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Differential
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accommodation
accomodation, abnormal
adolescent medicine
aggression
agitation
akinesia of eyelid function
algorithm
alien hand syndrome
alpha-fetoprotein
amenorrhea
ammonia
amphotericin B
anemia
Angelman syndrome
angiography, cerebral
ankle edema
anorexia
anticholinergic drugs
applause sign
apraxia
apraxia of eyelid opening
apraxia, constructional
arm swing, reduced
ascites
aspiration
asterixis
astrocytoma
ataxia
ataxia telangiectasia
ataxic gait
athetosis
attention span
atypical
autoantibodies
autonomic dysfunction
basal ganglia, degeneration
basal ganglia, lesion of
basal ganglia, lesion, bilateral
behavior, combative
behavioral disorder
belching
blepharophimosis
blepharospasm
blinking
blinking, reduced
bone marrow transplantation
brachycephaly
bradykinesia
bradykinesia, facial
bradyphrenia
brain damage
bruxism
calcification, intracranial
callosal angle
camptocormia
carbon monoxide poisoning
CAT scan, angiography
CAT scan, angiography, false negative
CAT scan, emission, abnormal
CAT scan, pelvis
CAT scan, venography
cataracts
cerebellar ataxia, children
cerebellar atrophy, primary
cerebral cortex
cerebral cortical atrophy
cerebral edema
cerebral infarction
cerebral palsy
cerebrospinal fluid, abnormal
cerebrospinal fluid, cytology
cerebrospinal fluid, drainage of
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, oligoclonal IgG in
cerebrovascular accident
cerebrovascular accident, young adult
cerebrovascular disease
ceruloplasmin, serum
Charcot's sign
chelation therapy
children
cholelithiasis
chorea
choreoathetosis
chromosomal abnormality
chromosome 15
cingulate island sign
cirrhosis
Clinical Pathologic Conference(C.P.C.)
clubbing of fingers
coat-hanger pain
cognition, slowed
cogwheel rigidty
coma
compulsivity
confusion
congenital heart disease
conjugate gaze, forced
contractures, joint
convergence
convergence, impaired
cortical-basal ganglionic degeneration
cough
creatine phosphokinase(CPK)elevated
crying, pathologic
cyst, ovary
degenerative diseases of CNS
delay in diagnosis
dementia
dementia, familial
dementia, rapidly progressive
dementia, reversible
dementia, thalamic
depression
developmental milestones
developmental milestones, loss of
developmental retardation
dexterity, impaired
diagnostic criteria
diet
differential diagnosis
difficulty climbing stairs
diplopia
dizziness
DNA sequencing
dopa responsive dystonia
dopamine agonist
downward gaze
driving
drooling
drowsiness
dural arteriovenous malformation
dysarthria
dysdiadochokinesia
dyskinesia
dyskinesia, buccal lingual facial
dysmorphic
dysphagia
dysphonia
dystonia
dystonia, cervical
dystonia, face
ear, abnormal
edema, pedal
electroencephalogram, abnormalities of
electromyogram
electron microscopy
emotional lability
encephalitis
encephalitis, autoimmune
encephalitis, paraneoplastic
encephalitis, viral
encephalopathy
encephalopathy, delayed
encephalopathy, metabolic
enolase
erectile dysfunction
esophageal varices
ethics in neurology
executive dysfunction
extrapyramidal movement disorder, progressive
eye movement, disorders of
facial appearance, abnormal
facial expression abnormality
facial hallucinations
facial weakness
facial weakness, bilateral
falling
familial
fatigue
feeding disorder
fine motor function, impaired
fish
fistula, arterio-venous, dural
fluorescene in situ hybridization
fracture, long bone
frontal lobe, anatomy and physiology
frontal lobe, pathologic signs of
gait disorder
gait, apraxic
gait, festinating
gait, magnetic
gangliosidosis GM1
gaze palsy
gaze palsy, supranuclear
gaze palsy, vertical
Gegenhaulten
gene
gene mutation
genetic counselling
genetic diagnosis, prenatal
genetic neurologic disorders
genetic testing
Gilles de la Tourette syndrome
Gilles de la Tourette syndrome, late-onset
glabellar sign
Gowers maneuver
grasp reflex
grimacing
gynecomastia
gyrus, abnormal
hallucination
hallucination, visual
haloperidol
handwriting
head injury
headache
hearing loss
hemorrhage, thalamic
hepatic encephalopathy
hepatic encephalopathy, acute
hepatic failure
hepatitis
hepatolenticular degeneration(Wilson's disease)
hepatolenticular degeneration(Wilson's disease), presymptomatic
hepatolenticular degeneration(Wilson's disease), screening for
hepatomegaly
hepatosplenomegaly
hip dysplasia
hummingbird sign
Huntington's chorea
hydrocephalus
hydrocephalus, normal pressure
hyperactivity
hyperbilirubinemia
hypercalcemia
hyperreflexia
hypersomnia
hypertension
hypoalbuminemia
hypoglycorrhachia
hypometric saccades
hypophonia
hypopigmentation of skin
hyporeflexia
hyposmia
hypotension, neurologic causes of
hypotonia
hypotonia, infants
hypoxia
hypoxic encephalopathy
ideomotor apraxia
imbalance
imbalance, postural
immunodeficiency
inclusion bodies, intranuclear
incontinence, fecal
infection
intellectual deficit
intellectual deterioration
Jakob-Creutzfeldt disease
jaundice
jaw contractures
jaw jerk, abnormal
Kayser-Fleischer ring
kinesia paradoxica
laughing, pathologic
L-dopa
leg dragging
lethargy
leucine rich glioma inactivated 1 antibodies
leukemia, neurologic findings assoc.with
leukoencephalopathy
leukopenia
level of consciousness, decreased
Lewy body
life support, withdrawal of
limbic encephalitis
liver biopsy
liver disease
liver function enzymes
liver transplantation
lobar atrophy
logopenia
lumbar puncture, complications of
macrocephaly
macrognathia
manganese intoxication
marche a petits pas
masked facies
memory, defect of recent
memory, impairment of
meningismus
mental retardation
metabolic disorder, primary
microcephaly
micrographia
microhemorrhage, intracerebral
midbrain
midbrain, atrophy
mimics
miosis
misdiagnosis
mitral valve lesion
molecular genetics
mood change
mortality
movement disorder
movement disorder, extrapyramidal
MRI
MRI, abnormal
MRI, angiography
MRI, angiography, false negative
MRI, contrast enhanced
MRI, diffusion weighted
MRI, high signal foci on
MRI, high signal intensity of basal ganglia
MRI, mouse ears
MRI, negative
MRI, T1 weighted high signal foci
MRI, venography
multiple system atrophy
muscle biopsy
muscle stiffness
muscle weakness
muscle weakness, proximal
muscular dystrophy
muscular dystrophy, congenital
muscular dystrophy, LAMA2
mutism
myasthenia gravis
myasthenia gravis, infantile and juvenile
myoclonus
myopathy
myotonia
nasal speech
nausea and vomiting
neck pain
neck weakness
neoplasm, primary of CNS
neurologic complications
neurologic disease, diagnoses of
neurologic signs
neuron specific enolase
neuronal intranuclear inclusion disease
neuroophthalmology
neuropathology
neuropathy
NMDA antagonists
noncommunicative
obsessive-compulsive disorder
ocular myopathy
ocular myopathy, differential diagnosis
opened mouth
ophthalmoplegia
opsoclonus
orthostatic hypotension
Parkinson disease
Parkinson disease, atypical
Parkinson disease, axial symptoms
Parkinson disease, diagnosis
Parkinson disease, dystonia with
Parkinson disease, familial
Parkinson disease, freezing phenomena in
Parkinson disease, juvenile
Parkinson disease, L-dopa nonresponsive
Parkinson disease, pathogenesis of
Parkinson disease, surgical treatment of
Parkinson disease, treatment of
Parkinson disease, tremor, absence of
Parkinsonism syndrome
penguin silhouette sign
penicillamine
persistent vegetative state
personality change
phencyclidine poisoning
picking at skin
pinched face
plasmacytoma of brain
pleocytosis of cerebrospinal fluid
pneumonia
polycythemia, secondary
portal caval shunt
postural abnormality
pregnancy, neurologic complications in
prion disease
PRKN gene
prognathism
prognosis
progressive neurologic disorder
progressive supranuclear palsy
prosopometamorphopsia
protein 14-3-3, cerebrospinal fluid
protein 14-3-3, cerebrospinal fluid, false negative
pseudobulbar palsy
psychiatric disorder
psychiatric problems in neurologic disorders
psychomotor retardation
psychosis
psychosis, acute
psychotic behavior
ptosis
pulmonary infection
pupil
pupil, abnormality in neurologic disorders
rapidly progressing neurologic illness
release phenomena
remote effect of cancer on the nervous system
renal failure
renal stones
retrocollis
retropulsion
Rett's syndrome
reversible neurologic disorder
review article
Reye's syndrome
rhabdomyolysis
rickets
rigidity
rigidity, axial
risk factors
risus sardonicus
rivastigmine
running
saccadic eye movements, abnormal
salivation, excessive
schizophrenia
Schwartz-Jampel syndrome
seizure
sensorineural hearing loss
sequencing difficulty
short stature
shoulder, pain in
shunt procedure, lumboperitoneal
shunt procedure, ventricular
sinemet
skin, darkening of
skin, lesions in neurologic disorders
sleep pathology and physiology
slit lamp examination
smiling
SNCA duplication
somnolence
speech disorder
speech disorder, childhood
speech, delayed development of
speech, soft
spitting
splenomegaly
spongy degeneration of brain
stare
startle reaction
stooped posture
stuporous
suck reflex
suicide
sweating
syncope
tau protein
tauopathy
teeth, wide-spaced
telangiectases
temporal lobe, lesion
temporal lobe, lesion, bilateral
teratoma, ovarian
thalamus, lesion of
thalamus, lesion of-bilateral
thrombocytopenia
tic
tongue, protrusion of
tonic foot response
treatment of neurologic disorder
tremor
tremor, postural
tremor, resting
trientine dihydrochloride
twins
urinary incontinence
urine test for metabolic disorders
urine test in toxic screen
venous hypertension
venous ischemia
ventricular enlargement
vision, blurred
visual symptoms
visuospatial disturbance
voice, abnormality of
walking, difficulty with
weakness
weakness, generalized
weight loss
wheelchair
white matter disease
wide based gait
Williams syndrome
workup
zinc
Showing articles 3250 to 3300 of 13819 << Previous Next >>

Functional Contrast-Enhanced CT for Evaluation of Acute Ischemic Stroke Does not Increase the Risk of Contrast-Induced Nephropathy
AJNR 31:817-821, Lima,F.O., 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

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

Ascending Paralysis from Malignant Leptomeningeal Melanomatosis
JNNP 81:449-450, Burrows,A.M., et al, 2010

Leptomeningeal Metastases in the MRI Era
Neurol 74:1449-1454, Clarke,J.L., et al, 2010

NMDA Receptor Encephalitis Mimicking Seronegative Neuromyelitis Optica
Neurol 74:1473-1475, Kruer,M.C., et al, 2010

A Comparison of MRI Criteria for Diagnosing Pediatric ADEM and MS
Neurol 74:1412-1415, 1404, Ketelslegers,I.A., et al, 2010

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

MRI Versus CT for Detection of Acute Vascular Lesions in Patients Presenting with Stroke Symptoms
Stroke 41:e427-e428, Brazzelli,M., et al, 2010

Teaching NeuroImages: MRI Reversal in Wilson Disease With Trientine Treatment
Neurol 74:e72, Park,H.K., et al, 2010

Prevalence of Superficial Siderosis in Patients with Cerebral Amyloid Angiopathy
Neurol 74:1346-1350, Linn,J., et al, 2010

Cognitive Impairment and Dementia in Neurocysticercosis: A Cross-Sectional Controlled Study
Neurol 74:1288-1295, Ciampi de Andrade,D., et al, 2010

Copper Deficiency as a Treatable Cause of Poor Balance
BMJ 340:864-866, Khaleeli,Z., et al, 2010

Clinicopath Conf., Progressive Multifocal Leukoencephalopathy
NEJM 362:1431-1437, Case 11-2010, 2010

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

Cryptococcal Meningoencephalitis in Immunocompetent Patients: Changing Trends in Canada
Neurol 74:1233-1235, Bestard,J. &Siddiqi,Z.A., 2010

Transoesophageal Echocardiography in Patients with Acute Stroke with Sinus Rhythm and No Cardiac Disease History
JNNP 81:412-415, Cho,H.-J., et al, 2010

Clinicopath Conf., Brain Abscess, Pulmonary Arteriovenous Malformation Due to Hereditary Hemorrhagic Telangiectasia
NEJM 362:1326-1333, Case 10-2010, 2010

Is the Diagnosis at Hand?
The Lancet 375:1134, Holmes,M.V., et al, 2010

Prognostication After Cardiac Arrest and Hypothermia: A Prospective Study
Ann Neurol 67:301-307, 5, Rossetti,A.O., 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

Severe Encephalopathy with Swine Origin Influenza A H1N1 Infection in Childhood: Case Reports
Neurol 74:1077-1078, 1020, Webster,R.I., et al, 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

Progressive Multifocal Leukoencephalopathy in Individuals with Minimal or Occult Immunosuppression
JNNP 81:247-254, Gheuens,S., et al, 2010

Multiple Cervical Artery Dissection in a Volleyball Player
Arch Neurol 67:1024-1025, Slankamenac,P., et al, 2010

Natalizumab and Progressive Multifocal Leukoencephalopathy: What are the Causal Factors and Can It be Avoided?
Arch Neurol 67:923-930, Warnke,C., et al, 2010

Longitudinally Extensive Transverse Myelitis Following Vaccination With Nasal Attenuated Novel Influenza A (H1N1) Vaccine
Arch Neurol 67:1018-1020, Akkad,W., et al, 2010

Transverse Myelitis
NEJM 363:564-572, Frohman,E.M. &Wingerchuk,D.M., 2010

A Case of Neurosarcoidosis Successfully Treated with Rituximab
Neurol 75:568-570, Bomprezzi,R., et al, 2010

Zonisamide Discontinuation Due to Psychiatric and Cognitive Adverse Events: A Case-Control Study
Neurol 75:513-518, White,J.R., et al, 2010

How Beneficial is Surgery for Cervical Radiculopathy and Myelopathy?
BMJ 341:200-202, Fouyas,I.P., et al, 2010

Characterization of Carotid Plaque Hemorrhage: A CT Angiography and MR Intraplaque Hemorrhage Study
Stroke 41:1623-1629, U-King-Im,J.M., et al, 2010

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

Status Epilepticus Migrainosus: Clinical, Electrophysiologic, and Imaging Characteristics
Neurol 75:373-374, Perucca,P., et al, 2010

Clinicopath Conf, Inflamatory Cerebral Amyloid Angiopathy,
NEJM 363:373-381, Case 22-2010, 2010

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

Clinicopath Conf, Oocyte Retrieval After Anoxic Brain Injury
NEJM: 363:276-283, Case 24-2010, 2010

Evidence-Based Guideline: The Role of Diffusion and Perfusion MRI for the Diagnosis of Acute Ischemic Stroke: Report of the Therapeutics and Technology Assessment Subcommittee of the American Academy of Neurology
Neurol 75:177-185, Schellinger,P.D., et al, 2010

Serial MRI and CSF Biomarkers in Normal Aging, MCI, and AD
Neurol 75:143-151, Vemuri,P., et al, 2010

Artery of Percheron Infarction: Imaging Patterns and Clinical Spectrum
AJNR 31:1283-1289, Lazarro,N.A., et al, 2010

Pneumonias Link With the Head and Neck
Lancet 376:388, Mariotti,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

Acute and Preventive Pharmacologic Treatment of Cluster Headache
Neurol 75:463-473, Francis,G.J., et al, 2010

Neuropsychological Dysfunction and Neuroimaging Abnormalities in Neurologically Intact Adults With Sickle Cell Anemia
JAMA 303:1823-1831, Vichinsky,E.P., et al, 2010

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

Acute Necrotizing Encephalopathy During Novel Influenza A (H1N1) Virus Infection
Ann Neurol 68:111-114, Mariotti,P., et al, 2010

Posterior Reversible Encephalopathy Syndrome: Long-Term Follow-Up
JNNP 81:773-777, Roth,C. &Ferbert,A., 2010

Isolated Ischaemic Lesions in the Foot Motor Area Mimic Peripheral Lower-Limb Palsy
JNNP 81:822-823, Alonso,A., et al, 2010

The Case Against Confirmatory Tests for Determining Brain Death in Adults
Neurol 75:77-83, Wijdicks,E.F.M., 2010



Showing articles 3250 to 3300 of 13819 << Previous Next >>