ReviewJournal of clinical pathology2000
ACP Best Practice No 163. Wilson's disease: acute and presymptomatic laboratory diagnosis and monitoring.
Review in Journal of clinical pathology, 2000. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
11 citing papers in PubMed.
- Current Management of Neurological Wilson's Disease.Tremor and other hyperkinetic movements (New York, N.Y.) · 2025Review
- Article
- Unilateral K-F ring in Wilson's disease.GMS ophthalmology cases · 2023Article
- A review and current perspective on Wilson disease.Journal of clinical and experimental hepatology · 2013Review
- Atomic Absorption Spectrometry in Wilson's Disease and Its Comparison with Other Laboratory Tests and Paraclinical Findings.Iranian journal of pediatrics · 2012Article
- A Case of Wilson's Disease in Patient with Mildly Elevated Liver Enzymes.Korean journal of family medicine · 2011Article
- High ceruloplasmin levels are associated with obsessive compulsive disorder: a case control study.Behavioral and brain functions : BBF · 2008Article
- P wave dispersion is prolonged in patients with Wilson's disease.World journal of gastroenterology · 2008Article
- Copper:caeruloplasmin ratio.Journal of clinical pathology · 2007Article
- Adjusting copper concentrations for caeruloplasmin levels in routine clinical practice.Journal of clinical pathology · 2006Article
- Electronic publishing and internet learning.Journal of clinical pathology · 2002Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
3 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Wilson's disease, the most common inherited disorder of copper metabolism, is a recessive genetic condition. The clinical presentation of Wilson's disease is very variable. It is characterised by low serum copper and caeruloplasmin concentrations coupled with the pathological accumulation of copper in the tissues. However, there are diagnostic difficulties and these are discussed. The current value of DNA diagnosis, both in gene tracking in families or as applied to de novo cases, is examined. Wilson's disease can be treated successfully but treatment must be life long. Patients are best treated by specialist centres with experience and expertise in the condition.
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Registered trials
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