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Differential
(Click to cross reference)
abducens nerve paralysis
abducens nerve paralysis, bilateral
Addison's disease
adverse drug reaction
amenorrhea
ammonia
aneurysm
aneurysm, intracranial
aphasia
aqueduct of Sylvius, stenosis
aqueductal stenosis
arcuate scotoma, differential diagnosis of
ataxia, cerebellar
bitemporal visual field defect
bromocriptine
calcification, intracranial
carcinoembryonic antigen
carcinoma of rectum
carpo-pedal spasm
CAT scan
CAT scan, abnormal
CAT scan, base of skull
CAT scan, false negative
CAT scan, metrizamide
CAT scan, skull bone changes
cavernous hemangioma
cerebral cortex
chiasmal syndromes
children
Chvostek sign
cingulate gyrus
cisternogram, metrizamide
Clinical Pathologic Conference(C.P.C.)
clivus
coma
coma, sudden onset
complicated migraine
confusion
craniopharyngioma
Cushing's syndrome
diabetes insipidus
diabetes mellitus
diabetes mellitus, neurologic manifestations of
diplopia
diplopia, monocular
dopamine agonist
empty sella syndrome
encephalopathy
encephalopathy, acute
ethambutol
exome sequencing
exophthalmus
familial
fasciculation
fever
fundus, abnormality of
funduscopic exam
galactorrhea
genetic neurologic disorders
growth retardation
hallucination, auditory
Hand-Schuller-Christian disease
head injury
headache
headache, severe
headache, sudden onset of
hemiachromatopsia, homonymous
hemianopia
hemianopia, homonymous
hemianopia, monocular
HHH syndrome
hydrocephalus
hydrocephalus, non-communicating(obstructive)
hyperadrenalism
hyperammonemic encephalopathy
hypercalcemia
hyperinsulinism
hyperkalemia
hyperparathyroidism
hyperthyroidism
hypokalemic periodic paralysis
hypoparathyroidism
hypopituitarism
hypothalamus
hypothalamus, disturbance of
hypothalamus, neoplasm of
hypothyroidism
iatrogenic neurologic disorders
impotence
infection
insular cortex
insular cortex, lesion
intracranial pressure, increased
intrinsic hand muscles, wasting of
islet cell tumor
Leber's hereditary optic neuropathy
level of consciousness, decreased
libido
libido, decreased
malformation, vascular
malformation, vascular, cryptic
memory, impairment of
meningismus
meningitis
meningitis, iatrogenic
meningitis, TB
migraine
misdiagnosis
mitochondrial disease
molecular genetics
motor neuron disease
MRI
MRI, abnormal
MRI, CAT scan compared to
MRI, contrast enhanced
MRI, diffusion weighted
multiple sclerosis
muscle weakness
muscle weakness, causes of
myasthenia gravis
myoclonus
myoedema
myopathy
myxedema coma
myxedema, neurologic manifestations of
nausea and vomiting
neoplasm, metastatic to CNS
neoplasm, pituitary
neoplasm, pituitary, incidental
neoplasm, pituitary, treatment of
neoplasm, primary of CNS
neoplasm, primary of CNS-children
neoplasm, primary of CNS-incidence of
neoplasm, primary of CNS-metastasizing to subarachnoid space
neoplasm, primary of CNS-treatment of
neuroendocrinology
neurologic disease, diagnoses of
nose blowing
nystagmus
nystagmus, see-saw
obesity
ophthalmoplegia
ophthalmoplegia, total
optic atrophy
optic chiasm
optic chiasm, hemorrhage in
optic chiasm, herniation
optic chiasm, lesion of
optic neuropathy
optic neuropathy, bilateral
optic neuropathy, hereditary
optic tract
optic tract, lesion of
ornithine transcarbamylase deficiency
pain, periorbital
papilledema
paranoia
parathyroid adenoma
pheochromocytoma
photophobia
pinealoma
pituitary, adenoma
pituitary, apoplexy
pituitary, enlargement
pituitary, lesion of
pituitary, metastasis to
pituitary, microadenoma
polyuria
postoperative neurologic complications
primary aldosteronism
prolactinoma
psychosis
quadrantanopsia, homonymous
review article
Riddoch phenomenon
scotoma
scotoma, central
scotoma, paracentral-homonymous
seizure
sella turcica, enlargement of
short stature
skull bone, erosion
spinal cord, metastasis to
suprasellar lesion
temporal lobe, lesion
temporal lobe, lesion, bilateral
tetany
third nerve palsy
thyrotoxicosis
treatment of neurologic disorder
Trousseau's sign
tuberculoma
urea-cycle enzymopathies
urinary frequency
vertigo
vision, blurred
vision, failure of in childhood
visual acuity
visual acuity, decreased
visual acuity, decreased, monocular
visual evoked response
visual field defect
visual field defect, altitudinal
visual field defect, monocular
visual loss
visual loss, sudden
weight gain
weight loss
Showing articles 2100 to 2150 of 4627 << Previous Next >>

Mutations in Each of the Five Subunits of Translation Initiation Factor eIF2B Can Cause Leukoencephalopathy with Vanishing White Matter
Ann Neurol 51:264-270, van der Knaap,M.S.,et al, 2002

Epilepsy Presenting as AD: Neuroimaging, Electroclinical Features, and Response to Treatment
Neurol 58:298-301, Hogh,P.,et al, 2002

Clinicopath Conf, Bilateral, Diffuse Uveal Melanocytic Proliferation, Metastatic Endometrial Carcinoma
NEJM 346:189-195, Case 2-2002, 2002

Clinicopath Conf,Mucormycosis, rhino-orbital
NEJM 346:924-929, Case 9-2002, 2002

Spinocerebellar Ataxia Type 10 is Rare in Populations Other Than Mexicans
Neurol 58:983-984, Matsuura,T.,et al, 2002

Recent Developments in Neurology
BMJ 324:656-660, Wiebe,S.,&Nicolle,M.W., 2002

Clinicopath Conf., Cerebral Venous Thrombosis, Resulting in Hemorrhagic Infarction of the Posterior Left Temporal Lobe
NEJM 346:1651-1658, Case 16-2002, 2002

Lead Encephalopathy: CT and MR Findings
J Comput Assist Tomogr 26:479-481, Tuzun,M.,et al, 2002

Subarachnoid Hemorrhage
Stroke 33:1321-1326, Kissela,B.M.,et al, 2002

Familial Temporal Lobe Epilepsy with Febrile Seizures
Neurol 58:1429-1433, Depondt,C.,et al, 2002

Earl Grey Tea Intoxication
Lancet 359:1484-1485, Finsterer,J., 2002

Patients with Multiple Sclerosis and Risk of Type 1 Diabetes Mellitus in Sardinia,Italy: A Cohort Study
Lancet 359:1461-1465,1450, Marrosu,M.G.,et al, 2002

A Tourist With Dengue Fever and Visual Loss
Lancet 360:1070, Haritoglou,C.,et al, 2002

Familial Infantile Bilateral Striatal Necrosis
Neurol 59:983-989, Straussberg,R.,et al, 2002

Potentially Reversible Conditions in 1000 Consecutive Memory Clinic Patients
JNNP 73:390-394, Hejl,A.,et al, 2002

New Evidence for Stroke Prevention
JAMA 288:1388-1395, Straus,S.E.,et al, 2002

Goosebumps
Lancet 360:690, Cutts,J.,et al, 2002

Neurological Presentation of Fabry's Disease in a 52 Year Old Man
JNNP 73:340-342, Mohanraj,R.,et al, 2002

Tinnitus
NEJM 347:904-910, Lockwood,A.H.,et al, 2002

Thrombolysis in Stroke Beyond Three Hours: Targeting Patients With Diffusion and Perfusion MRI
Ann Neurol 51:11-13,28, Warach,S., 2002

Mild Therapeutic Hypothermia to Improve the Neurologic Outcome After Cardiac Arrest
NEJM 346:549-556,612,546, The Hypothermia After Cardiac Arrest Study Group, 2002

Temporal Arteritis
JAMA 287:2996-3000,3034, Hellmann,D.B., 2002

Unexplained Sudden Amnesia
Arch Neurol 59:1310-1313, Fisher,C.M., 2002

Occurrence of Hemispheric and Retinal Ischemia in Atrial Fibrillation Compared with Carotid Stenosis
Stroke 33:1963-1968, Anderson,D.C.,et al, 2002

Dermoid Inclusion Cysts and Early Spinal Cord Tethering After Fetal Surgery for Myelomeningocele
NEJM 347:256-259,230, Mazzola,C.A.,et al, 2002

Orbital Infarction After Cocaine Use
Neurol 59:642, Van Stavern,G.P. &Gorman,M., 2002

Proposed Diagnostic Criteria and Nosology of Acute Transverse Myelitis
Neurol 59:499-505, Transverse Myelitis Consortium Working Group, 2002

Valproate Embryopathy in Three Sets of Siblings: Further Proof of Hereditary Susceptibility
Neurol 59:630-633, Malm,H.,et al, 2002

Is Patent Foramen Ovale a Family Trait?
Stroke 32:1563-1566, Arquizan,C.,et al, 2001

Cerebrovascular Manifestations in 321 Cases of Hereditary Hemorrhagic Telangiectasia
Stroke 32:877-882, Maher,C.O.,et al, 2001

Spontaneous Intracerebral Hemorrhage
NEJM 344:1450-1460, Qureshi,A.I.,et al, 2001

Amyotrophic Lateral Sclerosis
NEJM 344:1688-1700, Rowland,L.P. & Shneider,N.A., 2001

Atrial Fibrillation
NEJM 344:1067-1078, Falk,R.H., 2001

Memory Impairment in Abstinent MDMA ("Ecstasy") Users: A Longitudinal Investigation
Neurol 56:966-969, Zakzanis,K.K. & Young,D.A., 2001

Adverse Long-term Effects of Brain Radiotherapy in Adult Low-grade Glioma Patients
Neurol 56:1285-1290,1255, Surma-aho,O.,et al, 2001

Impact of the Human Genome Projects and Identification of a Stroke Gene
Stroke 32:1239-1241, Alberts,M.J., 2001

Diagnostic Investigation of Patients with Chronic Polyneuropathy: Evaluation of a Clinical Guideline
JNNP 71:205-209,147, Rosenberg, N.R.,et al, 2001

Hereditary Benign Chorea
Neurol 57:106-110, Fernandez,M.,et al, 2001

Recommended Diagnostic Criteria for Multiple Sclerosis: Guidelines from the International Panel on the Diagnosis of Multiple Sclerosis
Ann Neurol 50:121-127, McDonald,W.I.,et al, 2001

Subclinical Dopaminergic Dysfunction in Asymptomatic Parkinson's Disease Patients' Relatives with a Decreased Sense of Smell
Ann Neurol 50:34-41, Berendse,H.W.,et al, 2001

The Clinical Spectrum of Familial Hemiplegic Migraine Associated with Mutations in a Neuronal Calcium Channel
NEJM 345:17-24,57, Ducros,A.,et al, 2001

Impact of Folic Acid Fortification of the US Food Supply on the Occurrence of Neural Tube Defects
JAMA 285:2981-2986,3022, Honein,M.A.,et al, 2001

Fits and Strokes
Lancet 358:120, Sharma,P.,et al, 2001

Complete Genomic Screen in Parkinson Disease
JAMA 286:2239-2244, Scott,W.K.,et al, 2001

Adult-Onset Leukoencephalopathy with Vanishing White Matter Presenting with Dementia
Ann Neurol 50:665-668, Prass,K.,et al, 2001

Human Herpesvirus 6 Limbic Encephalitis After Stem Cell Transplantation
Ann Neurol 50:612-619, Wainwright,M.S.,et al, 2001

Should Stroke Subtype Influence Anticoagulation Decisions to Prevent Recurrence in Stroke Patients with Atrial Fibrillation?
Stroke 32:2828-2832, Evans,A.,et al, 2001

Late Cardiopulmonary Complication of Ventriculo-atrial Shunt
Lancet 358:1608,1569, Milton,C.A.,et al, 2001

Prospective Follow-up of 33 Asymptomatic Patients with Familial Cerebral Cavernous Malformations
Neurol 57:1825-1828, Labauge,P.,et al, 2001

Spinocerebellar Ataxia Type 2 Presenting as Familial Levodopa-Responsive Parkinsonism
Ann Neurol 50:812-815, Shan,D.,et al, 2001



Showing articles 2100 to 2150 of 4627 << Previous Next >>