ArticleJournal of genetics2010
Middle-aged heterozygous carriers of Wilson's disease do not present with significant phenotypic deviations related to copper metabolism.
Article in Journal of genetics, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers, 1 of them a synthesis that pooled it.
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
19 citing papers in PubMed, 1 synthesis or guideline pooled it.
- Biomarkers for diagnosis of Wilson's disease.The Cochrane database of systematic reviews · 2019Pooled it
- An incidental heterozygous ATP7B nonsense variant leading to a diagnostic pitfall for Wilson disease: a pediatric case report.BMC gastroenterology · 2026Article
- Macrothrombocytopenia with leukocyte inclusions in a patient with Wilson disease: a case report and literature review.BMC medical genomics · 2024Review
- Monitoring of Copper in Wilson Disease.Diagnostics (Basel, Switzerland) · 2023Review
- Antioxidant Capacity Is Decreased in Wilson's Disease and Correlates to Liver Function.Biological trace element research · 2023Article
- Wilson's Disease-Genetic Puzzles with Diagnostic Implications.Diagnostics (Basel, Switzerland) · 2023Review
- Re-evaluation of the existing health-based guidance values for copper and exposure assessment from all sources.EFSA journal. European Food Safety Authority · 2023Article
- Article
- Management Perspective of Wilson's Disease: Early Diagnosis and Individualized Therapy.Current neuropharmacology · 2021Article
- Transcranial sonography changes in heterozygotic carriers of the ATP7B gene.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2020Article
- Article
- Critical Review of Exposure and Effects: Implications for Setting Regulatory Health Criteria for Ingested Copper.Environmental management · 2020Review
- Biochemical Markers for the Diagnosis and Monitoring of Wilson Disease.The Clinical biochemist. Reviews · 2019Review
- Difficulties in diagnosis and treatment of Wilson disease-a case series of five patients.Annals of translational medicine · 2019Article
- New tools for Wilson's disease diagnosis: exchangeable copper fraction.Annals of translational medicine · 2019Review
- Population screening and diagnostic strategies in screening family members of Wilson's disease patients.Annals of translational medicine · 2019Review
- Distinct phenotype of a Wilson disease mutation reveals a novel trafficking determinant in the copper transporter ATP7B.Proceedings of the National Academy of Sciences of the United States of America · 2014Article
- Treatment with D-penicillamine or zinc sulphate affects copper metabolism and improves but not normalizes antioxidant capacity parameters in Wilson disease.Biometals : an international journal on the role of metal ions in biology, biochemistry, and medicine · 2014Article
- Challenges and Recent Advances in Diagnosing Wilson Disease.Journal of clinical and experimental hepatologyReview
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
6 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
PubMed holds no abstract for this paper.
Indexed as
Identifiers
21273697What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.