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Differential
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accommodation
accomodation, abnormal
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
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
difficulty climbing stairs
diplopia
dizziness
DNA sequencing
dopamine agonist
downward gaze
driving
drooling
drowsiness
dural arteriovenous malformation
dysarthria
dysdiadochokinesia
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 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, 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
hyposmia
hypotension, neurologic causes of
hypoxia
hypoxic encephalopathy
ideomotor apraxia
imbalance
imbalance, postural
immunodeficiency
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
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
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, proximal
mutism
myasthenia gravis
myasthenia gravis, infantile and juvenile
myoclonus
myotonia
nasal speech
nausea and vomiting
neck pain
neoplasm, primary of CNS
neurologic complications
neurologic disease, diagnoses of
neurologic signs
neuron specific enolase
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, familial
Parkinson disease, freezing phenomena in
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
prognathism
prognosis
progressive neurologic disorder
progressive supranuclear palsy
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
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
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
treatment of neurologic disorder
tremor
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
Williams syndrome
workup
zinc
Showing articles 50 to 100 of 13026 << Previous Next >>

Spinal Muscular Atrophy
UpToDate, Oct, Bodamer,O.A., 2022

Updates on Sturge-Weber Syndrome
Stroke 53:3769-3779, Yeom,S.E.&Comi,A.M., 2022

Bilateral Complete Ophthalmoplegia in a 50-Year-Old Man
JAMA Neurol 79:724-725, Arora, N.,et al, 2022

Clinicopathologic Conference, Granulomatosis with Polyangiitis
NEJM 387:1022-1032, Case 28-2022, 2022

Sturge-Weber Syndrome
www.UptoDate.com,Dec, Patterson,M.C., 2022

A 56-Year-Old Man with Unusual Presentation of Subacute Encephalopathy and Seizure
Neurol 98:e95-e102, Wang, T.,et al, 2022

Myotonic Dystrophy: Etiology, Clinical Features, and Diagnosis
UptoDate 2022 Jan, Darras, B.T., 2022

Ocular Findings in the Sturge-Weber Syndrome
NEJM 385:e68, Sherman, S.V., 2021

Multiple Facial Ulcers Following a Stroke
JAMA Neurol 78:1393-1394, Linnemann, B.E.,et al, 2021

Frequency and Characterization of Movement Disorders in Anti-IgLON5 Disease
Neurol 97:e1367-e1381, Gaig, C.,et al, 2021

Facial Numbness, Dysarthria, Muscle Atrophy, and Weakness in a Young Patient
JAMA Neurol 78:1273-1274, Liu, Y.,et al, 2021

An Unusual Presentation of Prolonged Delirium
BMJ 373:N1423, Bume, R.,et al, 2021

Asymmetrical Facial Flushing and Sweating Associated with Anisocoria
BMJ 373:m796, Michonidou, A. & Atan, D., 2021

CLOVES Syndrome
Neurol 96:e1487-e1488, Collins, M.,et al, 2021

A 64-Year-Old Man with Multiple Cranial Neuropathies
Neurol 97:e215-e221, Lefland, A.,et al, 2021

A 47-Year-Old With Headache, Vertigo, and Double Vision
Neurol 97:e535-e539, Frey, J.,et al, 2021

Genetics of Cluster Headache Takes a Leap
Ann Neurol 90:191-192, Palotie, A., 2021

A 42-Year-Old Woman with Mysterious Monocytic Meningitis
Neurol 97:449-454, Nothem, M.E., et al, 2021

The Tolosa-Hunt Syndrome
NJJP 71:577-582, Kline,L.B. & Hoyt,W.F., 2021

Cervical Discopathy in Idiopathic Trigeminal Neuralgia:More than a Coincidence?
Egy Spine J 40:53-64, Boru, U.T.,et al, 2021

Sensory Ganglionopathy
NEJM 383:1657-1662, Amato, A.A. & Ropper, A.H., 2020

Migraine, hearing loss, and blurred vision in a young woman
Neurol 95:e2945-e2950, Sasikumar, S.,et al, 2020

An 81-year-old Woman with Decreased Consciousness and Fluctuating Right Facial Droop
Neurol 94:843-848, Van Ommeren, R.,et al, 2020

Clinicopathologic Conference, LGI1 autoimmune encephalitis
NEJM 382:1943-1950, Case 15-2020, 2020

Severe Neurological Toxicity of Immune Checkpoint Inhibitors: Growing Spectrum
Ann Neurol 87:659-669, Dubey, D.,et al, 2020

The Face of Myasthenia Gravis
Neurol 95:89-90, Ruiter, A.M.,et al, 2020

Facial Nerve Palsy in COVID-19 Infection
Neurol 95:364-367, Goh, Y.,et al, 2020

A 14-Year-Old Boy with Acute Weakness, Parethesias, and Headache
Neurol 95:e1285-e1289, Seese, R.R.,et al, 2020

Rapidly Progressive Gait Disorder and Cranial Nerves Involvement in a 9-year-old boy
Neurol 94:e330-e334, Lipp, A.,et al, 2020

A Rare Presentation of Whipple Disease
Neurol 94:e758-e761, Koek, A.T.,et al, 2020

Clinicopathologic Conference, AA Amyloidosis, Complicated by Cerebral Mucormycosis
NEJM 382:1457-1466, Case 11-2020, 2020

Orofacial Dyskinesia in a Young Man
JAMA Neurol 76:1517-1518, Tian, X.,et al, 2019

Lyme Disease: What the Neuroradiologist Needs to Know
AJNR 40:1998-2000, Valand, H.A.,et al, 2019

Oculodentodigital Dysplasia: A Hypomyelinating Leukodystrophy with a Characteristic MRI Pattern of Brain Stem Involvement
AJNR 40:903-907, Hartin, I.,et al, 2019

Recurrent Involuntary Contractions of the Face, Arm, and Leg in an Elderly Man
JAMA Neurol 76:728-729, Kim, D.D.,et al, 2019

Global Orbital Infarction Syndrome after a Carotid Artery Dissection
JAMA Neurol 76:111-112, Larrosa Campo, D.,et al, 2019

Contemporary Reversal of Oral Anticoagulation in Intracerebral Hemorrhage
Stroke 50:529-536, Bower, M.M.,et al, 2019

A Pregnant Woman with Chin Numbness
Neurol 92:e996-e999, Arnold, A.J.,et al, 2019

Clinicopathologic Conference, Ocular Syphilis
NEJM 380:1062-1071, Case 8-2019, 2019

Behcet Disease
emedicine.medscape.com Dec, Davey-Ranasinghe, N. & Diamond, H.S., 2018

Clinicopathologic Conference, Granulomatosis with Polyangiitis
NEJM 379:2452-2461, Case 39-2018, 2018

A Child with Arthrogryposis
Neurol 91:e995-e998, Irumudomom, O. & Ghosh, P.S., 2018

Precentral Gyrus Infarct Presenting as Isolated Contralateral Peripheral-Type Facial Palsy
Neurol 91:421-422, Hebant, B.,et al, 2018

Clnicopathologic Conference Anti-N-Methyl-D-Aspartate (NMDA) Receptor Encephalitis
NEJM 379:870-878, CASE 27-2018, 2018

Proptosis and Double Vision in a Child
JAMA Neurol 75:1142-1143, Lu, A.J.,et al, 2018

Clinical Presentation and Cranial MRI Findings of Listeria Monocytogenes Encephalitis
Neurologist 23:198-203, Arslan, F.,et al, 2018

Numb Chin Syndrome
UptoDate.com Sept, Robertson, C.E., 2018

Clinicopathologic Conference, Intracranial Hypertension Associated with Systemic Lupus Erythematosus and Steroid Use
NEJM 378:282-289, Case 2-2018, 2018

Antibody-Mediated Encephalitis
NEJM 378:840-851, Dalmau, J.,et al, 2018

Gasperini Syndrome
Neurol 90:e261, Lorio, R., 2018



Showing articles 50 to 100 of 13026 << Previous Next >>