Onset than ataxia. Medical search. Frequent questions

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Anatomy12

Cerebellum Purkinje Cells Brain Intranuclear Inclusion Bodies Neurons Cell Line Cerebellar Nuclei Brain Stem Fibroblasts Cells, Cultured Chromosomes, Human, Pair 19 Cerebellar Cortex

Organisms4

Mice, Neurologic Mutants Mice, Transgenic Mice, Knockout Mice, Inbred C57BL

Diseases39

Ataxia Cerebellar Ataxia Friedreich Ataxia Spinocerebellar Ataxias Gait Ataxia Ataxia Telangiectasia Machado-Joseph Disease Cerebellar Diseases Ocular Motility Disorders Syndrome Dysarthria Fragile X Syndrome Apraxias Myoclonic Cerebellar Dyssynergia Nystagmus, Pathologic Olivopontocerebellar Atrophies Disease Models, Animal Heredodegenerative Disorders, Nervous System Multiple System Atrophy Atrophy Myoclonus Nervous System Diseases Neurodegenerative Diseases Vitamin E Deficiency Nerve Degeneration Disease Progression Reflex, Abnormal Epilepsies, Myoclonic Ophthalmoplegia Fasciculation Miller Fisher Syndrome Spastic Paraplegia, Hereditary Intellectual Disability Myoclonic Epilepsies, Progressive Optic Atrophy Seizures Hypoalbuminemia Chorea Muscle Spasticity

Chemicals and Drugs16

Ataxia Telangiectasia Mutated Proteins Iron-Binding Proteins Cell Cycle Proteins Tumor Suppressor Proteins Protein-Serine-Threonine Kinases Nerve Tissue Proteins DNA-Binding Proteins Fragile X Mental Retardation Protein Nuclear Proteins Kv1.1 Potassium Channel Gliadin Calcium Channels, Q-Type Calcium Channels, P-Type Checkpoint Kinase 2 Shaw Potassium Channels Phosphotransferases (Alcohol Group Acceptor)

Analytical, Diagnostic and Therapeutic Techniques and Equipment13

Pedigree Magnetic Resonance Imaging Disease Models, Animal Neurologic Examination Reflex, Abnormal DNA Mutational Analysis Severity of Illness Index Electroencephalography Chromosome Mapping Case-Control Studies Genetic Testing Rotarod Performance Test Fatal Outcome

Psychiatry and Psychology2

Apraxias Intellectual Disability

Phenomena and Processes26

Trinucleotide Repeat Expansion Trinucleotide Repeats Mutation Time Factors Genes, Recessive DNA Damage DNA Repeat Expansion Genes, Dominant Phenotype Mutation, Missense Labor Onset Homozygote Heterozygote Genetic Linkage Alleles DNA Repair Genotype Reflex, Abnormal Consanguinity Radiation, Ionizing Base Sequence Haplotypes Phosphorylation Chromosomes, Human, Pair 19 DNA Breaks, Double-Stranded Amino Acid Sequence

Information Science4

Molecular Sequence Data Base Sequence Fatal Outcome Amino Acid Sequence

Health Care7

Age of Onset Severity of Illness Index Family Health Case-Control Studies Genetic Testing Age Factors Fatal Outcome

Anatomy Organisms Diseases Chemicals and Drugs Analytical, Diagnostic and Therapeutic Techniques and Equipment Psychiatry and Psychology Phenomena and Processes Information Science Health Care

Ataxia Cerebellar Ataxia Friedreich Ataxia Spinocerebellar Ataxias Gait Ataxia Ataxia Telangiectasia Ataxia Telangiectasia Mutated Proteins Iron-Binding Proteins Machado-Joseph Disease Trinucleotide Repeat Expansion Trinucleotide Repeats Cerebellum Cell Cycle Proteins Pedigree Tumor Suppressor Proteins Mutation Purkinje Cells Protein-Serine-Threonine Kinases Cerebellar Diseases Nerve Tissue Proteins Ocular Motility Disorders Magnetic Resonance Imaging Syndrome Dysarthria Fragile X Syndrome Apraxias DNA-Binding Proteins Time Factors Genes, Recessive Age of Onset Fragile X Mental Retardation Protein DNA Damage Myoclonic Cerebellar Dyssynergia Brain Nystagmus, Pathologic Nuclear Proteins DNA Repeat Expansion Genes, Dominant Mice, Neurologic Mutants Kv1.1 Potassium Channel Phenotype Olivopontocerebellar Atrophies Intranuclear Inclusion Bodies Mutation, Missense Disease Models, Animal Labor Onset Neurologic Examination Heredodegenerative Disorders, Nervous System Homozygote Multiple System Atrophy Atrophy Myoclonus Nervous System Diseases Heterozygote Gliadin Neurodegenerative Diseases Molecular Sequence Data Vitamin E Deficiency Genetic Linkage Alleles Nerve Degeneration Calcium Channels, Q-Type Mice, Transgenic DNA Repair Neurons Disease Progression Calcium Channels, P-Type Genotype Reflex, Abnormal DNA Mutational Analysis Checkpoint Kinase 2 Epilepsies, Myoclonic Severity of Illness Index Consanguinity Ophthalmoplegia Mice, Knockout Fasciculation Miller Fisher Syndrome Family Health Radiation, Ionizing Spastic Paraplegia, Hereditary Base Sequence Intellectual Disability Myoclonic Epilepsies, Progressive Electroencephalography Cell Line Cerebellar Nuclei Optic Atrophy Seizures Brain Stem Haplotypes Hypoalbuminemia Chromosome Mapping Fibroblasts Phosphorylation Cells, Cultured Chromosomes, Human, Pair 19 Chorea Shaw Potassium Channels Phosphotransferases (Alcohol Group Acceptor)

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