Differential (Click to cross reference) accommodation accomodation, abnormal advances in neurology adverse drug reaction ammonia ANA anasarca anesthesia, general angiokeratoma ankle edema anorexia anterior tibial muscle weakness anticonvulsants anticonvulsants, untoward effects of antiviral agents areflexia arrhythmia, cardiac arthralgia arthritis arthrogryposis multiplex ascites ataxia ataxic gait atrial fibrillation atrial paralysis atrioventricular block attention deficit disorder with hyperactivity autoantibodies autoimmune disease autonomic dysfunction Babinski sign basal ganglia, calcification of biopterin deficiency blinking blinking, reduced bone marrow transplantation bradycardia bradykinesia brain atrophy brainstem, atrophy Brown-Vialetto-Van Laere syndrome burning paresthesia cachexia calcification, intracranial calf hypertrophy carcinoma cardiomegaly cardiomyopathy cardiovascular disease caries carpal tunnel syndrome CAT scan, abnormal cataracts causalgia central core disease cerebellar atrophy, primary cerebral cortical atrophy cerebral embolism cerebral embolism, carotid origin cerebral palsy cerebrospinal fluid, abnormal cerebrospinal fluid, gammaglobulin of cerebrospinal fluid, oligoclonal IgG in cerebrovascular accident cerebrovascular accident, cardiac disease causing cerebrovascular accident, young adult ceruloplasmin, serum cervical spine cervical spine abnormality Charcot-Marie-Tooth children cholelithiasis chorea chromosomal abnormality chromosome 14 chromosome 17 Clinical Pathologic Conference(C.P.C.) clubbing of fingers clubfoot as related to neurologic disease Cockayne's syndrome cognition cogwheel rigidty collagen vascular disease complications congenital infection, CNS congenital myopathy congenital myopathy, inflammatory congestive heart failure consanguinity contractures, joint contrast agents, neurotoxicity of convergence convergence, impaired cornea, opacity of corpus callosum, lesion of cough cranial neuropathy cranial neuropathy, multiple crawl regression C-reactive protein, elevated creatine phosphokinase MB isoenzyme elevation creatine phosphokinase(CPK)elevated cry, weak cryptorchidism cytomegalovirus infection cytomegalovirus infection, congenital D-dimer decision analysis dementia dermatomyositis developmental disability developmental milestones developmental milestones, loss of developmental retardation diabetes mellitus dialysis diamond on quadriceps differential diagnosis difficulty climbing stairs difficulty going down stairs disability rating scale, neurological disability, neurological dislocated hip, congenital distal muscle atrophy distal muscle weakness diurnal variation dopa responsive dystonia drooling drug induced neurologic disorders Dupuytren's contractures dysarthria dysmorphic dysostosis multiplex dysphagia dyspnea dyspraxia dystonia dystonia, children dystonia, treatment of dystrophic calcification dystrophin electrocardiogram, abnormal electromyogram Emery-Dreifuss muscular dystrophy encephalopathy encephalopathy, progressive endemic area enzyme, defect enzyme, muscle disease eosinophilia eosinophilia-myalgia syndrome eosinophilic fasciitis epidemiology of neurology epileptic encephalopathy equinovarus exercise exome sequencing eyes, sunken facial appearance, abnormal facial weakness failure to thrive falling familial FARS2 deficiency fasciculation fatigue feeding disorder fetal movements, reduced fetus fever fibrillations fine motor function, impaired floppy infant foot deformity foot drop fracture, long bone fucosidosis gadolinium gait disorder gait, festinating gait, spastic gait, waddling galactorrhea gamma amino butyric acid gene gene mutation gene therapy genetic counselling genetic neurologic disorders genetic testing glabellar sign glutamic acid decarboxylase, antibody glycoprotein Gowers maneuver grimacing groove sign growth retardation Guillain Barre syndrome hammertoes hand deformity hand pain hand weakness handwriting headache hearing loss heart block heart block, complete heart murmur hepatic failure hepatitis hepatolenticular degeneration(Wilson's disease) hepatomegaly hepatosplenomegaly high arched feet histochemistry histochemistry of muscle hyperpigmentation of skin hyperreflexia hypertonia hypogonadism hypoparathyroidism hypophonia hyporeflexia hypotonia hypotonia, infants iatrogenic neurologic disorders imbalance immunosuppressive agents implantable cardioverter defibrillator inclusion body myositis infection, recurrent influenza A virus influenza B virus injection neuropathy intellectual deficit intellectual deterioration intrauterine intrauterine infection intrauterine infection, viral intrauterine infection, viral of CNS intrinsic hand muscles, wasting of jaw contractures joint hypermobility Kayser-Fleischer ring kinesia paradoxica Krabbe's disease kyphoscoliosis, neurologic causes of lactic dehydrogenase(LDH) lateral cutaneous nerve of forearm L-dopa Ledderhose disease leg dragging leg swelling leprosy leukocytosis leukodystrophy life expectancy limb-girdle weakness liver disease liver function enzymes liver transplantation lordosis L-tryptophan lymphadenopathy lymphadenopathy, axillary lymphadenopathy, paraaortic lysosomal storage disease malignant hyperpyrexia marche a petits pas masked facies median neuropathy meningitis, CSF cell count-normal mental retardation merosin microcephaly micrographia misdiagnosis mitochondrial disease mitral valve prolapse molecular genetics monoclonal antibodies mortality movement disorder movement disorder, extrapyramidal MRI MRI, abnormal MRI, complications with MRI, contraindications MRI, contrast enhanced multiple system atrophy muscle atrophy, progressive muscle atrophy, static muscle biopsy muscle cramp muscle pain muscle spasm muscle stiffness muscle strength, testing muscle tenderness muscle weakness muscle weakness, proximal muscular dystrophy muscular dystrophy, Becker muscular dystrophy, Becker, carrier muscular dystrophy, cardiovascular changes with muscular dystrophy, central nervous system abnormality muscular dystrophy, classification muscular dystrophy, congenital muscular dystrophy, congenital, Fukuyama type muscular dystrophy, congenital, Ullrich muscular dystrophy, differential diagnosis of muscular dystrophy, Duchenne muscular dystrophy, Duchenne, carrier muscular dystrophy, limb-girdle muscular dystrophy, pattern of muscle involvement myasthenia gravis myasthenia gravis, familial incidence of myasthenic syndrome myocardial biopsy myocarditis myoglobinuria myopathy myopathy, hypocalcemic myopathy, quadriceps myositis myositis, acute of childhood myositis, post infectious myotonia dystrophica myotonic discharges mysoline neck extension neck weakness nephrogenic systemic fibrosis nerve conduction studies nerve enlargement nerve hypertrophy nerve injury neurocutaneous disease neuroendocrinology neurologic complications of, systemic disease neurologic disease, diagnoses of neuromuscular disease, electrodiagnosis of neuropathology neuropathy neuropathy, demyelinating neuropathy, hereditary peripheral neuropathy, hypertrophic neuropathy, iatrogenic neuropathy, peripheral neurotoxic nystagmus optic atrophy optic neuropathy orange peel appearance of skin overlap syndrome pacemaker, cardiac-transvenous pain pain, calf pain, leg paraparesis, familial spastic paraparesis, familial spastic, classification paraparesis, familial spastic, variants paraparesis, spastic paresthesias paresthesias, feet paresthesias, hands Parkinson disease Parkinson disease, diagnosis Parkinson disease, differential diagnosis of Parkinson disease, juvenile Parkinsonism syndrome periventricular leukomalacia personality change pes cavus Peyronie's disease phenobarbital phlebotomy photosensitivity, skin pigmentary retinopathy pneumonia polymerase chain reaction polymyalgia rheumatica polymyositis pons, atrophy positive sharp waves practice guidelines prayer sign premature infant prenatal diagnosis by amniocentesis prognosis progressive neurologic disorder prolactin, elevated proximal muscle atrophy pruritus pseudohypertrophy psychiatric problems in neurologic disorders psychomotor retardation pulmonary infiltrates pyramidal tract dysfunction rash Red flags reflex sympathetic dystrophy renal failure renal tubular acidosis repetitive nerve stimulation respiratory failure retinopathy retropulsion review article rhabdomyolysis riboflavin transporter deficiency rickets rigid spine syndrome rigidity rippling muscle disease safety Samoa sarcoglycan sarcoglycanopathy sarilumab scoliosis scoliosis, neurologic association with sedimentation rate sedimentation rate, elevated seizure seizure, children seizure, neonatal sensorineural hearing loss serositis short stature shoulder, frozen shoulder, pain in sinemet skin, biopsy skin, lesions in neurologic disorders skin, thickened spastic diplegia spasticity speech disorder speech disorder, childhood splenomegaly stare steppage gait steroid steroid therapy, CNS treatment and complications with stiff joints stiff man syndrome stillbirth stooped posture suck, poor sudden death systemic illness systemic juvenile idiopathic arthritis tandem gait, ataxic tenderness thrombocytosis tocilizumab toe walking toxic oil syndrome treatment of neurologic disorder tremor tremor, intention tremor, postural tremor, resting tripping type 1 muscle fiber type 2 muscle fiber tyrosine hydroxylase deficiency urea-cycle enzymopathies uremia urine test for metabolic disorders urine, dark viral infection viral myopathy vital capacity voice, abnormality of Walker-Warburg syndrome walking walking frame walking, delayed walking, difficulty with weakness weakness, congenital weakness, generalized weakness, progressive weakness, proximal web sites weight loss wheelchair white matter disease wide based gait winging of scapula workup wrist drop x-ray, cervical spine

Showing articles 50 to 55 of 55 << Previous Congenital Myotonic Dystrophy Arch Neurol 37:693-696, Argov,Z.,et al, 1980 Emery-Dreifuss Muscular Dystrophy Ann Neurol 5:111-117, Rowland,L.P.,et al, 1979 Familial Neuromuscular Disease with Type 1 Fiber Hypoplasia, Tubular Aggregates, Cardiomyopathy, & Myasthenic Features Neurol 28:1135-1140, Dobkin,B.H.,et al, 1978 The Spectrum of Mild X-Linked Recessive Muscular Dystrophy Arch Neurol 34:408, Ringer,S.P.,et al, 1977 Rigid Spine Syndrome:A Type I Fiber Myopathy Arch Neurol 34:119, Seay,A.R.,et al, 1977 Parkinson's Disease In Handbk of Clinical Neurology, Vinken, P. J. & Bruyn, G. W. , Ed, North-Holland Publ Co, Amsterdam, 6:173, 1968. Selby, G., 1968 Showing articles 50 to 55 of 55 << Previous