Neurodegenerative diseases parkinson disease. Medical search. Frequent questions

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Anatomy33

Neurons Brain Lewy Bodies Substantia Nigra Dopaminergic Neurons Inclusion Bodies Mitochondria Microglia Subthalamic Nucleus Corpus Striatum Putamen Mesencephalon Pedunculopontine Tegmental Nucleus Cells, Cultured Astrocytes Cerebral Cortex Globus Pallidus Neurofibrillary Tangles Cell Line Hippocampus PC12 Cells Central Nervous System Motor Neurons Lysosomes Neuroglia Neostriatum Basal Ganglia HEK293 Cells Axons Intranuclear Inclusion Bodies Spinal Cord Cerebellum Cell Line, Tumor

Organisms7

Mice, Transgenic Mice, Inbred C57BL Animals, Genetically Modified Mice, Knockout Cycas Rats, Sprague-Dawley Drosophila melanogaster

Diseases62

Parkinson Disease Neurodegenerative Diseases Parkinsonian Disorders Nerve Degeneration Parkinson Disease, Secondary Alzheimer Disease Amyotrophic Lateral Sclerosis Huntington Disease Lewy Body Disease Disease Models, Animal Multiple System Atrophy Supranuclear Palsy, Progressive MPTP Poisoning Dementia Tauopathies Gait Disorders, Neurologic Heredodegenerative Disorders, Nervous System Proteostasis Deficiencies REM Sleep Behavior Disorder Prion Diseases Spinocerebellar Ataxias Frontotemporal Lobar Degeneration Essential Tremor Genetic Predisposition to Disease Frontotemporal Dementia Friedreich Ataxia Movement Disorders Gaucher Disease Neuronal Ceroid-Lipofuscinoses Hypokinesia Nervous System Diseases Postmortem Changes Disease Progression Motor Neuron Disease Mitochondrial Diseases Central Nervous System Diseases Muscular Atrophy, Spinal Pick Disease of the Brain Manganese Poisoning Gliosis Tremor Olfaction Disorders Dyskinesias Plaque, Amyloid Sleep Arousal Disorders Primary Dysautonomias Atrophy TDP-43 Proteinopathies Neuroaxonal Dystrophies Ataxia Dyskinesia, Drug-Induced Pure Autonomic Failure Encephalitis Trauma, Nervous System Creutzfeldt-Jakob Syndrome Neuroblastoma Machado-Joseph Disease Brain Diseases Spinocerebellar Degenerations Neurotoxicity Syndromes Sweat Gland Diseases Scrapie

Chemicals and Drugs71

alpha-Synuclein Antiparkinson Agents tau Proteins Levodopa Glucosylceramidase Neuroprotective Agents Nerve Tissue Proteins Dopamine 1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine Synucleins Oxidopamine Prions Amyloid beta-Peptides beta-Synuclein Ubiquitin-Protein Ligases Amyloid Tyrosine 3-Monooxygenase 1-Methyl-4-phenylpyridinium Neurotoxins Ubiquitin Proteasome Endopeptidase Complex Oncogene Proteins Rotenone Superoxide Dismutase Pergolide Maneb Peptides Paraquat Reactive Oxygen Species Carbidopa Mitochondrial Proteins Benzothiazoles Dopamine Agents Iron-Binding Proteins Dopamine Plasma Membrane Transport Proteins Thiazoles Antioxidants Biological Markers 3,4-Dihydroxyphenylacetic Acid Molecular Chaperones Mutant Proteins RNA-Binding Protein FUS Tropanes Glial Cell Line-Derived Neurotrophic Factor Green Fluorescent Proteins Protein-Serine-Threonine Kinases Nuclear Proteins Intracellular Signaling Peptides and Proteins PrPSc Proteins Amino Acids, Diamino Electron Transport Complex I Peptide Fragments Cyclin-Dependent Kinase 5 Dopamine Agonists Herbicides Neurofilament Proteins Amyloid beta-Protein Precursor Adrenergic Agents PrPC Proteins Sodium Benzoate Hydrogen Peroxide RNA, Messenger Glial Fibrillary Acidic Protein Nitro Compounds Amyloidogenic Proteins Pemoline Selenoprotein W Iron Vesicular Monoamine Transport Proteins DNA, Mitochondrial Protein Kinases

Analytical, Diagnostic and Therapeutic Techniques and Equipment24

Disease Models, Animal Deep Brain Stimulation Dance Therapy Models, Biological Gait Case-Control Studies Immunohistochemistry Analysis of Variance Positron-Emission Tomography Blotting, Western Magnetic Resonance Imaging Severity of Illness Index Genetic Testing Genome-Wide Association Study Neurologic Examination Autopsy Reproducibility of Results Rotarod Performance Test DNA Mutational Analysis Cohort Studies Transfection Amino Acid Substitution Stereotaxic Techniques Risk Factors

Psychiatry and Psychology23

Alzheimer Disease Huntington Disease Lewy Body Disease Dementia REM Sleep Behavior Disorder Dance Therapy Frontotemporal Lobar Degeneration Frontotemporal Dementia Neuropsychological Tests Cognition Disorders Introversion (Psychology)Motor Activity Pick Disease of the Brain Apathy Sleep Arousal Disorders Cognition Creutzfeldt-Jakob Syndrome Mental Status Schedule Mild Cognitive Impairment Psychomotor Performance Motor Skills Reality Therapy Behavior, Animal

Phenomena and Processes44

Mutation Oxidative Stress Autophagy Cell Death Postural Balance Aging Protein Folding Genetic Predisposition to Disease Trinucleotide Repeat Expansion Gait DNA Repeat Expansion Cell Survival Gene Expression Regulation Signal Transduction Apoptosis Mutation, Missense Phenotype Protein Binding Proteolysis Time Factors Axonal Transport Motor Activity Trinucleotide Repeats Amino Acid Sequence Cytoprotection Mitochondrial Degradation Phosphorylation Protein Multimerization Genotype Polymorphism, Single Nucleotide Protein Transport Oxidation-Reduction Protein Structure, Tertiary Ubiquitination Transfection Gene Expression Dose-Response Relationship, Drug Psychomotor Performance Up-Regulation Amino Acid Substitution Protein Structure, Secondary Penetrance Neurogenesis Hormesis

Disciplines and Occupations1

Immunohistochemistry

Anthropology, Education, Sociology and Social Phenomena1

Information Science3

Molecular Sequence Data Amino Acid Sequence Image Processing, Computer-Assisted

Health Care10

Age of Onset Case-Control Studies Analysis of Variance Severity of Illness Index Genetic Testing Genome-Wide Association Study Reproducibility of Results Age Factors Cohort Studies Risk Factors

Geographicals1

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 Geographicals

Parkinson Disease Neurodegenerative Diseases alpha-Synuclein Antiparkinson Agents Parkinsonian Disorders Nerve Degeneration Neurons Brain Lewy Bodies Parkinson Disease, Secondary Alzheimer Disease Substantia Nigra tau Proteins Levodopa Amyotrophic Lateral Sclerosis Glucosylceramidase Huntington Disease Lewy Body Disease Neuroprotective Agents Disease Models, Animal Nerve Tissue Proteins Dopaminergic Neurons Dopamine 1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine Multiple System Atrophy Synucleins Deep Brain Stimulation Inclusion Bodies Mutation Supranuclear Palsy, Progressive Oxidopamine Mitochondria MPTP Poisoning Dementia Tauopathies Microglia Oxidative Stress Prions Amyloid beta-Peptides Subthalamic Nucleus Autophagy Gait Disorders, Neurologic beta-Synuclein Mice, Transgenic Cell Death Heredodegenerative Disorders, Nervous System Ubiquitin-Protein Ligases Proteostasis Deficiencies Corpus Striatum Postural Balance Amyloid Tyrosine 3-Monooxygenase REM Sleep Behavior Disorder Prion Diseases Dance Therapy Putamen Spinocerebellar Ataxias 1-Methyl-4-phenylpyridinium Neurotoxins Frontotemporal Lobar Degeneration Essential Tremor Models, Biological Ubiquitin Proteasome Endopeptidase Complex Age of Onset Aging Mesencephalon Protein Folding Genetic Predisposition to Disease Trinucleotide Repeat Expansion Frontotemporal Dementia Neuropsychological Tests Mice, Inbred C57BL Pedunculopontine Tegmental Nucleus Friedreich Ataxia Cells, Cultured Cognition Disorders Oncogene Proteins Astrocytes Movement Disorders Gait DNA Repeat Expansion Gaucher Disease Rotenone Superoxide Dismutase Neuronal Ceroid-Lipofuscinoses Guam Pergolide Cerebral Cortex Hypokinesia Nervous System Diseases Cell Survival Case-Control Studies Gene Expression Regulation Maneb Globus Pallidus Immunohistochemistry Peptides Postmortem Changes Neurofibrillary Tangles

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