Common coordination ataxia. Medical search. Frequent questions

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Anatomy24

Cerebellum Purkinje Cells Hand Brain Fingers Neurons Arm Intranuclear Inclusion Bodies Extremities Cerebellar Nuclei Cerebellar Cortex Cell Line Spinal Cord Joints Muscle, Skeletal Brain Stem Cells, Cultured Motor Neurons Fibroblasts Mitochondria Forelimb Ganglia, Invertebrate Parietal Lobe Cell Nucleus

Organisms6

Mice, Neurologic Mutants Mice, Knockout Mice, Transgenic Mice, Inbred C57BL Saccharomyces cerevisiae Escherichia coli

Diseases41

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

Chemicals and Drugs49

Ataxia Telangiectasia Mutated Proteins Coordination Complexes Iron-Binding Proteins Cell Cycle Proteins Tumor Suppressor Proteins Protein-Serine-Threonine Kinases Zinc Nerve Tissue Proteins DNA-Binding Proteins Iron Copper Organometallic Compounds Nuclear Proteins Metals Ligands Fragile X Mental Retardation Protein Heme Histidine Cobalt Kv1.1 Potassium Channel Transition Elements Lanthanoid Series Elements Metalloproteins Nickel DNA Manganese Gliadin Iron-Sulfur Proteins Hemeproteins Peptides Calcium Channels, Q-Type Cadmium Calcium Channels, P-Type Water Checkpoint Kinase 2 Ions Cations, Divalent Histones Phosphotransferases (Alcohol Group Acceptor)Ferrous Compounds Transcription Factors RNA, Messenger Oxygen Proteins Sulfur Tumor Suppressor Protein p53 Chelating Agents Shaw Potassium Channels Bacterial Proteins

Analytical, Diagnostic and Therapeutic Techniques and Equipment26

Models, Molecular Pedigree Rotarod Performance Test Crystallography, X-Ray X-Ray Absorption Spectroscopy Gait Electron Spin Resonance Spectroscopy Magnetic Resonance Imaging Models, Biological Spectrum Analysis Electromyography Neurologic Examination Hand Strength Magnetic Resonance Spectroscopy Spectrum Analysis, Raman Analysis of Variance Spectrophotometry Disease Models, Animal Reflex, Abnormal Models, Chemical Circular Dichroism Mutagenesis, Site-Directed DNA Mutational Analysis Spectroscopy, Mossbauer Models, Organizational Chromosome Mapping

Psychiatry and Psychology16

Psychomotor Performance Motor Skills Disorders Motor Skills Motor Activity Apraxias Functional Laterality Behavior, Animal Psychomotor Disorders Task Performance and Analysis Cooperative Behavior Proprioception Apraxia, Ideomotor Feedback, Sensory Reaction Time Intellectual Disability Interdisciplinary Communication

Phenomena and Processes67

Psychomotor Performance Trinucleotide Repeat Expansion Trinucleotide Repeats Movement Mutation Musculoskeletal Physiological Phenomena Biomechanical Phenomena Motor Activity Locomotion Binding Sites Postural Balance Amino Acid Sequence Gait Phenotype DNA Damage Protein Binding Functional Laterality Genes, Recessive Time Factors Protein Conformation Protein Structure, Tertiary DNA Repeat Expansion Molecular Structure Hand Strength Mutation, Missense Signal Transduction Posture Periodicity X-Rays DNA Repair Base Sequence Eye Movements Kinetics Genes, Dominant Saccades Oxidation-Reduction Catalytic Domain Deglutition Head Movements Homozygote Reflex, Abnormal Molecular Conformation Catalysis Walking Cell Cycle Phosphorylation Alleles Hydrogen Bonding Fixation, Ocular Heterozygote Proprioception Feedback, Sensory Radiation, Ionizing DNA Breaks, Double-Stranded Sequence Homology, Amino Acid Reaction Time DNA Replication Protein Structure, Secondary Genetic Linkage Point Mutation Adaptation, Physiological Hydrogen-Ion Concentration Swimming Gamma Rays Consanguinity Gene Expression Regulation Thermodynamics

Disciplines and Occupations1

Anthropology, Education, Sociology and Social Phenomena2

Walking Swimming

Information Science8

Molecular Sequence Data Amino Acid Sequence Base Sequence Feedback, Sensory Video Recording Handwriting Interdisciplinary Communication Feedback

Health Care9

Age of Onset Continuity of Patient Care Patient Care Management Analysis of Variance Patient Care Team Delivery of Health Care, Integrated Patient-Centered Care Interinstitutional Relations Models, Organizational

Anatomy Organisms Diseases Chemicals and Drugs Analytical, Diagnostic and Therapeutic Techniques and Equipment Psychiatry and Psychology Phenomena and Processes Disciplines and Occupations Anthropology, Education, Sociology and Social Phenomena Information Science Health Care

Ataxia Cerebellar Ataxia Friedreich Ataxia Spinocerebellar Ataxias Gait Ataxia Ataxia Telangiectasia Ataxia Telangiectasia Mutated Proteins Coordination Complexes Iron-Binding Proteins Machado-Joseph Disease Psychomotor Performance Motor Skills Disorders Cerebellum Trinucleotide Repeat Expansion Trinucleotide Repeats Movement Mutation Purkinje Cells Cell Cycle Proteins Motor Skills Tumor Suppressor Proteins Models, Molecular Musculoskeletal Physiological Phenomena Biomechanical Phenomena Cerebellar Diseases Protein-Serine-Threonine Kinases Zinc Motor Activity Locomotion Molecular Sequence Data Nerve Tissue Proteins Binding Sites Pedigree DNA-Binding Proteins Ocular Motility Disorders Postural Balance Rotarod Performance Test Apraxias Iron Crystallography, X-Ray Hand Copper Amino Acid Sequence X-Ray Absorption Spectroscopy Organometallic Compounds Gait Phenotype Electron Spin Resonance Spectroscopy DNA Damage Fragile X Syndrome Magnetic Resonance Imaging Protein Binding Mice, Neurologic Mutants Models, Biological Age of Onset Nuclear Proteins Brain Metals Dysarthria Functional Laterality Ligands Fragile X Mental Retardation Protein Spectrum Analysis Heme Electromyography Genes, Recessive Fingers Histidine Syndrome Myoclonic Cerebellar Dyssynergia Continuity of Patient Care Cobalt Time Factors Nystagmus, Pathologic Protein Conformation Behavior, Animal Neurologic Examination Protein Structure, Tertiary DNA Repeat Expansion Kv1.1 Potassium Channel Molecular Structure Hand Strength Magnetic Resonance Spectroscopy Mutation, Missense Movement Disorders Spectrum Analysis, Raman Signal Transduction Neurons Patient Care Management Posture Arm Periodicity Intranuclear Inclusion Bodies Transition Elements Olivopontocerebellar Atrophies Lanthanoid Series Elements X-Rays Metalloproteins Mice, Knockout DNA Repair

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