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Differential
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acanthocytosis
acne vulgaris
aneurysm, pulmonary
arcuate scotoma, differential diagnosis of
arthralgia
arthritis
aspirin
ataxia, cerebellar
Bassen-Kornzweig syndrome
Behcet's syndrome
blindness
brain atrophy
brainstem, lesion of
buphthalmos
calcarine artery
calcification, gyral
calcification, intracranial
cardiac arrest and resuscitation
CAT scan, abnormal
cataracts
cerebral infarction
cerebral venous infarction
cerebral venous thrombosis
cerebrovascular accident
chiasmal syndromes
children
Cockayne's syndrome
complications
consanguinity
cornea, abnormal
deafmute
deafness
developmental retardation
diagnostic criteria
differential diagnosis
dwarfism
electroencephalogram, abnormalities of
emotional lability
erythema nodosum
facial nevus
fluorescein angiography
Friedreich's ataxia
fundus, abnormality of
gadolinium
gargoylism
gastrointestinal bleeding
gastrointestinal disease, neurologic complications
gene
gene mutation
genetic neurologic disorders
genital ulcerations
glaucoma
glaucoma, low tension
glaucoma, visual field defects in
GNAQ gene
gyrus, abnormal
Hallgren's syndrome
headache
heart block
hemangioma
hemangioma, facial
hemangioma, leptomeningeal
hemiparesis
heralding manifestation
heterochromia iridis
Hurler's syndrome
hydrocephalus
hypopyon
intellectual deficit
iridocyclitis
Kearns-Sayre syndrome
keratoconus
Laurence-Moon-Bardet-Biedl syndrome
malformation, CNS, congenital
malformation, vascular
malformation, vascular, cerebral
memory, impairment of
meningeal enhancement
meningoencephalitis
mental retardation
mental status, abnormal
MRI
MRI, abnormal
MRI, contrast enhanced
mucopolysaccharidoses
myocardial infarction
myopia
neuritis
neurocutaneous disease
neurologic complications of, systemic disease
neurologic disease, diagnoses of
nystagmus
obesity
occipital lobe, infarction
occipital lobe, infarction, bilateral
occipital lobe, lesion of
ocular myopathy
optic atrophy
optic disc
optic neuritis
optic neuropathy
optic neuropathy, ischemic
oral ulcerations
pain, periorbital
papilledema
photophobia
polydactyly
port wine nevus
precipitating factors
prognosis
progressive neurologic disorder
pseudoretinitis pigmentosa
psychiatric disorder
quadrantanopsia, homonymous
retinal artery occlusion
retinal detachment
retinal vasculitis
retinitis pigmentosa
retinopathy
review article
schizophrenia
scotoma
seizure
seizure, children
seizure, focal
seizure, intractable
seizure, neonatal
shock, hypovolemic
skin, lesions in neurologic disorders
Spielmeyer Vogt syndrome
spontaneous remission
strokelike episodes
Sturge-Weber syndrome
systemic illness
thrombophlebitis
transient neurologic deficit
treatment of neurologic disorder
Usher's syndrome
uveitis
vasculitides
vasculopathy
venous thrombosis, non-cerebral
vertebral artery occlusion
vision, blurred
visual field defect
visual field defect, altitudinal
visual fields, constricted
visual loss
workup
Showing articles 2550 to 2600 of 4581 << Previous Next >>

Familial Temporal Lobe Epilepsy:A Common Disorder Identified in Twins
Ann Neurol 40:227-235, Berkovic,S.F.,et al, 1996

Epstein-Barr Virus-Associated Acute Autonomic Neuropathy
Ann Neurol 40:453-455, Bennett,J.L.,et al, 1996

Adjusted-Dose Warfarin Vs Low-Intens
Fixed-Dose Warfarin+Aspirin for High-Risk Pts with Atrial Fib, SPAFIII Invest, Lancet 348:633-638996, , 1996

Risk Factors for Creutzfeldt-Jakob Disease:A Reanalysis of Case-Control Studies
Neurol 46:1287-1291, Wientjens,D.P.W.M.,et al, 1996

A New Variant of Creutzfeldt-Jakob Disease in the UK
Lancet 347:921-925, 915, 916, 91796., Will,R.G.,et al, 1996

Creutzfeldt-Jakob Disease in a Young Woman
Lancet 347:945-948, Tabrizi,S.J.,et al, 1996

Intravenous IgG in Guillain-Barre Syndrome
BMJ 313:376-377, Hughes,R.A.C., 1996

Neuroradiologic Findings in Polyarteritis Nodosa
AJNR 17:1119-1126, Provenzale,J.M.&Allen,N.B., 1996

Evidence-Based Medicine, Critical Pathways, Practice Guidelines, & Managed Care:Prevention & Care of Stroke
Arch Neurol 53:867-871, Ringel,S.P.&Hughes,R.L., 1996

Memory, Attention, and Executive Function in Chronic Fatigue Syndrome
JNNP 60:495-503, Joyce,E.,et al, 1996

Routine Transesophageal Echocardiograhy for Cerebral Ischemia
Arch Int Med 156:1719-1723, Warner,M.F.&Kingson,I.M., 1996

Multiple Cerebral Lesions Complicating Therapy with Interleukin-2
Neurol 47:417-424, Karp,B.I.,et al, 1996

An Analysis of Lowest Effective Intensity of Prophylactic Anticoagulation for Pts with Nonrheumatic Atrial Fib
NEJM 335:540-546, 5871996., Hylek,E.M.,et al, 1996

Recurrent Spontaneous Arterial Dissections-Risk in Familial Vs Nonfamilial Disease
Stroke 27:662-624, Schievink,W.,et al, 1996

Implementation of an Acute Stroke Program Decreases Hospitalization Costs and Length of Stay
Stroke 27:1040-1043, Wentworth,D.A.&Atkinson,R.P., 1996

Results of a Computerized Screening of Stroke Patients for Unjustified Hospital Stay
Stroke 27:639-644, Goldman,R.S.,et al, 1996

Cerebral Venous Sinus Thrombosis Associated with Factor V Gene Mutation
JNNP 61:204-205, Kimber,T.,et al, 1996

The Challenge of the Dementias
Lancet 347:1301-1307, Eastwood,R.,et al, 1996

Hearing Loss in a Memory Disorders Clinic:A Specially Vulnerable Population
Arch Neurol 53:922-928, Gold,M.,et al, 1996

Misdiagnosis of the Vegetative State:Retrospective Study in a Rehabilitation Unit
BMJ 313:13-16, 51996., Andrews,K.,et al, 1996

An 85-Year-Old Woman with a History of Falls
JAMA 276:59-66, Lipsitz,L.A., 1996

Motor Changes in Presymptomatic Huntington Disease Gene Carriers
Arch Neurol 53:487-492, Siemers,E.,et al, 1996

Bilateral Optic Neuropathy Associated with Influenza Vaccination
J Neuro-Ophthalmol 16:182-184, Ray,C.L.&Dreizin,I.J., 1996

Evidence for Genetic Basis of Multiple Sclerosis
Lancet 347:1728-1730, Sadovnick,A.D.,et al, 1996

Clinical and Subclinical Neurological Involvement in Children of Conjugal Multiple Sclerosis Patients
Multiple Sclerosis 1:170-172, Constantinescu,C.S.,et al, 1996

Apolipoprotein E Genotyping in Alzheimer's Disease
Lancet 347:1091-1095, Tanzi,R.,et al, 1996

Presynaptic Dopaminergic Deficits in Lesch-Nyhan Disease
NEJM 334:1568-1572, 16021996., Ernst,M.,et al, 1996

Fatal Insomnia in a Case of Familial Creutzfeldt-Jakob Disease with the Codon 200Lys Mutation
Neurol 46:758-761, Chapman,J.,et al, 1996

Clinical, Neuroimaging, and Pathologic Features of Progressive Nonfluent Aphasia
Ann Neurol 39:166-173, Turner,R.S.,et al, 1996

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

Familial Migraine with Vertigo and Essential Tremor
Neurol 46:458-460, Baloh,R.W.,et al, 1996

Diagnosis of Merosin (Laminin-2) Deficient Congenital Muscular Dystrophy by Skin Biopsy
Lancet 347:582-584, Sewry,C.A.,et al, 1996

From Enigmatic to Problematic:The New Molecular Genetics of Childhood Spinal Muscular Atrophy
Neurol 46:335-340, Crawford,T.O., 1996

Cerebrospinal Fluid in Acute Optic Neuritis:Experience of the Optic Neuritis Treatment Trial
Neurol 46:368-372, Rolak,L.A.,et al, 1996

Optic Neuropathy
Neurol 46:315-322, Newman,N.J., 1996

Multifocal Motor Neuropathy with Conduction Block and Campylobacter Jejuni
Neurol 46:562-563, White,J.R.,et al, 1996

Infarction of Superior Cerebellar Artery Presenting as Cerebellar Symptoms
Stroke 27:1679-1681, Terao,S.,et al, 1996

Idiopathic Dysautonomia Treated with Intravenous Gammaglobulin
Lancet 347:28-29, Heafield,M.T.E.,et al, 1996

Silent Brain Infarction in Nonrheumatic Atrial Fibrillation
EAFT Study Group, Neurol 46:159-1651996., , 1996

Bleeding During Antithrombotic Therapy in Patients with Atrial Fibrillation
Stroke Prevention in Atrial Fib Invest, Arch Int Med 156:409-4161996., , 1996

Subjective Memory Complaints May Announce Dementia
Neurol 46:121-125, Schmand,B.,et al, 1996

Differential Effect of Aspirin Vs Warfarin on Clinical Stroke Types in Pts with Atrial Fibrillation
Neurol 46:238-240, Miller,V.T.,et al, 1996

Familial Hemiplegic Migraine, Nystagmus and Cerebellar Atrophy
Ann Neurol 39:100-106, Elliott,M.A.,et al, 1996

MR Evaluation of Patients with Congenital Hyposmia or Anosmia
AJR 166:439-443, Yousem,D.M.,et al, 1996

Antiepileptic Drugs
NEJM 334:168-175, Brodie,M.J.&Dichter,M.A., 1996

Brief Report:Deficiency of a Dystrophin-Assoc Glycoprotein (Adhalin) in Pt with Muscular Dystrophy & Cardiomyopathy
NEJM 334:362-366, Fadic,R.,et al, 1996

Bent Spine Syndrome
JNNP 60:51-54, Serratrice,G.,et al, 1996

Stroke in Williams Syndrome
Stroke 27:143-146, Wollack,J.B.,et al, 1996

Neurotoxicity Related to the Use of Topical Tretinoin (Retin-A)
Ann Int Med 124:227-228, Bernstein,A.L.&Leventhal-Rochon,J.L., 1996

Chronic Lymphocytic Leukemia and the Central Nervous System:A clinical and Pathological Study
Neurol 46:19-25, Cramer,S.C.,et al, 1996



Showing articles 2550 to 2600 of 4581 << Previous Next >>