Differential (Click to cross reference) acanthocytosis acquired immunodeficiency syndrome activated protein C resistance addiction, heroin adrenoleukodystrophy adverse drug reaction alcohol Alexanders disease algorithm aminoacidopathies aminoacidurias amniocentesis amphotericin B anticardiolipin antibodies anticoagulant, treatment antiphospholipid antibodies antithrombin III deficiency archery arylsulfatase B aspirin ataxia, cerebellar atlanto-axial subluxation Bassen-Kornzweig syndrome Behcet's syndrome birth injury blindness blood dyscrasias, neurologic findings with bone biopsy bone marrow transplantation bow hunter's stroke brainstem, infarction of carbenoxolone cardiac arrest cardiac arrest and resuscitation cardiomyopathy CAT scan CAT scan, abnormal CAT scan, angiography CAT scan, delta sign, empty CAT scan, venography cataracts cerebellar infarction cerebral cortical atrophy cerebral embolism cerebral infarction cerebral ischemia cerebral venous infarction cerebral venous thrombosis cerebral venous thrombosis, deep cerebral venous thrombosis, etiology cerebral venous thrombosis, recurrent cerebro hepato renal syndrome cerebrovascular accident cerebrovascular accident, acute management of cerebrovascular accident, cost of cerebrovascular accident, familial occurrence cerebrovascular accident, infancy and childhood cerebrovascular accident, prevention of cerebrovascular accident, recurrent cerebrovascular accident, thrombolytic agents in treatment cerebrovascular accident, women cerebrovascular accident, work up for cerebrovascular accident, young adult cerebrovascular disease, risk factors in cerebrovascular disease, treatment of cervical osteophyte cervical spine children chiropractic manipulation chiropractic manipulation, neurologic complications with chloroquine cholesterol chromosomal abnormality cisterna magna, enlarged Clinical Pathologic Conference(C.P.C.) clofibrate coagulopathy Cockayne's syndrome complications compression neuropathy conjunctival biopsy consanguinity cornea cornea, abnormal cornea, opacification in infancy-causes of cornea, opacity of corneal dystrophy corpus callosum corpus callosum, lesion of cost effectiveness craniectomy, decompressive cyst, arachnoid D-dimer deafmute deafness degenerative diseases of CNS dementia developmental milestones, loss of developmental retardation dipyridamole disseminated intravascular coagulation(DIC) dissociated sensory loss diuretic dizziness DNA probes drug induced neurologic disorders dural sinus thrombosis dwarfism dysmorphic dyspraxia efficacy electrocardiogram, abnormal electroencephalogram, abnormalities of electron microscopy electronystagmography electroretinograph embolism, platelet embolism, vertebral-basilar artery encephalopathy endovascular therapy enolase enzyme, defect enzyme, muscle disease epidemiology of neurology epsilon-aminocaproic acid(E.A.C.A.) evidence-based research Factor V Leiden false negative familial fibrinolytic agents fibrinolytic agents, intra-venous local infusion foam cells Friedreich's ataxia fundus, abnormality of gadolinium gangliosidosis GM1 gangliosidosis, generalized gargoylism gene mutation gene therapy genetic diagnosis, prenatal genetic linkage genetic neurologic disorders genetic testing genu valgum glaucoma glycogen storage disease growth retardation Hallervorden Spatz disease Hallgren's syndrome head injury head injury, pediatric head turning head turning, neurologic complications with headache headache, persistent headache, severe hearing loss heart block hemiparesis hemoglobin abnormality, neurologic complications of hepatosplenomegaly human immunodeficiency virus type 1 Hunter's syndrome Hurler's syndrome hydrocephalus hypercholesterolemia hypokalemia hypotonia hypotonia, infants hypoxic encephalopathy incidence infantile hemiplegia interobserver agreement intracranial hypertension, benign intracranial pressure, increased ipecac Kearns-Sayre syndrome keratoconus Krabbe's disease kyphoscoliosis, neurologic causes of Laurence-Moon-Bardet-Biedl syndrome leukemia leukemia, neurologic findings assoc.with leukodystrophy level of consciousness, decreased lipid lowering agent lipid storage disorder of CNS lipid storage myopathy lipids liquorice lupus anticoagulant lysosomal storage disease lysosomes, abnoral macrocephaly macular degeneration malformation, CNS, congenital meningitis mental retardation metabolic disorder, primary metachromatic leukodystrophy middle cerebral artery territory infarction middle cerebral artery, occlusion of mimics misdiagnosis Morquio syndrome mortality MRI MRI, abnormal MRI, CAT scan compared to MRI, contrast enhanced MRI, disappearing lesion on MRI, false negative MRI, high signal foci on MRI, negative MRI, venography MRS mucopolysaccharidoses mucopolysacchariduria muscle pain muscle swelling muscle tenderness muscle weakness muscle weakness, causes of myelopathy myeloproliferative disorder myoglobinuria myopathy myopathy, acute myopathy, alcoholic myopathy, drug-induced myopathy, hypokalemic myopathy, mitochondrial myopathy, proximal myopathy, steroid induced myopia nausea and vomiting neck flexion neuritis neuroaxonal dystrophy neurologic complications of, systemic disease neurologic disease, diagnoses of neurologic examination, focal neuron specific enolase neuronal ceroid-lipofuscinosis neuropathology neuropathy neuropathy, hereditary peripheral Niemann-Pick disease night blindness nonsteroidal anti-inflammatory drug obesity occipitalization of the atlas ocular myopathy ophthalmoplegia, plus syndrome optic atrophy optic nerve optic neuropathy oral contraceptives oral contraceptives, cerbrovascular disease and oral contraceptives, neurologic complications with osteoporosis papilledema paraparesis, spastic paroxysmal nocturnal hemoglobinuria pectus carinatum perhexiline maleate peroxisomal disease pigmentary retinopathy pitfalls plasminogen deficiency platelet inhibiting drugs polycythemia, primary polydactyly practice guidelines pregnancy, neurologic complications in prenatal diagnosis by amniocentesis prethrombotic state primary thrombocythemia prognosis protein C deficiency protein S deficiency pseudoretinitis pigmentosa psychiatric disorder pulmonary embolism quadriparesis quadriplegia radiculopathy refractive errors Refsum's disease respiratory failure retinal degeneration retinal lesion retinitis pigmentosa retinopathy review article RFLPs rhabdomyolysis risk factors S-100 protein safety Sanfilippo syndrome schizophrenia seizure sensorineural hearing loss short neck short stature sickle cell disease skin, biopsy sphingolipodoses Spielmeyer Vogt syndrome spinal cord, compression of spinocerebellar degeneration sports medicine, neurology of stem cell transplantation steroid straight sinus sulfinpyrazone superior sagittal sinus thrombosis tapetoretinal degeneration thalamus, infarction of thrombocytopenia thrombophlebitis tissue plasminogen activator, intravenous tongue, enlarged transient ischemic attack transient ischemic attack, treatment of treatment of neurologic disorder triglycerides Usher's syndrome vertebral artery vertebral artery injury vertebral artery occlusion vertebral-basilar insufficiency vincristine neurotoxicity visual acuity, decreased visual field defect visual fields, constricted visual loss white matter disease workup

Showing articles 50 to 51 of 51 << Previous Prenatal Genetic Diagnosis NEJM 283:1370, Milunsky,A.,et al, 1970 Morquio's Disease, A Radiologic & Morphologic Study Pediatrics 34:839-850, Schenk,E.A.&Haggerty,J., 1964 Showing articles 50 to 51 of 51 << Previous