Atrophy 1. Medical search. Frequent questions

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Anatomy13

Muscle, Skeletal Brain Muscle Fibers, Skeletal Temporal Lobe Motor Neurons Fundus Oculi Hippocampus Anterior Horn Cells Cerebral Cortex Choroid Cerebellum Cerebral Ventricles Gastric Mucosa

Organisms2

Mice, Transgenic Helicobacter pylori

Diseases35

Atrophy Muscular Atrophy Optic Atrophy Muscular Atrophy, Spinal Multiple System Atrophy Spinal Muscular Atrophies of Childhood Olivopontocerebellar Atrophies Gyrate Atrophy Geographic Atrophy Muscular Disorders, Atrophic Optic Atrophy, Autosomal Dominant Bulbo-Spinal Atrophy, X-Linked Gastritis, Atrophic Optic Atrophies, Hereditary Cerebellar Ataxia Alzheimer Disease Uveal Diseases Supranuclear Palsy, Progressive Facial Hemiatrophy Shy-Drager Syndrome Disease Models, Animal Spinocerebellar Degenerations Disease Progression Myoclonic Epilepsies, Progressive Dementia Brain Diseases Macular Degeneration Cerebellar Diseases Celiac Disease Nerve Degeneration Neurodegenerative Diseases Frontotemporal Dementia Muscle Weakness Motor Neuron Disease Gastritis

Chemicals and Drugs13

Survival of Motor Neuron 1 Protein SMN Complex Proteins Survival of Motor Neuron 2 Protein SKP Cullin F-Box Protein Ligases Muscle Proteins Ornithine-Oxo-Acid Transaminase Neuronal Apoptosis-Inhibitory Protein Pepsinogen A Myostatin Nerve Tissue Proteins Cyclic AMP Response Element-Binding Protein Pepsinogen C RNA-Binding Proteins

Analytical, Diagnostic and Therapeutic Techniques and Equipment9

Magnetic Resonance Imaging Hindlimb Suspension Organ Size Muscle Denervation Disease Models, Animal Immobilization Pedigree Fluorescein Angiography Biopsy

Psychiatry and Psychology5

Alzheimer Disease Cognition Disorders Dementia Frontotemporal Dementia Mild Cognitive Impairment

Phenomena and Processes2

Organ Size Aging

Information Science1

Image Processing, Computer-Assisted

Health Care1

Hindlimb Suspension

Anatomy Organisms Diseases Chemicals and Drugs Analytical, Diagnostic and Therapeutic Techniques and Equipment Psychiatry and Psychology Phenomena and Processes Information Science Health Care

Atrophy Muscular Atrophy Optic Atrophy Muscular Atrophy, Spinal Multiple System Atrophy Spinal Muscular Atrophies of Childhood Olivopontocerebellar Atrophies Gyrate Atrophy Geographic Atrophy Survival of Motor Neuron 1 Protein Muscular Disorders, Atrophic Magnetic Resonance Imaging Optic Atrophy, Autosomal Dominant SMN Complex Proteins Survival of Motor Neuron 2 Protein Hindlimb Suspension Muscle, Skeletal Bulbo-Spinal Atrophy, X-Linked Brain Gastritis, Atrophic SKP Cullin F-Box Protein Ligases Optic Atrophies, Hereditary Cerebellar Ataxia Alzheimer Disease Uveal Diseases Organ Size Supranuclear Palsy, Progressive Muscle Proteins Facial Hemiatrophy Ornithine-Oxo-Acid Transaminase Shy-Drager Syndrome Muscle Denervation Muscle Fibers, Skeletal Cognition Disorders Disease Models, Animal Spinocerebellar Degenerations Disease Progression Temporal Lobe Neuronal Apoptosis-Inhibitory Protein Pepsinogen A Myoclonic Epilepsies, Progressive Dementia Immobilization Aging Brain Diseases Macular Degeneration Motor Neurons Fundus Oculi Myostatin Image Processing, Computer-Assisted Cerebellar Diseases Hippocampus Nerve Tissue Proteins Pedigree Cyclic AMP Response Element-Binding Protein Anterior Horn Cells Fluorescein Angiography Celiac Disease Pepsinogen C Nerve Degeneration Neurodegenerative Diseases Frontotemporal Dementia Cerebral Cortex Choroid Biopsy Muscle Weakness Cerebellum Mild Cognitive Impairment Motor Neuron Disease Mice, Transgenic Cerebral Ventricles RNA-Binding Proteins Helicobacter pylori Gastritis Gastric Mucosa

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