Differential (Click to cross reference) aminoacidurias ammonia anatomy of anorexia Arnold Chiari malformation ataxia ataxia telangiectasia ataxia, cerebellar ataxia, truncal ataxic gait Babinski sign basal ganglia basal ganglia, calcification of basal ganglia, degeneration basal ganglia, lesion of basal ganglia, lesion, bilateral basilar artery occlusion Behcet's syndrome beriberi beriberi, infantile blood dyscrasias, neurologic findings with brain atrophy brainstem brainstem, lesion of bulimia calcification, intracranial Canavan's disease carbon monoxide poisoning cardiomyopathy CAT scan CAT scan, abnormal CAT scan, contrast enhanced CAT scan, false negative cataracts caudate nucleus caudate nucleus, lesion of caudate nucleus, lesion of, bilateral central nervous system, infection of central pontine myelinolysis cerebellar ataxia, children cerebellar ataxia, children, differential diagnosis of cerebellar atrophy, secondary cerebellar lesion cerebral cortex cerebral infarction cerebral venous thrombosis cerebral venous thrombosis, deep cerebrospinal fluid, lactic acid concentration cerebrovascular accident cerebrovascular accident, mimics cerebrovascular accident, nonvascular territory cerebrovascular accident, young adult children chorea chronic progressive external ophthalmoplegia Clinical Pathologic Conference(C.P.C.) coenzyme Q10 deficiency cognition color vision, impaired crying cultured skin fibroblasts cytochrome c oxidase cytochrome c oxidase, deficiency deafness deafness, congenital deep gray nuclei degenerative diseases of CNS dementia dentate nuclei dentate nuclei, lesion of developmental milestones developmental milestones, loss of developmental retardation diabetes mellitus differential diagnosis dizziness dysarthria dystonia electron microscopy encephalitis encephalitis, Japanese encephalitis, viral encephalopathy encephalopathy, neonatal enkephalins enzyme, defect eye movement, disorders of Fabry's disease Fahr disease failure to thrive familial flavivirus fontanel, bulging Friedreich's ataxia gadolinium gene gene mutation gene therapy genetic counselling genetic neurologic disorders glioma glutaric acidemia gyrus, abnormal head injury head lag headache hearing loss heart block hepatolenticular degeneration(Wilson's disease) hepatomegaly hiccoughs histochemistry histochemistry of muscle hyperglycemia hyperphagia hyperreflexia hypoglycemia hyponatremia hypothermia hypotonia hypotonia, infants hypoxic encephalopathy iatrogenic neurologic disorders inborn errors of metabolism infant and newborn with distress, neurologic prognosis in infant, evaluation of intellectual deterioration internuclear ophthalmoplegia internuclear ophthalmoplegia, unilateral intestinal pseudoobstruction intraventricular hemorrhage iron, brain irritability Jakob-Creutzfeldt disease Kearns-Sayre syndrome lactic acidemia 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 lipid storage disorder of CNS liver disease magnetic susceptibility maple syrup urine disease Marinesco-Sjogren syndrome MELAS syndrome mental retardation MERRF syndrome metabolic disorder, primary metabolic disorder, primary-screening tests metronidazole microhemorrhage, intracerebral midbrain, lesion of mitochondrial disease mitochondrial encephalomyopathy mitochondrial recessive ataxic syndrome MNGIE syndrome molecular genetics mortality movement disorder movement disorder, extrapyramidal MRI MRI, abnormal MRI, CAT scan compared to MRI, complications with MRI, contrast enhanced MRI, diffusion weighted MRI, paramagnetic effect MRI, serial MRI, spinal cord MRI, T1 weighted high signal foci MRI, target sign MRS multiple sclerosis multiple sclerosis, differential diagnosis of muscle biopsy muscle pain myelitis, longitudinal myelopathy myoclonic jerks myoclonus myoclonus, epilepsy myopathy myopathy, mitochondrial neoplasm, primary of CNS neurofibromatosis 1 neurologic complications of, systemic cancer neurologic disease, diagnoses of neurologic signs neuropathology neuropathology, brain neuropathy neuropathy, ataxia, retinitis pigmentosa neuropathy, peripheral neurotoxin nutritional deficiency nystagmus nystagmus, rotary ophthalmoplegia ophthalmoplegia, progressive external optic atrophy optic atrophy, hereditary optic neuropathy osmotic demyelination syndrome overlap syndrome owl's eye sign of spinal cord pancytopenia paraparesis, spastic Parkinson disease pes cavus pigmentary retinopathy POLG1 gene polyneuropathy pons, lesion of progressive infantile poliodystrophy psychiatric problems in neurologic disorders psychomotor retardation ptosis putamen, lesion of putamen, lesion of, bilateral pyramidal tract dysfunction pyruvate dehydrogenase deficiency pyruvate metabolism, abnormality of quadriparesis ragged-red fibers remote effect of cancer on the nervous system respiratory failure restless leg syndrome retinopathy review article Romberg's sign seizure seizure, children sensorineural hearing loss sensory loss short stature spasticity speech, loss of spinal cord spinal cord, lesion of spinocerebellar degeneration spongy degeneration of brain status epilepticus striatonigral degeneration striatonigral degeneration, infantile striatum, lesion of striatum, lesion of, bilateral strokelike episodes substantia nigra suck, poor symmetric brain lesions term infant thalamic tumors thalamic tumors, bilateral thalamus thalamus, infarction of thalamus, infarction, bilateral thalamus, lesion of thalamus, lesion of-bilateral thiamine deficiency titubation tonic spasms treatment of neurologic disorder tremor tremor, intention urine test for metabolic disorders visual acuity, decreased vitamin deficiency Von Hippel Lindau weakness weakness, progressive weight loss Wernicke's encephalopathy white matter disease white matter disease, periventricular wide based gait workup

Showing articles 750 to 763 of 763 << Previous Clinical Cases-Dx:Functional Approach to Neuroanatomy pp 477-490 Earl Lawrence House McGraw Hill 1967., , 1967 Bacterial Meningitis, A Review of Selected Aspects (Cont. ) NEJM 272:842, Swartz,M.N.,et al, 1965 Inherited Aminoacidopathies Demonstrating Vitamin Dependency NEJM 281:145, Rosenberg,L., 1965 SLE Case Report-Pathology of the Cardiac Conduction System in SLE Am J Med 264:255, 1972 Ann Int Med 63:4021965., James,T.,et al, 1965 Thyrotoxicosis & Vitamin B-12 Lancet Sept. 22, 1962, p. 616, George,W.K.,et al, 1962 Neuro CPC of MGH Cerebral Embolism & Infarction, NEJM 267:1084-109162., , 1962 Neuro CPC of MGH Jacob-Creutzfeldt Disease, NEJM 264:1359-13641961., , 1961 Recurrent Meningitis Associated With Congenital Dermal Sinus Ann Int Med 54:503-509, Mendez-Cashion,D.,et al, 1961 Recurrent Attacks of Bacterial Meningitis Am J Med 29:465-475, Boe,J.,et al, 1960 Clinical Picture in Creutzfeldt-Jakob Disease Trans of Amer Neuro Assn 5:l47, Fisher,C.M., 1960 Neuro CPC of MGH Acute Bacterial Endocarditis with Cerebral Emboli, NEJM 260:1085-10881959., , 1959 The Significance of Nonbacterial Thrombotic Endocarditis:An Autopsy & Clinical Study of 78 Cases Ann Int Med 46:255, MacDonald,R.A.,et al, 1957 Failure of Vision in Childhood Proc Royal Soc Medicine, pp 494-500., , 1850 Neurology & Psychiatry Section-Year book of Pediatrics Pediatr Abstract p. 406-449., , 1850 Showing articles 750 to 763 of 763 << Previous