Studies on levels of penicillamine-induced cupriuresis in heterozygotes of Wilson's disease-Reference-Cited by-同舟云学术

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Studies on levels of penicillamine-induced cupriuresis in heterozygotes of Wilson's disease

Published:1967-06 Issue:6 Volume:16 Page:507-513
ISSN:0026-0495
Container-title:Metabolism
language:en
Short-container-title:Metabolism

Author:

Tu Jun-Bi,Blackwell R.Quentin

Publisher

Elsevier BV

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism

Reference23 articles.

1. Genetic considerations in Wilson's disease;Bearn,1961

2. Wilson's disease;Scheinberg;Ann. Rev. Med.,1965

3. Genetic and biochemical aspects of Wilson's disease;Bearn;Amer. J. Med.,1953

4. A genetic, biochemical and clinical study of Wilson's disease among Chinese in Taiwan;Tu;Acta Paediat. Sinica,1963

Cited by 38 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's Disease;Seminars in Neurology;2023-08

2. Benefits of using exchangeable copper and the ratio of exchangeable copper in a real‐world cohort of patients with Wilson disease;Journal of Inherited Metabolic Disease;2023-06-08

3. Monitoring of Copper in Wilson Disease;Diagnostics;2023-05-23

4. Wilson Disease and Alpha1-Antitrypsin Deficiency: A Review of Non-Invasive Diagnostic Tests;Diagnostics;2023-01-10

5. A multidisciplinary approach to the diagnosis and management of Wilson disease: 2022 Practice Guidance on Wilson disease from the American Association for the Study of Liver Diseases;Hepatology;2022-12-07

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