Differential (Click to cross reference) abdominal cramps acid maltase deficiency acid maltase deficiency, adult acral sensory symptoms adrenoleukodystrophy adrenomyeloneuropathy agalsidase alfa alpha glucosidase aminoacidopathies aminoacidurias amniocentesis angina pectoris angiokeratoma anhidrosis anterior horn cell disease anterior tibial muscle weakness antiviral agents Arnold Chiari malformation arthropathy arthropathy, neuropathic arylsulfatase A aspartate aminotransferase aspiration asymptomatic ataxia ataxia telangiectasia ataxia, cerebellar ataxia, progressive athetosis atidarsagene autotemcel attention deficit disorder with hyperactivity attention span autonomic dysfunction axonal spheroid Babinski sign basal ganglia, lesion of basal ganglia, lesion, bilateral basilar impression behavioral disorder blindness blood dyscrasias, neurologic findings with bone marrow biopsy bone marrow transplantation brain atrophy brain biopsy brain biopsy, complications of brain biopsy, false negative brain biopsy, indication brainstem, infarction of burning feet burning feet, differential diagnosis of burning hands burning paresthesia cardiomyopathy CAT scan CAT scan, abnormal CAT scan, false negative cataplexy cataracts cerebellar ataxia, children cerebellar ataxia, children, differential diagnosis of cerebellar infarction cerebral cortical atrophy cerebral ischemia cerebrospinal fluid, gammaglobulin of cerebrotendinous xanthomatosis cerebrovascular accident cerebrovascular accident, cryptogenic cerebrovascular accident, familial occurrence cerebrovascular accident, non atherosclerotic cause of cerebrovascular accident, young adult cerebrovascular disease cerebrovascular disease, cardiovascular disease with cherry red spot cherry red spot-myoclonus syndrome children chorea choreoathetosis chromosomal abnormality chronic graft versus host disease Clinical Pathologic Conference(C.P.C.) coagulopathy cognition complications compression fracture congestive heart failure consanguinity contractures, joint cornea, abnormal cornea, opacification in infancy-causes of cornea, opacity of corneal dystrophy corpus callosum corpus callosum, hypoplastic corpus callosum, lesion of creatine phosphokinase(CPK)elevated creatinine, elevated cry, abnormal cultured skin fibroblasts cystinosis degenerative diseases of CNS delay in diagnosis dementia dementia, childhood dementia, diagnostic evaluation of developmental disability developmental milestones, loss of developmental retardation diarrhea differential diagnosis difficulty going down stairs diplopia distal muscle weakness drooling dropped head syndrome dysarthria dysmorphic dysostosis multiplex dysphagia dystonia dystonia, face dystonia, focal dystonic lipidosis echocardiogram efficacy electroencephalogram electroencephalogram, abnormalities of electromyogram electron microscopy enzyme treatment enzyme, defect episodic disorders episodic neurologic deficits exercise intolerance exome sequencing eye movement, disorders of Fabry's disease facial appearance, abnormal falling familial Farber's disease fever foam cells fracture, pathologic Friedreich's ataxia fucosidosis gait disorder galactosidase gangliosidosis GM1 gangliosidosis GM2 gargoylism Gaucher's disease gaze palsy gaze palsy, supranuclear gaze palsy, vertical gene gene mutation gene therapy genetic counselling genetic diagnosis genetic diagnosis, prenatal genetic neurologic disorders genetic screening genetic testing glucocerebrosidase glycogen storage disease glycoprotein growth retardation hand pain head injury hearing loss heat intolerance hemorrhagic diathesis hepatic failure hepatitis hepatolenticular degeneration(Wilson's disease) hepatomegaly hepatosplenomegaly heralding manifestation hexosaminidase-A hexosaminidase-A and B high arched feet Hurler's syndrome hydrocephalus hyperreflexia hypertonia hypohidrosis hypomyelination hypotonia hypotonia, infants inattention inborn errors of metabolism inborn errors of metabolism, screening inclusion bodies, intracytopasmic incoordination infection, recurrent intellectual deficit intellectual deterioration intelligence quotient intrathecal medication Jakob-Creutzfeldt disease jaundice Jewish klippel feil syndrome Krabbe's disease kyphoscoliosis, neurologic causes of lactic acidemia lead poisoning learning disability, in children Leigh's disease leukocyte enzyme abnormality leukodystrophy Lewy body disease, diffuse life expectancy limb-girdle weakness lipid storage disorder of CNS liver disease lymphadenopathy lysosomal storage disease lysosomes, abnoral macrocephaly Marinesco-Sjogren syndrome megalencephaly memory, impairment of meningitis, chronic mental retardation metabolic disorder, primary metabolic disorder, primary-screening tests metachromatic leukodystrophy metachromatic leukodystrophy, adult onset metachromatic leukodystrophy, juvenile metachromatic leukodystrophy, late-infantile misdiagnosis mitral valve prolapse molecular genetics mortality motor neuron disease movement disorder movement disorder, extrapyramidal MRI MRI, abnormal MRI, hypointense signal foci on MRS mucopolysaccharidoses multiple sclerosis multiple sclerosis, differential diagnosis of muscle biopsy muscle spasm muscle wasting, diffuse muscle weakness muscle weakness, proximal muscular dystrophy, Duchenne myelopathy myocardial infarction myoclonus myopathy myopathy, vacuolar N-acetyl-L-aspartic acid neonatal screening, genetic neurologic disorders neoplasm, primary of CNS neuraminidase deficiency neuroaxonal dystrophy neuroaxonal dystrophy, infantile neurofibrillary degeneration neurolipidosis IV neurologic complications of, systemic disease neurologic disease neurologic disease, diagnoses of neurologic testing neuronal ceroid-lipofuscinosis neuroophthalmology neuropathic pain scale neuropathology neuropathy neuropathy, demyelinating neuropathy, painful neuropathy, small-fiber neuropathy, small-fiber, painful sensory neurosis next-generation sequencing Niemann-Pick disease ophthalmoplegia optic atrophy optokinetic nystagmus, abnormal osteopetrosis pain pain, neuropathic Parkinsonism syndrome paroxysmal neurologic deficits patient in waiting pediatric neurology peroxisomal disease pes cavus photophobia polymerase chain reaction polyneuropathy Pompe's disease of glycogen storage precipitating factors preclinical prenatal diagnosis by amniocentesis prevention of neurologic disorders prognosis progressive neurologic disorder proteinuria psychiatric problems in neurologic disorders psychological testing psychological testing, children psychomotor retardation psychosis quadriparesis quadriplegia rectal biopsy remote effect of cancer on the nervous system renal failure respiratory failure respiratory tract infection retinal degeneration retinopathy retropulsion review article rigidity safety Salla disease Sandhoff's disease schizophrenia scoliosis, neurologic association with screening sea-blue histiocytes seizure seizure, children seizure, laughing as manifestation sensorineural hearing loss short stature sick sinus syndrome skin, biopsy skin, lesions in neurologic disorders slit lamp examination small vessel disease spasticity speech, delayed development of sphingomyelin spinal cord, compression of spinocerebellar degeneration splenomegaly startle reaction stem cell transplantation subdural hematoma systemic illness tandem gait, ataxic Tay-Sachs disease thalamus, lesion of thalamus, lesion of-bilateral thrombocytopenia toe walking tone, muscle, increased tongue, enlarged treatment of neurologic disorder tremor tremor, intention tripping urea-cycle enzymopathies urinary sulfatidase excretion urine test for metabolic disorders vasculopathy ventricular enlargement vertebral-basilar insufficiency vertigo vision, failure of in childhood visual acuity, decreased visual fields, constricted visual loss visual loss, transient Von Hippel Lindau walking, delayed walking, difficulty with weakness weakness, proximal white matter disease wide based gait

Showing articles 50 to 65 of 65 << Previous A Progressive Neurologic Disorder with Supranuclear Vertical Gaze Paresis & Distinctive Bone Marrow Cells Mayo Clin Proc 59:404-410, Yan-go,F.L.,et al, 1984 Infantile Osteopetrosis & Neuronal Storage Disease Neurol 33:437-441, Ambler,M.W.,et al, 1983 Adult Dystonic Lipidosis, Clin Histo & Biochem Findings of a Neurovisceral Storage Dis Neurol 32:1295-1299, Longstreth,W.T.Jr.,et al, 1982 Inborn Errors of Metabolism Ann Neurol 11:221-232, Kolodny,E.H.,et al, 1982 Computed Tomography in Cerebrotendinous Xanthomatosis Neurol 31:1463-1465, Berginer,V.M.,et al, 1981 Adrenoleukodystrophy:Elevated C26 Fatty Acid in Cultured Skin Fibroblasts Ann Neurol 7:542-549, Moser,H.W.,et al, 1980 Prenatal Genetic Diagnosis in 3000 Amniocenteses NEJM 300:157-163, Golbus,M.S.,et al, 1979 Adult Type Neuronal Storage Disease with Neuraminidase Deficiency Ann Neurol 6:232-244, Miyatake,T.,et al, 1979 Chronic Hexosaminidase A & B Deficiency et al. , Ann Neurol 2:156977., Goldie,W.D., 1977 Diagnosis of Fabry's Disease by Tear-Galactosidase A-Correspondence NEJM 290:57 1974., , 1974 Niemann-Pick Disease Correspondence NEJM 289:590, Dacremont,G.,et al, 1973 Tay-Sachs Disease-The Use of Tears for the Detection of Heterozygotes NEJM 289:1072, Carmody,P.,et al, 1973 Progressive Paresis of Vertical Gaze in Lipid Storage Disease Neurol 21:896, Grover,W., 1971 Abnormal Head Size, In Neurology In Pediatrics (Ed) , 1970 Year Book Med. Publishers, p. 61., Bray,P.F., 1970 Prenatal Genetic Diagnosis NEJM 283:1370, Milunsky,A.,et al, 1970 Cerebellar Ataxia in Children Handout & References., Gilbert,J.J., 1850 Showing articles 50 to 65 of 65 << Previous