Ataxia neurological impairments. Medical search. Frequent questions

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Anatomy17

Brain Thoracic Vertebrae Cervical Vertebrae Cerebral Cortex Cerebellum Purkinje Cells Hippocampus Neurons Intranuclear Inclusion Bodies Cells, Cultured Mitochondria Cell Line Cerebellar Nuclei Fibroblasts Brain Stem Cerebellar Cortex Chromosomes, Human, Pair 19

Organisms7

Mice, Inbred C57BL Mice, Neurologic Mutants Mice, Knockout Mice, Transgenic Rats, Sprague-Dawley Rats, Wistar Mice, Mutant Strains

Diseases82

Ataxia Nervous System Diseases Cerebellar Ataxia Friedreich Ataxia Brain Diseases, Metabolic, Inborn Spinocerebellar Ataxias Somatosensory Disorders Quadriplegia Gait Ataxia Cerebral Palsy Ataxia Telangiectasia Stroke Brain Diseases Intellectual Disability Spinal Fractures Brain Injuries Epilepsy Spinal Cord Injuries Disease Models, Animal Acute Disease Machado-Joseph Disease Memory Disorders Vision Disorders Apraxias Alzheimer Disease Cerebellar Diseases Atrophy Dementia Ocular Motility Disorders Amnesia Syndrome Fragile X Syndrome Dysarthria Language Disorders Hearing Loss Vision, Low Nystagmus, Pathologic Myoclonic Cerebellar Dyssynergia Movement Disorders Language Development Disorders Psychomotor Disorders Hearing Disorders Sensation Disorders Blindness Learning Disorders Neurodegenerative Diseases Disease Progression Nerve Degeneration Olivopontocerebellar Atrophies Hearing Loss, Sensorineural Multiple System Atrophy Heredodegenerative Disorders, Nervous System Speech Disorders Reflex, Abnormal Olfaction Disorders Parkinson Disease Vitamin E Deficiency Paresis Deafness Peripheral Nervous System Diseases Spastic Paraplegia, Hereditary Myoclonus Gait Disorders, Neurologic Muscle Spasticity Epilepsies, Myoclonic Ophthalmoplegia Optic Atrophy Dementia, Vascular Fasciculation Miller Fisher Syndrome Myoclonic Epilepsies, Progressive Seizures Mitochondrial Diseases Perceptual Disorders Chronic Disease Gait Apraxia Huntington Disease Hypoalbuminemia Eye Diseases Chorea Parkinsonian Disorders Renal Insufficiency

Chemicals and Drugs20

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 Nuclear Proteins Kv1.1 Potassium Channel Gliadin Calcium Channels, Q-Type Calcium Channels, P-Type Checkpoint Kinase 2 Amyloid beta-Peptides Scopolamine Hydrobromide RNA, Messenger Phosphotransferases (Alcohol Group Acceptor)Peptides Shaw Potassium Channels

Analytical, Diagnostic and Therapeutic Techniques and Equipment35

Neurologic Examination Magnetic Resonance Imaging Severity of Illness Index Analysis of Variance Disability Evaluation Treatment Outcome Retrospective Studies Activities of Daily Living Disease Models, Animal Follow-Up Studies Case-Control Studies Prospective Studies Risk Factors Cohort Studies Prognosis Pedigree Rotarod Performance Test Prevalence Reflex, Abnormal Cross-Sectional Studies Gait Geriatric Assessment Longitudinal Studies DNA Mutational Analysis Visual Acuity Questionnaires Reproducibility of Results Electroencephalography Chromosome Mapping Statistics, Nonparametric Reference Values Brain Mapping Genetic Testing Immunohistochemistry Audiometry

Psychiatry and Psychology46

Cognition Disorders Intellectual Disability Mild Cognitive Impairment Neuropsychological Tests Memory Disorders Apraxias Alzheimer Disease Dementia Amnesia Memory Cognition Maze Learning Psychomotor Performance Psychomotor Disorders Learning Disorders Motor Activity Executive Function Behavior, Animal Mental Status Schedule Language Tests Motor Skills Disorders Memory, Short-Term Reaction Time Psychiatric Status Rating Scales Motor Skills Verbal Learning Developmental Disabilities Visual Acuity Schizophrenia Avoidance Learning Attention Recognition (Psychology)Dementia, Vascular Intelligence Tests Mental Recall Spatial Behavior Intelligence Schizophrenic Psychology Perceptual Disorders Functional Laterality Learning Psychometrics Exploratory Behavior Gait Apraxia Space Perception Huntington Disease

Phenomena and Processes39

Time Factors Trinucleotide Repeat Expansion Trinucleotide Repeats Mutation Phenotype Genes, Recessive Aging Psychomotor Performance DNA Damage Motor Activity DNA Repeat Expansion Genes, Dominant Mutation, Missense Homozygote Postural Balance Heterozygote Reflex, Abnormal Gait Reaction Time Consanguinity Genetic Linkage DNA Repair Genotype Oxidative Stress Phosphorylation Alleles Visual Acuity Dose-Response Relationship, Drug Signal Transduction Base Sequence Radiation, Ionizing Functional Laterality Haplotypes Recovery of Function Chromosomes, Human, Pair 19 Point Mutation Amino Acid Sequence DNA Breaks, Double-Stranded Apoptosis

Disciplines and Occupations1

Immunohistochemistry

Anthropology, Education, Sociology and Social Phenomena4

Activities of Daily Living Geriatric Assessment Quality of Life Spatial Behavior

Humanities1

Quality of Life

Information Science6

Prevalence Geriatric Assessment Molecular Sequence Data Questionnaires Base Sequence Amino Acid Sequence

Named Groups3

Infant, Newborn Visually Impaired Persons Disabled Persons

Health Care21

Severity of Illness Index Analysis of Variance Treatment Outcome Retrospective Studies Activities of Daily Living Follow-Up Studies Case-Control Studies Prospective Studies Risk Factors Cohort Studies Age of Onset Age Factors Prevalence Cross-Sectional Studies Geriatric Assessment Longitudinal Studies Questionnaires Reproducibility of Results Family Health Statistics, Nonparametric Genetic Testing

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

Ataxia Nervous System Diseases Cerebellar Ataxia Friedreich Ataxia Brain Diseases, Metabolic, Inborn Spinocerebellar Ataxias Neurologic Examination Somatosensory Disorders Quadriplegia Gait Ataxia Brain Cognition Disorders Cerebral Palsy Ataxia Telangiectasia Stroke Brain Diseases Intellectual Disability Thoracic Vertebrae Magnetic Resonance Imaging Cervical Vertebrae Ataxia Telangiectasia Mutated Proteins Severity of Illness Index Infant, Newborn Spinal Fractures Analysis of Variance Brain Injuries Disability Evaluation Treatment Outcome Epilepsy Retrospective Studies Spinal Cord Injuries Time Factors Activities of Daily Living Disease Models, Animal Follow-Up Studies Acute Disease Case-Control Studies Cerebral Cortex Prospective Studies Risk Factors Cohort Studies Mild Cognitive Impairment Iron-Binding Proteins Prognosis Mice, Inbred C57BL Machado-Joseph Disease Neuropsychological Tests Trinucleotide Repeat Expansion Cerebellum Memory Disorders Trinucleotide Repeats Pedigree Mutation Tumor Suppressor Proteins Cell Cycle Proteins Vision Disorders Purkinje Cells Apraxias Protein-Serine-Threonine Kinases Alzheimer Disease Cerebellar Diseases Age of Onset Nerve Tissue Proteins Atrophy Dementia Visually Impaired Persons Ocular Motility Disorders Amnesia Memory Syndrome Fragile X Syndrome Phenotype Cognition Maze Learning Genes, Recessive Dysarthria Language Disorders DNA-Binding Proteins Fragile X Mental Retardation Protein Hearing Loss Aging Psychomotor Performance DNA Damage Vision, Low Mice, Neurologic Mutants Nystagmus, Pathologic Hippocampus Myoclonic Cerebellar Dyssynergia Movement Disorders Language Development Disorders Psychomotor Disorders Hearing Disorders Nuclear Proteins Sensation Disorders Blindness Learning Disorders Motor Activity DNA Repeat Expansion Genes, Dominant Executive Function

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