Muscle weakness infantile muscular atrophy spinal. Medical search. Frequent questions

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Anatomy62

Spinal Cord Muscles Muscle, Skeletal Motor Neurons Muscle Fibers, Skeletal Anterior Horn Cells Respiratory Muscles Muscle, Smooth Muscle, Smooth, Vascular Muscle Fibers, Slow-Twitch Diaphragm Muscle Fibers, Fast-Twitch Spinal Nerve Roots Neuromuscular Junction Quadriceps Muscle Chromosomes, Human, Pair 5 Mitochondria, Muscle Spinal Nerves Coiled Bodies Spinal Canal Myocytes, Smooth Muscle Neck Muscles Oculomotor Muscles Axons Muscle, Striated Muscle Spindles Cells, Cultured Papillary Muscles Myofibrils Abdominal Muscles Facial Muscles Muscle Cells Peripheral Nerves Hindlimb Sural Nerve Masseter Muscle Masticatory Muscles Intercostal Muscles Motor Endplate Satellite Cells, Skeletal Muscle Ganglia, Spinal Brain Myoblasts Inclusion Bodies Sarcomeres Ulnar Nerve Spine Leg Thoracic Vertebrae Pectoralis Muscles Cervical Vertebrae Cell Line Sciatic Nerve Intranuclear Inclusion Bodies Lumbosacral Region Thigh Arm Neurons Fibroblasts Lumbar Vertebrae Spliceosomes Psoas Muscles

Organisms8

Mice, Transgenic Mice, Inbred C57BL Mice, Knockout Rats, Sprague-Dawley Mice, Inbred mdx Animals, Newborn Rats, Wistar Rabbits

Diseases85

Muscular Atrophy, Spinal Muscle Weakness Spinal Muscular Atrophies of Childhood Atrophy Muscular Atrophy Muscular Disorders, Atrophic Bulbo-Spinal Atrophy, X-Linked Spinal Cord Injuries Muscular Diseases Myopathies, Nemaline Neuromuscular Diseases Motor Neuron Disease Spinal Cord Diseases Disease Models, Animal Optic Atrophy Myositis Polymyositis Muscular Dystrophies Charcot-Marie-Tooth Disease Respiratory Paralysis Bulbar Palsy, Progressive Dermatomyositis Hypokalemic Periodic Paralysis Myopathies, Structural, Congenital Multiple System Atrophy Ophthalmoplegia Myasthenia Gravis Spinal Cord Neoplasms Contracture Neuromuscular Junction Diseases Spinal Cord Compression Amyotrophic Lateral Sclerosis Spinal Diseases Postpoliomyelitis Syndrome Myasthenic Syndromes, Congenital Spinal Neoplasms Myositis, Inclusion Body Muscle Hypotonia Muscular Dystrophy, Duchenne Spinal Stenosis Muscular Dystrophies, Limb-Girdle Hereditary Sensory and Motor Neuropathy Syndrome Nerve Degeneration Paralysis Distal Myopathies Rhabdomyolysis Arthrogryposis Muscular Dystrophy, Animal Olivopontocerebellar Atrophies Vocal Cord Paralysis Myotonic Dystrophy Lambert-Eaton Myasthenic Syndrome Hypokalemia Quadriplegia Scoliosis Spinal Injuries Muscle Spasticity Gyrate Atrophy Glycogen Storage Disease Type II Reflex, Abnormal Myotonia Disease Progression Spinal Cord Ischemia Paralyses, Familial Periodic Paraplegia Nervous System Diseases Fasciculation Geographic Atrophy Respiratory Insufficiency Paralysis, Hyperkalemic Periodic Pain Brachial Plexus Neuritis Myotonic Disorders Muscular Dystrophy, Oculopharyngeal Peripheral Nervous System Diseases Muscular Dystrophy, Facioscapulohumeral Mitochondrial Myopathies Myoclonic Epilepsies, Progressive Respiratory Aspiration Hematoma, Epidural, Spinal Polyneuropathies Tuberculosis, Spinal Neoplasms, Connective Tissue Sensation Disorders

Chemicals and Drugs24

Survival of Motor Neuron 1 Protein SMN Complex Proteins Survival of Motor Neuron 2 Protein Neuronal Apoptosis-Inhibitory Protein Muscle Proteins Cyclic AMP Response Element-Binding Protein RNA-Binding Proteins Nerve Tissue Proteins Ribonucleoproteins, Small Nuclear DEAD Box Protein 20 Receptors, Androgen snRNP Core Proteins Myosin Heavy Chains RNA, Messenger Glycine-tRNA Ligase Receptors, Cholinergic Creatine Kinase Monocrotophos Dystrophin Actins Calcium Desmin NAV1.4 Voltage-Gated Sodium Channel Tropomyosin

Analytical, Diagnostic and Therapeutic Techniques and Equipment35

Electromyography Disease Models, Animal Muscle Strength Muscle Denervation Pedigree Injections, Spinal Muscle Strength Dynamometer Anesthesia, Spinal Magnetic Resonance Imaging Spinal Fusion Heterozygote Detection Electric Stimulation Immunohistochemistry Reflex, Abnormal Hand Strength Blotting, Western Biopsy Severity of Illness Index Treatment Outcome Inspiratory Capacity Hindlimb Suspension Myelography DNA Mutational Analysis Laminectomy Analysis of Variance Breathing Exercises Polymerase Chain Reaction Gait Chromosome Mapping Models, Biological Prenatal Diagnosis Genetic Therapy Retrospective Studies Neurologic Examination Genetic Testing

Psychiatry and Psychology2

Motor Activity Pain

Phenomena and Processes42

Muscle Contraction Muscle Strength Muscle Development Muscle Fatigue Exons Chromosomes, Human, Pair 5 Phenotype Neural Conduction Isometric Contraction Mutation Time Factors Motor Activity Genes, Recessive Homozygote Muscle Relaxation Genes, Dominant Genetic Linkage Gene Deletion Biomechanical Phenomena Gene Expression Regulation Base Sequence Trinucleotide Repeat Expansion RNA Splicing Mutation, Missense Reflex, Abnormal Hand Strength Aging Inspiratory Capacity Torque Gene Dosage Trinucleotide Repeats Amino Acid Sequence Heterozygote Pain Alternative Splicing Gait Gene Expression Action Potentials Locomotion Inhalation Genotype Recovery of Function

Disciplines and Occupations3

Immunohistochemistry Chemistry, Analytic Genetic Counseling

Information Science3

Molecular Sequence Data Base Sequence Amino Acid Sequence

Health Care8

Age of Onset Severity of Illness Index Treatment Outcome Hindlimb Suspension Analysis of Variance Retrospective Studies Genetic Testing Genetic Counseling

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

Muscular Atrophy, Spinal Muscle Weakness Spinal Muscular Atrophies of Childhood Survival of Motor Neuron 1 Protein Atrophy Muscular Atrophy SMN Complex Proteins Survival of Motor Neuron 2 Protein Spinal Cord Muscles Muscle, Skeletal Muscular Disorders, Atrophic Bulbo-Spinal Atrophy, X-Linked Spinal Cord Injuries Motor Neurons Neuronal Apoptosis-Inhibitory Protein Muscle Fibers, Skeletal Muscle Proteins Muscular Diseases Cyclic AMP Response Element-Binding Protein Myopathies, Nemaline Anterior Horn Cells Neuromuscular Diseases Respiratory Muscles Muscle Contraction RNA-Binding Proteins Muscle, Smooth Motor Neuron Disease Electromyography Spinal Cord Diseases Nerve Tissue Proteins Muscle, Smooth, Vascular Disease Models, Animal Muscle Strength Muscle Development Muscle Fatigue Optic Atrophy Myositis Polymyositis Muscle Fibers, Slow-Twitch Muscle Denervation Ribonucleoproteins, Small Nuclear Muscular Dystrophies Diaphragm Muscle Fibers, Fast-Twitch Exons DEAD Box Protein 20 Charcot-Marie-Tooth Disease Pedigree Spinal Nerve Roots Neuromuscular Junction Quadriceps Muscle Respiratory Paralysis Bulbar Palsy, Progressive Injections, Spinal Chromosomes, Human, Pair 5 Phenotype Mitochondria, Muscle Mice, Transgenic Dermatomyositis Neural Conduction Spinal Nerves Isometric Contraction Hypokalemic Periodic Paralysis Muscle Strength Dynamometer Mutation Myopathies, Structural, Congenital Coiled Bodies Multiple System Atrophy Ophthalmoplegia Anesthesia, Spinal Myasthenia Gravis Magnetic Resonance Imaging Spinal Cord Neoplasms Contracture Neuromuscular Junction Diseases Receptors, Androgen Spinal Cord Compression Spinal Canal snRNP Core Proteins Amyotrophic Lateral Sclerosis Spinal Diseases Postpoliomyelitis Syndrome Time Factors Myasthenic Syndromes, Congenital Spinal Neoplasms Myositis, Inclusion Body Myocytes, Smooth Muscle Neck Muscles Oculomotor Muscles Muscle Hypotonia Axons Muscular Dystrophy, Duchenne Muscle, Striated Spinal Stenosis Motor Activity Muscle Spindles Muscular Dystrophies, Limb-Girdle Hereditary Sensory and Motor Neuropathy Spinal Fusion

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