Area of weakness. Medical search. Frequent questions

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Anatomy23

Muscle, Skeletal Diaphragm Respiratory Muscles Quadriceps Muscle Muscle Fibers, Skeletal Muscles Neuromuscular Junction Cervical Vertebrae Sural Nerve Shoulder Motor Neurons Spinal Cord Peripheral Nerves Facial Muscles Thigh Thoracic Vertebrae Spinal Nerve Roots Cauda Equina Muscle Fibers, Slow-Twitch Phrenic Nerve Arm Oculomotor Muscles Lower Extremity

Organisms1

Mice, Inbred mdx

Diseases108

Muscle Weakness Muscular Diseases Neuromuscular Diseases Myopathies, Nemaline Hypokalemic Periodic Paralysis Muscular Atrophy Myositis Myasthenia Gravis Polymyositis Respiratory Paralysis Polyneuropathies Brachial Plexus Neuritis Motor Neuron Disease Postpoliomyelitis Syndrome Myositis, Inclusion Body Dermatomyositis Paralysis Muscle Hypotonia Myasthenic Syndromes, Congenital Muscular Dystrophies Myopathies, Structural, Congenital Distal Myopathies Charcot-Marie-Tooth Disease Guillain-Barre Syndrome Lambert-Eaton Myasthenic Syndrome Hypesthesia Muscular Dystrophies, Limb-Girdle Ophthalmoplegia Paresthesia Rhabdomyolysis Myotonia Paresis Hypokalemia Paralyses, Familial Periodic Sensation Disorders Paralysis, Hyperkalemic Periodic Reflex, Abnormal Bulbar Palsy, Progressive Muscular Atrophy, Spinal Hereditary Sensory and Motor Neuropathy Myotonic Dystrophy Syndrome Peripheral Nervous System Diseases Nervous System Diseases Respiratory Insufficiency Spinal Cord Compression Sarcopenia Dysarthria Neuromuscular Junction Diseases Muscular Dystrophy, Duchenne Glycogen Storage Disease Type II Hemiplegia Ataxia Spinal Cord Diseases Quadriplegia Polyradiculoneuropathy Spinal Cord Neoplasms Muscular Dystrophy, Oculopharyngeal Myoglobinuria Muscular Dystrophy, Facioscapulohumeral Amyotrophic Lateral Sclerosis Paraparesis Asthenia Spastic Paraplegia, Hereditary Facial Paralysis Fatigue Polyradiculopathy Spinal Muscular Atrophies of Childhood Brachial Plexus Neuropathies Lameness, Animal Nerve Compression Syndromes Disease Models, Animal Myotonic Disorders Femoral Neuropathy Myotonia Congenita Contracture Syringomyelia Neoplasms, Connective Tissue Movement Disorders Myelitis, Transverse Critical Illness Muscle Spasticity Thyrotoxicosis Paraneoplastic Syndromes Pain Radiculopathy Muscular Dystrophy, Animal Myopathy, Central Core Mitochondrial Myopathies Demyelinating Diseases Hematoma, Epidural, Spinal Paraplegia Stroke Dyspnea Myasthenia Gravis, Autoimmune, Experimental Gait Disorders, Neurologic Epidural Abscess Blepharoptosis Dog Diseases Infarction, Anterior Cerebral Artery Mobius Syndrome Camurati-Engelmann Syndrome Snake Bites Spinal Neoplasms Deglutition Disorders Tongue Diseases Beriberi Acute Disease

Chemicals and Drugs15

Pyridostigmine Bromide Receptors, Cholinergic Immunoglobulins, Intravenous Muscle Proteins Creatine Kinase Edrophonium NAV1.4 Voltage-Gated Sodium Channel Monocrotophos Carbimazole Cholinesterase Inhibitors Prednisolone Anti-Dyskinesia Agents Myosin Heavy Chains Dystrophin Thymopoietins

Analytical, Diagnostic and Therapeutic Techniques and Equipment35

Muscle Strength Electromyography Magnetic Resonance Imaging Neurologic Examination Muscle Strength Dynamometer Reflex, Abnormal Pedigree Fatal Outcome Treatment Outcome Electrodiagnosis Early Ambulation Laminectomy Biopsy Hand Strength Severity of Illness Index Tomography, X-Ray Computed Disease Models, Animal Gait Myelography Respiration, Artificial Inspiratory Capacity Retrospective Studies Enzyme Therapy Physical Therapy Modalities Follow-Up Studies Range of Motion, Articular Myasthenia Gravis, Autoimmune, Experimental Research Design Decompression, Surgical Orthotic Devices Reproducibility of Results Breathing Exercises Bed Rest Prospective Studies Respiratory Function Tests

Psychiatry and Psychology3

Conversion Disorder Pain Motor Activity

Phenomena and Processes20

Muscle Strength Neural Conduction Muscle Contraction Reflex, Abnormal Isometric Contraction Muscle Fatigue Phenotype Hand Strength Time Factors Mutation Gait Torque Inspiratory Capacity Biomechanical Phenomena Recovery of Function Pain Range of Motion, Articular Genes, Dominant Motor Activity Pressure

Disciplines and Occupations2

Evidence-Based Medicine Research Design

Information Science1

Health Care10

Fatal Outcome Treatment Outcome Severity of Illness Index Age of Onset Benchmarking Retrospective Studies Intensive Care Units Follow-Up Studies Reproducibility of Results Prospective Studies

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

Muscle Weakness Muscular Diseases Neuromuscular Diseases Myopathies, Nemaline Muscle, Skeletal Hypokalemic Periodic Paralysis Muscular Atrophy Diaphragm Myositis Respiratory Muscles Muscle Strength Myasthenia Gravis Polymyositis Electromyography Respiratory Paralysis Polyneuropathies Brachial Plexus Neuritis Motor Neuron Disease Postpoliomyelitis Syndrome Myositis, Inclusion Body Dermatomyositis Paralysis Muscle Hypotonia Myasthenic Syndromes, Congenital Muscular Dystrophies Myopathies, Structural, Congenital Distal Myopathies Charcot-Marie-Tooth Disease Quadriceps Muscle Guillain-Barre Syndrome Neural Conduction Lambert-Eaton Myasthenic Syndrome Hypesthesia Muscular Dystrophies, Limb-Girdle Ophthalmoplegia Paresthesia Rhabdomyolysis Myotonia Paresis Magnetic Resonance Imaging Hypokalemia Paralyses, Familial Periodic Muscle Contraction Sensation Disorders Neurologic Examination Muscle Strength Dynamometer Conversion Disorder Paralysis, Hyperkalemic Periodic Reflex, Abnormal Bulbar Palsy, Progressive Evidence-Based Medicine Muscular Atrophy, Spinal Hereditary Sensory and Motor Neuropathy Myotonic Dystrophy Syndrome Muscle Fibers, Skeletal Peripheral Nervous System Diseases Isometric Contraction Muscle Fatigue Pedigree Nervous System Diseases Respiratory Insufficiency Spinal Cord Compression Muscles Fatal Outcome Sarcopenia Treatment Outcome Dysarthria Electrodiagnosis Neuromuscular Junction Diseases Pyridostigmine Bromide Muscular Dystrophy, Duchenne Glycogen Storage Disease Type II Hemiplegia Ataxia Spinal Cord Diseases Quadriplegia Early Ambulation Polyradiculoneuropathy Spinal Cord Neoplasms Neuromuscular Junction Cervical Vertebrae Muscular Dystrophy, Oculopharyngeal Myoglobinuria Muscular Dystrophy, Facioscapulohumeral Amyotrophic Lateral Sclerosis Laminectomy Biopsy Receptors, Cholinergic Phenotype Paraparesis Asthenia Hand Strength Severity of Illness Index Spastic Paraplegia, Hereditary Facial Paralysis Time Factors Tomography, X-Ray Computed Sural Nerve Fatigue

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