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Differential
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acquired immunodeficiency syndrome

acquired immunodeficiency syndrome dementia complex

acquired immunodeficiency syndrome, congenital

acquired immunodeficiency syndrome, infants and children

advances in neurology

Aicardi-Goutieres syndrome

Alexanders disease

aneurysm, asymptomatic

aneurysm, intracranial

apraxia of eye movements

aqueduct of Sylvius, stenosis

arm swing, reduced

ataxia, truncal

autoimmune epilepsy

B 12 deficiency

B 12 deficiency, infants

basal ganglia, calcification of

basal ganglia, lesion of

basal ganglia, lesion, bilateral

biologic markers

black toenail sign

blood transfusion

bone marrow biopsy

Brown-Vialetto-Van Laere syndrome

calcification, gyral

calcification, intracranial

Canavan's disease

CAT scan, abnormal

cerebellar lesion

cerebral cortex

cerebral cortical atrophy

cerebral ischemia

cerebral vasculature

cerebral venous infarction

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, proteincytologic dissociation

cerebrovascular accident

cerebrovascular accident, mimics

cerebrovascular disease

cherry red spot

cherry red spot-myoclonus syndrome

choreoathetosis

chromosomal abnormality

Clinical Pathologic Conference(C.P.C.)

cold hands sign

congenital infection, CNS

contractures, joint

controversies in neurology

corpus callosum, atrophy of

corpus callosum, thinning

cranial nerve enhancement

cranial nerve enlargement

cranial neuropathy

cranial neuropathy, multiple

crawl regression

cultured skin fibroblasts

cyst, parenchymal

decision analysis

deep gray nuclei

degenerative diseases of CNS

delay in diagnosis

dementia, childhood

demyelinating disease

dentate nuclei, lesion of

developmental milestones

developmental milestones, loss of

developmental retardation

diagnostic criteria

differential diagnosis

difficulty climbing stairs

dopa responsive dystonia

dropped head syndrome

dystonia, children

electroencephalogram, abnormalities of

encephalitis, autoimmune

encephalomalacia

encephalopathy, neonatal

encephalopathy, progressive

endoscopic surgery

epileptic encephalopathy

episodic disorders

evoked potentials

eye movement, disorders of

facial weakness

facial weakness, bilateral

failure to thrive

FARS2 deficiency

feeding disorder

fine motor function, impaired

fontanel, bulging

frontal bossing

fundus, abnormality of

gangliosidosis GM2

Gaucher's disease

gaze palsy, supranuclear

genetic counselling

genetic neurologic disorders

genetic testing

glucocerebrosidase

glutamic acid decarboxylase, antibody

granular osmiphilic material

growth retardation

gyrus, abnormal

Hallervorden Spatz disease

head circumference

hepatic failure

hepatosplenomegaly

hexosaminidase-A

human immunodeficiency virus type 1

human immunodeficiency virus type 1, infants and children

hydrocephalus, complications with

hydrocephalus, etiology

hydrocephalus, fetal

hydrocephalus, non-communicating(obstructive)

hydrocephalus, treatment of

hyperhomocysteinemia

hyperpigmentation of skin

hypomyelination

hypotonia, infants

immunomodulation

inborn errors of metabolism

infant, evaluation of

infantile spasm

infantile tremor syndrome

intellectual deficit

intellectual deterioration

interferon alpha

intracranial pressure, increased

Krabbe's disease

lactic acidemia

laminar necrosis, cortical

Leigh's disease

leukocyte enzyme abnormality

leukoencephalopathy

leukoencephalopathy, differential diagnosis

life expectancy

lipid storage disorder of CNS

liver function enzymes

lymphadenopathy

lymphadenopathy, axillary

lymphadenopathy, paraaortic

lysosomal storage disease

malformation, CNS, congenital

malformation, vascular

meconium staining

memory, impairment of

meningeal enhancement

meningitis, CSF cell count-normal

mental retardation

metabolic disorder, primary

metabolic disorder, primary-screening tests

metachromatic leukodystrophy

metachromatic leukodystrophy, late-infantile

midbrain, lesion of

mitochondrial disease

mitochondrial encephalomyopathy

monoclonal antibodies

movement disorder

movement disorder, extrapyramidal

MRI lesion location

MRI, angiography

MRI, contrast enhanced

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, gyral swelling

MRI, hypointense signal foci on

MRI, paramagnetic effect

MRI, T1 weighted high signal foci

mucopolysaccharidoses

myasthenia gravis

myasthenia gravis, infantile and juvenile

myelination of nervous system

myoclonus, epilepsy

myoclonus, multifocal

myoclonus, treatment of

nausea and vomiting

nerve conduction studies

neuroaxonal dystrophy

neurocutaneous disease

neurofibrillary degeneration

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neurologic disease, tempo

neurologic examination

neurologic signs

neuronal ceroid-lipofuscinosis

neuroophthalmology

neuropathology, brain

Niemann-Pick disease

nystagmus, rotary

ophthalmoplegia

opportunistic infection

opportunistic infection, CNS

optic chiasm, enlarged

optic nerve, enlarged

paraparesis, familial spastic

paraparesis, spastic

PAS positive material in the brain

pediatric neurology

pleocytosis of cerebrospinal fluid

port wine nevus

postural abnormality

progressive myoclonic epilepsy

progressive neurologic disorder

prolactin, elevated

psychological testing

psychomotor retardation

pulmonary infiltrates

pyramidal tract

pyramidal tract dysfunction

pyruvate dehydrogenase deficiency

pyruvate metabolism, abnormality of

renal tubular acidosis

retinal degeneration

retinitis pigmentosa

Rett's syndrome

reversible neurologic disorder

riboflavin transporter deficiency

Rosenthal fibers

scoliosis, neurologic association with

sedimentation rate, elevated

seizure, children

seizure, crying as manifestation of

seizure, drug resistance

seizure, intractable

shunt procedure, ventricular

shunt procedure, ventricular-complications of

skin, lesions in neurologic disorders

spastic diplegia

speech disorder

speech disorder, childhood

speech, loss of

spinal muscular atrophy

spongy degeneration of brain

spontaneous remission

startle reaction

status epilepticus

stereotyped behavior

striatonigral degeneration

striatonigral degeneration, infantile

strokelike episodes

Sturge-Weber syndrome

subacute sclerosing panencephalitis(S.S.P.E.)Dawson's disease

substantia nigra

symmetric brain lesions

systemic illness

systemic juvenile idiopathic arthritis

Tay-Sachs disease

temporal lobe, lesion, bilateral

thalamus, lesion of

thalamus, lesion of-bilateral

tone, muscle, increased

tongue, fasciculations of

toxoplasmosis, CNS

transient neurologic deficit

treatment of neurologic disorder

tremor, intention

trichopoliodystrophy

tuberous sclerosis

tumor necrosis factor

tyrosine hydroxylase deficiency

ventricular enlargement

ventriculostomy

ventriculostomy, endoscopic

visual acuity, decreased

visual evoked response

visual field defect

visual fields, constricted

visual impairment

vitamin deficiency

vomiting, episodic

vomiting, recurrent

walking, difficulty with

weakness, generalized

weakness, progressive

Werdnig-Hoffman disease

white matter disease

wide based gait

x-linked hydrocephalus

Showing articles 1200 to 1250 of 2307 << Previous Next >>

Progressive Familial Leukodystrophy of Late Onset
Neurol 46:429-434, Knopman,D.,et al, 1996

Cognitive Dysfunction as the Major Presenting Feature of Becker's Muscular Dystrophy
Neurol 46:461-465, North,K.N.,et al, 1996

Lewy Body Disease and Dementia
Arch Int Med 156:487-493, Kalra,S.,et al, 1996

Valproic Acid Hepatic Fatalities. III. U. S. Experience Since 1986
Neurol 46:465-469, Bryant,A.E.&Dreifuss,F., 1996

Clinicopath Conf
Focal Cortical Dysplasia, Case 7-1996, NEJM 334:586-592996., , 1996

Cognitive Impairment & Mortality in a Cohort of Elderly People
BMJ 312:608-611, Gale,C.R.,et al, 1996

Meningeal Gliomatosis Presenting as Multiple Cerebral Infarcts:A Case Report
Neurol 46:1760-1762, Moonis,M.&Smith,T.W., 1996

Ultrasonographic Assess of Carotid Wall Characteristics & Cognitive Functions in Community Sample of 59-to 71-Yr-Olds
Stroke 27:1290-1295, Auperin,A.,et al, 1996

Leukoencephalopathy-Related Cerebral Amyloid Angiopathy with Cystatin C Deposition
Stroke 27:1417-1419, Shimode,K.,et al, 1996

Low Blood Pressure and Dementia in Elderly People:The Kungsholmen Project
BMJ 312:805-808, 7931996., Guo,Z.,et al, 1996

Is the Cognitive Function of Older Pts Affected by Antihypertensive Treatment? Med Res Council's Treat Trial
BMJ 312:801-805, 7931996., Prince,M.J.,et al, 1996

15-Year Longitudinal Study of Blood Pressure and Dementia
Lancet 347:1141-1145, 11301996., Skoog,I.,et al, 1996

Apolipoprotein E and Cognitive Decline in Alzheimer's Disease
Neurol 47:317-320, Plassman,B.L.&Breitner,J.C.S., 1996

Effects of HIV on Cognitive & Motor Devel in Children Born to HIV-Seropositive Women with no Reported Drug Use:Birth-24 mo
Pediatrics 96:1078-1082, Gay,C.L.,et al, 1995

Assessment:Neurological Evaluation of Male Sexual Dysfunction
Report of the Therapeutics & Tech Assess Subcommittee of the AAN, Neurol 45:2287-229295., , 1995

Regional Distrib of Neurofibrillary Tangles & Senile Plaques in Cerebral Cortex of Very Old Pts
Arch Neurol 52:1150-1159, Gioannakopoulos,P.,et al, 1995

Clinical, Neuropath & Genetic Studies of Large Spinocerebellar Ataxia Type 1 (SCA1) Kindred: (CAG) n Early Premonitory Signs & Symp
Neurol 45:24-30, Genis,D.,et al, 1995

Neurodevelopmental Outcome of Infants with Hypoplastic Left Heart Syndrome
J Pediatr 126:496-498, Rogers,B.T.,et al, 1995

The Synd of Autosomal Recessive Pontocerbellar Hypoplasia, Microcephaly, & Extrapyr Dyskinesia (Pontocereb Hypopl Type 2)
Neurol 45:311-317, Barth,P.G.,et al, 1995

A Novel Mutation in Exon 3 of the Proteolipid Protein Gene in Pelizaeus-Merzabacher Disease
Neurol 45:394-395, Pratt,V.M.,et al, 1995

Correlation Between Changes in Disability and T2-Weighted Brain MRI Activity in Multiple Sclerosis:A Follow-up Study
Neurol 45:255-260, Filippi,M.,et al, 1995

Identification of Comatose Patients at High Risk for Death or Severe Disability
JAMA 273:1842-1848, Hamel,M.B.,et al, 1995

Autosomal Dominant Migraine with MRI White-Matter Abnormalities Mapping to the CADASIL Locus
Neurol 45:1086-1091, Chabriat,H.,et al, 1995

Interferon Beta-1b in the Trtm of MS:Outcome of the Randomized Controlled Trial
IFNB Study Gr, Neurol 45:1277-12851995., , 1995

Clinical and Genetic Studies of Fatal Familial Insomnia
Neurol 45:1068-1075, Reder,A.T.,et al, 1995

Dentatorubral-Pallidoluysian Atrophy:Clin Features Closely Related to Unstable Expansion of Trinucleotide (CAG) Repeat
Ann Neurol 37:769-775, Ikeuchi,T.,et al, 1995

Apolipoprotein E Genotyping in the Differential Diagnosis, Not Prediction, of Alzheimer's Disease
Ann Neurol 38:6-14, Roses,A.D., 1995

Apolipoprotein E Genotyping in the Diagnosis of Alzheimer's Disease:A Cautionary View
Ann Neurol 38:2-4, Bird,T.D., 1995

Effectiveness & Safety of Velnacrine for Treatment of Alzheimer's Disease:A Double Blind, Placebo-Controlled Study
Arch Int Med 155:1766-1772, Antuono,P.G.,et al, 1995

Prevalence of Alzheimer's Disease and Vascular Dementia:Association with Education:The Rotterdam Study
BMJ 310:970-973, 9511995., Ott,A.,et al, 1995

Alzheimer and Vascular Dementias and Driving:A Prospective Road and Laboratory Study
JAMA 273:1360-1365, Fitten,L.J.,et al, 1995

Prospective CT Confirms Differnces Between Vascular and Alzheimer's Dementia
Stroke 26:735-742, Meyer,J.S.,et al, 1995

Relation Between Education and Dementia:The Role of Test Bias Revisited
JNNP 59:170-174, Schmand,B.,et al, 1995

Decreased Brain Choline Uptake in Older Adults:An In Vivo Proton Magnetic Resonance Spectroscopy Study
JAMA 274:902-907, Cohen,B.M.,et al, 1995

Reflex Sympathetic Dystrophy
BMJ 310:1645-1648, Paice,E., 1995

Neuropsychiatric Aspects of HIV Infection
JNNP 58:399-402, Everall,I.P., 1995

Encephalopathy in Children with Perinatally Acquired Immunodeficiency Virus Infection
J Pediatr 126:710-715, Lobato,M.N.,et al, 1995

Neuropsychologic Impairment in Early HIV Infection:A Risk Factor for Work Disability
Arch Neurol 52:525-530, Albert,S.M.,et al, 1995

The Value of Brain Imaging in Children with Headaches
Pediatrics 96:413-416, Maytal,J.,et al, 1995

Mild Traumatic Brain Injury:Pathophysiology, Natural History, and Clinical Management
Neurol 45:1253-1260, 12511995., Alexander,M.P., 1995

Cerebrospinal Fluid Concentration of Neuron-specific Enolase in Diagnosis of Creutzfeldt-Jakob Disease
Lancet 345:1609-1610, Zerr,I.,et al, 1995

Dementia Associated with the Acquired Immunodeficiency Syndrome
NEJM 332:934-940, Lipton,S.A.&Gendelman,H.E., 1995

Adverse Outcomes of Bacterial meningitis in School-Age Survivors
Pediatrics 95:646-655, Grimwood,K.,et al, 1995

Deficiency of Brain Synaptic Dystrophin in Human Duchenne Muscular Dystrophy
Ann Neurol 38:446-449, Kim,T.W.,et al, 1995

Brain Abnormalities in Duchenne Muscular Dystrophy:Phosphorus-31 Magnetic Resonance Spectroscopy & Neuropsych Study
Lancet 345:1260-1264, Tracey,I.,et al, 1995

Mitochondrial DNA and Disease
NEJM 333:638-644, Johns,D.R., 1995

The Eosinophilia-Myalgia Syndrome:Status of 205 Patients and Results of Treatment 2 Years After Onset
Ann Int Med 122:851-855, Hertzman,P.A.,et al, 1995

Natural History in Proximal Spinal Muscular Atrophy
Arch Neurol 52:518-523, Zerres,K.&Rudnik-Schoneborn,R., 1995

Persistence of MRI Hyperintensity of the Globus Pallidus in Cirrhotic Patients:A 2-year Follow-up Study
Neurol 45:995-997, Kulisevsky,J.,et al, 1995

MR of Oculomotor Nerve Plasy
AJNR 16:1665-1672, Blake,P.Y.,et al, 1995

Showing articles 1200 to 1250 of 2307 << Previous Next >>