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MYO5B Gene Mutations: A Not Negligible Cause of Intrahepatic Cholestasis of Infancy With Normal Gamma-Glutamyl Transferase Phenotype.
Matarazzo, Lorenza; Bianco, Anna Monica; Athanasakis, Emmanouil; Serveres, Marco; Francalanci, Paola; Cenacchi, Giovanna; Maggiore, Giuseppe; D'Adamo, Adamo Pio.
Afiliación
  • Matarazzo L; Department of Medicine, Surgery, and Health Sciences, University of Trieste.
  • Bianco AM; lnstitute for Maternal and Child Health, IRCCS "Burlo Garofolo", Trieste.
  • Athanasakis E; lnstitute for Maternal and Child Health, IRCCS "Burlo Garofolo", Trieste.
  • Serveres M; Pediatric Hepatology and Pediatric Liver Transplantation, ISMETT, University of Pittsburgh Medical Center Italy, Palermo.
  • Francalanci P; Department of Pathology, IRCCS Bambino Gesu Children's Hospital-IRCCS, Rome.
  • Cenacchi G; Department of Biomedical and Neuromotor Sciences, Alma Mater, University of Bologna and IRCCS Policlinico di S.Orsola, Bologna.
  • Maggiore G; Hepatology, Gastroenterology, Nutrition and Liver Transplant Unit Bambino Gesu Children's Hospital-IRCCS, Rome, Italy.
  • D'Adamo AP; Department of Medicine, Surgery, and Health Sciences, University of Trieste.
J Pediatr Gastroenterol Nutr ; 74(5): e115-e121, 2022 05 01.
Article en En | MEDLINE | ID: mdl-35129155

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Colestasis / Colestasis Intrahepática / Miosina Tipo V Tipo de estudio: Diagnostic_studies / Observational_studies / Prognostic_studies Límite: Humans Idioma: En Revista: J Pediatr Gastroenterol Nutr Año: 2022 Tipo del documento: Article Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Colestasis / Colestasis Intrahepática / Miosina Tipo V Tipo de estudio: Diagnostic_studies / Observational_studies / Prognostic_studies Límite: Humans Idioma: En Revista: J Pediatr Gastroenterol Nutr Año: 2022 Tipo del documento: Article Pais de publicación: Estados Unidos