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Clinical Heterogeneity of Immune Dysregulation, Polyendocrinopathy, Enteropathy, X-Linked Syndrome: A French Multicenter Retrospective Study.
Duclaux-Loras, R; Charbit-Henrion, F; Neven, B; Nowak, J; Collardeau-Frachon, S; Malcus, C; Ray, P F; Moshous, D; Beltrand, J; Goulet, O; Cerf-Bensussan, N; Lachaux, A; Rieux-Laucat, F; Ruemmele, F M.
Afiliación
  • Duclaux-Loras R; Department of Paediatric GastroenterologyHepatology and Nutrition, Hospices Civils de Lyon, Hôpital Femme Mère Enfant, Bron, France. Remi.duclaux-loras@inserm.fr.
  • Charbit-Henrion F; Université Paris Descartes-Sorbonne Paris Cité, Paris, France. Remi.duclaux-loras@inserm.fr.
  • Neven B; INSERM, UMR1163, Laboratory of Intestinal Immunityand Imagine Institute, Paris, France. Remi.duclaux-loras@inserm.fr.
  • Nowak J; Université Paris Descartes-Sorbonne Paris Cité, Paris, France.
  • Collardeau-Frachon S; INSERM, UMR1163, Laboratory of Intestinal Immunityand Imagine Institute, Paris, France.
  • Malcus C; Department of Pediatric, Gastroenterology Assistance Publique-Hôpitaux de Paris, Hôpital Necker-Enfants Malades, Paris, France.
  • Ray PF; Université Paris Descartes-Sorbonne Paris Cité, Paris, France.
  • Moshous D; Assistance Publique - Hôpitaux de Paris, Hôpital Necker-Enfants Malades, Paediatric Haemato-Immunology Unit, Paris, France.
  • Beltrand J; Department of Pediatric Gastroenterology and Metabolic Diseases, Poznan University of Medical Sciences, Poznan, Poland.
  • Goulet O; Department of Pathology, Hospices Civils de Lyon, Hôpital Femme Mère Enfant, Bron, France.
  • Cerf-Bensussan N; Hospices Civils de Lyon, Hôpital Edouard Herriot, Laboratory of Immunology, Lyon, France.
  • Lachaux A; Genetic Epigenetic and Therapies of Infertility, Institute for Advanced Biosciences, Inserm U1209, CNRS UMR 5309, Université Grenoble Alpes, 38000, Grenoble, France.
  • Rieux-Laucat F; CHU de Grenoble, UF de Biochimie Génétique et Moléculaire, Grenoble, F-38000, France.
  • Ruemmele FM; Université Paris Descartes-Sorbonne Paris Cité, Paris, France.
Clin Transl Gastroenterol ; 9(10): 201, 2018 11 02.
Article en En | MEDLINE | ID: mdl-30385752

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Poliendocrinopatías Autoinmunes / Enfermedades Genéticas Ligadas al Cromosoma X / Factores de Transcripción Forkhead / Enfermedades Intestinales Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Child / Child, preschool / Humans / Infant / Male / Newborn País/Región como asunto: Europa Idioma: En Año: 2018 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Poliendocrinopatías Autoinmunes / Enfermedades Genéticas Ligadas al Cromosoma X / Factores de Transcripción Forkhead / Enfermedades Intestinales Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Child / Child, preschool / Humans / Infant / Male / Newborn País/Región como asunto: Europa Idioma: En Año: 2018 Tipo del documento: Article