Differential (Click to cross reference) abdominal distention abdominal muscle paralysis abdominal protrusion abducens nerve paralysis abducens nerve paralysis, bilateral acanthocytosis acetylcholine receptor antibody acid maltase deficiency acid maltase deficiency, adult acquired immunodeficiency syndrome acquired immunodeficiency syndrome-related complex acromegaly acute intermittant porphyria acyl CoA dehydrogenase deficiency addiction, heroin Addison's disease adverse drug reaction alcohol alcohol, heart involvement with alcohol, neurologic complications with alcoholism aldolase alpha glucosidase amaurosis fugax amphotericin B amyloid amyloidosis amyotrophic lateral sclerosis amyotrophic lateral sclerosis, bulbar amyotrophic lateral sclerosis, differential diagnosis amyotrophic lateral sclerosis, familial amyotrophic lateral sclerosis, misdiagnosis ANA anemia aneurysm angiotensin-converting enzyme ankle edema anterior horn cell disease anterior tibial muscle weakness anti HMGCR antibody anti Jo1 antibody anti Ku antibody anti Mi2 antibody anti signal recognition particle antibody antibodies to voltage-gated calcium channels anticonvulsants, hypersensitivity syndrome anticonvulsants, untoward effects of aphasia aphonia areflexia arm weakness arrhythmia, cardiac arthralgia arthritis arthrogryposis multiplex Asians aspartate aminotransferase asthma asymptomatic ataxia ataxia, cerebellar ataxia, progressive ataxia, sensory ataxia, truncal ataxic gait atrial fibrillation atrioventricular block atypical autoantibodies autoimmune disease autonomic dysfunction axonal degeneration azidodeoxythymidine Balint's syndrome beta adrenergic blocker biologic markers blepharophimosis blepharospasm bone biopsy bone marrow transplantation bone pain bone scanning botulism brachial plexus neuropathy bradycardia brain natriuretic peptide bulbar palsy bulbar palsy, progressive burning feet burning paresthesia cachexia CAG repeats calcification, intracranial calf atrophy calf hypertrophy camptocormia cancer associated myopathy canned food carbenoxolone carcinoma carcinoma of esophagus carcinoma of lung cardiomegaly cardiomyopathy cardiotoxicity cardiovascular disease carnitine deficiency carnitine deficiency myopathy carpal tunnel syndrome case studies CAT scan CAT scan, abnormal CAT scan, chest CAT scan, emission, abnormal CAT scan, false negative cataracts cauda equina, enhancement central core disease cerebellar atrophy, secondary cerebellar degeneration cerebral cortical atrophy cerebral embolism cerebral infarction cerebral venous thrombosis cerebrospinal fluid cerebrospinal fluid, elevated protein of cerebrospinal fluid, lactic acid concentration cerebrovascular accident cerebrovascular accident, mimics cerebrovascular accident, multiple cerebrovascular accident, recurrent cerebrovascular accident, young adult cerebrovascular disease Charcot-Marie-Tooth chemotherapy, CNS treatment and complications with chest pain chewing, impaired children chloroquine chorea chromosomal abnormality chromosome 19 chromosome 3 chromosome 5 chronic graft versus host disease chronic progressive external ophthalmoplegia cigarette smoking Clinical Pathologic Conference(C.P.C.) clofibrate clubfoot as related to neurologic disease Coats syndrome colchicine collagen vascular disease coma complications conduction block confidentiality confusion congenital heart disease congenital myasthenic syndromes congenital myopathy congestive heart failure consanguinity constipation contractures, joint corticotropin level corticotropin-releasing factor cortisol, elevated cranial nerve palsies cranial neuropathy cranial neuropathy, multiple creatine kinase creatine phosphokinase(CPK)elevated critical care unit cultured skin fibroblasts Cushing's syndrome deafness deep tendon reflexes delay in diagnosis dementia dementia, frontotemporal dementia, rapidly progressive depression dermatitis dermatomyositis descending paralysis developmental retardation diabetes mellitus diabetes mellitus, chemical diabetes mellitus, neurologic manifestations of diabetic amyotrophy diamond on quadriceps diaphragmatic paralysis diarrhea diarrhea, bloody differential diagnosis difficulty climbing stairs dilantin dilantin, hypersensitivity to diplegia, brachial diplopia disability, neurological dislocated hip, congenital disorientation distal muscle atrophy distal muscle weakness diuretic docetaxel dropped head syndrome drug induced neurologic disorders dysarthria DYSF gene dysferlin dysferlinopathy dysphagia dysphonia dyspnea dyspraxia dystrophic calcification dystrophin ear, abnormal echocardiogram echocardiogram, LVH edema, leg electrocardiogram, abnormal electromyogram electromyogram, decremental response electromyogram, fasciculation potentials electromyogram, incremental response electron microscopy Emery-Dreifuss muscular dystrophy encephalopathy encephalopathy, progressive entrapment neuropathy enzyme treatment enzyme, defect enzyme, muscle disease enzyme, serum eosinophilia eosinophilia-myalgia syndrome epidemiology of neurology epsilon-aminocaproic acid(E.A.C.A.) evoked potentials exercise exercise intolerance exercise-induced neurologic dysfunction exercise-related muscle strength increase exome sequencing extraocular muscle lesion eye closure eye movement, disorders of face, elongated facial appearance, abnormal facial hair, excessive facial nerve palsy facial nerve palsy, recurrent facial weakness facial weakness, bilateral facioscapulohumeral syndrome falling false negative familial fasciculation fatigable chewing fatigue fever fibrillations finger flexor weakness finger weakness Fisher's syndrome fluctuate flu-like illness food poisoning foot drop foot ulcer, neuropathic Fragile-X associated tremor/ataxia-syndrome fragile-X syndrome fragile-X syndrome, carrier gag reflex, depressed gait disorder gait speed gait, waddling gammaglobulin therapy, intravenous gastrocnemius muscle weakness gastrointestinal disease, neurologic complications gastrointestinal motility gastroparesis gender gene gene mutation gene therapy genetic counselling genetic diagnosis genetic diagnosis, prenatal genetic linkage genetic neurologic disorders genetic screening genetic testing glucose tolerance test, abnormal glycogen debranching enzyme deficiency glycogen storage disease gout Gowers maneuver granulomatosis with polyangiitis granulomatosis, allergic granulomatous disease Guillain Barre syndrome Guillain Barre syndrome, ataxic form Guillain Barre syndrome, differential diagnosis of Guillain Barre syndrome, ophthalmoplegia in Guillain Barre syndrome, variant forms of gynecomastia hallucination hallucination, auditory hammertoes hand pain hand weakness headache hearing loss heart block heart block, complete heart murmur heat intolerance hemianopia hepatomegaly hepatosplenomegaly heralding manifestation high arched feet high arched palate hip dysplasia hip flexor weakness hip pain hirsutism Hispanics histochemistry of muscle HLA HMGcoA reductase inhibitors hoarseness hot bath test H-reflex testing human immunodeficiency virus type 1 hung reflex hyperadrenalism hypercalcemia hypereosinophilic syndrome(HES) hypergammaglobulinemia hyperparathyroidism hyperparathyroidism, secondary hyperphosphatasia hyperreflexia hypersensitivity reaction hypertension hyperthyroidism hypoglycemia hypokalemia hypokalemic periodic paralysis hypomagnesemia hyponatremia hypoosmolality of serum hypoparathyroidism hypophonia hypopituitarism hyporeflexia hypothyroidism hypotonia hypotonia, infants hypoxia iatrogenic neurologic disorders idiopathic inflammatory myopathy ileus, paralytic imbalance immune checkpoint inhibitors immune-related adverse events immunohistochemistry immunomodulation immunosuppressive agents impotence impulsivity inability to stand on tiptoes inappropriate antidiuretic(A.D.H.)hormone, CNS involvement with inclusion bodies inclusion bodies, eosinophilic intranuclear inclusion body myositis insecticides insulin intellectual deficit interstitial pulmonary fibrosis intestinal pseudoobstruction intrinsic hand muscles, wasting of ipecac ipilimumab ischemic exercise test klippel feil syndrome Kugelberg-Welander syndrome kyphoscoliosis, neurologic causes of lactic acidemia lactic dehydrogenase(LDH) leg atrophy leg numbness leg swelling leg weakness, bilateral leg weakness, unilateral lethargy leukocytosis leukodystrophy lid closure, weakness of life expectancy limb-girdle weakness lipid storage myopathy lipoma of skin lipomatosis lipomatosis, multiple symmetrical liquorice livedo reticularis liver disease liver function enzymes lordosis lumbosacral radiculopathy lung transplantation lymphadenopathy lymphocytic meningoradiculitis lymphopenia lysosomal storage disease lysosomes, abnoral malabsorption malabsorption syndrome malignancy screen malignant hyperpyrexia McArdle's disease McArdle's disease, adult onset McLeod syndrome MELAS syndrome Melkersson's syndrome memory, impairment of meningitis meningitis, aseptic mental retardation mental status, abnormal mestinon metabolic acidosis metabolic alkalosis methotrexate middle cerebellar peduncle migraine mimics misdiagnosis mitochondrial disease mitochondrial encephalomyopathy mitral valve prolapse MNGIE syndrome molecular genetics monoclonal antibodies monoclonal gammopathy monoclonal gammopathy of uncertain significance mononeuritis multiplex mononeuropathy mononeuropathy multiplex monoparesis mortality motor neuron disease movement disorder MRI MRI, abnormal MRI, brachial plexus MRI, disappearing lesion on MRI, muscle multicore myopathy multiple myeloma multiple sclerosis muscle atrophy, progressive muscle atrophy, static muscle biopsy muscle cramp muscle diseases, characteristics of muscle hypertrophy muscle pain muscle phosphorylase deficiency muscle spasm muscle stiffness muscle strength, testing muscle swelling muscle tenderness muscle wasting, diffuse muscle weakness muscle weakness, insidious onset of muscle weakness, proximal muscle weakness, sudden onset of muscle, metabolic disorders of muscular dystrophy muscular dystrophy, Becker muscular dystrophy, cardiovascular changes with muscular dystrophy, central nervous system abnormality muscular dystrophy, classification muscular dystrophy, congenital muscular dystrophy, congenital, Fukuyama type muscular dystrophy, differential diagnosis of muscular dystrophy, distal, Miyoshi muscular dystrophy, Duchenne muscular dystrophy, Duchenne, carrier muscular dystrophy, dystrophin normal muscular dystrophy, facioscapulohumeral muscular dystrophy, female occurrence of muscular dystrophy, limb-girdle muscular dystrophy, pattern of muscle involvement myasthenia gravis myasthenia gravis, congenital myasthenia gravis, diagnosis myasthenia gravis, differential diagnosis myasthenia gravis, distal weakness myasthenia gravis, drug induced myasthenia gravis, etiology of myasthenia gravis, familial incidence of myasthenia gravis, limb-girdle myasthenia gravis, misdiagnosis of myasthenia gravis, neuromuscular junction in myasthenia gravis, treatment of myasthenic crisis myasthenic syndrome myasthenic syndrome, treatment of myelopathy myelopathy, chronic progressive myocarditis myoclonus myoedema myoglobinuria myoneuropathy myopathy myopathy, acquired myopathy, acute myopathy, alcoholic myopathy, amyloid myopathy, autoimmune myopathy, carcinomatous myopathy, critically ill myopathy, drug-induced myopathy, glycogen storage myopathy, hereditary myopathy, hypocalcemic myopathy, hypokalemic myopathy, inclusion body myopathy, inclusion body with Paget's disease myopathy, inflammatory myopathy, metabolic myopathy, mitochondrial myopathy, myofibrillar myopathy, necrotizing myopathy, necrotizing, autoimmune myopathy, necrotizing, immune-mediated myopathy, painful myopathy, proximal myopathy, quadriceps myopathy, scleromyxedema myopathy, steroid induced myopathy, steroid responsive myopathy, thyroid disease causing myopathy, toxic myopathy, vacuolar myositis myositis, focal myositis, granulomatous myositis, ocular myotonia myotonia dystrophica myotonia dystrophica, classification myotonia dystrophica, type 2 myotonic discharges myxedema, neurologic manifestations of nasal speech nausea and vomiting neck weakness negative Nelson's syndrome nemaline rod myopathy nemaline rod myopathy, adult onset neoplasm, hormone producing, ectopic neoplasm, metastatic to muscle nerve biopsy nerve conduction studies nerve root enhancement neuritis, causes of neuroendocrinology neurologic complications of, surgery neurologic complications of, systemic cancer neurologic complications of, systemic disease neurologic disease, diagnoses of neurologic examination, focal neurologic signs neuromuscular blockade neuromuscular disease, electrodiagnosis of neuromuscular junction neuromuscular junction, abnormality of neuroophthalmology neuropathology, brain neuropathy neuropathy, diabetic neuropathy, medication induced neuropathy, motor neuropathy, motor, multifocal neuropathy, painful neuropathy, peripheral neuropathy, peripheral, treatment neuropathy, recurrent neuropathy, sensory neuropathy, short-fiber neuropathy, toxic neuropathy, vasculitic, systemic neurotoxin neutropenia next-generation sequencing night sweats nivolumab normal nusinersen nystagmus ocular myopathy oculopharyngeal muscular dystrophy old age, neurology of opened mouth ophthalmoplegia ophthalmoplegia, plus syndrome ophthalmoplegia, progressive external ophthalmoplegia, total optic atrophy optic neuritis oral contraceptives orthopnea osteomalacia overlap syndrome pacemaker, cardiac-transvenous Paget's disease pain pain, abdominal pain, back pain, calf pain, leg pain, thigh palpitations paralysis, acute areflexic paranoia paraparesis paraproteinemia paraspinal muscle paraspinal muscle weakness parathyroid adenoma paresthesias paresthesias, feet paresthesias, hands Parkinsonism syndrome parotid gland swelling parvovirus pathognomonic pembrolizumab perhexiline maleate pericarditis periodic paralysis periodic paralysis, thyrotoxic peripheral blood smear personality change pinched face plasma cell dyscrasia plasmapheresis pleocytosis of cerebrospinal fluid pleurisy pneumonia poison, neurologic problems with poison, organophosphate poliomyelitis polymerase chain reaction polymyositis polymyositis, eosinophilic polyneuritis polyneuropathy polyneuropathy, chronic inflammatory demyelinating polyneuropathy, chronic inflammatory demyelinating, variant form polyneuropathy, chronic inflammatory demyelinating-pure motor syn polyneuropathy, chronic inflammatory demyelinating-sens atax var polyneuropathy, chronic inflammatory demyelinating-variant forms polyradiculoneuropathy polyuria Pompe's disease of glycogen storage porphyria positive sharp waves postpartum potassium precipitating factors pregnancy, neurologic complications in prenatal diagnosis by amniocentesis prognosis progressive neurologic disorder propranolol proteinuria proximal muscle atrophy proximal myotonic myopathy pseudohypertrophy pseudomyotonia psychiatric problems in neurologic disorders psychosis psychosis, acute psychotic behavior ptosis ptosis, bilateral pulmonary embolism pulmonary function tests pulmonary hypertension pulmonary infiltrates purkinje cell cytoplastic autoantibody quadriceps atrophy quadriceps weakness quadriparesis quadriparesis, acute radiculitis radionuclide imaging, heart ragged-red fibers rapidly progressing neurologic illness rash Raynaud's phenomenon recurrent regional enteritis remote effect of cancer on the nervous system renal failure renal stones repetitive nerve stimulation respirator respiratory failure respiratory tract infection retina, abnormal retinal lesion reversible neurologic disorder review article rhabdomyolysis rheumatoid arthritis rheumatoid arthritis factor(R.A.factor) rifampin rigid spine syndrome risk factors safety sarcoglycan sarcoglycanopathy sarcoidosis schizophrenia Schwartz-Jampel syndrome scleroderma sclerosis, bone scoliosis scoliosis, neurologic association with screening sedimentation rate, elevated seizure seizure, focal sensorineural hearing loss sensory loss serum alanine aminotransferase sex reassignment surgery short stature shoulder, pain in single-fiber electromyography sinusitis Sjogren's syndrome Sjogren's syndrome, neurologic manifestations of skin, biopsy skin, lesions in neurologic disorders sleep apnea sloped shoulders SMN1 gene spinal muscular atrophy spinal muscular atrophy, adult onset spinal muscular atrophy, classification spinal muscular atrophy, intermediate form spinocerebellar degeneration spirochete infection splenomegaly splinter hemorrhages standing difficulty starvation, therapeutic statin therapy statin therapy, discontinuation status asthmaticus status epilepticus stem cell transplantation steroid steroid therapy, CNS treatment and complications with stiff joints stiff man syndrome stooped posture strokelike episodes subarachnoid hemorrhage subcutaneous edema sudden death suicide survival motor neuron gene systemic illness systemic lupus erythematosus tachycardia tandem gait, ataxic taxol telangiectases telangiectases, periungual temporal lobe, lesion temporalis muscle wasting tensilon test, false positive thirst thyroid function tests thyroiditis thyrotoxicosis tick bite toe walking tongue, enlarged tongue, fasciculations of tongue, weakness torticollis toxins, nervous system transgender transient ischemic attack transverse smile treatment of neurologic disorder tremor tremor, intention trinucleotide repeats type 1 muscle fiber type 2 muscle fiber ulcerative colitis undiagnosed upgaze, paralysis of uremia urinary frequency urine osmolality, elevated urine, dark vasculitides vecuronium vestibular migraine vincristine neurotoxicity viral infection viral myopathy vision, blurred vital capacity vitamin deficiency vitamin E vitamin E deficiency walking frame walking, difficulty with Watson-Schwartz reaction weakness weakness, acute weakness, episodic weakness, fatiguable weakness, fluctuating weakness, generalized weakness, progressive weakness, proximal weakness, rapidly progressive weaning from respirator, failure to weight loss Werdnig-Hoffman disease wheelchair white matter disease winging of scapula workup xerostomia X-linked bulbospinal neuronopathy X-linked myopathy x-linked myopathy with excessive autophagy

Showing articles 1050 to 1051 of 1051 << Previous Muscular Dystrophy Am J Med 35:632, Pearson,C.M., 1963 Neuro CPC of MGH Myopathy, Severe, Generalized, Chronic, NEJM 258:388-3938., , 1958 Showing articles 1050 to 1051 of 1051 << Previous