Differential (Click to cross reference) abdominal distention acanthocytosis adrenoleukodystrophy adverse drug reaction agammaglobulinemia aminoacidopathies aminoacidurias ammonia anatomy of aneurysm, intracranial, familial anorexia anticonvulsants anticonvulsants, selection of aphasia areflexia arginine Arnold Chiari malformation arrhythmia, cardiac arteriopathy asymptomatic ataxia ataxia telangiectasia ataxia, cerebellar ataxia, progressive ataxia, truncal ataxic gait auditory and vestibular pathways autoimmune disease Babinski sign basal ganglia basal ganglia, calcification of basal ganglia, degeneration basal ganglia, infarction basal ganglia, lesion of basal ganglia, lesion, bilateral basilar artery occlusion Bassen-Kornzweig syndrome Behcet's syndrome Behr's optic atrophy beriberi beriberi, infantile bitemporal visual field defect black toenail sign blindness blindness, sudden blood dyscrasias, neurologic findings with botulism brain atrophy brain biopsy brainstem brainstem, lesion of bulimia cachexia calcification, intracranial Canavan's disease carbon monoxide poisoning carcinoma cardiomegaly cardiomyopathy CAT scan CAT scan, abnormal CAT scan, contrast enhanced CAT scan, dense artery sign CAT scan, disappearing lesion on CAT scan, emission CAT scan, emission, abnormal CAT scan, false negative CAT scan, gyral swelling CAT scan, xenon-enhanced cataracts caudate nucleus caudate nucleus, lesion of caudate nucleus, lesion of, bilateral cause of death central nervous system, infection of central pontine myelinolysis cerebellar ataxia, children cerebellar ataxia, children, differential diagnosis of cerebellar ataxia, primary 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 embolism cerebral embolism, cardiac origin cerebral glucose metabolism cerebral infarction cerebral infarction, small, deep cerebral ischemia cerebral venous thrombosis cerebral venous thrombosis, deep cerebro hepato renal syndrome cerebrospinal fluid, abnormal cerebrospinal fluid, elevated protein of cerebrospinal fluid, lactic acid concentration cerebrospinal fluid, oligoclonal IgG in 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 cherry red spot-myoclonus syndrome children chorea chromosomal abnormality chronic progressive external ophthalmoplegia Chvostek sign Clinical Pathologic Conference(C.P.C.) Cockayne's syndrome coenzyme Q10 coenzyme Q10 deficiency cognition color vision color vision, impaired coma complications congenital birth defects congenital heart disease congestive heart failure consanguinity cornea, abnormal corpus callosum, lesion of cortical blindness cortical blindness, transient cortical infarction cortical ribbon sign cranial neuropathy, multiple creatine phosphokinase(CPK)elevated cricopharyngeal bar crying cultured skin fibroblasts cyanide poison cyst, parenchymal cytochrome c oxidase cytochrome c oxidase, deficiency deafmute deafness deafness, congenital deep gray nuclei degenerative diseases of CNS delay in diagnosis dementia dementia, rapidly progressive dentate nuclei dentate nuclei, lesion of dentatorubral-pallidoluysian atrophy depression developmental milestones developmental milestones, loss of developmental retardation diabetes mellitus diagnostic criteria diarrhea differential diagnosis diplegia, brachial diplopia dizziness DNA probes drug induced neurologic disorders dwarfism dysarthria dyschromatopsia dysphagia dyspraxia dystonia echocardiogram Ekbom's Syndrome electrocardiogram, abnormal electroencephalogram, abnormalities of electromyogram electron microscopy electronystagmography electroretinograph encephalitis encephalitis, Japanese encephalitis, viral encephalomalacia encephalomyopathy encephalopathy encephalopathy, metabolic encephalopathy, neonatal encephalopathy, progressive enkephalins enzyme, defect epilepsia partialis continua exercise exercise intolerance exome sequencing extraocular muscle atrophy extraocular muscle lesion eye closure eye movement, disorders of Fabry's disease facial nerve palsy facial nerve palsy, bilateral facial nerve, lesion of facial weakness Fahr disease failure to thrive falling false negative familial fatigue fever fibrillations flaccid paralysis flavivirus fontanel, bulging fourth ventricle, enlargement of Friedreich's ataxia fundus, abnormality of funduscopic exam gadolinium gait disorder gargoylism gastrointestinal disease, neurologic complications gastrointestinal motility gastroparesis gaze palsy gene gene mutation gene therapy genetic counselling genetic linkage genetic neurologic disorders genetic screening genetic testing glaucoma glioma glutaric acidemia gray matter growth retardation gyrus, abnormal Hallervorden Spatz disease Hallgren's syndrome head injury head lag 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 hepatic failure hepatolenticular degeneration(Wilson's disease) hepatomegaly heralding manifestation herpes simplex encephalitis herpes simplex encephalitis, differential diagnosis of herpes simplex encephalitis, recurrent hiccoughs hirsutism histochemistry histochemistry of muscle HLA human immunodeficiency virus type 1 Huntington's chorea Hurler's syndrome hydrocephalus hydrocephalus, viral induced hyperglycemia hyperphagia hyperreflexia hypocalcemia hypoglycemia hypomagnesemia hyponatremia hypoparathyroidism hypoparathyroidism, idiopathic hypothermia hypothyroidism hypotonia hypotonia, infants hypoxic encephalopathy iatrogenic neurologic disorders ileus, paralytic imbalance impulsivity inborn errors of metabolism infant and newborn with distress, neurologic prognosis in infant, evaluation of intellectual deficit intellectual deterioration intelligence quotient internuclear ophthalmoplegia internuclear ophthalmoplegia, unilateral intestinal pseudoobstruction intracranial hypertension, benign intraventricular hemorrhage iron, brain irritability Jakob-Creutzfeldt disease Kearns-Sayre syndrome keratoconus lactate lactic acidemia Lafora's disease laminar necrosis, cortical Laurence-Moon-Bardet-Biedl syndrome Leber's hereditary optic neuropathy leg numbness leg weakness, bilateral Leigh's disease Leigh's disease, adult variety lenticular nucleus, lesion of lenticular nucleus, lesion of, bilateral lethargy leukocyte enzyme abnormality leukodystrophy leukoencephalopathy lid closure, weakness of lipid storage disorder of CNS liver disease macular degeneration magnetic susceptibility malformation, CNS, congenital manic-depressive maple syrup urine disease Marcus Gunn pupil Marinesco-Sjogren syndrome MELAS syndrome Melkersson's syndrome memory, impairment of meningeal enhancement meningioma mental retardation mental status, abnormal MERRF syndrome mesial temporal lobe metabolic acidosis metabolic disorder, primary metabolic disorder, primary-screening tests methanol intoxication metronidazole microangiopathy, brain microhemorrhage, intracerebral midbrain, lesion of middle cerebellar peduncle, lesion middle cerebellar peduncle, lesion, bilateral migraine migratory lesion pattern mimics misdiagnosis mitochondrial disease mitochondrial disease, pathogenesis mitochondrial encephalomyopathy mitochondrial recessive ataxic syndrome MNGIE syndrome molecular genetics mortality movement disorder movement disorder, extrapyramidal MRI MRI lesion location MRI pattern MRI, abnormal MRI, ADC maps MRI, CAT scan compared to MRI, complications with MRI, contrast enhanced MRI, diffusion weighted MRI, disappearing lesion on MRI, gyral enhancement MRI, gyral swelling MRI, linear enhancement MRI, optic nerve MRI, paramagnetic effect MRI, serial MRI, spinal cord MRI, spinal cord, increased intramedullary cord signal MRI, T1 weighted high signal foci MRI, target sign MRS mucopolysaccharidoses multiple sclerosis multiple sclerosis, differential diagnosis of muscle biopsy muscle biopsy, extraocular muscle cramp muscle pain muscle weakness muscle weakness, proximal muscular dystrophy muscular dystrophy, congenital myasthenia gravis myasthenia gravis, differential diagnosis myasthenia gravis, misdiagnosis of myasthenia gravis, ocular myasthenia gravis, seronegative myasthenic syndrome myelitis myelitis, longitudinal myelopathy myoclonic jerks myoclonus myoclonus, epilepsy myoglobinuria myopathy myopathy, mitochondrial myopia myotonia myotonia dystrophica nausea and vomiting neck weakness negative neoplasm, primary of CNS nephrotic syndrome neuritis neuroendocrinology neurofibromatosis 1 neurologic complications of, systemic cancer neurologic complications of, systemic disease neurologic disease neurologic disease, diagnoses of neurologic examination, focal neurologic signs neurologic symptoms neuromuscular blockade neuromuscular junction, abnormality of neuronal ceroid-lipofuscinosis neurons neuroophthalmology neuropathology neuropathology, brain neuropathy neuropathy, ataxia, retinitis pigmentosa neuropathy, hereditary peripheral neuropathy, peripheral neuroradiology neurotoxin next-generation sequencing night blindness normal nutritional deficiency nystagmus nystagmus, rotary obesity occipital lobe occipital lobe, infarction occipital lobe, infarction, bilateral occipital lobe, lesion of ocular motility, disorders of ocular myopathy ocular myopathy, differential diagnosis oculopharyngeal muscular dystrophy ophthalmoplegia ophthalmoplegia, plus syndrome ophthalmoplegia, progressive external optic atrophy optic atrophy, bilateral optic atrophy, hereditary optic chiasm optic chiasm, enlarged optic chiasm, lesion of optic disc edema optic glioma optic nerve optic nerve, compression of optic nerve, enhancement optic nerve, lesion of optic nerve, neoplasm of optic neuritis optic neuritis, bilateral optic neuritis, treatment of optic neuropathy optic neuropathy, bilateral optic neuropathy, hereditary optic neuropathy, ischemic optic neuropathy, nutritional optic neuropathy, toxic optic tract, lesion of orbicularis oculi muscle osmotic demyelination syndrome overlap syndrome owl's eye sign of spinal cord pain, abdominal pancytopenia paraparesis paraparesis, spastic Parkinson disease Parkinsonism syndrome patient information and support peroxisomal disease personality change pes cavus pigmentary retinopathy PLEDs PLEDs, bilateral independent PLEDs, etiology of POLG1 gene polydactyly polymerase chain reaction polymerase chain reaction, false negative polymerase chain reaction, false positive polyneuropathy pons, lesion of posterior cerebral artery territory infarction prevention of neurologic disorders prognosis progressive infantile poliodystrophy progressive myoclonic epilepsy progressive neurologic disorder prostigmine proteinuria pseudomyasthenia pseudoretinitis pigmentosa psychiatric disorder psychiatric problems in neurologic disorders psychological testing psychomotor retardation psychosis psychosis, acute ptosis ptosis, bilateral putamen, lesion of putamen, lesion of, bilateral pyramidal tract dysfunction pyruvate dehydrogenase deficiency pyruvate metabolism, abnormality of quadriparesis radiation therapy, CNS treatment and complications with radiculopathy ragged-red fibers rapidly progressing neurologic illness recurrent red free light red free light, fundus exam with refractive errors Refsum's disease remote effect of cancer on the nervous system renal failure renal tubular acidosis respiratory failure respiratory tract infection restless leg syndrome retina, abnormal retinal degeneration retinal lesion retinal nerve fiber layer retinitis pigmentosa retinopathy reversible neurologic disorder review article RFLPs Romberg's sign Schilder's disease schizophrenia scotoma scotoma, central screening seizure seizure, children seizure, focal seizure, paradoxical seizure, treatment of sensorineural hearing loss sensory loss seronegative short stature single photon emission computed tomography small vessel disease Southern immunoblot test spasticity speech, loss of Spielmeyer Vogt syndrome spinal cord spinal cord, lesion of spinocerebellar degeneration spongy degeneration of brain spontaneous remission standing difficulty status epilepticus Stephens syndrome steroid therapy, CNS treatment and complications with striatal encephalitis striatonigral degeneration striatonigral degeneration, infantile striatum, lesion of striatum, lesion of, bilateral strokelike episodes subependymal nodules substantia nigra succinate dehydrogenase deficiency suck, poor sudden death sumatriptan symmetric brain lesions systemic illness tachycardia tapetoretinal degeneration temporal lobe, lesion temporal lobe, lesion, bilateral term infant tetany thalamic tumors thalamic tumors, bilateral thalamus thalamus, infarction of thalamus, infarction, bilateral thalamus, lesion of thalamus, lesion of-bilateral thiamine deficiency titubation tonic spasms transient neurologic deficit treatment of neurologic disorder tremor tremor, intention trinucleotide repeats triptans tuberous sclerosis Unverricht-Lundborg disease upgaze, paralysis of uremic encephalopathy urine test for metabolic disorders Usher's syndrome vasculopathy viral infection, CNS visceral neuropathy vision loss, sequential vision, blurred vision, failure of in childhood visual acuity, decreased visual acuity, decreased, monocular visual evoked response visual field defect visual fields, constricted visual loss visual loss, progressive visual loss, slow visual loss, sudden vitamin deficiency Von Hippel Lindau walking, difficulty with weakness weakness, fatiguable weakness, generalized weakness, progressive weaning from respirator, failure to web sites weight loss Wernicke's encephalopathy white matter disease white matter disease, pattern white matter disease, periventricular whole genome sequencing wide based gait Wolff-Parkinson-White syndrome workup

Showing articles 200 to 203 of 203 << Previous Neuropathy & Mitochondrial Myopathy Ann Neurol 7:262-268, Peyronnard,M.J.,et al, 1980 Lactic Acidemia, Mitochondrial Myopathy, & Basal Ganglia Calcification Neurol 29:1057-1061, Markesbery,Wm.R., 1979 A Familial Mitochondrial Myopathy With Central Defect in Neural Transmission Arch Neurol 36:553-556, Barron,S.A.,et al, 1979 The Facioscapulohumeral Synd, in Clinical Studies in Myology, Amsterdam, Excerpta Medica p498-501, VanWijngaarden,G.K.&Bethlem,J., 1973 Showing articles 200 to 203 of 203 << Previous