Corinne; Vorona, Elena; Araújo-Vilar, David; Wabitsch, Martin.
Afiliación
  • von Schnurbein J; Division of Paediatric Endocrinology and Diabetes, Department of Paediatrics and Adolescent Medicine, Centre for Rare Endocrine Disorders, Ulm University Medical Centre, Eythstraße 24, 89075, Ulm, Germany.
  • Adams C; University of Cambridge Metabolic Research Laboratories, Cambridge, UK.
  • Akinci B; Dokuz Eylul University School of Medicine, Izmir, Turkey.
  • Ceccarini G; Obesity and Lipodystrophy Center, Endocrine Unit, University Hospital of Pisa, Pisa, Italy.
  • D'Apice MR; Medical Genetics Laboratory, Policlinico Tor Vergata, Rome, Italy.
  • Gambineri A; Endocrinology Unit, Department of Clinical and Medical Science, S. Orsola-Malpighi Hospital, University of Bologna, Bologna, Italy.
  • Hennekam RCM; Department of Paediatrics, Amsterdam University Medical Centre, Amsterdam, Netherlands.
  • Jeru I; Inserm U938, AP-HP, National Reference Center for Rare Diseases of Insulin Secretion and Insulin Sensitivity (PRISIS), Departments of Endocrinology, Diabetology and Reproductive Endocrinology, and Molecular Biology and Genetics, Sorbonne University, Saint-Antoine University Hospital, Paris, France.
  • Lattanzi G; CNR Institute of Molecular Genetics "Luigi Luca Cavalli-Sforza", Unit of Bologna, Bologna, Italy.
  • Miehle K; Medical Department III - Endocrinology, Nephrology, Rheumatology, University of Leipzig, Leipzig, Germany.
  • Nagel G; Institute of Epidemiology and Medical Biometry, Ulm University, Ulm, Germany.
  • Novelli G; Department of Biomedicine and Prevention, University of Rome Tor Vergata - Policlinico Tor Vergata, Rome, Italy.
  • Santini F; Neuromed IRCCS Institute, Pozzilli, IS, Italy.
  • Santos Silva E; Obesity and Lipodystrophy Center, Endocrine Unit, University Hospital of Pisa, Pisa, Italy.
  • Savage DB; Pediatric Gastroenterology Unit, Pediatrics Division, Centro Materno Infantil do Norte (CMIN), Centro Hospitalar Universitário do Porto, Porto, Portugal.
  • Sbraccia P; Instituto de Ciências Biomédicas Abel Salazar (ICBAS), Universidade do Porto, Porto, Portugal.
  • Schaaf J; UCIBIO, REQUIMTE, Laboratory of Biochemistry, Faculdade de Farmácia do Porto, Porto, Portugal.
  • Sorkina E; University of Cambridge Metabolic Research Laboratories, Cambridge, UK.
  • Tanteles G; Internal Medicine Unit and Obesity Center, Department of Systems Medicine, University of Rome Tor Vergata, Rome, Italy.
  • Vantyghem MC; Medical Informatics Group, University Hospital Frankfurt, Frankfurt, Germany.
  • Vatier C; Endocrinology Research Centre, Moscow, Russia.
  • Vigouroux C; Clinical Genetics Clinic, Cyprus Institute of Neurology & Genetics, 1683, Nicosia, Republic of Cyprus.
  • Vorona E; CHU Lille, Department of Endocrinology, Diabetology and Metabolism, Inserm, Translational Research for Diabetes, UMR-1190, European Genomic Institute for Diabetes, University of Lille, 59000, Lille, France.
  • Araújo-Vilar D; Inserm U938, AP-HP, National Reference Center for Rare Diseases of Insulin Secretion and Insulin Sensitivity (PRISIS), Departments of Endocrinology, Diabetology and Reproductive Endocrinology, and Molecular Biology and Genetics, Sorbonne University, Saint-Antoine University Hospital, Paris, France.
  • Wabitsch M; Inserm U938, AP-HP, National Reference Center for Rare Diseases of Insulin Secretion and Insulin Sensitivity (PRISIS), Departments of Endocrinology, Diabetology and Reproductive Endocrinology, and Molecular Biology and Genetics, Sorbonne University, Saint-Antoine University Hospital, Paris, France.
Orphanet J Rare Dis ; 15(1): 17, 2020 01 15.
Article en En | MEDLINE | ID: mdl-31941540
Asunto(s)
Palabras clave
Texto completo
Añadir a Mi BVS
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Sistema de Registros / Enfermedades Raras / Lipodistrofia Límite: Humans Idioma: En Revista: Orphanet J Rare Dis Asunto de la revista: MEDICINA Año: 2020 Tipo del documento: Article País de afiliación: Alemania Pais de publicación: Reino Unido
Texto completo
Añadir a Mi BVS
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Sistema de Registros / Enfermedades Raras / Lipodistrofia Límite: Humans Idioma: En Revista: Orphanet J Rare Dis Asunto de la revista: MEDICINA Año: 2020 Tipo del documento: Article País de afiliación: Alemania Pais de publicación: Reino Unido