Spinal amyotrophic lateral sclerosis. Medical search. Frequent questions

Home page Questions and answers Statistics Donations Contact

Anatomy22

Spinal Cord Motor Neurons Inclusion Bodies Anterior Horn Cells Brain Neurons Astrocytes Microglia Pyramidal Tracts Axons Mitochondria Spinal Nerve Roots Neuroglia Central Nervous System Neuromuscular Junction Muscle, Skeletal Motor Cortex Chromosomes, Human, Pair 9 Spinal Nerves Cells, Cultured Brain Stem Spinal Canal

Organisms5

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

Diseases32

Amyotrophic Lateral Sclerosis Motor Neuron Disease Multiple Sclerosis Frontotemporal Dementia Frontotemporal Lobar Degeneration Disease Models, Animal Nerve Degeneration Neurodegenerative Diseases Fasciculation Spinal Cord Injuries TDP-43 Proteinopathies Sclerosis Bulbar Palsy, Progressive Disease Progression Tuberous Sclerosis Pseudobulbar Palsy Sialorrhea Muscular Atrophy, Spinal Neuromuscular Diseases Muscle Weakness Paralysis Scleroderma, Systemic Dementia Parkinson Disease Gliosis Atrophy Spinal Cord Diseases Genetic Predisposition to Disease Respiratory Insufficiency Nervous System Diseases Multiple Sclerosis, Chronic Progressive Muscular Atrophy

Chemicals and Drugs20

Superoxide Dismutase RNA-Binding Protein FUS Riluzole Neurofilament Proteins Lithium Carbonate Neuroprotective Agents Excitatory Amino Acid Transporter 2 DNA-Binding Proteins Mutant Proteins Ribonuclease, Pancreatic Amino Acids, Diamino Nerve Tissue Proteins Peripherins Glial Fibrillary Acidic Protein Glutamic Acid Copper Ubiquitin Glycine Pyrazolones Proteins

Analytical, Diagnostic and Therapeutic Techniques and Equipment14

Disease Models, Animal Rotarod Performance Test Noninvasive Ventilation Amino Acid Substitution Injections, Spinal Case-Control Studies Electromyography Magnetic Resonance Imaging Immunohistochemistry Pedigree Communication Aids for Disabled Tracheostomy Anesthesia, Spinal Neuroimaging

Psychiatry and Psychology5

Frontotemporal Dementia Frontotemporal Lobar Degeneration Laughter Dementia Motor Activity

Phenomena and Processes14

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

Disciplines and Occupations1

Immunohistochemistry

Health Care2

Age of Onset Case-Control Studies

Geographicals2

Anatomy Organisms Diseases Chemicals and Drugs Analytical, Diagnostic and Therapeutic Techniques and Equipment Psychiatry and Psychology Phenomena and Processes Disciplines and Occupations Health Care Geographicals

Amyotrophic Lateral Sclerosis Superoxide Dismutase Spinal Cord Motor Neuron Disease Motor Neurons RNA-Binding Protein FUS Multiple Sclerosis DNA Repeat Expansion Frontotemporal Dementia Guam Riluzole Frontotemporal Lobar Degeneration Inclusion Bodies Mice, Transgenic Disease Models, Animal Nerve Degeneration Neurodegenerative Diseases Mutation Fasciculation Anterior Horn Cells Spinal Cord Injuries TDP-43 Proteinopathies Sclerosis Bulbar Palsy, Progressive Neurofilament Proteins Disease Progression Rats, Transgenic Brain Age of Onset Neurons Tuberous Sclerosis Astrocytes Mutation, Missense Lithium Carbonate Microglia Cycas Neuroprotective Agents Pyramidal Tracts Excitatory Amino Acid Transporter 2 DNA-Binding Proteins Axons Pseudobulbar Palsy Mutant Proteins Sialorrhea Rotarod Performance Test Muscular Atrophy, Spinal Axonal Transport Noninvasive Ventilation Amino Acid Substitution Ribonuclease, Pancreatic Injections, Spinal Neuromuscular Diseases Animals, Genetically Modified Case-Control Studies Electromyography Muscle Weakness Magnetic Resonance Imaging Mitochondria Amino Acids, Diamino Spinal Nerve Roots Paralysis Cell Death Nerve Tissue Proteins Neuroglia Central Nervous System Peripherins Phenotype Protein Folding Scleroderma, Systemic Neuromuscular Junction Laughter Dementia Mice, Inbred C57BL Glial Fibrillary Acidic Protein Muscle, Skeletal Immunohistochemistry Pedigree Parkinson Disease Gliosis Glutamic Acid Communication Aids for Disabled Copper Tracheostomy Italy Atrophy Motor Cortex Time Factors Spinal Cord Diseases Ubiquitin Chromosomes, Human, Pair 9 Spinal Nerves Glycine Genetic Predisposition to Disease Respiratory Insufficiency Nervous System Diseases Pyrazolones Oxidative Stress Cell Survival Motor Activity Anesthesia, Spinal

No FAQ available that match "spinal amyotrophic lateral sclerosis"