Differential (Click to cross reference) acanthocytosis adrenoleukodystrophy adverse drug reaction Alexanders disease aminoacidopathies aminoacidurias amniocentesis arylsulfatase B ataxia, cerebellar atlanto-axial subluxation Bassen-Kornzweig syndrome birth injury blindness bone biopsy bone marrow transplantation CAT scan CAT scan, abnormal cataracts cerebral cortical atrophy cerebro hepato renal syndrome chromosomal abnormality cisterna magna, enlarged Clinical Pathologic Conference(C.P.C.) Cockayne's syndrome 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 cyst, arachnoid deafmute deafness degenerative diseases of CNS dementia developmental milestones, loss of developmental retardation dissociated sensory loss DNA probes drug induced neurologic disorders dwarfism dysmorphic dyspraxia efficacy electroencephalogram, abnormalities of electron microscopy electronystagmography electroretinograph encephalopathy enzyme, defect foam cells Friedreich's ataxia fundus, abnormality of gangliosidosis GM1 gangliosidosis, generalized gargoylism gene therapy genetic diagnosis, prenatal genetic linkage genetic neurologic disorders genu valgum glaucoma glycogen storage disease growth retardation Hallervorden Spatz disease Hallgren's syndrome hearing loss heart block hepatosplenomegaly Hunter's syndrome Hurler's syndrome hydrocephalus hypotonia hypotonia, infants Kearns-Sayre syndrome keratoconus Krabbe's disease kyphoscoliosis, neurologic causes of Laurence-Moon-Bardet-Biedl syndrome leukodystrophy lipid storage disorder of CNS lipid storage myopathy lysosomal storage disease lysosomes, abnoral macrocephaly macular degeneration malformation, CNS, congenital mental retardation metabolic disorder, primary metachromatic leukodystrophy Morquio syndrome MRI MRI, abnormal MRI, disappearing lesion on MRI, high signal foci on MRS mucopolysaccharidoses mucopolysacchariduria myelopathy myopathy, mitochondrial myopia neuritis neuroaxonal dystrophy neurologic disease, diagnoses of neuronal ceroid-lipofuscinosis neuropathology neuropathy neuropathy, hereditary peripheral Niemann-Pick disease night blindness obesity ocular myopathy ophthalmoplegia, plus syndrome optic atrophy optic nerve optic neuropathy osteoporosis papilledema paraparesis, spastic pectus carinatum peroxisomal disease pigmentary retinopathy polydactyly pregnancy, neurologic complications in prenatal diagnosis by amniocentesis prognosis pseudoretinitis pigmentosa psychiatric disorder quadriparesis quadriplegia radiculopathy refractive errors Refsum's disease respiratory failure retinal degeneration retinal lesion retinitis pigmentosa retinopathy review article RFLPs safety Sanfilippo syndrome schizophrenia seizure sensorineural hearing loss short neck short stature skin, biopsy sphingolipodoses Spielmeyer Vogt syndrome spinal cord, compression of spinocerebellar degeneration stem cell transplantation tapetoretinal degeneration tongue, enlarged treatment of neurologic disorder Usher's syndrome visual acuity, decreased visual field defect visual fields, constricted visual loss white matter disease

Showing articles 50 to 57 of 57 << Previous The Role of HTLV in HIV-1 Neurologic Disease Neurol 41:197-202, Berger,J.R.,et al, 1991 Multiple Sclerosis, Retroviruses, and PCR Neurol 41:335-343, Ehrlich,G.D.,et al, 1991 Clinicopath Conf Myopathy Due to Adult Acid Maltase Deficiency, 36-1986, NEJM 315:694-701986., , 1986 Acid Maltase Deficiency Engel, A. G. in Engel and Banker, Myology, McGraw-Hill Co, New York, Ch 55, p. 1629-1651, , 1986 Carbonic Anhydrase II Deficiency in 12 Families with Osteopetrosis with Renal Tubular Acidosis & Cerebral Calcification NEJM 313:139-181, Sly,W.S.,et al, 1985 Studies Of A Patient With Megaloblastic Anemia & An Abnormal Transcobalamin II NEJM 303:1209-1212, Seligman,P.A.,et al, 1980 The Ultrastructure of the Sural Nerve in Pompe's Disease Ann Neurol 2:111, Goebel,H.H.,et al, 1977 The Adult Form of Acid Maltase (a-1, 4-Glucosidase) Deficiency Ann Neurol 1:276, Karpati,G.,et al, 1977 Showing articles 50 to 57 of 57 << Previous