Type ataxia. Medical search. Frequent questions

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Anatomy6

Cerebellum Purkinje Cells Intranuclear Inclusion Bodies Brain Cerebellar Nuclei Chromosomes, Human, Pair 19

Organisms1

Mice, Neurologic Mutants

Diseases35

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

Chemicals and Drugs16

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

Analytical, Diagnostic and Therapeutic Techniques and Equipment5

Pedigree Magnetic Resonance Imaging Neurologic Examination Reflex, Abnormal Disease Models, Animal

Psychiatry and Psychology2

Apraxias Intellectual Disability

Phenomena and Processes19

Trinucleotide Repeat Expansion Trinucleotide Repeats Mutation Genes, Recessive DNA Damage DNA Repeat Expansion Phenotype Genes, Dominant Mutation, Missense Homozygote DNA Repair Radiation, Ionizing Heterozygote Genetic Linkage Reflex, Abnormal Consanguinity Alleles DNA Breaks, Double-Stranded Chromosomes, Human, Pair 19

Information Science1

Molecular Sequence Data

Health Care1

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 Tumor Suppressor Proteins Cell Cycle Proteins Purkinje Cells Pedigree Protein-Serine-Threonine Kinases Cerebellar Diseases Mutation Ocular Motility Disorders Nerve Tissue Proteins Fragile X Syndrome Apraxias Age of Onset Dysarthria DNA-Binding Proteins Fragile X Mental Retardation Protein Genes, Recessive Syndrome DNA Damage Myoclonic Cerebellar Dyssynergia Nystagmus, Pathologic DNA Repeat Expansion Kv1.1 Potassium Channel Magnetic Resonance Imaging Phenotype Mice, Neurologic Mutants Nuclear Proteins Intranuclear Inclusion Bodies Olivopontocerebellar Atrophies Genes, Dominant Heredodegenerative Disorders, Nervous System Mutation, Missense Multiple System Atrophy Brain Gliadin Vitamin E Deficiency Neurologic Examination Calcium Channels, Q-Type Homozygote Myoclonus Calcium Channels, P-Type Neurodegenerative Diseases Atrophy DNA Repair Nervous System Diseases Checkpoint Kinase 2 Radiation, Ionizing Nerve Degeneration Fasciculation Miller Fisher Syndrome Heterozygote Myoclonic Epilepsies, Progressive Genetic Linkage Reflex, Abnormal Spastic Paraplegia, Hereditary Consanguinity Cerebellar Nuclei Epilepsies, Myoclonic Intellectual Disability Ophthalmoplegia Optic Atrophy Hypoalbuminemia Phosphotransferases (Alcohol Group Acceptor)Disease Models, Animal Shaw Potassium Channels Alleles Molecular Sequence Data DNA Breaks, Double-Stranded Chromosomes, Human, Pair 19

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