Neurology Specific Literature Search   
 
[home][thesaurus]
    

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 3000 to 3050 of 4581 << Previous Next >>

Familial Rectal Pain:A Type of Reflex Epilepsy?
Ann Neurol 32:824-826, Schubert,R.&Cracco,J.B., 1992

Familial Creutzfeldt-Jakob Disease (Codon 200 Mutation) with Supranuclear Palsy
Bertoni. J. M. , et al, JAMA 268:2413-2415., , 1992

Cortical Blindness after Nifedipine Treatment
BMJ 305:693, Morton,C.&Hickey-Dwyer,M., 1992

Familial Alzheimer's Disease:Second Gene Locus Located, Markers for Familial Disease May be Available
BMJ 305:1108-1109, Mullan,M., 1992

The Psychological Consequences of Predictive Testing for Huntington's Disease
NEJM 327:1401-1405, 14491992., Wiggins,S.,et al, 1992

Multiple Sclerosis in 54 Twinships:Concordance Rate is Independent of Zygosity
French Res. Gr. of MS, Ann Neurol 32:724-727, 7222., , 1992

Analysis of the Prion Protein Gene in Thalamic Dementia
Neurol 42:1859-1863, Petersen,R.B.,et al, 1992

Twinning and Neurologic Morbisity
Am J Dis Child 146:1110-1113, Scheller,J.M.&Nelson,K.B., 1992

Intracranial Aneurysms in Autosom Dominant Polycystic Kidney Disease
NEJM 327:916-920, 9531992., Chapman,A.B.,et al, 1992

The Diagnostic Reliability of Magnetically Evoked Motor Potentials In Multiple Sclerosis
Neurol 42:1296-1301, Ravnborg,M.,et al, 1992

Acute Toxic Reaction to Carbamazepine:Clinical Effects and Serum Concentrations
J Pediatr 121:295-299, Tibballs,J., 1992

Juvenile Myoclonic Epilepsy, Underdiagnosed and Treatment May Have to be Life Long
BMJ 305:4-5, Timmings,P.L.&Richens,A., 1992

Ictal Hemimacropsia
Neurol 42:1119-1120, Mendez,M.F., 1992

Effects of Intravent Hemorrhage & Socioecon Status on NEur Status of Low Birth Weight Inf at 5 yrs of age
J Pediatr 121:280-285, Vohr,B.,et al, 1992

The Changing Epidemiology of Neural Tube Defects, United STates, 1968-1989
Am J Dis Child 146:857-861, Yen,I.H.,et al, 1992

Matrnal Heat Exposure and Neural Tube Defects
JAMA 268:882-885, Milunsky,A.,et al, 1992

The Biology of Developmental Dyslexia
JAMA 268:912-915, Rumsey,J.M., 1992

Causal Heterogeneity in Isolated Lissencephaly
Neurol 42:1375-1388, Dobyns,W.B.,et al, 1992

Population Screening for Fragile X
Lancet 339:1210-1213, Turner,G.,et al, 1992

Infants with Anencephaly as Organ Sources:Ethical Considerations
Committee on Bioethics, Pediatrics 89:1116-11191992., , 1992

Clinicopath Conf
Emery-Dreifus Muscular Dystrophy, NEJM 327:548-5571992., , 1992

Abnormalities in Color Vision and Contrast Sensitivity in Parkinson's Disease
Neurol 42:887-890, Price,M.J.,et al, 1992

Parkinson's Disease in Twins
Neurol 42:1453-1461, Vieregge,P.,et al, 1992

Clinicopath Conf
Metastatic Malignant Melanoma, "Encephalitic"Form, in Leptomeninges and Cerebral Cortex, Case 28-199, , NE27:107-116,1992., 1992

Periodic Alternating Gaze Deviation in Infancy
Neurol 42:1740-1743, Legge,R.H.,et al, 1992

Delayed Encephalopathy after Acute Carbon Monoxide Intoxication:MR Imaging Features & Cerebral White Matter Lesions
Radiology 184:117-122, Chang,K.H.,et al, 1992

Neurological Complications Following Liver Transplantation
Ann Neurol 31:644-649, Stein,D.P.,et al, 1992

Neurologic Syndrome in 25 Workers from an Aluminim Smelting Plant
Arch Int Med 152:1443-1448, White,D.M.,et al, 1992

Coronary Vasospasm Induced by Subcutaneous Sumatriptan
BMJ 304:1415, Willett,F.,et al, 1992

Detection of Full Fragile X Mutation
Lancet 339:271-272, Pergolizzi,R.G.,et al, 1992

Cerebromeningeal Haemophagocytic Lymphohistiocytosis
Lancet 239:104-107, Henter,J.&Elinder,G., 1992

Intra-arterial Cisplatin-Associated Optic and Otic Toxicity
Arch Neurol 49:83-86, Maiese,K.,et al, 1992

Frequent Involvement of the Optic Radiation in Patients with Acute Isolated Optic Neuritis
Neurol 42:77-79, Hornabrook,R.S.L.,et al, 1992

Girls with Fragile X Syndrome:Physical and Neurocognitive Status and Outcome
Pediatrics 89:395-400, Hagerman,R.J.,et al, 1992

GM1 Gangliosidosis in Adults:Clinical and Molecular Analysis of 16 Japanese Patients
Ann Neurol 31:328-332, Yoshida,K.,et al, 1992

A Randomized, Controlled Trial of Corticosteroids in the Treatment of Acute Optic Neuritis
NEJM 326:581-588, 6341992., Beck,R.W.,et al, 1992

Corticosteroid Treatment of Acute Optic Neuritis
NEJM 326:634-635, Lessell,S., 1992

Multifocal Demyelinating Motor Neuropathy:Cranial Nerve Involvement and Immunoglobulin Therapy
Neurol 42:506-509, Kaji,R.,et al, 1992

Multifocal Motor Neuropathy with Conduction Block:Is It a Distinct Clinical Entity?
Neurol 42:497-505, Lange,D.J.,et al, 1992

Familial Intracranial Haemorrhage Due to Factor V Deficiency
JNNP 55:227-228, Wadia,R.S.,et al, 1992

A Familial Disorder with Subcortical Ischemic Strokes, Dementia, and Leukoencephalopathy
Neurol 42:1015-1019, Mas,J.L.,et al, 1992

Effect of Cocaine Use On the Fetus
NEJM 327:399-407, Volpe,J.J., 1992

Presymptomatic Testing for Huntington's Disease in the United Kingdom
BMJ 304:1593-1596, Tyler,A.,et al, 1992

New Research in Tuberous Sclerosis, Probably More Common with More Adult Complications
BMJ 304:1647-1648, Mitchell,S.&Bradbeer,C., 1992

Wilson Disease
Medicine 71:139-164, Brewer,G.J.&Yuzbasiyan-Gurkan,V., 1992

Wilson's Disease:Current Status
Am J Med 92:643-654, Yarze,J.C.,et al, 1992

Prenatal Diagnosis of Wilson's Disease by Analysis of DNA Polymorphism
NEJM 327:57, Cossu,P.,et al, 1992

Multiple Sclerosis as a Cause of Atrial Fibrillation and Electrocardiographic Changes
Arch Neurol 49:422-424, Schroth,W.S.,et al, 1992

Clinicopath Conf
Infantile Striatonigral Regeneration, with Cerebellar Degeneration, Familial, Case 30-1992, NEJM 327, 261-1992., 1992

The Older Driver, Clinical Assessment and Injury Prevention
Arch Int Med 152:735-740, Underwood,M., 1992



Showing articles 3000 to 3050 of 4581 << Previous Next >>