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A AAA syndrome AARS A-β-lipoproteinemia Absent muscles ACAD9 Acanthosis Nigricans Acetylcholine & ACh Receptors Acetylcholine Receptor   Antibodies   Disorders   Epsilon subunit   Myasthenia Gravis Achondroplasia Acid Maltase Aconitase Acromegaly Acromutilation (Ulceromutilation) Acrylamide Actin Acute   Immune neuropathies   Motor Neuropathies   Myopathies   Neuropathies   Quadriplegic myopathies   Weakness Acyl-CoA dehydrogenase disorders   hydroxy   long chain   medium chain   very long chain   Multiple deficiency Adenosine receptors Adhalin Adhesion molecules Adrenal Adrenomyeloneuropathy α-Dystroglycan disorders Age & Muscle Agrin Alanine-repeat disorders Alcoholic (Ethanol) polyneuropathy Aldolase A deficiency Alexander disease   Adult onset   Mitochondrial Allgrove syndrome All-Trans-Retinoic Acid Allyl chloride Alpers-Huttenlocher α-Methylacyl-CoA racemase (AMACR) Almitrine neuropathy Alpers α-galactosidase α-tocopherol transfer protein ALS ALS Association Alsin AMACR AMAN Aminoacyl-tRNA synthetase e-Amino Caproic Acid Amiodarone neuropathy Ammonia AMPDA deficiency Amphiphysin Amyloidosis Amyotrophic Lateral Sclerosis (ALS)   Hereditary   Sporadic An-α-lipoproteinemia ANCA Andermann Syndrome Andersen disease Andersen periodic paralysis Androgen Receptor Angiogenin Angiotropic lymphoma Anhidrosis Anion exchangers Ankylosing spondylitis ANO10 Anterior interosseus nerve Anterior primary rami Antibodies   Acetylcholine Receptor   Connective tissue disease   Decorin (BJ)   Glutamic acid decarboxylase   GM1 Ganglioside   Hu   Jo-1   MAG   M-protein   Monoclonal   Muscle   Nerve   Polymyositis   Polyspecific   Striational (Muscle)   Sulfatide   tRNA Synthetase   Tubulin   Yo Antibody testing   Requisition Form   Instructions Apamin APECED Apoptosis   Congenital myopathy + Apoptosis Arachnoiditis Arm predominance   Myopathy   Neuropathy Arnold-Chiari Malformation ARS Arsenic Arthrogryposis ARVD Asymmetric   Neuropathies   Myopathies Ataxias   Ataxia Telangectasia   Ataxia Telangectasia-like   Autosomal Dominant   Autosomal Recessive   Congenital   DNA repair defects   Episodic   Metabolic disorders   Multisystem disorders   SCA   Sensory   Treatments   X-linked Atlanto-Axial instability ATP ATPase 6 ATPase Disorders Atrial septal defect Atrophy, type 2 muscle fibers Autonomic Disorders   Syndromes   Cardiac   Sweating   Hypotension   Urinary   Sexual   Ocular Autophagy   Differential diagnosis   Excessive   General features   Pathology AVSF   Pathology Axenfeld-Rieger anomaly Axillary nerve Axonal   Neuropathies - Immune   Transport Axons: Characteristics Azathioprine AZT myopathy B B12, vitamin β-Enolase BAG3 Baltic myoclonus Barium Barnes's myopathy Barth syndrome Basal Lamina: Muscle Baseball Basement membrane BCIM Becker Muscular Dystrophy Becker Myotonia Bee stings Behçet Behr syndrome Bell's Palsy Benign acute childhood myositis Bent spine syndrome Bethlem myopathy β-galactosidase Bickerstaff brainstem encephalitis Biemond Congenital Anesthesia Biochemical-genetic testing Biopsy   Muscle   Nerve   Pictures   Quiz   Results: Differential diagnosis Biotinidase deficiency BJ (Decorin) antibodies & myopathy Björnstad syndrome Black widow spider toxin Bodybuilding Bone morphogenetic proteins Bortezomib (Velcade) Botulism Brachial Amyotrophic Diplegia Brachial Plexopathy Brachial plexus: Innervation Branching Enzyme Brachio-Cervical Inflammatory Myopathy   Pathology Broad A-band disease Brody's Syndrome Brown-Vialetto-van Laere Brucellosis Brugada BSMA (X-linked) Buckthorn Bulbar weakness Bulbospinal Neuronopathy (X-linked) Bungarotoxins: α; β; κ Burning mouth syndrome Burning feet syndrome Burns & neuropathy C C1-C2 instability c9orf72 c20orf7 CADASIL (Multi-infarct dementia) Cadherins CADM-140 Cadmium Calciphylaxis Calcium Channels   Antibodies   Disorders Calpain 3 Camera-Marugo-Cohen Syndrome CAMOS Camurati-Engelmann CANOMAD CANVAS Cap myopathy CAPOS syndrome Carbohydrate Deficient Glycoproteins Carbon disulphide Cardiac Disorders   with myopathy   heart only; hereditary Cardiomyopathy: Dilated Carey-Fineman-Ziter syndrome Carnitine Carnitine-acylcarnitine translocase Carnitine palmitoyltransferase II Carpal tunnel syndrome Cartilage-Hair hypoplasia Caspr2 Cataract & Facial disorder: HMSN Catecholamines Cavanagh's sensory neuropathy Caveolin-3 CDG CEDNIK Celiac disease Central Core Central European encephalitis Central Nervous System (CNS) + ...   Myopathy   Neuropathy Centromere antibodies Centronuclear Myopathy Cerebral palsy, Spastic quadriplegic Cerebral palsy: Symmetric Cerebrotendinous Xanthomatosis CFEOM Chagas' Channel Disorders (Ion) Chaperones Charcot joints Charcot-Marie-Tooth (CMT) Charlevoix-Saguenay   Andermann Syndrome   Charlevoix-Saguenay syndrome   Spastic Ataxias Chediak-Higashi CHILD syndrome Childhood-onset   Myopathy   Neuropathy Chloramphenicol Chloride Channels   Disorders Chloroquine Chlorophenoxy toxicity Cholesterol emboli Chorea-Acanthocytosis Chronic Fatigue Syndrome Chronic Immune Demyelinating Neuropathy Churg-Strauss CIDP Ciguatoxin cis-platinum neuropathy CK Cleidocranial dysplasia Clevudine Club foot CMT COACH syndrome Cocaine Cockayne syndrome: A; B Coenzyme Q10 deficiency   Ataxia Coffin-Lowry Colchicine   Myopathy   Neuropathy Cold   Induced sweating 1   Induced sweating 2   Sensation Collagen   Collagen, Type IV   Collagen, Type VI     Bethlem     OPLL     Ullrich Collagen vascular diseases Common peroneal nerve Complement Complex regional pain syndrome Complex repetitive discharges Conduction Block Congenital   Disorders of glycosylation   Fiber type     Disorders     1 atrophy     2 atrophy   Muscle absence   Muscular Dystrophy   Myopathy   Neuropathy Congenital myopathy with apoptosis Congenital Sensory Neuropathy + Anhydrosis Connective tissue diseases: Immune Connective tissue molecules Connexin-31 Connexin-32 Contractures Copper deficiency & disorders Cores Cores + Rods Corticosteroid   Disorders   Treatment Cough Cowchock Syndrome CPEO CPSQ CPT II Cramps Cramp & Neuropathy syndrome Cranial Nerve Disorders Creatine treatment Creatine Kinase   Low   Unexpectedly High   Very High CREST Creutzfeldt-Jakob Crisponi syndrome Critical illness myopathy Critical illness polyneuropathy CRMP-5 syndromes Crohn's disease Cryoglobulins Cuban neuropathy Cushing syndrome CV-2 Cyanide Cyclophosphamide   Indications - Motor Neuropathies   Orders, IV   Protocol   Treatment   Cyclophosphamide + Plasma Exchange Cyclosporine   Myopathies   Treatment Cytochrome oxidase deficiency   Benign Infantile Myopathy   Fatal Infantile Myopathy   Leigh's Syndrome Cytokines Cytomegalovirus Cytoplasmic body myopathies   Distal   Limb-Girdle Syndromes D Danon's disease (LAMP-2) Dapsone neuropathy Davidenkow d4T neuropathy ddC neuropathy ddI neuropathy Deafness   Achondroplasia   Connexin-26   Dystonia   Hereditary Neuropathies   Mitochondrial   Morquio   Myosin: Unconventional Debranching Enzyme Decorin antibodies & myopathy Deflazacort Degradation: Protein Dejerine-Sottas Delayed onset muscle soreness (DOMS) Deltoid Demyelinating Neuropathies   Differential Diagnosis   Immune Dentatorubral-Pallidoluysian Atrophy (DRPLA) Dermatologic changes Dermatomyositis desert hedgehog Desmin myopathies   Cardiac Failure   Myofibrillar myopathies   Respiratory Failure Diabetes   Muscle infarction   Neuropathy   NIDDM Diaphragm, Congenital defects Diaphyseal Dysplasia 20,25-Diazacholesterol Diethylene glycol Differential diagnosis   Cerebellar   Muscle biopsy   Myopathy   Neuropathy   Spinal   Syndromes Dimethylamine Borane Dimethylaminopropionitrile Dioxins Diphtheria Disc disease Disclaimer Distal Myopathies Distal SMA (HMN) Distal Ulnar-Median Muscular Atrophy Disulfiram neuropathy DM3: See IBMPFD DNA repeat disorders Docetaxel Dok-7 DOMS Dopamine Dopamine β-hydroxylase Dopamine receptor D4 Dorsal scapular nerve Doxorubicin Drug-induced neuropathies Duane's syndrome Duchenne Muscular Dystrophy DUX4 Dyggve-Melchior-Clausen disease Dynactin Dynamin   Dynamin 2   Related Disorders Dysautonomia Dysferlin Dysphagia Dysthyroid ophthalmopathy Dystonia-Spasticity Dystroglycan   α-Dystroglycan disorders Dystrophinopathies   Gene   Protein Dystrophin-associated Glycoproteins E e-Amino Caproic Acid Early Growth response (EGR) genes Ehlers-Danlos Elejalde EMARDD Emery-Dreifuss Dystrophies Emetine Encephalomyopathy Endocrine Endplate spikes β-Enolase Eosinophilia-myalgia syndrome Eosinophilic fasciitis Eosinophils Epidermal growth factors Epidermolysis Bullosa & Congenital MD Epinephrine Epiphyseal dysplasia with myopathy (EDM3) Episodic ataxias   Episodic Ataxia/Myokymia Syndrome Erabutoxin Erb's palsy Erythromelalgia (Erythermalgia) Escobar Ethambutol neuropathy Ethanol: Myopathy; Neuropathy Ethionamide neuropathy Ethylene glycol Ethylene oxide Excessive Autophagy Evaluation of neuromuscular disease: Guidelines Extra-ocular muscle weakness F Fabry's Facial   Bell's Palsy   with myopathy   Nerve Facioscapulohumeral (FSH) Dystrophy Fasciculations Fasciitis Fatigue Syndrome: Chronic Fatty acid oxidation Fatty acid transport Fazio-Londe Femoral nerve FHL1 Fiber type Disorders   1 atrophy   1 predominance   2 atrophy   Size disproportion Fibrillation Fibroblast growth factors Fibroblast growth factor receptor-3 Fibromyalgia Fibrosing myopathy: Focal Fibrosis of EOM Filamin C Finnish encephalopathy FKRP Flier's Syndrome Fludarabine Focal fibrosing myopathy Focally folded myelin FOSMN FOXRED1 Freezing muscle: Methods Friedreich Ataxia FSH dystrophy FSP Fukuyama congenital MD Fumarate hydratase FUS FXTAS G Galactosamine sulfatase Galactosidase: α; β GALOP Syndrome γ-Glutamyl Cysteine Synthetase Gangliosides & glycolipids Gap junctions GARS Gasoline Neuropathy Gastric bypass Gastrointestinal   Gastric bypass   Myopathy   Neuropathy GBS Gemcitabine Germanium myopathy Gerstmann-Straüssler-Schienker Giant Axonal Neuropathy Glucose tolerance Glue Neuropathy Glutaricaciduria IIA Gluten enteropathy Glutethimide neuropathy Glycine Glycine receptors Glycogen Storage Disorders Glycosylation disorders   Glycosylation deficiency, Ia   Muscle-Eye-Brain syndrome GM1   Antibodies   Ganglioside GM2 gangliosidosis Gold neuropathy Goldberg-Shprintzen Gonadal dysgenesis: HSN; HMSN Gossypol Gowers distal myopathy GRACILE syndrome Graft-vs-host Granulomatous Myopathy Griscelli Guillain-Barré Gynecomastia H H-reflex Hamstring injury HANAC Hand weakness (pure motor) Harlequin syndrome Haw River Syndrome Hearing loss Hemifacial spasm Hemochromatosis Hemophagocytic lymphohistiocytosis Hemophilia Hemosiderin Heparan sulfate Heparin-binding growth factors Hepatic disease Hepatitis C Hereditary   Ataxias   Liability to Pressure Palsies   Distal Ulnar-Median Muscular Atrophy   Motor Syndromes   Motor-Sensory Neuropathies     IA; IB; IX; II; III; 4A     Focally folded myelin sheaths     Sensory > Motor + Ulcero-mutilation   Myopathies   Sensory Neuropathy     I, II, III, IV     Large Fiber     Large + Small Fiber     Small Fiber     With spasticity   Spinal Cord Syndromes Heroin Herpes Zoster Hexachlorophene Hexacarbons Hexagonally cross-linked crystalloid inclusions Hexosaminidase A HHH Syndrome HIBM Hidrosis Hirayama's syndrome Hirschsprung's Histiocytoid cardiomyopathy HIV HLA: Disease associations   Myasthenia gravis   Myositis HMG-CoA Reductase Inhibitors HMN (Distal SMA) HMSN HMSN-Russe (HMSNR) HNA HNPP Hoarse voice Holmes-Adie syndrome Holmes Ataxia Horner's syndrome HSAN HSP HTLV-1 Hu Human immune globulin Human Immunodeficiency Virus (HIV) Humor Hyaline body myopathy Hydralazine neuropathy Hydroxychloroquine Hydroxyurea Hymenoptera venom Hyperekplexia Hyperhidrosis Hyperkalemic Periodic Paralysis Hyperornithinemia-hyperammonemia-homocitrullinuria Hypoglycemia + Neuropathy Hypokalemic Periodic Paralysis I IBMPFD Ichthyosiform erythroderma Idiopathic neuropathy Ifosfamide neuropathy Illustrations: Index Immune disorders: Treatment strategies Immunoglobulin Superfamily Immunomodulating therapies IMPP Inability to experience pain Inclusion Body Myopathies (Hereditary)   Dominant: IBM1; IBM3; IBMPFD   Recessive: IBM2   Types Inclusion Body Myositis Inclusions Infantile   Myopathy   Neuropathy Infections   Myelopathy   Neuropathy Infantile Onset Spinocerebellar Ataxia (IOSCA) Infarction, Diabetic Muscle Inflammatory bowel disease Inflammatory Myopathies IMAM Injections & Myopathy Insulin-like growth factors Insulinoma + Neuropathy Integrins   Integrin α7 Intensive care (Critical illness) neuropathy Interferon-α: Neuropathy Intermediate filament disorders Interstitial lung disease Intravascular lymphoma Intravenous immunoglobulin Ion Channel Disorders   General concepts Ipecac Iron Isaac's Syndrome Isoniazid neuropathy Isotretinoin Itch ITP J Jensen syndrome JMP syndrome Jo-1   Myopathy Joint Contractures Joubert syndromes K KARS Kearns-Sayre Kennedy's Syndrome King-Denborough Klippel-Trenaunay-Weber Köbberling-Dunnigan Syndrome Konzo Krabbe L L1CAM L-2 Hydroxyglutaric acidemia Laboratory   Antibody tests   Certification   Pathology (Muscle & Nerve) tests Lactate Lactate dehydrogenase, M (muscle) subunit Lafora disease Lambert-Eaton Syndrome Lamin A/C Lamin B1 Laminin-α2 Laminin-β2 LAMP-2 Large Muscles Large Nerves Lateral femoral cutaneous nerve Latrotoxin LCAD LCHADD Lead Leber's Optic Atrophy Leflunomide Leigh's Syndrome LEMS Leprosy Lethal congenital contracture Lethal congenital myopathy Leukodystrophy Leukoencephalopathy Lewis-Sumner LGMD LHON Licorice Lidocaine Ligament of Struthers Limb-Girdle Muscular Dystrophy Lipid   Disorders     Carnitine     Classification (Biochemical)     Myopathies     Storage disorders   Lowering agents Lipodystrophy   Acquired   Syndromes Lithium Long QT Syndromes   K+ Channel   Na+ Channel Disorders Long thoracic nerve Lower Motor Neuron syndromes LRP4 Lumbosacral plexopathies Lung disease, Interstitial Lyme disease Lymphoma   Intravascular M Ma Machado-Joseph Macroglossia Macrophagic myofasciitis MADD Madelung syndrome Madras motor neuron disease MADSAM MAG Magnesium Malignant Hyperthermia Maple syrup urine disease Marine toxins Marinesco-Sjögren Markesbery Martin-Gruber anastomosis MASA Syndrome Masticator myopathy MCAD McArdle's MELAS McLeod Syndrome MECP2 protein Median nerve Megaconial Melkersson-Rosenthal syndrome Meralgia paresthetica Mercury Merosin: Deficient; Abnormal MERRF Metabolic syndrome Metachromatic Leukodystrophy Methotrexate Methyl bromide 5,10 Methylenetetrahydrofolate Reductase Metronidazole neuropathy MGUS MHC-I Mi-2 antibody Microscopic polyangiitis (MPA) Migrant sensory neuritis Miller Fisher Miniature endplate potential Minicore myopathy Minifascicles: HSN; HMSN Minipolymyoclonus MIRAS Misonidazole neuropathy Mitochondria   Complexes   Disorders   DNA breakage syndrome   Pathology Mitofusin 2 Miyoshi distal myopathy MLASA MMN MNGIE Möbius Syndrome Mohr-Tranebjaerg syndrome Molecules Monensin Monoclonal Antibodies (M-proteins) Monomelic Amyotrophy Mononeuritis multiplex Morquio Morvan's fibrillary chorea Motor Syndromes   Hereditary Motor Neuropathies Mowat-Wilson Mountain sickness MPP1 M-proteins MRI, Muscle patterns MSCAE mtDNA depletion MTHFR MTPAP Mulibrey Nanism Multicore myopathy Multifocal Motor Neuropathy Multi-Infarct dementia Multiple acyl–CoA dehydrogenase (MADD) Multiple Endocrine Neoplasia Multiple Epiphyseal Dysplasia (MED) Multiple Symmetric Lipomatosis Multiple Myeloma Multiple Systems Atrophy Muscle   Absence (Congenital)   Biopsy   Development   Hypertrophy   Innervation     Upper extremity     Lower extremity   Pain   Structural Proteins Muscle biopsy Muscle biopsy stains Muscle-Eye-Brain Disease Muscle infarction: Diabetic Muscle spindle Muscular Dystrophy Muscular Dystrophy Association Musculocutaneous nerve Mushroom intoxication Musicians MuSK antibodies Muzolimine Myasthenia Gravis   Associated disorders   Autoimmune   Syndromes Myasthenic Syndromes   Lambert-Eaton MYBPC1 Mycophenolate mofetil Mycoplasma pneumoniae Myelin-Associated Glycoprotein (MAG) Myelination: Neuropathies with abnormal Myelin components Myelocerebellar Myeloma Myelopathies MYH7 Myhre Syndrome Myoadenylate deaminase deficiency Myoedema Myofibrillar (Desmin) myopathies Myogenesis Myoglobinuria MYH7 Myokymia   Differential diagnosis Myopathy   Differential Diagnosis   with Neuropathy   Syndromes Myosclerosis Myosin   Binding protein (MYBPC)   Cardiomyopathies   Deficiency Myopathies   Disorders   Hearing loss   Heavy chain   Light chain   Non-muscle myosin Myosin loss myopathy Myositis   Antibodies Myostatin Myotilin Myotonia   Acetazolamide-responsive   Congenita (Becker)   Congenita (Thomsen)   Fluctuans   Permanens   Treatment Myotonic Dystrophy   DM1   DM2 Myotoxins Myotubular Myopathy N NARP Native American Myopathy Navajo neuropathy with arthropathy Navajo neuropathy with corneal ulceration Nebulin Neck weakness   Posterior Necrosis Necrotizing myopathy   Paraneoplastic   Pipestem capillaries Nemaline Myopathy Neonatal Perifascicular Myopathy Nerve Biopsy (Indications) Nerves   Upper extremity   Lower extremity Nesprins: 1; 2 Neuralgic Amyotrophy Neuroacanthocytosis Neuroaxonal Dystrophy Neurofilaments: Motor neuron disease Neurofilament antibodies Neurofibroma Neurofibromatosis: 1; 2 Neuroleptic-Malignant Syndrome Neuromuscular Disease: Typical Patterns Neuromuscular: Evaluation guidelines Neuromuscular Junction Disorders Neuromuscular Laboratory   Antibody tests   Certification   Pathology (Muscle & Nerve) tests Neuromyotonia Neuronal Intranuclear Inclusion Disease (NIID) Neuronopathy Neuropathy   Childhood   Chronic immune axonal   Chronic immune demyelinating   with CNS disease   Differential Diagnosis   Syndromes Neurotoxic esterase Neurotransmitters Neurotrophins n-Hexane Niemann-Pick, Type C Nitrofurantoin neuropathy Nitrous oxide neuropathy Nonaka distal myopathy NOS NS6S NUBPL Nuclear envelope Nucleoside neuropathy Nucleosome, Antibodies O O'Sullivan-McLeod syndrome Oculopharyngeal Muscular Dystrophy Oculopharyngodistal myopathy OMIM Ophthalmoplegia Opsoclonus-Myoclonus Optic Nerve Optic neuropathy: Hereditary Organophosphorous esters Ornithine aminotransferase Ossification of posterior longitudinal ligament Osteosclerotic Myeloma Oxaliplatin P P1 receptors P2 receptors p97 p140 p155/140 Paget disease Pain   General principles   Medications   Myopathy   Neuropathy Palmaris brevis spasm Palytoxin Pantothenate kinase 2 (PANK2) Paraganglioma Paramyotonia congenita Paraneoplastic syndromes Paraspinous muscle weakness Parathyroid Paroxysmal   Cerebellar Ataxia (EA2)   Choreoathetosis/Spasticity   Extreme Pain Pathology: Index Patient information & resources Patterns: Neuromuscular Disease PCARP PCH Pearson's Pectoral muscle aplasia Pelizaeus Merzbacher Pelizaeus Merzbacher-like: 1; 2 Penicillamine Pentaborane PEO Perhexiline neuropathy Periaxin Perimysial pathology Perimyositis Perineurioma Perineuritis Periodic fever + Focal myositis Periodic paralysis   Hyperkalemic   Hypokalemic Peripheral axons: Characteristics Peripheral nerve tumors Perlecan Peroneal nerve Peroxisomes: Refsum PEX10 PHARC Phenylketonuria Phenytoin neuropathy Phosphoglycerate Kinase Phosphoglycerate Mutase, M subunit Phosphofructokinase, M subunit Phospholipase A2 proteins Phospholipid antibodies Phosphorylase (McArdle's) Phosphorylase b Kinase Physical examination Pipecolic acid Pipestem capillaries Plasma exchange Plectin Plexopathy   Brachial   Lumbar   Neoplastic   Radiation PLS PMA PMP-22 PNPLA6 P0 Protein Podophyllin POEMS Poland syndrome POLG Polio Polyarteritis nodosa Polychlorinated biphenyls (PCBs) Polyglucosan   Polyglucosan body disease   Deposition Polymyalgia Rheumatica Polymyositis Polyneuropathy Pompe Pontocerebellar hypoplasia Porcine brain-associated neuropathy Porphyria Positive sharp wave Posterior column ataxia + Retinitis pigmentosa Posterior neck weakness Posterior tibial nerve Post-paralysis paralysis Post-polio syndrome Postural hypotension Postural orthostatic tachycardia (POTS) Potassium Channels   Antibodies   Disorders POTS Prednisone Pressure Palsies, Hereditary Liability to Presynaptic proteins Primary lateral sclerosis Primary muscular atrophy Prion Progressive External Ophthalmoplegia (PEO) PROMM Pronator syndrome Propofol Proteasome Protein degradation Proteoglycans Proteolipid protein (PLP) Proximal   Arms - Myopathy   Motor Neuropathy   Sensory Neuropathy Proximal Myotonic Myopathy (PROMM) Psoas, hypoplasia Pterygium, Multiple Pyomyositis Pyridoxine   Deficiency   Intoxication Pyruvate dehydrogenase Q QT Syndromes, Long   K+ Channel Disorders   Na+ Channel Disorders Quadriceps weakness Quadrilateral space syndrome Quadriplegic myopathy, Acute R Rabies Radial nerve Radiation   Brachial Plexopathy   Lumbar Plexopathy   Myelopathy Ramsay-Hunt Rapsyn Recent revisions Reducing body myopathies Reflex sympathetic dystrophy Reflexes, Tendon Refsum Relapsing Renal disease Respiratory Failure Rett syndrome Rhabdomyolysis Rheumatoid arthritis Rhomboid Ri antibody Riboflavin Ribonucleoprotein (RNP) Rigid spine Riley-Day Ringed fiber myopathy Rippling Muscle Syndrome Rituximab   Orders   Protocol   Treatment RNA: Splicing RNF170 Rod Myopathy Roots   Upper extremity   Lower extremity Ross syndrome Rucksack paralysis Ryanodine receptor S Sacsin Salla syndrome Sarcocystis Sarcoglycans   Disorders Sarcoid Sarcotubular Satoyoshi Saxitoxin SBMA (X-linked) SCA SCAD Scapular winging Scapuloperoneal syndromes Scheie syndrome Schwann cell components Schwannoma Schwartz-Jampel Scleroderma Scleromyxedema SECISBP2 Selectins Selenium   Deficiency   Selenoprotein N 1 (SEPN1) Semaphorins Senataxin Sengers Sensory   Ataxia   Idiopathic   Large Fiber   Large & Small Fiber   Neuronopathies   Small Fiber SEPN1 Serotonin syndrome Serratus anterior SeSAME SGPG SH3TC2 Shoulder Shy-Drager Sickle cell disease Siderosis Signal recognition particle Silver syndrome Sjögren-Larsson Sjögren's Skeletal disorders Skin changes SMA SMA-LED SMNA Snake venom toxins SNAX1 snRNP SOD1 Sodium Channels   Disorders Sodium cyanate neuropathy Solumedrol treatment   Orders Spanish toxic oil SPAR Spastic   Ataxias   Dystonia   Paraplegias SPG Spheroid body myopathy Spinal accessory nerve Spinal Cord Disorders   Hereditary   Systemic Causes   Trauma   Vascular Spinal cord syndromes   Anterior cord   Brown-Séquard   Cauda Equina   Conus medullaris   Hemicord   Posterior cord Spinal Muscular Atrophies   Benign congenital with contractures   Bulbo-Spinal Muscular Atrophy     X-linked (Kennedy's)     Autosomal Dominant   Distal SMA     HMN 1; 2; 5     Diaphragmatic paralysis & Neonatal     Distal Ulnar-Median     Recessive     Upper limb predominance     Vocal cord involvement   Congenital with leg weakness   Dominant, Proximal     SMALED   Scapuloperoneal syndromes   SMA 5q     Congenital with arthrogryposis     Werdnig-Hoffmann     Kugelberg-Welander   Spinal muscular atrophy 2   X-linked Infant SMA & Arthrogryposis Spindle excess + Congenital myopathy Spindle, muscle Spine disorders Spliceosomes Spontaneous Muscle Activity Sports disorders   Backpacking   Baseball   Bicycle   Bodybuilding   Bowling   Football   Mountain climbing   Surfing   Volleyball Spurling test SSA SSc Stains: Muscle biopsy Statins   Myopathy   Neuropathy Stiffman Syndrome Strachan syndrome Striational Antibodies Struthers, Ligament Strychnine Stuve-Wiedemann syndrome Substance P and Tachykinins Succinate Dehydrogenase   Leigh's Syndrome   Rhabdomyolysis SUCLA2 SUCLG1 Sudden infant death (SIDS) Sulfatide Superficial siderosis Superior oblique myokymia Superoxide Dismutase Suprascapular nerve Suramin neuropathy SURF-1 Surfing Sweating disorders Sydenham chorea Synaptic Proteins   Presynaptic   Postsynaptic SYNE: 1; 2 Syntrophin Syphilis Syringomyelia Systemic lupus erythematosis T Ta TACH Tangier disease Tarsal tunnel Tarsal tunnel, anterior TATA binding protein Taxol neuropathy Tay-Sachs T-cells TDP-43 Telbivudine Telethionin Tel Hashomer camptodactyly Tellurium Tendon reflexes Test forms Tetanus Tetany Tetrodotoxin Thalidomide neuropathy Thallium Thermoanalgesia Thenar motor neuropathy Thiamine Thomsen Thoracic outlet syndrome Thymoma Thyroid Tick paralysis Titin   Antibodies   Muscle Tomaculae   Differential diagnosis   Pathology Toxic myopathies Toxic neuropathies Toxins: Snake venom TPM3 Transforming growth factors β Transmitters Transverse myelitis Trapezius TRAPS Treatment strategies Trichinosis Trichloroethylene Trigeminal neuralgia Triglycerides TRIM32 Triorthocresyl phosphate (TOCP) Triosephosphate isomerase Trisulfated heparin disaccharide tRNA synthetase Trophic factors Tropical   Ataxic neuropathy   Pyomyositis   Spastic paraparesis Tropomyosin Troponin T (Cardiac) Troyer syndrome TRP ion channels   TRPV4 TS-HDS TTID Tuberculosis Tubular aggregates Tubulin, Antibodies Tubulin-reactive crystalline inclusions, Myopathy Tumor-like disorders Tumor necrosis factor-α Tumor necrosis factor receptor 1A Tumors: Peripheral nerve Twinkle Type 2 muscle fiber atrophy Tyrosine kinase receptor ligands Tyrosinemia U Ubiquitin Udd Ulcerative colitis Ulcero-mutilation   with Hereditary neuropathy Ullrich CMD Ulnar nerve Urea cycle Uruguay Facio-Cardio-Musculo-Skeletal Syndrome Utrophin V Vacor Vacuoles: Muscle Vanishing white matter Vasculitis VCP VEGF Velcade (Bortezomib) Venoms: Snake Toxins Venous insufficiency Ventricular fibrillation Vernant's disease Very long chain acyl-CoA dehydrogenase Vibration VII nerve Vinca alkaloid neuropathy Visual field disorders Visual loss   Optic neuropathy   Paraneoplastic Vitamin disorders   B12 deficiency   D deficiency   E: Deficiency & Intoxication VLCAD Vocal cord disorders Voice, hoarse Von Hippel-Lindau W Waldenström's macroglobulinemia Walker-Warburg Wallerian degeneration Wartenberg's sensory neuritis Weakness, acute Wegener's Weight lifting Welander Werdnig-Hoffmann West Nile Virus Whipple's disease Williams-Beuren syndrome Wilson's Disease Winging (Scapular) Wolfram syndrome Worster-Drought syndrome X XK membrane transport protein X-linked HMSN XMEA Xp21 microdeletion syndromes with Duchenne MD Y YARS Yo Z ZASP Z-disk Zimeldine Zinc Zoster

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