Differential (Click to cross reference) acquired immunodeficiency syndrome acute intermittant porphyria addiction, heroin addiction, heroin-neurologic complications with advances in neurology adverse drug reaction agitation alcohol alcoholism anemia anemia, megaloblastic anesthesia, general ankle, swelling of anorexia anticholinergic drugs anticholinergic drugs, side effects of areflexia arrhythmia, cardiac arthralgia ascites aspartate aminotransferase aspergillosis asterixis asymptomatic ataxia ataxia, cerebellar ataxic gait autoantibodies autonomic dysfunction azidodeoxythymidine B 12 deficiency brain natriuretic peptide bulbar palsy bulimia bulimia nervosa burning hands burning paresthesia calf hypertrophy carbon monoxide poisoning cardiomyopathy cardiovascular disease carnitine deficiency carnitine deficiency myopathy CAT scan CAT scan, muscle CAT scan, pelvis catatonia catatonia, lethal cathartic cerebrovascular accident cervical spondylosis children chromosome 19 Clinical Pathologic Conference(C.P.C.) clofibrate coenzyme Q10 coenzyme Q10 deficiency colchicine coma compartment syndrome compartment syndrome, gluteal complications compression neuropathy confusion confusional state, acute congenital myopathy conjunctivitis contractures, joint contraindications C-reactive protein, elevated creatine phosphokinase(CPK)elevated critical care unit cultured skin fibroblasts dantrolene sodium deafness delay in diagnosis delirium depression dermatomyositis developmental retardation dexterity, impaired diabetes insipidus diagnostic criteria diamond on quadriceps differential diagnosis difficulty climbing stairs drug abuse drug abuse, neonatal abstinence syndrome with drug abuse, neurologic complications of drug addiction drug induced neurologic disorders drug induced neurologic disorders in children drug interactions drug withdrawal dysphagia dystonia dystonia musculorum deformens dystrophin eating disorder ECHO virus electrocardiogram, abnormal electromyogram emergencies, neurologic encephalomyopathy encephalopathy encephalopathy, metabolic endophthlamitis enterovirus enzyme, defect enzyme, muscle disease enzyme, serum epsilon-aminocaproic acid(E.A.C.A.) exercise exercise intolerance eye, pain in facial weakness falling familial fatigue fever fibrillations fine motor function, impaired fungal infection gait disorder gait, waddling gasoline sniffing gene gene mutation genetic neurologic disorders genetic screening genetic testing glycogen storage disease Gowers maneuver hand weakness head injury hearing loss hematuria, microscopic hepatolenticular degeneration(Wilson's disease) histochemistry of muscle HMGcoA reductase inhibitors human immunodeficiency virus type 1 hung reflex hypercapnia hypernatremia hypersegmented polys hyperthermia hypokalemia hyporeflexia hypothyroidism iatrogenic neurologic disorders inborn errors of metabolism inclusion body myositis injection neuropathy intellectual deterioration intravenous drug abuse ischemic exercise test jaundice lactic acidemia lactic dehydrogenase(LDH) learning disability learning disability, in children leg weakness, bilateral leg weakness, unilateral leukocytosis level of consciousness, decreased limb-girdle weakness lipid lowering agent lithium liver function enzymes malignant hyperpyrexia McArdle's disease McArdle's disease, adult onset mental status, abnormal metabolic acidosis metabolic disorder, primary methylmalonic acid, serum mimics misdiagnosis mitochondrial disease molecular genetics mononeuropathy mononeuropathy multiplex mood change mortality movement disorder MRI MRI, muscle MRI, spine muscle atrophy, progressive muscle atrophy, static muscle biopsy muscle cramp muscle pain muscle phosphofructokinase deficiency muscle phosphorylase deficiency muscle stiffness muscle tenderness muscle weakness muscle weakness, proximal muscular dystrophy muscular dystrophy, Becker muscular dystrophy, cardiovascular changes with muscular dystrophy, central nervous system abnormality muscular dystrophy, Duchenne muscular dystrophy, limb-girdle muscular dystrophy, pattern of muscle involvement myelopathy myoclonus myocytolysis myoedema myoglobinuria myopathy myopathy, acute myopathy, drug-induced myopathy, metabolic myopathy, mitochondrial myopathy, necrotizing myopathy, necrotizing, autoimmune myopathy, proximal myopathy, toxic myositis myotonia dystrophica myxedema, neurologic manifestations of nephrotic syndrome neuroleptic neuroleptic malignant syndrome neurologic complications of, surgery neurologic complications of, systemic disease neurologic disease, diagnoses of neuropathy neuropathy, acute neuropathy, painful neuropathy, peripheral neuropathy, sensory ochronosis osteoarthrosis osteoporosis pain pain, abdominal pain, buttock pain, leg paraparesis, spastic paresthesias paresthesias, hands PAS positive periarteritis nodosa periodic paralysis peripheral blood smear, abnormal pernicious anemia personality change phosphorylase b kinase deficiency polyneuropathy polyneuropathy, chronic inflammatory demyelinating porphyria precipitating factors prevention of neurologic disorders prognosis progressive neurologic disorder proteinuria proximal muscle atrophy pruritus psychiatric problems in neurologic disorders psychosis psychosis, acute ptosis quadriplegia recurrent red eye renal failure renal failure, acute renal stones respiratory failure review article rhabdomyolysis rigidity risk factors Romberg's sign sarcoglycan sarcoglycanopathy sciatic neuropathy sclerae, hyperpigmented second wind phenomena seizure seizure, neonatal seizure, neonatal abstenence syndrome selective serotonin reuptake inhibitors sensorineural hearing loss serotonin syndrome serum alanine aminotransferase sex reassignment surgery sleep apnea speech disorder speech disorder, childhood speech, delayed development of speech, slowed spondylolysis statin therapy status epilepticus strychnine poisoning stuporous subdural hematoma systemic illness tachycardia 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Showing articles 200 to 216 of 216 << Previous Neurologic Manifest. of Infective Endocarditis:A Review Stroke 4:958, Greenlee,J.E.,et al, 1973 Case Record of MGH-NEJM Atheromatous Emboli to Brain Kidney, 286:11461972., , 1972 Pediatric Neurology Psych Annals 2:1, , 1972 Dumbbell Anterolateral Spinocranial Neurofibroma with a Note on Thigh Muscle Atrophy & Fasciculation Neurochir 4:143, Bartal,A.D.,et al, 1972 Urine Tests for Morphine-Correspondence NEJM 286:895, Mani,G., 1972 Encephalomyelopathy of Leigh Editorial BMJ 238, 1971, May., , 1971 New Kind of PKU Pediatrics Consultant Sept 1971, pp 68-70., Johnson,C., 1971 Spinal Epidural Hematoma and the Brown-Sequard Syndrome Neurol 21:1066-1068, Russman,B.S.&Kazi,K.H., 1971 Prenatal Genetic Diagnosis NEJM 283:1370, Milunsky,A.,et al, 1970 Expanding Intraspinal Lesions Hosp Med, Sept 1969 p. 31., Nugent,G.R., 1969 Clinical Cases-Dx:Functional Approach to Neuroanatomy pp 477-490 Earl Lawrence House McGraw Hill 1967., , 1967 Screening for Inborn Errors of Metabolism Associated with Mental Deficiency or Neurologic Disorders or Both NEJM 274:384, Renuart,A., 1966 Neurological Complications of Wegener's Granulomatosis Arch Neurol l8:45, 1963, Drachman,D., 1963 Metabolic Defects Associated with Mental Retardation Am J Dis Child 104:401, Garell,D., 1962 Candida Endocarditis-Clinical & Pathologic Studies Am J Med 32:251-285, 1962, Andriole,V.T.,et al, 1962 The Significance of Nonbacterial Thrombotic Endocarditis:An Autopsy & Clinical Study of 78 Cases Ann Int Med 46:255, MacDonald,R.A.,et al, 1957 Seizure Disorder Lead Poisoning, Case Study-Rocom Laboratories., , 1850 Showing articles 200 to 216 of 216 << Previous