Disease or amyotrophic. Medical search. Frequent questions

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Anatomy17

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

Organisms5

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

Diseases21

Amyotrophic Lateral Sclerosis Motor Neuron Disease Frontotemporal Dementia Frontotemporal Lobar Degeneration Nerve Degeneration Neurodegenerative Diseases Disease Models, Animal Fasciculation TDP-43 Proteinopathies Bulbar Palsy, Progressive Disease Progression Pseudobulbar Palsy Sialorrhea Neuromuscular Diseases Muscle Weakness Dementia Paralysis Parkinson Disease Muscular Atrophy, Spinal Gliosis Respiratory Insufficiency

Chemicals and Drugs19

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

Analytical, Diagnostic and Therapeutic Techniques and Equipment9

Disease Models, Animal Rotarod Performance Test Amino Acid Substitution Noninvasive Ventilation Electromyography Case-Control Studies Pedigree Tracheostomy Communication Aids for Disabled

Psychiatry and Psychology4

Frontotemporal Dementia Frontotemporal Lobar Degeneration Dementia Laughter

Phenomena and Processes10

DNA Repeat Expansion Mutation Mutation, Missense Amino Acid Substitution Axonal Transport Protein Folding Cell Death Phenotype Chromosomes, Human, Pair 9 Oxidative Stress

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 Health Care Geographicals

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

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