The dilemma to diagnose Wilson disease by genetic testing alone-Reference-Cited by-同舟云学术

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The dilemma to diagnose Wilson disease by genetic testing alone

Published:2019-06-20 Issue:8 Volume:49 Page:
ISSN:0014-2972
Container-title:European Journal of Clinical Investigation
language:en
Short-container-title:Eur J Clin Invest

Author:

Stättermayer Albert Friedrich¹^ORCID,Entenmann Andreas²,Gschwantler Michael³,Zoller Heinz⁴,Hofer Harald¹⁵,Ferenci Peter¹

Affiliation:

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

2. Department of Pediatrics Innsbruck Medical University Innsbruck Austria

3. Department of Internal Medicine IV Wilhelminenspital Vienna Austria

4. Department of Medicine I, Gastroenterology, Hepatology and Endocrinology Innsbruck Medical University Innsbruck Austria

5. Department of Internal Medicine I Klinikum Wels‐Grieskirchen Wels Austria

Publisher

Wiley

Subject

Clinical Biochemistry,Biochemistry,General Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/eci.13147

Reference33 articles.

1. EASL Clinical Practice Guidelines: Wilson’s disease

2. Wilson disease

3. Hepatic copper metabolism: Insights from genetic disease

4. Function and Regulation of the Mammalian Copper-transporting ATPases: Insights from Biochemical and Cell Biological Approaches

5. Wilson Disease: Clinical Presentation, Treatment, and Survival

Cited by 34 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Wilson Disease (Hepato-Lenticular Degeneration);Reference Module in Life Sciences;2024

2. Developmental and Inherited Liver Disease;MacSween's Pathology of the Liver;2024

3. Significant heterogeneity in the diagnosis and long-term management of Wilson disease: Results from a large multicenter Spanish study;Gastroenterología y Hepatología (English Edition);2023-10

4. Metallothionein: a game changer in histopathological diagnosis of Wilson disease;Histopathology;2023-09-04

5. Clinical spectrum and genotype-phenotype associations in Finnish patients with Wilson's disease;Journal of the Neurological Sciences;2023-05

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