Pediatric and Adult Liver Disease in Alpha-1 Antitrypsin Deficiency.


Journal

Seminars in liver disease
ISSN: 1098-8971
Titre abrégé: Semin Liver Dis
Pays: United States
ID NLM: 8110297

Informations de publication

Date de publication:
Aug 2023
Historique:
medline: 3 11 2023
pubmed: 5 7 2023
entrez: 4 7 2023
Statut: ppublish

Résumé

Alpha-1 antitrypsin deficiency (AATD) arises due to inherited variants in

Identifiants

pubmed: 37402396
doi: 10.1055/a-2122-7674
doi:

Types de publication

Review Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

258-266

Subventions

Organisme : Deutsche Forschungsgemeinschaft (DFG)
ID : SFB 1382 (ID 403224013) and STR 1095/6-1

Informations de copyright

Thieme. All rights reserved.

Déclaration de conflit d'intérêts

M.R. received advisory board fees and lecture fees from Takeda, advisory board fees from Grifols, lecture fees from CSL Behring. P.S. received grant support and lecture fees from Grifols and CSL Behring; grant support and advisory board fees from Arrowhead Pharmaceuticals and Dicerna Pharmaceuticals; grant support from Vertex Pharmaceuticals; advisory board fees from GSK, Intellia Pharmaceuticals, Novo Nordisk, Takeda, and Ono Pharmaceuticals; and is supported by the Deutsche Forschungsgemeinschaft (DFG) grants SFB 1382 (ID 403224013) and STR 1095/6–1.

Auteurs

Mathias Ruiz (M)

Hépatologie, Gastroentérologie et Nutrition Pédiatriques, Hôpital Femme Mère Enfant, Hospices civils de Lyon, Health Care Provider of the European Reference Network on Rare Liver Disorders (ERN RARE LIVER), Lyon, France.

Florence Lacaille (F)

Service de Gastroentérologie-Nutrition Pédiatriques et Unité d'Hépatologie Pédiatrique Hôpital Universitaire Necker-Enfants Malades, Health Care Provider of the European Reference Network on Rare Liver Disorders (ERN RARE LIVER), Paris, France.

Christina Schrader (C)

Medical Clinic III, Gastroenterology, Metabolic Diseases and Intensive Care, University Hospital RWTH Aachen, Health Care Provider of the European Reference Network on Rare Liver Disorders (ERN RARE LIVER), Aachen, Germany.

Monica Pons (M)

Liver Unit, Hospital Universitari Vall d'Hebron, Vall d'Hebron Research Institute (VHIR), Universitat Autonoma de Barcelona, Health Care Provider of the European Reference Network on Rare Liver Disorders (ERN RARE LIVER), Barcelona, Spain.
Centro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas (CIBERehd), Instituto de Salud Carlos III, Madrid, Spain.

Piotr Socha (P)

The Children's Memorial Health Institute, Department of Gastroenterology, Hepatology, Nutritional Disorders and Pediatrics, Al. Dzieci Polskich, Warszawa, Poland.

Aleksander Krag (A)

Department of Gastroenterology and Hepatology, Odense University Hospital, Odense, Denmark.

Ekkehard Sturm (E)

Pediatric Gastroenterology and Hepatology, University Children's Hospital Tübingen, Member Center of the European Reference Network on Rare Liver Disorders (ERN RARE LIVER), Tübingen, Germany.

Marion Bouchecareilh (M)

University of Bordeaux, CNRS, INSERM, BRIC, U1312, Bordeaux, France.

Pavel Strnad (P)

Medical Clinic III, Gastroenterology, Metabolic Diseases and Intensive Care, University Hospital RWTH Aachen, Health Care Provider of the European Reference Network on Rare Liver Disorders (ERN RARE LIVER), Aachen, Germany.

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Classifications MeSH