Amyotrophic sclerosis. Medical search. Frequent questions

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Anatomy25

Motor Neurons Spinal Cord Inclusion Bodies Brain Anterior Horn Cells Astrocytes Microglia Axons Central Nervous System Neurons Pyramidal Tracts Myelin Sheath Mitochondria Nerve Fibers, Myelinated Neuroglia Cells, Cultured Neuromuscular Junction Oligodendroglia Chromosomes, Human, Pair 9 Motor Cortex Muscle, Skeletal Cerebral Cortex Hyalin Brain Stem Cell Line

Organisms5

Mice, Transgenic Rats, Transgenic Cycas Mice, Inbred C57BL Animals, Genetically Modified

Diseases44

Amyotrophic Lateral Sclerosis Multiple Sclerosis Sclerosis Tuberous Sclerosis Motor Neuron Disease Scleroderma, Systemic Multiple Sclerosis, Chronic Progressive Frontotemporal Dementia Frontotemporal Lobar Degeneration Disease Models, Animal Nerve Degeneration Neurodegenerative Diseases Disease Progression Fasciculation TDP-43 Proteinopathies Bulbar Palsy, Progressive Encephalomyelitis, Autoimmune, Experimental Scleroderma, Diffuse Demyelinating Diseases Diffuse Cerebral Sclerosis of Schilder Atrophy Optic Neuritis Scleroderma, Limited Pseudobulbar Palsy Sialorrhea Neuromuscular Diseases Genetic Predisposition to Disease Nervous System Diseases Raynaud Disease Muscle Weakness Angiomyolipoma Peritoneal Fibrosis Epilepsy, Temporal Lobe Scleroderma, Localized Dementia Gliosis Paralysis Parkinson Disease Neuromyelitis Optica Respiratory Insufficiency Muscular Atrophy, Spinal Rhabdomyoma Central Nervous System Diseases Brain Diseases

Chemicals and Drugs30

Superoxide Dismutase RNA-Binding Protein FUS Riluzole Neurofilament Proteins Neuroprotective Agents Lithium Carbonate DNA-Binding Proteins Excitatory Amino Acid Transporter 2 Myelin Basic Protein Mutant Proteins Oligoclonal Bands Interferon-beta Ribonuclease, Pancreatic Myelin-Oligodendrocyte Glycoprotein Glial Fibrillary Acidic Protein Amino Acids, Diamino Peripherins Nerve Tissue Proteins Myelin Proteins Copper Biological Markers Glutamic Acid Myelin-Associated Glycoprotein Proteins Ubiquitin Pyrazolones Autoantibodies Myelin Proteolipid Protein Immunologic Factors Glycine

Analytical, Diagnostic and Therapeutic Techniques and Equipment21

Disease Models, Animal Magnetic Resonance Imaging Encephalomyelitis, Autoimmune, Experimental Case-Control Studies Rotarod Performance Test Disability Evaluation Amino Acid Substitution Noninvasive Ventilation Immunohistochemistry Severity of Illness Index Pedigree Electromyography Neurologic Examination Cohort Studies Communication Aids for Disabled Tracheostomy Autopsy Diffusion Tensor Imaging Follow-Up Studies Neuroimaging Reproducibility of Results

Psychiatry and Psychology6

Frontotemporal Dementia Frontotemporal Lobar Degeneration Laughter Dementia Neuropsychological Tests Cognition Disorders

Phenomena and Processes15

DNA Repeat Expansion Mutation Mutation, Missense Amino Acid Substitution Axonal Transport Phenotype Genetic Predisposition to Disease Cell Death Time Factors Protein Folding Chromosomes, Human, Pair 9 Oxidative Stress Cell Survival Gene Expression Regulation Anisotropy

Disciplines and Occupations1

Immunohistochemistry

Anthropology, Education, Sociology and Social Phenomena1

Information Science1

Molecular Sequence Data

Health Care6

Age of Onset Case-Control Studies Severity of Illness Index Cohort Studies Follow-Up Studies Reproducibility of Results

Geographicals2

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

Amyotrophic Lateral Sclerosis Multiple Sclerosis Sclerosis Superoxide Dismutase Tuberous Sclerosis Motor Neuron Disease Motor Neurons Scleroderma, Systemic RNA-Binding Protein FUS Spinal Cord DNA Repeat Expansion Multiple Sclerosis, Chronic Progressive Frontotemporal Dementia Guam Riluzole Mice, Transgenic Inclusion Bodies Frontotemporal Lobar Degeneration Disease Models, Animal Nerve Degeneration Neurodegenerative Diseases Mutation Brain Disease Progression Fasciculation TDP-43 Proteinopathies Anterior Horn Cells Neurofilament Proteins Magnetic Resonance Imaging Bulbar Palsy, Progressive Age of Onset Encephalomyelitis, Autoimmune, Experimental Scleroderma, Diffuse Astrocytes Microglia Demyelinating Diseases Diffuse Cerebral Sclerosis of Schilder Rats, Transgenic Case-Control Studies Axons Neuroprotective Agents Cycas Atrophy Mutation, Missense Optic Neuritis Central Nervous System Scleroderma, Limited Neurons Lithium Carbonate DNA-Binding Proteins Pyramidal Tracts Excitatory Amino Acid Transporter 2 Myelin Basic Protein Rotarod Performance Test Mutant Proteins Pseudobulbar Palsy Disability Evaluation Amino Acid Substitution Mice, Inbred C57BL Sialorrhea Oligoclonal Bands Axonal Transport Interferon-beta Myelin Sheath Phenotype Noninvasive Ventilation Neuromuscular Diseases Genetic Predisposition to Disease Nervous System Diseases Ribonuclease, Pancreatic Myelin-Oligodendrocyte Glycoprotein Cell Death Raynaud Disease Mitochondria Muscle Weakness Immunohistochemistry Nerve Fibers, Myelinated Animals, Genetically Modified Angiomyolipoma Glial Fibrillary Acidic Protein Amino Acids, Diamino Neuroglia Cells, Cultured Peritoneal Fibrosis Severity of Illness Index Pedigree Electromyography Laughter Time Factors Italy Epilepsy, Temporal Lobe Peripherins Nerve Tissue Proteins Protein Folding Scleroderma, Localized Dementia Gliosis Paralysis Myelin Proteins Copper

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