Latest papers

[Haplotype analysis and possible founder effect at the R778L mutation of the ATP7B gene in Korean patients with Wilson's disease]

[Haplotype analysis at R778L mutation of ATP7B gene in Korean patients with Wilson disease]

Solution structures of the actuator domain of ATP7A and ATP7B, the Menkes and Wilson disease proteins.

Comment on: Acute cholecystitis in Wilson's disease.

Diagnosis and epidemiology of cirrhosis.

Impact of the discovery of human zinc deficiency on health.

Wilson's disease: a case report and a historical review.

Copper in Alzheimer's disease: too much or too little?

Diagnosis of Wilson's disease.

Potential Feasibility of Early Bone Marrow Cell Injection Into the Spleen for Creating Functional Hepatocytes

The impact of inherited thrombophilia on liver transplantation.

The soluble metal-binding domain of the copper transporter ATP7B binds and detoxifies cisplatin

RNA analysis of consensus sequence splicing mutations: implications for the diagnosis of Wilson disease.

Torticolis révélant une maladie de Wilson

[Wilson's disease: pediatric experience in Costa Rica].

[Probing into indication of living-related liver transplantation for Wilson's disease].

Acquired hepatocerebral degeneration

Mimicry of acute cholecystitis from Wilson's disease.

Outcomes of Living-Related Liver Transplantation for Wilson’s Disease: A Single-Center Experience in China

[Father would have never wanted this. Substituted judgement from family members about the treatment of Wilson disease patients].