Differential (Click to cross reference) acanthocytosis adult polyglucosan body disease adult-onset leukodystrophy, with neuroaxonal spheroids alternating hemiplegia alternating hemiplegia of childhood amimia ammonia amyloid angiopathy, cerebral amyloid angiopathy, cerebral, Dutch type anterior tibial muscle weakness antiviral agents aphasia areflexia arthrogryposis multiplex ataxia ataxia, cerebellar ataxia, progressive ataxic gait ataxic-dystonia syndromes ATP1A3 gene attention deficit disorder with hyperactivity atypical autonomic dysfunction Babinski sign basal ganglia, lesion, bilateral behavioral disorder beta-D-glucon bladder dysfunction brain atrophy brain biopsy brainstem, atrophy bronchoscopy bulbar palsy calcification, gyral calcification, intracranial candida albicans cardiomyopathy CAT scan, abnormal CAT scan, emission, abnormal catalepsy cataplexy cerebellar ataxia, children cerebellar atrophy, primary cerebellar atrophy, secondary cerebellar degeneration cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy cerebral cortex cerebral cortical atrophy cerebral palsy cerebral palsy, etiology cerebral palsy, work up cerebrospinal fluid, beta-D-glucan cerebrospinal fluid, lactic acid concentration cerebrospinal fluid, proteincytologic dissociation cerebrovascular accident cerebrovascular accident, cryptogenic cerebrovascular accident, nonvascular territory cerebrovascular accident, young adult chest x-ray, abnormal children chorea choreoathetosis chromosomal abnormality cingulate gyrus Clinical Pathologic Conference(C.P.C.) clonus clubfoot as related to neurologic disease Coats plus cobalamin C deficiency coma coma, sudden onset complications confusion congenital myasthenic syndromes consanguinity corpus callosum corpus callosum, hypoplastic corpus callosum, lesion of corpus callosum, thinning cortical ribbon sign cranial nerve enhancement creatine phosphokinase(CPK)elevated cyst cyst, benign intracranial cyst, cortical parenchyma cyst, parenchymal deafness delay in diagnosis dementia dementia, presenile developmental disability developmental retardation diabetes mellitus diagnostic criteria diet differential diagnosis difficulty climbing stairs difficulty going down stairs disease modifying agents distal muscle atrophy distal muscle weakness DNA sequencing double-cortex syndrome dysarthria dysmetria dysmorphic dysphagia dystonia electromyogram encephalopathy encephalopathy, acute eosinophilia executive dysfunction exome sequencing Fabry's disease facial appearance, abnormal facial weakness falling false negative familial fatal familial insomnia fatigue feeding disorder fever fish floppy infant fourth ventricle, compression fungal infection fungal infection, CNS gait disorder gait speed gait, spastic GAMT gene gaze palsy, supranuclear gaze palsy, vertical gene gene mutation genetic counselling genetic neurologic disorders genetic screening genetic testing globus pallidus, lesion of, bilateral gram positive cocci gray hair hammertoes headache headache, awakening with headache, positional headache, progressive hearing loss helminthic infection of CNS hemianopia, homonymous hemiparesis, transient hemophagocytic lymphohistiocytosis hepatomegaly hepatosplenomegaly heterotopia HHH syndrome high arched feet high arched palate human genome hydrocephalus hydrocephalus, non-communicating(obstructive) hyperammonemic encephalopathy hyperhomocysteinemia hyperreflexia hypoglycorrhachia hypogonadism hypogonadism, hypogonadotropic hyporeflexia hypotonia hypotonia, causes of hypotonia, infants imbalance immunotherapy inborn errors of metabolism inclusion bodies, intranuclear incoordination India infection insomnia insular cortex insular cortex, lesion intellectual deficit interstitial pulmonary fibrosis intracerebral hemorrhage intravenous drug abuse intrinsic hand muscles, wasting of jaundice Jewish Krabbe's disease lactic acidemia Leber's hereditary optic neuropathy leg weakness, bilateral leukodystrophy leukoencephalopathy leukoencephalopathy with calcification and cysts level of consciousness, decreased lid lid abnormalities life expectancy linear lesion lipid storage disorder of CNS lung nodule lung-brain syndromes lysosomal storage disease malformation, CNS, congenital McLeod syndrome megalencephaly MELAS syndrome memory, impairment of meningeal enhancement meningeal sarcomatosis meningitis meningitis, basilar meningitis, candida meningitis, chronic meningitis, fungal meningitis, neutrophilic mental retardation mestinon metabolic acidosis methylmalonic acidemia microcephaly microhemorrhage, intracerebral middle cerebellar peduncle middle cerebellar peduncle, lesion middle cerebellar peduncle, lesion, bilateral miglustat mimics mineralization misdiagnosis mitochondrial disease mitochondrial encephalomyopathy molecular genetics movement disorder moyamoya moyamoya, adult MRI, abnormal MRI, blooming effect MRI, contrast enhanced MRI, diffusion weighted MRI, mass effect on MRI, muscle MRI, negative MRI, nodular enhancement MRI, spinal cord muscle biopsy muscle weakness, proximal mutism myelomalacia myeloneuropathy myelopathy myoclonus myopathy nasal speech nausea and vomiting needle tracks neonatal intensive care unit neonatal screening, genetic neurologic disorders neurologic complications of, systemic disease neurologic disease neurologic disease, diagnoses of neuronal intranuclear inclusion disease neuroophthalmology neuropathy neuropathy, demyelinating newborn, evaluation of next-generation sequencing Niemann-Pick disease night blindness normal NOTCH2NLC nystagmus occipital lobe ocular motility, disorders of opened mouth ophthalmoplegia organomegaly ornithine transcarbamylase deficiency ovarian dysgenesis pachygyria papilledema paragonimiasis paraparesis, familial spastic paraparesis, spastic parasitic infection, CNS Parkinsonism syndrome paroxysmal neurologic deficits peripheral blood smear Perrault syndrome pes cavus philtrum, tented phonophobia photophobia PICU pleocytosis of cerebrospinal fluid pleocytosis of cerebrospinal fluid, neutrophilic polyglucosan body disease polymicrogyria pons, lesion of precipitating factors prion disease prognosis progressive neurologic disorder psychiatric problems in neurologic disorders psychological testing psychomotor retardation psychosis psychotic behavior ptosis ptosis, bilateral pyramidal tract pyramidal tract dysfunction pyruvate dehydrogenase deficiency pyruvate metabolism, abnormality of quadriplegia ragged-red fibers recurrent ReNU syndrome respiratory tract infection retinopathy review article risk factors Romberg's sign salivation, excessive schizophrenia scissors gait scotoma screening sedimentation rate, elevated seizure seizure, focal seizure, laughing as manifestation sensorineural hearing loss short stature shunt procedure, ventricular shunt procedure, ventricular-complications of sleep pathology and physiology small vessel disease spastic ataxia spastic paraplegia, type 7 spasticity speech disorder speech, absence of spinal cord, lesion of spinocerebellar ataxia spinocerebellar ataxia type 28 spinocerebellar degeneration splenomegaly strokelike episodes symmetric brain lesions systemic illness tandem gait, ataxic telangiectases, retinal temporal lobe, lesion temporal lobe, lesion, bilateral thalamus, lesion of-bilateral tinnitus toe walking treatment of neurologic disorder tremor tremor, intention trinucleotide repeats tripping tumefactive lesion urea-cycle enzymopathies urinary urgency vasculitides vasculopathy vegetarianism vestibular migraine vision loss, sequential vision, blurred visual loss visual loss, transient visual obscurations, transient visuospatial disturbance walking, delayed walking, difficulty with weakness weakness, fatiguable weakness, progressive weakness, proximal weight loss wheelchair white matter disease white matter disease, unilateral whole genome sequencing wide based gait workup x-linked intellectual deficit x-linked mental retardation

Showing articles 300 to 305 of 305 << Previous The Fluorodeoxyglucose 18F Scan in Alzheimer's Disease & Multi-infarct Dementia Arch Neurol 40:711-714, Benson,D.F.,et al, 1983 Positron Computed Tomography for Studies of Myocardial & Cerebral Function Ann Int Med 98:339-359, Phelps,M.E.,et al, 1983 Alzheimer's Disease:Focal Cortical Changes Shown by Positron Emission Tomography Neurol 33:961-965, Foster,N.L.,et al, 1983 Regional Cerebral Metab. Alter. in Dementia of the Alzheimer Type:Positron Emission Tomogr J Comput Assist Tomogr 4:590-598, Friedland,R.P.,et al, 1983 Remission From Polymyositis After Total Body Irradiation BMJ 284:1915-1916, Hubbard,W.N.,et al, 1982 Emission & Transmission Brain Tomography BMJ 1:438-440, Ell,P.J.,et al, 1980 Showing articles 300 to 305 of 305 << Previous