Monozygotic female twins discordant for phenotype of Wilson's disease
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Summary
The phenotypic characteristics of Wilson's disease are possibly attributable to epigenetic/environmental factors, and the type of mutation in ATP7B only to some degree determines phenotypesic manifestation of WD.
- Type
- article
- Published
- 2009-05-15
- Cited by
- 129
- References
- 111
- OpenAlex
- https://openalex.org/W19306278
- Semantic Scholar
- https://api.semanticscholar.org/CorpusID:52854183
Keywords
Political science
References
- Proposed schizophrenia-related gene polymorphism: expression of the Ser9Gly mutant human dopamine D3 receptor with the Semliki Forest virus system.
- Predictors of Nursing Home Placement in Parkinson's Disease: A Population‐Based, Prospective Study
- Complications and limitations of drug therapy for Parkinson's disease.
- Tourette's syndrome.
- The epidemiology of tics and Tourette syndrome in children and adolescents.
- Attention-deficit hyperactivity disorder : a clinical workbook
- Studies of X inactivation and isodisomy in twins provide further evidence that the X chromosome is not involved in Rett syndrome.
- Projected number of people with Parkinson disease in the most populous nations, 2005 through 2030
- [Treatment of a case of generalised dystonia using subthalamic stimulation].
- Psychiatric Symptoms and Subthalamic Nucleus Stimulation in Parkinson's Disease. A Retrospective Study in Our Japanese Patients
- Subthalamic nucleus stimulation for primary dystonia and tardive dystonia.
- Dopamine D2 receptor gene polymorphism and the risk of levodopa-induced dyskinesias in PD.
- The Wilson's disease gene and phenotypic diversity.
- Association of specialist involvement and quality of care for Parkinson's disease
- Telemedicine for delivery of health care in Parkinson's disease
- Data protection in biomaterial banks for Parkinson's disease research: The model of GEPARD (Gene bank Parkinson's Disease Germany)
- Alleviation of camptocormia by bilateral subthalamic nucleus stimulation in a patient with Parkinson's disease.
- Amino acid substitution in the dopamine D3 receptor as a useful polymorphism for investigating psychiatric disorders
- l -Dopa-induced adverse effects in PD and dopamine transporter gene polymorphism
- Two‐year follow‐up of subthalamic deep brain stimulation in Parkinson's disease
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- Comprehensive analysis on clinical features of Wilson’s disease: an experience over 28 years with 133 cases
- Currently Clinical Views on Genetics of Wilson's Disease
- A genetic study of Wilson's disease in the United Kingdom.
- Systems biology approach to Wilson’s disease
- A feasibility study of conducting the Montreal Cognitive Assessment remotely in individuals with movement disorders
- Web‐based clinical assessments for Parkinson's disease: Reliable and feasible
- Gene variants encoding proteins involved in antioxidant defense system and the clinical expression of Wilson disease
- Potential reliability and validity of a modified version of the Unified Parkinson’s Disease Rating Scale that could be administered remotely
- Genetic variability in the methylenetetrahydrofolate reductase gene (MTHFR) affects clinical expression of Wilson's disease.
- Potentials of Telemedicine for Green Health Care
- Genetics of essential tremor: from phenotype to genes, insights from both human and mouse studies.
- Homozygous Mutations in the Conserved ATP Hinge Region of the Wilson Disease Gene: Association With Liver Disease
- Genetics of Wilson’s disease: a clinical perspective
- Wilson’s Disease: A Comprehensive Review of the Molecular Mechanisms
- Increasing access to specialty care: A pilot, randomized controlled trial of telemedicine for Parkinson's disease
- Maternal choline modifies fetal liver copper, gene expression, DNA methylation, and neonatal growth in the tx-j mouse model of Wilson disease
- Genotype-Phenotype Correlations in a Mountain Population Community with High Prevalence of Wilson’s Disease: Genetic and Clinical Homogeneity
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