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Differential
(Click to cross reference)
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 2600 to 2650 of 4581 << Previous Next >>

Thalamic Haemorrhage
Brain 119:1873-1886, Chung,C-S.,et al, 1996

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

Reversible Empty Sella in Idiopathic Intracranial Hypertension:An Indicator of Successful Therapy
AJNR 17:1953-1956, Zagardo,M.T.,et al, 1996

Management Protocol for an Enhancing Cerebral Lesion in HIV Infection
Conn Medicine 60:649-651, Finelli,P.F., 1996

Confirmation of Linkage of Oculopharyngeal Muscular Dystrophy to Chromosome 14q11. 2-q13
Ann Neurol 40:801-804, Stajich,J.M.,et al, 1996

Diagnostic Test for the Prader-Willi Syndrome by SNRPN Expression in Blood
Lancet 348:1068-1069, Wevrick,R.&Francke,U., 1996

An Emotional 13-Year Old Girl
Lancet 348:1000, Kanabar,D.J.,et al, 1996

A Gene for Parkinson's Disease
BMJ 313:1278, Hawkes,C., 1996

Clinical Genetic Analysis of Parkinson's Disease in the Contursi Kindred
Ann Neurol 40:767-775, Golbe,L.I.,et al, 1996

Genetic Factors in Alzheimer's Disease:A Review of Recent Advances
Ann Neurol 40:829-840, Levy-Lahad,E.&Bird,T.D., 1996

Elevated Risk of Alzheimer's Disease Among Workers with Likely Electromagnetic Field Exposure
Neurol 47:1477-1481, Sobel,E.,et al, 1996

Electromagnetic Field Exposure May Cause Increased Production of Amyloid Beta & Eventually lead to Alzheimer's Disease
Neurol 47:1594-1600, Sobel,E.&Davanipour,Z., 1996

Consensus Guidelines for Clin & Path Dx of Dementia with Lewy Bodies (DLB) :Report of DLB Intl Workshop
Neurol 47:1113-1114, 11241996., McKeith,I.G.,et al, 1996

Unusual Clinical Presentations of Cortical-Basal Ganglionic Degeneration
Ann Neurol 40:893-900, Bergeron,C.,et al, 1996

Age on Onset, Sex, & Cardiomyopathy as Predictors of Disability and Survival in Friedreich's Disease
Neurol 47:1260-1264, DeMichele,G.,et al, 1996

Clinical and Genetic Abnormalities in Patients with Friedreich's Ataxia
NEJM 335:1169-1175, 12221996., Durr,A.,et al, 1996

Clinicopath Conf
Distinguishing Acute Disseminated Encephalomyelitis from Multiple Sclerosis, BMJ 313:802-8041996., , 1996

Diagnosis of Patients Presenting to a Huntington Disease (HD) Clinic without a Family History of HD
Neurol 47:1578-1580, Nance,M.A.,et al, 1996

Cerebral Venous Thrombosis:Role of Activated Protein C Resistance and Factor V Gene Mutation
Stroke 27:1719-1720, Brey,R.L.&Coull,B.M., 1996

Restless Legs Syndrome:Clinicoetiologic Correlates
Neurol 47:1435-1441, Ondo,W.&Jankovic,J., 1996

Practice Parameter:Genetic Testing Alert
Pract Comm Genet Testing Task Force AAN, Neurol 47:1343-13441996., , 1996

The Effect on Memory of Chronic Prednisone Treatment in Patients with Systemic Disease
Neurol 47:1396-1402, Keenan,P.A.,et al, 1996

Charcot-Marie-Tooth Disease and Related Inherited Neuropathies
Medicine 75:233-250, Murakami,T.,et al, 1996

Stimulus-Evoked Sinus Arrest in Severe Guillain-Barre Syndrome:A Case Report
Neurol 47:1239-1242, Minahan,R.E.,et al, 1996

The Role of Lab Investig in the Dx & Management of Pts with Suspected Herpes Simplex Encephalitis:A Consensus Rpt
JNNP 61:339-345, Clinque,P.,et al, 1996

Clinicopath Conf
Granulomatous Encephalitis, Secondary to Schistosoma Mansoni Infection, Case 39-1996, NEJM 335:1906-, 91496., 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

Acute Low Back Pain:A New Paradigm for Management
BMJ 313:1343-1344, Deyo,R.A., 1996

Acute Phenytoin Toxicity Followed by Seizure Breakthrough From a Ticlopidine-Phenytoin Interaction
Arch Neurol 53:1191-1192, Privitera,M.&Welty,T.E., 1996

Visual Hallucinations Associated with Parkinson Disease
Arch Neurol 53:1265-1268, Sanchez-Ramos,J.R.,et al, 1996

Presymptomatic Diagnosis of Neurofibromatosis 2 Using Linked Genetic Markers, Neuroimging, and Ocular Examinations
Neurol 47:1269-1277, Baser,M.E., 1996

Paraneoplastic Limbic Encephalitis in Hodgkin's Disease
Can J Neurol Sci 23:138-140, Deodhare,S.,et al, 1996

Machado Joseph Disease Maps to Same Region of Chromosome 14 as Spinocerebellar Ataxia Type 3 Locus
J Med Genet 32:25-31, Twist,E.C.,et al, 1995

Benign Episodic Unilateral Mydriasis
Ophthalmol 102:1623-1627, Jacobson,D.M., 1995

Magnetic Resonance Imaging of the Brain in Nonarteritic Ischemic Optic Neuropathy
J Neuro-Ophthalmol 15:158-160, Arnold,A.C.,et al, 1995

Epidemic Optic Neuropathy in Cuba-Clinical Characterization and Risk FActors
NEJM 333:1176-1182, Bern,C.,et al, 1995

Multifocal Demyelinating Motor Neuropathy:Pathologic Evidence of Inflammatory Demyelinasting Polyradiculoneuropathy
Neurol 45:1828-1832, Oh,S.J.,et al, 1995

Clin Electrophy & Molec Correl in 13 Families with Hered Neurop with Liabil to Press Palsies & Chromosome 17p11. 2 Deletion
Neurol 45:2018-2023, Gouider,R.,et al, 1995

Folate Levels and Neural Tube Defects:Implications for Prevention
JAMA 274:1698-1702, 17171995., Daly,L.E.,et al, 1995

Canavan Disease:From Spongy Degeneration to Molecular Analysis
J Pediatr 127:511-517, Matalon,R.,et al, 1995

Hereditary Adult-Onset Alexander's Disease with Palatal Myoclonus, Spastic Paraparesis and Cerebellar Ataxia
Neurol 45:2266-2271, Schwankhaus,J.D.,et al, 1995

Anticonvulsant Hypersensitivity Syndrome
Arch Int Med 155:2285-2290, Vittorio,C.C.&Muglia,J.J., 1995

Hereditary Hemorrhagic Telangiectasia
NEJM 333:918-924, Guttmacher,A.E.,et al, 1995

Screening Family Members of Patients with Hereditary Hemorrhagic Telangiectasia
Am J Med 99:519-524, Haitjema,T.,et al, 1995

Adult-Onset Spinocerebellar Dysfunction Caused by a Mutation in the Gene for the a-Tocopherol-Transfer Protein
NEJM 333:1313-1318, 13511995., Gotoda,T.,et al, 1995

Digitalis-Induced Visual Disturbances with Therapeutic Serum Digitalis Concentrations
Ann Int Med 123:676-680, Butler,V.P.,et al, 1995

Optic Neuropathy, Headache, & Diplopia with MRI Suggestive of Cerebral Arteritis in Relapsing Polychondritis
J Neuro-Ophthalmol 15:171-175, Massry,G.G.,et al, 1995

Cerebrovascular Complications in Ehlers-Danlos Syndrome Type IV
Ann Neurol 38:960-964, North,K.N.,et al, 1995

Familial Acephalgic Migraine
Neurol 45:2293-2294, Ziegler,D.K., 1995

Acute Bacterial meningitis
Lancet 346:1675-1680, Tunkel,A.R.&Scheld,W.M., 1995



Showing articles 2600 to 2650 of 4581 << Previous Next >>