Differential (Click to cross reference) acoustic neurinoma acoustic neurinoma, bilateral acquired immunodeficiency syndrome adrenoleukodystrophy adrenomyeloneuropathy advances in neurology adverse drug reaction Alexanders disease algorithm alopecia alpha-fetoprotein Alzheimer's disease Alzheimer's disease, diagnosis of Alzheimer's disease, early onset Alzheimer's disease, familial amniocentesis amyloid angiopathy, cerebral amyloid angiopathy, hereditary cystatin C amyotrophic lateral sclerosis amyotrophic lateral sclerosis, familial anemia anemia, hemolytic anesthesia, general anosmia apolipoprotein E APP gene apraxia of eye movements arteriopathy ataxia ataxia telangiectasia ataxia, cerebellar ataxia, hereditary ataxia, truncal attention deficit disorder with hyperactivity autonomic dysfunction basal ganglia, degeneration basal ganglia, lesion of Bassen-Kornzweig syndrome benign familial neonatal convulsions brachial neuritis brachial plexus neuropathy brachial plexus neuropathy, familial brain biopsy brainstem, lesion of brainstem, neoplasms of bulbar palsy, progressive cafe au lait spots carcinoembryonic antigen carcinoma carcinoma of pancreas CAT scan CAT scan, abnormal cataracts cavernous hemangioma cerebellar ataxia, children cerebellar ataxia, hereditary cerebellar degeneration cerebellar lesion cerebellum, neoplasms of cerebral atherosclerosis cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy cerebral autosomal recessive arteriopathy with subcortical infarction and leukoencephalopathy cerebral infarction cerebral infarction, subcortical cerebral ischemia cerebro hepato renal syndrome cerebrovascular accident cerebrovascular accident, familial occurrence cerebrovascular accident, young adult Charcot-Marie-Tooth chorea choreoathetosis choreoathetosis, paroxysmal chromosomal abnormality chromosome 11 chromosome 14 chromosome 17 chromosome 2 chromosome 22 chromosome 3 chromosome 7 chromosome 9 clindamycin clonazepam clubfoot as related to neurologic disease Cockayne's syndrome coma compression neuropathy compression neuropathy, recurrent cost effectiveness creatine phosphokinase(CPK)elevated Creutzfeldt-Jakob disease, genetic cryptococcal meningitis cyst, neoplastic cerebellum cytomegalovirus infection degenerative diseases of CNS dementia dementia, familial dementia, presenile dementia, rapidly progressive dementia, transmissible dentate nuclei dentate nuclei, lesion of developmental retardation diabetes mellitus DNA probes drooling drug induced neurologic disorders dysarthria dysmorphic dystonia dystonia musculorum deformens dystonia, paroxysmal dystrophin ear, abnormal electroencephalogram electronystagmography electroretinograph encephalitis encephalitis, focal encephalitis, Rasmussen's encephalitis, viral enzyme, muscle disease epidemiology of neurology ethics in neurology eye movement, disorders of face, elongated facial appearance, abnormal familial fasciculation fatal familial insomnia fragile-X syndrome Friedreich's ataxia fundus, abnormality of gadolinium gait disorder gaze palsy gaze palsy, supranuclear gene gene mutation genetic counselling genetic diagnosis genetic diagnosis, prenatal genetic linkage genetic neurologic disorders genetic screening genetic testing Gerstmann-Straussler-Scheinker disease GFAP gene gonadotropin-releasing hormone growth retardation gynecomastia Hallervorden Spatz disease hallucination hamartoma headache headache, positional hearing loss hemangioblastoma hemiparesis hepatic failure hepatolenticular degeneration(Wilson's disease) hepatolenticular degeneration(Wilson's disease), presymptomatic hepatosplenomegaly Hispanics HTRA1 gene Hunter's syndrome huntingtin Huntington's chorea Huntington's chorea, genetic counselling Huntington's chorea, presymptomatic detection of hyperactivity hyperekplexia hyperhidrosis hyperkalemic periodic paralysis hyperreflexia hyperthermia hypogonadism hypotelorism hypotonia hypotonia, infants imbalance immunodeficiency immunohistochemistry immunoperoxidase staining immunosuppression in situ hybridization inclusion bodies, intracytopasmic insomnia intracerebral hemorrhage intracerebral hemorrhage, familial intracerebral hemorrhage, young adult Jakob-Creutzfeldt disease joint hypermobility Kallmann's syndrome Kearns-Sayre syndrome KRIT1 gene Kugelberg-Welander syndrome Laurence-Moon-Bardet-Biedl syndrome leukemia leukodystrophy leukoencephalopathy lymphoma macrocephaly macular degeneration malformation, vascular malformation, vascular, cerebral malformation, vascular, familial malignant hyperpyrexia manic-depressive medulla oblongata medulla oblongata, atrophy medulla oblongata, lesion of meningitis meningitis, recurrent meningitis, relapse mental retardation mental retardation, familial Mexican Mexico misdiagnosis molecular genetics mongolism mononeuropathy mononeuropathy, recurrent mortality motor neuron disease movement disorder movement disorder, extrapyramidal MRI MRI, abnormal MRI, contrast enhanced MRI, spinal cord MRI, spinal cord, increased intramedullary cord signal mucopolysaccharidoses mucopolysacchariduria multiple sclerosis multiple sclerosis, differential diagnosis of multiple sclerosis, familial multiple sclerosis, misdiagnosis multiple system atrophy muscle biopsy muscle spasm muscle stiffness muscular dystrophy muscular dystrophy, Becker muscular dystrophy, differential diagnosis of muscular dystrophy, Duchenne muscular dystrophy, Duchenne, carrier muscular dystrophy, Duchenne, neonatal screening muscular dystrophy, Duchenne, presymptomatic detection muscular dystrophy, female occurrence of muscular dystrophy, limb-girdle myelin basic protein gene myoclonus myopathy myopathy, mitochondrial myopathy, proximal myopia myotonia myotonia dystrophica neonatal screening, genetic neurologic disorders neoplasm, metastatic to CNS neoplasm, posterior fossa neoplasm, primary intracranial neoplasm, primary of CNS neurocutaneous disease neuroendocrinology neurofibroma neurofibromatosis 1 neurofibromatosis 2 neurofibromatosis 2, presymptomatic neurologic disease neurologic disease, diagnoses of neuronal ceroid-lipofuscinosis neuronal migration disorder neuropathology neuropathology, brain neuropathy neuropathy, amyloid neuropathy, hereditary peripheral neuropathy, peripheral night blindness Notch3 gene ocular motility, disorders of oculopharyngeal muscular dystrophy olfactory bulb optic atrophy optic glioma optic nerve optic neuropathy pain pain, flank paraparesis paraparesis, familial spastic paraparesis, spastic paroxysmal dystonic choreoathetosis paroxysmal neurologic deficits pathology patient information and support periodic paralysis peroxisomal disease pheochromocytoma pigmentary retinopathy polycystic kidneys polymerase chain reaction polyneuropathy, familial posterior fossa, lesion of practice guidelines prenatal diagnosis by amniocentesis prion disease progeria prognosis progressive multifocal leucoencephalopathy progressive spinal muscular atrophy proximal myotonic myopathy radiation hypersensitivity recombinant DNA recurrent refractive errors Refsum's disease renal cell carcinoma renal cyst retinal degeneration retinal hemangioma retinal lesion retinal tumor retinitis pigmentosa retinopathy review article RFLPs rigidity risk factors Rosenthal fibers seizure seizure, familial seizure, focal seizure, intractable, treatment of seizure, neonatal sensorineural hearing loss simian crease skin, lesions in neurologic disorders skull x-ray, abnormal sleep pathology and physiology small vessel disease Southern immunoblot test spasticity spinal cord spinal cord, lesion of spinal cord, neoplasm spinal muscular atrophy spine, metastasis to spinocerebellar ataxia spinocerebellar ataxia type 3/Machado Joseph disease spinocerebellar degeneration spondylosis spongy degeneration of brain startle reaction stuporous subarachnoid hemorrhage synkinesis tapetoretinal degeneration telangiectases testicular enlargement thalamus, lesion of tinnitus tomaculous neuropathy trauma treatment of neurologic disorder trinucleotide repeats Usher's syndrome ventricular garlands vibratory sensation, abnormal viral infection viral infection, CNS visual field defect visual loss Von Hippel Lindau Von Hippel Lindau, carrier Von Hippel Lindau, screening protocol for walking, difficulty with Werdnig-Hoffman disease Western immunoblot test wheelchair white matter disease X-linked bulbospinal neuronopathy x-linked mental retardation X-linked neuropathy

Showing articles 350 to 356 of 356 << Previous Neurologic Complications of Systemic Cancer In Neurologic Clinics 3:729-750, Patchell,R.A.&Posner,J.B., 1985 The Computer as Clinical Consultant Arch Int Med 140:313-314, Shortliffe,E.H.,et al, 1980 Cytogentic Diagnosis Of Meningeal Carcinomatosis NEJM 303:1479, Kristoffersson,U.,et al, 1980 NERVLINE, A Neuroscience Information Retrieval System Neurol 28:380, Finelli,P.F., 1978 Protocol-Based Computer Reminders, The Quality of Care & the Non-perfectability of Man NEJM 295:1351, McDonald,C.J., 1976 Computer Analysis of the Clinical Neurological Examination Comput Bio Med 3:111, Meyer,A.U.,et al, 1973 Medical Diagnosis:An Information-Processing Approach Comput & Biomed Research 5:315972., Wortman,P.M., 1972 Showing articles 350 to 356 of 356 << Previous