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Differential
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Addison's disease
adrenoleukodystrophy
adrenoleukodystrophy, adult onset
adrenoleukodystrophy, carrier
adrenomyeloneuropathy
adverse drug reaction
affect, inappropriate
akinetic mute
Alexanders disease
amniocentesis
asymptomatic
ataxia
attention deficit disorder with hyperactivity
auditory evoked brainstem potentials
Balint's syndrome
Bassen-Kornzweig syndrome
behavioral disorder
Binswanger disease
blindness
bone marrow transplantation
brain biopsy
brain scan, abnormal
calcification, intracranial
Canavan's disease
CAT scan
CAT scan, abnormal
CAT scan, contrast enhanced
CAT scan, demyelinating disease
cataracts
cerebellar lesion
cerebral autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy
cerebro hepato renal syndrome
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, gammaglobulin of
children
Clinical Pathologic Conference(C.P.C.)
Cockayne's syndrome
color vision
color vision, impaired
complications
conjunctival biopsy
corpus callosum, lesion of
cortical blindness
crying, pathologic
cultured skin fibroblasts
deafness
decerebrate posture
dementia
dementia, childhood
dementia, presenile
dementia, rapidly progressive
demyelinating disease
diet
DNA probes
drug induced neurologic disorders
dysarthria
dysarthria-clumsy hand syndrome
dysmorphic
dysphagia
dysphasia
dyspraxia
electroencephalogram, abnormalities of
electron microscopy
electronystagmography
electroretinograph
encephalopathy
enzyme, defect
epidemiology of neurology
erucic acid therapy
evoked potentials
familial
fatty acid, elevated plasma content
frontal lobe, pathologic signs of
fundus, abnormality of
gait disorder
gangliosidosis GM1
gangliosidosis, generalized
gender
gene
gene mutation
gene therapy
genetic counselling
genetic diagnosis, prenatal
genetic linkage
genetic neurologic disorders
genetic screening
genetic testing
grasp reflex
Hallervorden Spatz disease
hearing loss
hearing problems in children
hepatomegaly
HMGcoA reductase inhibitors
hormone replacement
hyperpigmentation of skin
hyperreflexia
hypogonadism
hypotonia
impotence
inattention
inborn errors of metabolism
inclusion bodies
inclusion bodies, intracytopasmic
intellectual deterioration
Kearns-Sayre syndrome
Kluver-Bucy syndrome
Krabbe's disease
Laurence-Moon-Bardet-Biedl syndrome
leukemia
leukodystrophy
leukoencephalopathy
leukoencephalopathy, differential diagnosis
lipid storage disorder of CNS
Lorenzo's oil
lovastatin
macular degeneration
mental retardation
metabolic disorder, primary
metachromatic leukodystrophy
misdiagnosis
mitochondrial disease
mortality
MRI
MRI, abnormal
MRI, CAT scan compared to
MRI, contrast enhanced
MRI, demyelinating disease
MRI, spinal cord
MRS
mucopolysaccharidoses
multiple sclerosis
multiple sclerosis, familial
multiple sclerosis, misdiagnosis
muscular dystrophy
myelodysplasia
myelomalacia
myopathy, mitochondrial
myopia
nerve biopsy
nerve conduction studies
neuroaxonal dystrophy
neuroendocrinology
neurologic disease
neurologic disease, diagnoses of
neurologic signs
neuronal ceroid-lipofuscinosis
neuropathology
neuropathy
neuropathy, hereditary peripheral
neuropathy, peripheral
Niemann-Pick disease
night blindness
oleic acid therapy
ophthalmoplegia, plus syndrome
optic atrophy
optic nerve
optic neuropathy
paraparesis
paraparesis, familial spastic
paraparesis, spastic
PAS positive
PAS positive material in the brain
Pelizaeus Merzbacher
peroxisomal disease
peroxisomes
personality change
pigmentary retinopathy
polyneuropathy
prenatal diagnosis by amniocentesis
prevention of neurologic disorders
prognosis
progressive multifocal leucoencephalopathy
progressive neurologic disorder
pseudobulbar palsy
psychiatric problems in neurologic disorders
psychomotor retardation
quadriparesis
refractive errors
Refsum's disease
retinal degeneration
retinal lesion
retinitis pigmentosa
retinopathy
review article
seizure
seizure, neonatal
sensorineural hearing loss
skin, biopsy
skin, darkening of
somatosensory evoked potentials
spinal cord, lesion of
spinal cord, pathologic exam of
spinocerebellar degeneration
spongy degeneration of brain
steroid therapy, CNS treatment and complications with
symmetric brain lesions
tapetoretinal degeneration
temporal lobe, lesion
temporal lobe, lesion, bilateral
testicular atrophy
testicular biopsy
treatment of neurologic disorder
ultrasonography
urinary incontinence
Usher's syndrome
very long chain fatty acids
visual evoked response
visual field defect
visual loss
visual loss, slow
weight loss
white matter disease
white matter disease, unilateral
x-linked hydrocephalus
x-linked mental retardation
Showing articles 250 to 300 of 577 << Previous Next >>

Bilat Periventricular Nodular Heterotopia with Mental Retard & Syndactyly in Boys:New X-Linked MR Synd
Neurol 49:1042-1047, Dobyns,W.B.,et al, 1997

Spinobulbar Muscular Atrophy Can Mimic ALS:The Importance of Genetic Testing in Male Patients with Atypical ALS
Neurol 49:568-572, Parboosingh,J.S.,et al, 1997

Lymphoproliferative Disorders and Motor Neuron Disease:An Update
Neurol 48:1671-1678, Gordon,P.H.,et al, 1997

The X-Linked Infantile Spasms Syndrome (MIM 308350) Maps to Xp11. 4-Xpter in Two Pedigrees
Ann Neurol 42:360-364, Claes,S.,et al, 1997

Cerebral Tuberculosis in Pts with AIDS, Report of 6 Cases & Review
Medicine 76:423-431, Lesprit,P.,et al, 1997

Cerebral Manifestation of Erdheim-Chester Disease:Clinical and Radiologic Findings
Neurol 49:1702-1705, Bohlega,S.,et al, 1997

Clinicopath Conf
Rocky Mountain Spotted Fever with Meningoencephalomyelitis, Vasculitis and Focal Myocarditis, Case 3, -17,NEJM 337:1149-1156,1997., 1997

X-Linked Vacuolated Myopathy:Membrane Attack Complex Depos on Muscle Fiber Membr with Calcium Accumul on Sarcolemma
Ann Neurol 41:117-120, Louboutin,J.P.,et al, 1997

Acute Demyelinating Polyneuropathy with Arsenic Ingestion
Muscle & Nerve 19:1611-1613996., Greenberg,S.A., 1996

A Simplified Six-Item Checklist for Screening for Fragile X Syndrome in the Pediatric Population
J Pediatr 129:611-614, Giangreco,C.A.,et al, 1996

Patterns of Ordering Diagnostic Tests for Patients with Acute Low Back Pain
Ann Int Med 125:807-814, Carey,T.S.,et al, 1996

Clinicopath Conf
T-Cell Lymphoma (Lymphomatoid Granulomatosis) , Case 36-1996, NEJM 335:1514-15216., , 1996

Distal WEakness in Dystrophin-Deficient Muscular Dystrophy
Muscle & Nerve 19:1608-1610996., Felice,K.J., 1996

Myasthenia Gravis and Sarcoidosis:Report of 2 Cases
Eur Neurol 36:326-327, DeBleecker,J.,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

Tuberculous Meningitis:Clin Charact & Comp with Cryptococ Mening in Pts with HIV Infect
Arch Neurol 53:671-676, Sanchez-Portocarrero,J.,et al, 1996

Tuberculous Meningitis Among Adults with and without HIV Infection
Arch Int med 156:1710-1716, Yechoor,V.K.,et al, 1996

Development of Cardiomyopathy in Female Carriers of Duchenne and Becker Muscular Dystrophies
JAMA 275:1335-1338, Politano,L.,et al, 1996

Investigation of Muscle Disease
JNNP 60:256-274, Mastaglia,F.L.&Laing,N.G., 1996

Diagnosing Motor Neurone Disease
BMJ 312:650-651, Chancellor,A.M., 1996

Brain Metastases from an Unknown Primary Tumour:Which Diagnostic Procedures are Indicated
JNNP 61:321-323, van de Pol,M.,et al, 1996

Intelligence and the X Chromosome
Lancet 347:1814-1815, Turner,G., 1996

X-Linked Malformation of Neuronal Migration
Neurol 47:331-339, Dobyns,W.B.,et al, 1996

Neuroradiologic Aspects of Chester-Erdheim Disease
AJNR 16:735-740, Caparros-Lefebvre,D.,et al, 1995

Leptomeningeal and Calvarial Sarcoidosis:CT and MR Appearances
J Comput Assist Tomogr 19:639-642, Finelli,D.A.,et al, 1995

Dopamine, Dystonia, and the Deficient Co-Factor
Lancet 345:1130, Williams,A.C., 1995

Diagnostic Yield of the Neurologic Assessment of the Developmentally Delayed Child
J Pediatr 127:193-199, Majnemer,A.&Shevell,M.I., 1995

Rapid Antibody Test for Fragile X Syndrome
Lancet 345:1147-1148, Willemsen,R.,et al, 1995

Carbamazepine Hypersensitivity Syndrome:Report of 4 Cases & Review of Literature
Medicine 74:144-151, DeVriese,A.S.P.,et al, 1995

Substantial Head Trauma:Value of Routine CT Examination of the Cervicocranium
Radiology 196:741-745, Link,T.M.,et al, 1995

Clinicopath Conf
Arteritis, Unclassified, with Giant-Cell Reaction & Multiple Infarcts of the Brain & Neuropathy, Cas, 5-199532:452-459,1995., 1995

Gene Analysis of L1 Neural Cell Adhesion Molecule in Prenatal Diagnosis of Hydrocephalus
Lancet 345:161-162, Jouet,M.&Kenwrick,S., 1995

Patients Who Reattend After Head Injury:A High Risk Group
BMJ 311:1395-1398, Voss,M.,et al, 1995

Diffuse Leptomeningeal Gliomatosis with Osteoblastic Metastases and No Evidence of Intraaxial Lesions
AJNR 16:1018-1020, Pingi,A.,et al, 1995

Evaluation of the Cardiomyopathy in Becker Muscular Dystrophy
Muscle & Nerve 18:283-291995., Nigro,G.,et al, 1995

Jaw Involvement in American Burkitt's Lymphoma
Cancer 53:1777-1782, Sariban,E.,et al, 1994

Antimicrobial Prophylaxis in Neurosurgery and After Head Injury
Lancet 344:1547-1551, deLouvois,J.,et al, 1994

Becker Muscular Dystrophy with Onset after 60 Years
Neurol 44:2388-2390, Heald,A.,et al, 1994

Trinucleotide Repeat Expansion in Neurological Disease
Ann Neurol 36:814-822, LaSpada,A.R.,et al, 1994

Clinicopath Conf
Multiple Myeloma with Epistaxis, Confusion and Central Retinal Vein Thrombosis, Case 13-1994, NEJM 3, 0:9927,1994., 1994

Rapid Direct Diagnosis of Deletions Carriers of Duchenne and Becker Muscular Dystrophies
Lancet 344:302-303, Fassati,A.,et al, 1994

Dopa-Responsive Dystonia:Pathological and Biochemical Observations in a Case
Ann Neurol 35:396-402, 3811994., Rajput,A.H.,et al, 1994

Do Young Boys with Fragile X Syndrome have Macroorchidism
Pediatrics 93:992-995, Lachiewicz,A.M.&Dawson,D.V., 1994

Neuroanatomy of Fragile X Syndrome:The Temporal Lobe
Neurol 44:1317-1324, Reiss,A.L.,et al, 1994

Head Injury in Sport
BMJ 308:1620-1624, McLatchie,G.&Jennett,B., 1994

POEMS Syndrome:A Study of 25 Cases and a Review of the Literature
Am J Med 97:543-553, Soubrier,M.J.,et al, 1994

Disseminated Active HIV-6 Infections in Patients with AIDS
Lancet 343:577-578, 5551994., Knox,K.K.&Carrigan,D.R., 1994

MR of Intracranial Langerhans Cell Histiocytosis
J Comput Assist Tomogr 18:295-297, George,J.C.,et al, 1994

Advances in Molecular Analysis of Fragile X Syndrome
552, Warren,W.T.&Nelson,D.L.JAMA 271:536-553, 1994

Rapid Fragile X Carrier Screening and Prenatal Diagnosis Using a Nonradioactive PCR Test
JAMA 270:1569-1575, Brown,W.,et al, 1993



Showing articles 250 to 300 of 577 << Previous Next >>