Wilson Disease

Wilson’s disease is an autosomal recessive disorder caused by mutation in the ATP7B gene and is characterized by copper build-up in the body. Discover the latest research on Wilson’s disease here.

May 23, 2020
Preprint
Open Access

Golgi-Dependent Copper Homeostasis Sustains Synaptic Development and Mitochondrial Content

BioRxiv : the Preprint Server for Biology
C. HartwigVictor M Faundez
June 4, 2020
Open Access

Oxylipin Profiles in Plasma of Patients with Wilson's Disease

Metabolites
Nadezhda V AzbukinaMarina G Sergeeva
June 11, 2020

Wilson disease

Current Opinion in Neurology
Annu Aggarwal, Mohit Bhatt
June 14, 2020
Case Report

Bodybuilding supplements leading to copper toxicity, encephalopathy, fulminant hepatic failure and rhabdomyolysis

The American Journal of Emergency Medicine
John R RichardsDaniel K Colby
May 21, 2020
Open Access

A rare case of Wilson disease associated with intracerebral hemorrhage

Korean journal of anesthesiology
Shalendra SinghVikas Marwah
June 14, 2020
Open Access

Early-onset Wilson disease caused by ATP7B exon skipping associated with intronic variant

Cold Spring Harbor Molecular Case Studies
Daniel C KoboldtRichard K Wilson
June 11, 2020

Pediatric Wilson Disease Presenting as Acute Liver Failure: An Individual Patient Data Meta-Analysis

Journal of Pediatric Gastroenterology and Nutrition
Shannon M VandrielBinita M Kamath
June 23, 2020
Open Access

Predictors of caregiver burden in patients with neurologic Wilson disease

The Journal of International Medical Research
Peng WuYuancheng Bao
May 7, 2020

Undulating Tongue and Wilson's Disease

Movement Disorders Clinical Practice
Hicham El Otmani
June 5, 2020
Open Access

WilsonGen a comprehensive clinically annotated genomic variant resource for Wilson's Disease

Scientific Reports
Mukesh KumarBinukumar Bk
July 7, 2020
Case Report

Oculo-Auricular Synkinesia Post Bell's Palsy Causing Unilateral Wilson's Phenomenon

Movement Disorders Clinical Practice
Douglas E Hobson, Andrew E Borys
July 7, 2020
Open Access

Cirrhosis in Wilson Disease is characterized by Impaired Hepatic Synthesis, Leukopenia and Thrombocytopenia

International Journal of Medical Sciences
Hao-Jie ZhongXing-Xiang He
May 14, 2020

A liver-targeting Cu(i) chelator relocates Cu in hepatocytes and promotes Cu excretion in a murine model of Wilson's disease

Metallomics : Integrated Biometal Science
Marie MonestierElisabeth Mintz
July 3, 2020
Review

Are the new genetic tools for diagnosis of Wilson disease helpful in clinical practice?

JHEP Reports : Innovation in Hepatology
Carmen Espinós, Peter Ferenci
July 4, 2020
Open Access

Wilson's Disease in Finland: A Nationwide Population-Based Study

Movement Disorders : Official Journal of the Movement Disorder Society
Jussi O T SipiläValtteri Kaasinen
May 14, 2020
Comment / Editorial

Liver transplant for neurologic Wilson disease: Hope or fallacy?

Neurology
Oliver BandmannPeter Hedera
June 10, 2020
Case Report
Open Access

ATP7B Mutation Analysis: Wilson Disease, A Difficult to Diagnose Case

Journal of the College of Physicians and Surgeons--Pakistan : JCPSP
Bibi ZubaidaMunir Akmal Lodhi
June 13, 2020
Case Report
Open Access

Zinc Monotherapy as an Alternative Treatment Option for Decompensated Liver Disease due to Wilson Disease?

Case Reports in Hepatology
Hansa HaftuTeklu Gebrehiwot

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