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1	Genetics of Progressive Multifocal Leukoencephalopathy and Acquired Immunodeficiency Syndrome Conditions: PML; AIDS	3042
2	Immunotherapy of the Paraneoplastic Syndromes Condition: Paraneoplastic Syndromes	3064
3	Caspofungin Acetate in Treating Aspergillosis in Patients With Hematologic Cancer or in Patients Who Have Undergone a Stem Cell Transplant Conditions: Cancer; Infection	3033
4	Dietary Supplements for the Treatment of Angelman Syndrome Conditions: Angelman Syndrome; Nervous System Diseases	3039
5	Use of Rituximab in Opsoclonus-Myoclonus in Children With Neuroblastoma Conditions: Neuroblastoma; Opsoclonus-Myoclonus	2928
6	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	2896
7	Phenotype/Genotype Correlations in Movement Disorders Condition: Movement Disorder	3266
8	Natural History, Genetic Bases and Phenotype-Genotype Correlations in Autosomal Conditions: Ataxia; Motor Neuron Disease; Muscular Disease; Muscular Dystrophy; Peripheral Nervous System Disease	3000
9	Study of Inherited Neurological Disorders Conditions: Ataxia; Motor Neuron Disease; Muscular Disease; Muscular Dystrophy; Peripheral Nervous System Disease	3050
10	Characteristics of Episodic Ataxia Syndrome Conditions: Episodic Ataxia Syndrome; Cerebellar Diseases	3039
11	Iron-Chelating Therapy and Friedreich Ataxia Condition: Friedreich Ataxia	3064
12	Clinical and Molecular Correlations in Spinocerebellar Ataxia Type 10 (SCA10) Condition: Hereditary Ataxia	2975
13	Clinical and Genetic Analysis of Cerebellar Ataxias and Spastic Paraplegias Conditions: Cerebellar Ataxias; Spastic Paraplegias	2905
14	Effect of Riluzole as a Symptomatic Approach in Patients With Chronic Cerebellar Ataxia Conditions: Hereditary Ataxia; Multiple Sclerosis; Cerebellar Ataxia	3070
15	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 ...	3188
16	Friedreich's ataxia Friedreich's ataxia (FA) is an inherited, progressive nervous system disorder causing loss of balance and coordination ...	3248
17	Ataxia Lack of coordination in the muscles.	3396
18	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 ...	3238
19	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 ...	3776
20	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...	3394
21	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...	3912
22	Ataxia Treatment	1526