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Hyperleptinemia in children with autosomal recessive spinal muscular atrophy type I-III.
Kölbel, Heike; Hauffa, Berthold P; Wudy, Stefan A; Bouikidis, Anastasios; Della Marina, Adela; Schara, Ulrike.
Afiliación
  • Kölbel H; Department of Neuropediatrics, Developmental Neurology and Social Pediatrics, Children's Hospital 1, University of Duisburg-Essen, Essen, Germany.
  • Hauffa BP; Department of Pediatric Endocrinology, Children's Hospital 2, University of Duisburg-Essen, Essen, Germany.
  • Wudy SA; Steroid Research and Mass Spectrometry Unit, Division of Pediatric Endocrinology and Diabetology, Center of Child and Adolescent Medicine, Justus Liebig University, Giessen, Germany.
  • Bouikidis A; Department of Pediatric Pulmonology, Children's Hospital 3, University of Duisburg-Essen, Essen, Germany.
  • Della Marina A; Department of Neuropediatrics, Developmental Neurology and Social Pediatrics, Children's Hospital 1, University of Duisburg-Essen, Essen, Germany.
  • Schara U; Department of Neuropediatrics, Developmental Neurology and Social Pediatrics, Children's Hospital 1, University of Duisburg-Essen, Essen, Germany.
PLoS One ; 12(3): e0173144, 2017.
Article en En | MEDLINE | ID: mdl-28278160
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Índice de Severidad de la Enfermedad / Atrofias Musculares Espinales de la Infancia / Leptina / Genes Recesivos / Enfermedades Metabólicas Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies Idioma: En Revista: PLoS One Asunto de la revista: CIENCIA / MEDICINA Año: 2017 Tipo del documento: Article
Texto completo
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Índice de Severidad de la Enfermedad / Atrofias Musculares Espinales de la Infancia / Leptina / Genes Recesivos / Enfermedades Metabólicas Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies Idioma: En Revista: PLoS One Asunto de la revista: CIENCIA / MEDICINA Año: 2017 Tipo del documento: Article