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Differential
(Click to cross reference)
abscess, sphenoid sinus
Adies pupil
allergy
alopecia
amaurosis fugax
amblyopia
anemia
angiography, cerebral
angiotensin-converting enzyme
anisocoria
anosmia
anosmia, unilateral
anticoagulant, treatment
Argyll Robertson pupil
arteritis, temporal
arthralgia
arthritis
aspartate aminotransferase
aspergillosis
ataxia
autoantibodies
autoimmune disease
blindness
border zone infarct
botulinum toxin
brain biopsy
carcinoma
carcinoma of breast
carotid artery disease
carotid artery stenosis
carotid artery stenosis, intracranial
carotid artery stenosis, tandem
carotid siphon
carotid-siphon stenosis
CAT scan
CAT scan, abnormal
CAT scan, contrast enhanced
CAT scan, orbits
CAT scan, venography
central retinal artery occlusion
cerebellar lesion
cerebral artery, encasement
cerebral embolism
cerebral infarction
cerebral venous thrombosis
cerebrospinal fluid, cytology
cerebrospinal fluid, cytology, false negative
cerebrovascular accident
cerebrovascular accident, acute management of
cerebrovascular accident, prevention of
cerebrovascular disease
chemosis
chemotherapy, CNS treatment and complications with
cherry red spot
chiasmal syndromes
children
chorioretinitis
Clinical Pathologic Conference(C.P.C.)
cold intolerance
color desaturation
color vision
color vision, impaired
complications
conjunctival injection
controversies in neurology
corneal ulceration
corpus callosum
corpus callosum, neoplasm of
cotton-wool spots
cranial nerve palsies
cranial nerve palsies, unilateral
cranial neuropathy
cranial neuropathy, multiple
craniopharyngioma
delay in diagnosis
depression
diabetes insipidus
diabetes mellitus
dialysis
diplopia
dyschromatopsia
dysthyroid ocularmyopathy
edema, periorbital
embolization, therapeutic
emergencies, neurologic
emergencies, ocular
eye movement, disorders of
eye, pain in
false negative
false negative VDRL
familial
fatigue
fistula, arterio-venous, dural
fluorescent treponema antibody absorption(FTA-ABS)
fundus, abnormality of
funduscopic exam
fungal infection
gadolinium
gene mutation
genetic testing
giant cell arteritis
Graves ophthalmopathy
hallucination
hallucination, visual
head injury
headache
headache, focal
headache, positional
headache, unilateral
hearing loss
hemiplegia
hemiplegia, progressive
heparin
Horner's syndrome
human immunodeficiency virus type 1
hyperphosphatasia
hyperreflexia
hypersomnia
hypertension
hyperthyroidism
hypotension, systemic
hypothermia
imbalance
internal carotid artery
iris, atrophy of
iritis
Leber's hereditary optic neuropathy
lens, dislocation of
lid lag
light-near dissociation, causes of
liver disease
liver function enzymes
lymphoma
lymphoma involving CNS
lymphoma, primary of CNS
Marcus Gunn pupil
meningeal enhancement
meningismus
meningitis, carcinomatous
middle cerebral artery, emboli to
miosis
mitochondrial disease
MRI
MRI, abnormal
MRI, CAT scan compared to
MRI, contrast enhanced
MRI, diffusion weighted
MRI, mass effect on
MRI, optic nerve
MRI, orbit
mucormycosis
multiple sclerosis
multiple sclerosis, differential diagnosis of
myopia
myopia, axial
myopia, unilateral
nasal stuffiness
negative
neoplasm, pituitary
neoplastic angioendotheliosis
neurologic disease, diagnoses of
neuroophthalmology
neuroretinitis
neurosyphilis
nocturia
non-arteritic antererior ischemic optic neuropathy
normal
obesity
ophthalmoplegia
ophthalmoplegia, total
optic atrophy
optic chiasm
optic disc edema
optic nerve
optic nerve sheath fenestration
optic nerve sheath hemorrhage
optic nerve, compression of
optic nerve, decompression of
optic nerve, enhancement
optic nerve, enlarged
optic nerve, lesion of
optic nerve, neoplasm of
optic neuritis
optic neuritis, bilateral
optic neuritis, treatment of
optic neuropathy
optic neuropathy, bilateral
optic neuropathy, hereditary
optic neuropathy, ischemic
optic neuropathy, ischemic, anterior
optic neuropathy, traumatic
orbit
orbit, cellulitis of
orbit, lesions of
orbital apex
orbital apex syndrome
pain
pain, abdominal
pain, periorbital
papilledema
papilledema, unilateral
papillitis
paresthesias
pleocytosis of cerebrospinal fluid
prevention of neurologic disorders
prognosis
prolactin, elevated
prolactinoma
proptosis
proptosis, unilateral
psoriatic arthritis
ptosis
ptosis, unilateral
Pulfrich phenomenon
pupil
pupil, abnormality in neurologic disorders
pupil, light reflex of
pupil, light reflex, abnormal
pupil, normal
pupil, tonic
pure motor hemiplegia
radiation therapy, CNS treatment and complications with
rash
rash, hand
recurrent
respiratory tract infection
reticulum cell sarcoma
retinal branch artery occlusion
retinal ischemia
retinitis pigmentosa
review article
risk factors
sarcoidosis
sarcoidosis, CNS
scotoma
scotoma, central
sedimentation rate
serologic test for syphilis
serum alanine aminotransferase
sheathing of retinal veins
sinus, biopsy of
sinuses, diseases of
sinusitis
skin, lesions in neurologic disorders
slurred speech
sphenoid sinus
sphenoid sinus biopsy
stem cell rescue
stem cell transplantation
stent, venous sinus
steroid therapy, CNS treatment and complications with
stroke, progression of
suprasellar lesion
syphilis, diagnosis and treatment
syphilis, neurologic complications with
syphilis, ocular
tabes dorsalis
tachycardia
temporal artery, biopsy
third nerve
third nerve misdirection
third nerve palsy
thyrotoxicosis
tinnitus
tinnitus, pulsatile
tissue plasminogen activator, intravenous
treatment of neurologic disorder
tremor
trigeminal neuropathy
trigeminal neuropathy, sensory
ultrasonography, orbit
uremia
urinary frequency
urinary urgency
uveitis
vision loss, sequential
vision, blurred
vision, cloudy
visual acuity, decreased
visual acuity, decreased, monocular
visual field defect
visual field defect, altitudinal
visual impairment
visual loss
visual loss, progressive
visual loss, slow-unilateral
visual loss, sudden
visual loss, sudden-unilateral
Westphal-Pilty phenomenon
white matter disease
wide based gait
workup
Showing articles 650 to 700 of 3113 << Previous Next >>

Intrauterine Exposure to Carbamazepine and Specific Congenital Malformations: Systematic Review and Case-Control Study
BMJ 341:c6581, 1229, Jentik,J.,et al, 2010

Association Between Familial Atrial Fibrillation and Risk of New-Onset Atrial Fibrillation
JAMA 304:2263-2269, Lubitz,S.A.,et al, 2010

Update on the Natural History of Cavernous Malformations and Factors Predicting Aggressive Clinical Presentation
Neurosurg Focus 29:E7, Washington,C.W.,et al, 2010

Dabigatran Challenges Warfarins Superiority for Stroke Prevention in Atrial Fibrillation
Stroke 41:1307-1309, Schwartz,N.E. &Albers,G.W., 2010

Optimal Screening Strategy for Familial Intracranial Aneurysms: A Cost-Effectiveness Analysis
Neurol 74:1671-1679, Bor,A.S.E., et al, 2010

Detection of Paroxysmal Atrial Fibrillation with Transtelephonic EKG in TIA or Stroke Patients
Neurol 74:1666-1670, 1662, e94, Gaillard,N., et al, 2010

Clincopath Conf, Pheochromocytoma
NEJM 362:1815-1823, Case 14-2010, 2010

Glucose Transporter-1 Deficiency Syndrome: The Expanding Clinical and Genetic Spectrum of a Treatable Disorder
Brain 133:655-670, Leen,W.G., et al, 2010

Screening for Intracranial Aneurysms in Patients with Bicuspid Aortic Valve
Neurol 74:1430-1433, Schievink,W.I., et al, 2010

Atypical Dementia
Lancet 376:656, Cohen-Bittan,J. et al, 2010

Prevalence and Predictors of Paroxysmal Atrial Fibrillation on Holter Monitor in Patients With Stroke or Transient Ischemic Attack
Stroke 41:2596-2600, Alhadramy,O.,et al, 2010

Efficacy and Safety of Dabigatran Compared With Warfarin at Different Levels of International Normalised Ratio Control for Stroke Prevention in Atrial Fibrillation: An Analysis of the RE-LY Trial
Lancet 376:975-983, Wallentin,L.,et al, 2010

Optimal Timing of Resumption of Warfarin After Intracranial Hemorrhage
Stroke 41:2860-2866, Majeed,A.,et al, 2010

Comparison of Clinical, Familial, and MRI Features of CADASIL and NOTCH3-Negative Patients
Neurol 74:57-63, Pantoni,L.,et al, 2010

A Case Report of Bilateral Superior Altitudinal Hemianopia with Cerebral Infarction
The Neurologist 16:132-135, Keklikoglu,H.D.,et al, 2010

Genetic Susceptibility to Stuttering
NEJM 362:750-752, Fisher,S.E. &Phil,D., 2010

Familial Versus Sporadic Cavernous Malformations: Differences in Developmental Venous Anomaly Association and Lesion Phenotype
AJNR 31:377-382, Petersen,T.A.,et al, 2010

The Spectrum of Mutations in Progranulin: A Collaborative Study Screening 545 Cases of Neurodegeneration
Arch Neurol 67:161-170,145, Yu,C.-E.,et al, 2010

Oral Fingolimod or Intramuscular Interferon for Relapsing Multiple Sclerosis
NEJM 362:402-415, 456, Cohen,J.A.,et al, 2010

A Placebo-Controlled Trial of Oral Fingolimod in Relapsing Multiple Sclerosis
NEJM 362:387-401, 456, Kappos, L.,et al, 2010

Clinicopath Conf, Infantile Krabbe Disease
NEJM 362:346-356, Case 3-2010, 2010

Incidence of Newly Detected Atrial Arrhythmias via Implantable Devices in Patients with a History of Thromboembolic Events
Stroke 41:256-260, Ziegler,P.D.,et al, 2010

Reversible Paraneoplpastic Limbic Encephalitis Associated with Antibodies to the AMPA Receptor
Neurol 74:265-267, Bataller,L.,et al, 2010

Familial Mediterranean Fever and Central Nervous System Involvement: A Case Series
Medicine 89:75-84, Kalyoncu,U.,et al, 2010

Diagnostic Accuracy of Confrontation Visual Field Tests
Neurol 74:1184-1190, Kerr,N.M., et al, 2010

Clinical Reasoning: Seizures in a Child With Sensorineural Deafness and Agitation
Neurol 74:e61-e63, Auvin,S., et al, 2010

Whole-Genome Sequencing in a Patient with Charcot-Marie-Tooth Neuropathy
NEJM 362:1181-1191, Lupski,J.R., et al, 2010

Prolactinomas
NEJM 362:1219-1226, Klibanski,A., 2010

Clinical Spectrum of CADASIL and the Effect of Cardiovascular Risk Factors on Phenotype: Study in 200 Consecutively Recruited Individuals
Stroke 41:630-634, Adib-Samii,P., et al, 2010

Absence Epilepsies With Widely Variable Onset are a Key Feature of Familial GLUT1 Deficiency
Neurol 75:432-440, Mullen,S.A., et al, 2010

Redefining Dysferlinopathy Phenotypes Based on Clinical Findings and Muscle Imaging Studies
Neurol 75:316-323,298, Paradas,C., et al, 2010

Familial Neuromyelitis Optica
Neurol 75:310-315, Matiello,M., et al, 2010

A Hereditary Moyamoya Syndrome With Multisystemic Manifestations
Neurol 75:259-264, Herv�,D., et al, 2010

Pediatric Moyamoya Disease: An Analysis of 410 Consecutive Cases
Ann Neurol 68:92-101, Kim,S.-K., et al, 2010

Cost-Effectiveness of Outpatient Cardiac Monitoring to Detect Atrial Fibrillation After Ischemic Stroke
Stroke 41:1514-1520, Kamel,H., et al, 2010

Incidence of Cerebral Microbleeds: A Longitudinal Study in Memory Clinic Population
Neurol 74:1954-1960, Goos,J.D.C., et al, 2010

Clinicopath Conf, Rapid-Onset-Dystonia-Parkinsonism Due to a Mutation in the ATP1A3 Gene
NEJM 362:2213-2219, Case 17-2010, 2010

Early Alzheimers Disease
NEJM 362:2194-2201, Mayeux,R., 2010

Valproic Acid Monotherapy in Pregnancy and Major Congenital Malformations
NEJM 362:2185-2193, Jentink,J., et al, 2010

Huntingtons Disease
BMJ 341:34-40, Novak,M.J. &Tabrizi,S.J., 2010

Delirious Deficiency
Lancet 376:1362, Olsen,R.Q &Regis,J.T., 2010

New Aspects on Patients Affected by Dysferlin Deficient Muscular Dystrophy
JNNP 81:946-953, Klinge,L.,et al, 2010

Quality of Anticoagulation Control in Atrial Fibrillation
Lancet 376:935-937, Lane,D.A. &Lip,G.Y.H., 2010

A Multidisciplinary Study of Patients with Early-Onset PD with and Without Parkin Mutations
Neurol 72:110-116,106, Lohmann,E.,et al, 2009

Clinicopath Conf., Adult Cerebral Form of X-Linked Adrenoleukodystrophy
NEJM 360:171-181, Case 1-2009, 2009

Persistent Fainting After Implantation of a "Curative" Pacemaker
NEJM 360:88-89, Kasim,S.,et al, 2009

Voltage-gated Potassium Channel-associated Limbic Encepahlitis in the West of Scotland:Case Reports and Literature Review
Scott Med J 54:27-31, Reid,J.M.,et al, 2009

Dabigatran Versus Warfarin in Patients with Atrial Fibrillation
NEJM 361:1139-1151, 1200, Connolly,S.,et al, 2009

Practice Parameter: Evaluation of the Child with Microcephaly (An Evidence-Based Review): Report of the Quality Standards Subcommittee of the American Academy of Neurology and the Practice Committee of the Child Neurology Society
Neurol 73:887-897, Ashwal,S.,et al, 2009

Diagnosis and Therapy in Neuromuscular Disorders: Diagnosis and New Treatments in Mitochondrial Diseases
JNNP 80:943-953, Rahman,S. &Hanna,M.G., 2009



Showing articles 650 to 700 of 3113 << Previous Next >>