Age and Sex but Not ATP7B Genotype Effectively Influence the Clinical Phenotype of Wilson Disease-Reference-Cited by-同舟云学术

Age and Sex but Not ATP7B Genotype Effectively Influence the Clinical Phenotype of Wilson Disease

Published:2019-03 Issue:4 Volume:69 Page:1464-1476
ISSN:0270-9139
Container-title:Hepatology
language:en
Short-container-title:Hepatology

Author:

Ferenci Peter¹^ORCID,Stremmel Wolfgang²,Członkowska Anna³,Szalay Ferenc⁴,Viveiros André⁵,Stättermayer Albert Friedrich¹,Bruha Radan⁶,Houwen Roderick⁷,Pop Tudor Lucian⁸^ORCID,Stauber Rudolf⁹,Gschwantler Michael¹⁰,Pfeiffenberger Jan²,Yurdaydin Cihan¹¹,Aigner Elmar¹²,Steindl‐Munda Petra¹,Dienes Hans‐Peter¹³,Zoller Heinz⁵,Weiss Karl Heinz²

Affiliation:

1. Department of Internal Medicine III, Gastroenterology and Hepatology Medical University of Vienna Vienna Austria

2. Department of Internal Medicine IV Medical University of Heidelberg Heidelberg Germany

3. Second Department of Neurology, Institute of Psychiatry and Neurology, and Department of Pharmacology Medical University of Warsaw Poland

4. First Department of Internal Medicine Semmelweis University Budapest Hungary

5. First Department of Internal Medicine Medical University Innsbruck Austria

6. Fourth Medical Department, First Faculty of Medicine Charles University Prague Czech Republic

7. Wilhelmina Children’s Hospital, University Medical Center Utrecht the Netherlands

8. Second Pediatric Clinic University of Medicine and Pharmacy “Iuliu Hatieganu” Cluj‐Napoca Romania

9. Department of Internal Medicine Medical University of Graz Graz Austria

10. Internal Medicine 4 Wilhelminen hospital Vienna Austria

11. Department of Gastroenterology and Hepatology Ankara University Medical School Ankara Turkey

12. Department of Internal Medicine I Paracelsus Medical University Salzburg Austria

13. Department of Clinical Pathology Medical University of Vienna Austria

Publisher

Wiley

Subject

Hepatology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/hep.30280

Reference47 articles.

1. Wilson's disease and other neurological copper disorders

2. Late-Onset Wilson’s Disease

3. Two families with Wilson disease in which siblings showed different phenotypes

4. Fulminant Wilson's Disease Requiring Liver Transplantation in One Monozygotic Twin Despite Identical Genetic Mutation

5. Homozygous Mutations in the Conserved ATP Hinge Region of the Wilson Disease Gene

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