Differential (Click to cross reference) aneurysm, intracranial, familial aphasia arginine arrhythmia, cardiac arteriopathy asymptomatic ataxia ataxia, progressive ataxic gait auditory and vestibular pathways basal ganglia basal ganglia, calcification of basal ganglia, infarction basal ganglia, lesion of basal ganglia, lesion, bilateral black toenail sign blindness, sudden brain atrophy brain biopsy brainstem, lesion of calcification, intracranial carbon monoxide poisoning carcinoma cardiomegaly cardiomyopathy CAT scan CAT scan, abnormal CAT scan, disappearing lesion on CAT scan, false negative CAT scan, gyral swelling CAT scan, xenon-enhanced cataracts caudate nucleus, lesion of cause of death cerebellar atrophy, secondary cerebellar degeneration cerebellar lesion cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy cerebral blood flow cerebral cortex cerebral cortical atrophy cerebral edema, cytotoxic cerebral infarction cerebral infarction, small, deep cerebral ischemia cerebral venous thrombosis, deep cerebrospinal fluid, lactic acid concentration cerebrovascular accident cerebrovascular accident, familial occurrence cerebrovascular accident, infancy and childhood cerebrovascular accident, location of cerebrovascular accident, mimics cerebrovascular accident, multiple cerebrovascular accident, non atherosclerotic cause of cerebrovascular accident, nonarterial territory cerebrovascular accident, nonvascular territory cerebrovascular accident, prevention of cerebrovascular accident, recurrent cerebrovascular accident, young adult children chromosomal abnormality chronic progressive external ophthalmoplegia Clinical Pathologic Conference(C.P.C.) coenzyme Q10 deficiency coma complications congenital heart disease corpus callosum, lesion of cortical blindness cortical blindness, transient cortical infarction cortical ribbon sign cyanide poison cyst, parenchymal deafness deep gray nuclei delay in diagnosis dementia dementia, rapidly progressive depression developmental retardation diabetes mellitus diagnostic criteria differential diagnosis diplopia dysphagia dystonia echocardiogram electrocardiogram, abnormal electroencephalogram, abnormalities of electron microscopy encephalomalacia encephalopathy encephalopathy, metabolic encephalopathy, progressive epilepsia partialis continua exercise intolerance eye movement, disorders of failure to thrive false negative familial fatigue fever fourth ventricle, enlargement of gadolinium gene mutation gene therapy genetic counselling genetic neurologic disorders genetic screening genetic testing gray matter growth retardation gyrus, abnormal Hallervorden Spatz disease headache headache, recurrent headache, sudden onset of headache, treatment of hearing loss hearing loss, bilateral heart block heart rate hemianopia hemianopia, alternating hemianopia, homonymous hemianopia, recurrent hemianopia, transient hemiparesis hemiparesis, transient hemiplegia heralding manifestation herpes simplex encephalitis herpes simplex encephalitis, differential diagnosis of herpes simplex encephalitis, recurrent hirsutism human immunodeficiency virus type 1 hydrocephalus ileus, paralytic imbalance impulsivity intellectual deficit intellectual deterioration intestinal pseudoobstruction Kearns-Sayre syndrome lactate lactic acidemia laminar necrosis, cortical Leber's hereditary optic neuropathy Leigh's disease lenticular nucleus, lesion of, bilateral leukocyte enzyme abnormality leukodystrophy leukoencephalopathy manic-depressive MELAS syndrome meningeal enhancement mental retardation mental status, abnormal MERRF syndrome mesial temporal lobe metabolic disorder, primary methanol intoxication middle cerebellar peduncle, lesion middle cerebellar peduncle, lesion, bilateral migraine migratory lesion pattern mimics misdiagnosis mitochondrial disease mitochondrial encephalomyopathy MNGIE syndrome molecular genetics mortality MRI MRI lesion location MRI pattern MRI, abnormal MRI, ADC maps MRI, CAT scan compared to MRI, contrast enhanced MRI, diffusion weighted MRI, disappearing lesion on MRI, gyral enhancement MRI, gyral swelling MRI, linear enhancement MRI, serial MRI, spinal cord MRI, spinal cord, increased intramedullary cord signal MRI, T1 weighted high signal foci MRI, target sign MRS multiple sclerosis, differential diagnosis of muscle biopsy muscle weakness muscle weakness, proximal myasthenia gravis, differential diagnosis myasthenia gravis, misdiagnosis of myelitis myelitis, longitudinal myelopathy myoclonus myoclonus, epilepsy myopathy myopathy, mitochondrial nausea and vomiting negative neuroendocrinology neurofibromatosis 1 neurologic complications of, systemic cancer neurologic disease, diagnoses of neurologic examination, focal neurons neuroophthalmology neuropathology neuropathy neuropathy, ataxia, retinitis pigmentosa neuroradiology neurotoxin next-generation sequencing normal occipital lobe occipital lobe, infarction occipital lobe, infarction, bilateral occipital lobe, lesion of ophthalmoplegia ophthalmoplegia, progressive external optic atrophy optic neuropathy overlap syndrome owl's eye sign of spinal cord pancytopenia patient information and support personality change pigmentary retinopathy PLEDs PLEDs, bilateral independent PLEDs, etiology of polymerase chain reaction posterior cerebral artery territory infarction prevention of neurologic disorders prognosis progressive neurologic disorder proteinuria psychiatric problems in neurologic disorders psychosis psychosis, acute ptosis putamen, lesion of, bilateral radiation therapy, CNS treatment and complications with ragged-red fibers rapidly progressing neurologic illness recurrent renal failure respiratory tract infection retinopathy reversible neurologic disorder review article Schilder's disease schizophrenia screening seizure seizure, children seizure, focal sensorineural hearing loss short stature single photon emission computed tomography small vessel disease spinal cord, lesion of spontaneous remission steroid therapy, CNS treatment and complications with striatal encephalitis striatum, lesion of, bilateral strokelike episodes subependymal nodules substantia nigra succinate dehydrogenase deficiency sumatriptan symmetric brain lesions systemic illness tachycardia temporal lobe, lesion temporal lobe, lesion, bilateral thalamus, lesion of thalamus, lesion of-bilateral transient neurologic deficit treatment of neurologic disorder triptans tuberous sclerosis upgaze, paralysis of uremic encephalopathy vasculopathy visual acuity, decreased visual field defect visual loss visual loss, progressive walking, difficulty with weakness weight loss white matter disease white matter disease, pattern whole genome sequencing Wolff-Parkinson-White syndrome workup

Showing articles 50 to 57 of 57 << Previous Magnetic Resonance Imaging in MELAS Syndrome Neuroradiology 32:168-171, Rosen,L.,et al, 1990 MELAS Syndrome:Characteristic Migrainous & Epileptic Features and Maternal Transmission Neurol 38:751-754, Montagne,P.,et al, 1988 Diagnosis & Follow-up of Mitochondrial Encephalomyopathy:CT and MR Studies J Comput Assist Tomogr 12:696-697, Taverni,N.,et al, 1988 Significance of Basal Ganglia Calcification on Computed Tomography in Children Pediatr Neurosci 14:64-70, Zimmerman,L.A.,et al, 1988 MELAS Syndrome Involving a Mother & Two Children Arch Neurol 44:971-973, Driscoll,P.F.,et al, 1987 Mitochondrial Myopathies Ann Neurol 17:521-538, DiMauro,S.,et al, 1985 Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, & Strokelike Episodes:A Distinctive Clinical Syndrome Ann Neurol 16:481-488, Pavlakis,S.G.,et al, 1984 Mitochondrial Encephalomyopathy:Fluctuating Symptoms & CT Neurol 34:1456-1460, Yamamoto,T.,et al, 1984 Showing articles 50 to 57 of 57 << Previous