Differential (Click to cross reference) acanthocytosis adrenoleukodystrophy adverse drug reaction alopecia Alzheimer's disease anisocoria anosmia antiretinal antibodies aphasia apraxia of eye movements areflexia Argyll Robertson pupil arrhythmia, cardiac ataxia ataxia, cerebellar ataxia, hereditary ataxia, progressive ataxic gait autoantibodies Babinski sign baclofen basal ganglia basal ganglia, calcification of basal ganglia, lesion of basal ganglia, lesion, bilateral Bassen-Kornzweig syndrome battered child syndrome behavioral disorder bladder dysfunction blepharospasm blindness bradykinesia brain atrophy brain biopsy brainstem, atrophy brainstem, hypoplasia bulbar palsy cachexia calcification, intracranial CAR syndrome carcinoma carcinoma of lung cardiomyopathy caries carotid artery occlusion, neck CAT scan CAT scan, abnormal CAT scan, false negative cataracts cerebellar ataxia, children cerebellar atrophy, primary cerebellar atrophy, secondary cerebellar degeneration cerebellar lesion cerebellar vermis cerebral cortical atrophy cerebro hepato renal syndrome cerebrospinal fluid, elevated protein of cerebrovascular accident cerebrovascular accident, young adult cherry red spot cherry red spot-myoclonus syndrome children chorea choreoathetosis chorioretinitis chromosomal abnormality chromosome 17 chromosome 20 chronic progressive external ophthalmoplegia cisterna magna, enlarged Clinical Pathologic Conference(C.P.C.) clubfoot as related to neurologic disease Cockayne's syndrome coenzyme Q10 deficiency color vision color vision, impaired cone-rod dystrophy conjunctival biopsy consanguinity contractures, joint cornea, abnormal cornea, opacity of corpus callosum corpus callosum, hypoplastic cranial nerve palsies craniopharyngioma cry, weak cryptorchidism cyst cyst, parenchymal cyst, subcortical cytochrome c oxidase cytochrome c oxidase, deficiency deafmute deafness deep gray nuclei degenerative diseases of CNS dementia developmental abnormality of brain developmental milestones, loss of developmental retardation diabetes insipidus diabetes mellitus diarrhea differential diagnosis diplegia, spastic cerebral DNA probes drug induced neurologic disorders dwarfism dysarthria dysmetria dysmorphic dysphagia dystonia electrocardiogram, abnormal electroencephalogram, abnormalities of electron microscopy electronystagmography electroretinograph enzyme, defect epidermal nevus syndrome eye injury eye movement, disorders of eyes, sunken facial appearance, abnormal falling false negative false negative VDRL familial fasciculation fatty acid dehydrogenase deficiency feeding disorder fingerprint bodies fluorescein angiography fluorescent treponema antibody absorption(FTA-ABS) foot deformity fourth ventricle, enlargement of Friedreich's ataxia fundus, abnormality of funduscopic exam gait disorder gargoylism gastrointestinal motility gaze palsy gaze palsy, supranuclear gene gene mutation gene therapy genetic counselling genetic diagnosis, prenatal genetic linkage genetic neurologic disorders genetic testing glare, light-induced glaucoma globus pallidus globus pallidus, lesion of globus pallidus, lesion of, bilateral growth retardation Hallervorden Spatz disease Hallervorden Spatz disease, late onset Hallgren's syndrome hand flapping headache hearing loss hearing loss, bilateral hearing loss, congenital heart block hepatomegaly Hurler's syndrome hydrocephalus hyperpigmentation of skin hyperreflexia hypocholesterolemia hypogonadism hypomagnesemia hypoparathyroidism hyposmia hypotonia imbalance immunosuppressive agents inborn errors of metabolism inclusion bodies inclusion bodies, intracytopasmic incoordination intellectual deficit intellectual deterioration internuclear ophthalmoplegia intestinal pseudoobstruction iris, atrophy of iron, brain Joubert syndrome Kearns-Sayre syndrome keratoconus kyphoscoliosis, neurologic causes of kyphosis lactic acidemia Laurence-Moon-Bardet-Biedl syndrome Leber's hereditary optic neuropathy Leigh's disease lens, dislocation of lenticular nucleus, lesion of, bilateral leukocyte enzyme abnormality leukodystrophy leukoencephalopathy light-near dissociation, causes of lymphocyte fingerprint profiles lysosomal storage disease macular degeneration malabsorption malformation, CNS, congenital malformation, vascular malformation, vascular, cerebral marche a petits pas Marcus Gunn pupil medial longitudinal fasciculus(MLF) MELAS syndrome memory, impairment of mental retardation MERRF syndrome microcephaly mitochondrial disease mitochondrial encephalomyopathy MNGIE syndrome molecular genetics mortality motor neuron disease movement disorder movement disorder, extrapyramidal MRI MRI, abnormal MRI, CAT scan compared to MRI, eye of tiger sign MRI, paramagnetic effect MRI, serial MRS mucopolysaccharidoses muscle atrophy, progressive muscle biopsy myelopathy myoclonic jerks myoclonus myopathy myopathy, mitochondrial myopia nausea and vomiting neuraminidase deficiency neuritis neurocutaneous disease neuroendocrinology neuroichthyosis neurolipidosis IV neurologic complications of, systemic cancer neurologic disease, diagnoses of neurologic signs neuronal ceroid-lipofuscinosis neuroophthalmology neuropathology neuropathology, brain neuropathy neuropathy, ataxia, retinitis pigmentosa neuropathy, ataxic neuropathy, hereditary peripheral neuropathy, hypertrophic neuropathy, onion bulb neuropathy, peripheral neurosyphilis nevus night blindness nystagmus nystagmus, pendular obesity ocular myopathy ophthalmoplegia ophthalmoplegia, progressive external optic atrophy optic atrophy, hereditary optic glioma optic nerve optic nerve, lesion of optic nerve, neoplasm of optic neuropathy optic neuropathy, hereditary optical coherence tomography palilalia pancytopenia PANK2 mutation paraparesis paraparesis, spastic Parkinson disease Parkinsonism syndrome peroxisomal disease peroxisomes pes cavus photophobia photosensitivity, eye photosensitivity, skin phytanic acid pigmentary retinopathy pleocytosis of cerebrospinal fluid polydactyly polyneuropathy Poretti-Boltshauser syndrome postural abnormality progeria prognosis progressive neurologic disorder pseudoretinitis pigmentosa psychiatric disorder psychiatric problems in neurologic disorders psychomotor retardation ptosis pupil pupil, abnormality in neurologic disorders pupil, light reflex, abnormal putamen, lesion of putamen, lesion of, bilateral pyramidal tract pyramidal tract dysfunction quadriparesis quadriplegia ragged-red fibers rash refractive errors Refsum's disease remote effect of cancer on the nervous system retina, abnormal retinal arteriole attenuation retinal degeneration retinal detachment retinal lesion retinitis pigmentosa retinoblastoma retinopathy retropulsion review article RFLPs rigidity Romberg's sign roving eye movements schizophrenia scotoma scotoma, central scotoma, paracentral-homonymous sea-blue histiocytes sedimentation rate, elevated seizure seizure, children seizure, neonatal sensorineural hearing loss sensory loss serologic test for syphilis sheathing of retinal veins short stature Sjogren-Larsson syndrome skin, biopsy skin, lesions in neurologic disorders skull x-ray, abnormal spastic diplegia spasticity speech disorder speech disorder, childhood Spielmeyer Vogt syndrome spinocerebellar ataxia spinocerebellar ataxia type 1 spinocerebellar ataxia type 7 spinocerebellar degeneration spongy degeneration of brain steatorrhea steroid steroid therapy, CNS treatment and complications with stooped posture substantia nigra sudden death syphilis, diagnosis and treatment syphilis, neurologic complications with syphilis, ocular tabes dorsalis Tangier's disease tapetoretinal degeneration third nerve palsy titubation trauma treatment of neurologic disorder tremor trinucleotide repeats Usher's syndrome uveitis ventricular enlargement vision loss, sequential vision, blurred vision, failure of in childhood visual acuity visual acuity, decreased visual acuity, decreased, monocular visual evoked response visual field defect visual field defect, altitudinal visual fields, constricted visual impairment visual loss visual loss, progressive visual loss, slow visual loss, sudden vitamin A vitamin deficiency vitamin E vitamin E deficiency vitamin K vitritis walking, difficulty with weakness weight loss white matter disease wide based gait Wolfram syndrome workup

Showing articles 100 to 104 of 104 << Previous Congenital Anomalies & Herpesvirus Infection Am J Dis Child 126:364, Montogomery,J.R.,et al, 1973 Unusual Cause of Progressive Head Enlargement Following Proteus Mirabilis Meningitis Develop Med Child Neurol 11:633, Mukhergee,S.K.,et al, 1969 Congenital Rubella Am J Dis Child 118:32-34, Menser,M.A.,et al, 1969 Neuro CPC of MGH Congenital Toxoplasmosis Involving CNS, NEJM 269:369-3741963., , 1963 Sarcoid of the Fundus Arch Ophthalmol 65:161, Gould,H.,et al, 1961 Showing articles 100 to 104 of 104 << Previous