Enlaces web      Genetics of Progressive Multifocal Leukoencephalopathy and Acquired Immunodeficiency Syndrome Conditions: PML; AIDS      Immunotherapy of the Paraneoplastic Syndromes Condition: Paraneoplastic Syndromes      Caspofungin Acetate in Treating Aspergillosis in Patients With Hematologic Cancer or in Patients Who Have Undergone a Stem Cell Transplant Conditions: Cancer; Infection      Dietary Supplements for the Treatment of Angelman Syndrome Conditions: Angelman Syndrome; Nervous System Diseases      Use of Rituximab in Opsoclonus-Myoclonus in Children With Neuroblastoma Conditions: Neuroblastoma; Opsoclonus-Myoclonus      Cyclophosphamide and Prednisone With or Without Immunoglobulin in Treating Abnormal Muscle Movement in Children With Neuroblastoma Conditions: Localized Resectable Neuroblastoma; Regional Neuroblastoma; Disseminated Neuroblastoma; Stage 4S Neuroblastoma; Localized Unresectable Neuroblastoma      Phenotype/Genotype Correlations in Movement Disorders Condition: Movement Disorder      Natural History, Genetic Bases and Phenotype-Genotype Correlations in Autosomal Conditions: Ataxia; Motor Neuron Disease; Muscular Disease; Muscular Dystrophy; Peripheral Nervous System Disease      Study of Inherited Neurological Disorders Conditions: Ataxia; Motor Neuron Disease; Muscular Disease; Muscular Dystrophy; Peripheral Nervous System Disease      Characteristics of Episodic Ataxia Syndrome Conditions: Episodic Ataxia Syndrome; Cerebellar Diseases      Iron-Chelating Therapy and Friedreich Ataxia Condition: Friedreich Ataxia      Clinical and Molecular Correlations in Spinocerebellar Ataxia Type 10 (SCA10) Condition: Hereditary Ataxia      Clinical and Genetic Analysis of Cerebellar Ataxias and Spastic Paraplegias Conditions: Cerebellar Ataxias; Spastic Paraplegias      Effect of Riluzole as a Symptomatic Approach in Patients With Chronic Cerebellar Ataxia Conditions: Hereditary Ataxia; Multiple Sclerosis; Cerebellar Ataxia      NINDS Ataxias and Cerebellar/Spinocerebellar Degeneration Information Page Ataxia often occurs when parts of the nervous system that control movement are damaged. People with ataxia experience a failure of muscle control in their arms and legs ...      Friedreich's ataxia Friedreich's ataxia (FA) is an inherited, progressive nervous system disorder causing loss of balance and coordination ...      Ataxia Lack of coordination in the muscles.      Supplemental support - vitamin E can reduce some ataxia symptoms - Brief Article According to research, vitamin E supplements can reduce symptoms of some types of hereditary ataxia (i.e., neurological disorders that result in uncontrollable ...      Vitaminlike compound eases rare disorder - cerebellar ataxia - Brief Article Researcher Salvatore DiMauro had never seen anything like it. An 11-year-old boy who had been wheelchair-bound for years was up and walking, thanks to some pills you can buy over the counter ...      Ataxia-telangiectasia Ataxia-telangiectasia (A-T), also called Louis-Bar syndrome, is a rare genetic disease. It affects multiple systems. Individuals with A-T usually die by...      Friedreich's ataxia: disease mechanisms, antioxidant and coenzyme Q10 therapy Cooper JM, Schapira AH, Biofactors 2003;18:163-171. Mitochondria clearly play a central role in the pathogenesis of Friedreich's ataxia. The most common genetic abnormality results in the deficie...

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