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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 1800 to 1850 of 13819 << Previous Next >>

Encephalitis with mGluR5 antibodies
Neurol 90:e1964-e1972, Spatola, M.,et al, 2018

Intracranial Arterial Dolichoectasia and Stenosis
Stroke 49:1135-1140, Zhai, F.,et al, 2018

Palatal tremor as a presenting symptom of amyotrophic lateral sclerosis
Neurol 90:801-802, Maghzi, A.,et al, 2018

Long-Term Risk of Hemorrhagic Stroke In Young Patients with Congenital Heart Disease
Stroke 49:1155-1162, Giang, K.W.,et al, 2018

Predicting Intracerebral Hemorrhage Expansion With Noncontrast Computed Tomography
Stroke 49:1163-1169, Morotti, A.,et al, 2018

A 30-year-old man with headache and sleep disturbance
Neurol 90:e1535-e1540, English, S.W.,et al, 2018

The critical role of histopathology in diagnosing cancer-associated necrotizing CNS vasculitis
Neurol 90:808-811, Sheehan, J.,et al, 2018

Toxidrome Recognition in Chemical - Weapons Attacks
NEJM 378:1611-1620, Ciottone, G.R., 2018

Acute Amnestic Syndrome Associated with Fentanyl Overdose
NEJM 378:1157-1158, Barash, J.A., et al, 2018

Acute demyelinating polyneuropathy induced by nivolumab
JNNP 89:435-437, Fukumoto, Y.,et al, 2018

Gummatous Neurosyphilis
Neurol 90:e913-e914, Silva, H.S.,et al, 2018

Clinical Reasoning: A Teenager with Left Arm Weakness
Neurol 90:e907-e910, Al-Ghamdi, F.,et al, 2018

Clinicopathologic Conference, Homocystinuria due to genetic mutations of the gene encoding cystathionine B-synthase (CBS)
NEJM 378:941-948, Case 7-2018, 2018

Atrophy Patterns in Cerebral Amyloid Angiopathy With and Without Cortical Superficial Siderosis
Neurol 90:e1751-e1758, Kim,J.,et al, 2018

Cerebral Venous Sinus Thrombosis in Homocystinuria: Dietary Intervention in Conjunction with Anticoagulation
Sage Open Med Case Reports 5:1-4, Yap, S.,et al, 2017

Intracranial Meningeal Enhancement Characterization
Rev Colomb Radiol 28:4709-4716, Mera, J.L.C.,et al, 2017

Guillain-Barre Syndrome following tuberculosis: A rare association
J Neurosci Rural Pract 8:296-299, Lakhotia, A.N.,et al, 2017

Disseminated Aspergillosis in an HIV-positive Cannabis user taking steroid treatment
Lancet Infect Dis 17:882, Salam, A.P. & Pozniak, A.L., 2017

Glial Fibrillary Acidic Protein Immunoglobulin G as Biomarker of Autoimmune Astrocytopathy: Analysis of 102 Patients
Ann Neurol 81:298-309, Flanagan, E.P.,et al, 2017

Clinicopathologic Conference, Paroxysmal Nocturnal Hemoglobinuria
NEJM 377:2581-2590, Case 40-2017, 2017

Huntington Disease: Clinical Features and Diagnosis
UptoDate Dec 2017, Oksana Suchowersky, 2017

Clinicopathologic Conference, Copper Deficiency Myelopathy
NEJM 377:1977-1984, Case 35-2017, 2017

Myeloperoxidase-Anti-Neutrophil Cytoplasmic Antibody-Positive Hypertrophic Pachymeningitis
Neurol 89:e253-e254, Culbertson, C.J.,et al, 2017

Evolution of DWI lesions in Cerebral Amyloid Angiopathy
Neurol 89:2136-2142, Van Veluw, S.J.,et al, 2017

An 82-year-old man with Worsening Gait
Neurol 89:e246-e252, Chew, S.,et al, 2017

Spaceflight-Induced Changes in White Matter Hyperintensity Burden in Astronauts
Neurol 89:2187-2191, Alperin, N.,et al, 2017

A Man with Paraesthesia, Headache, and Vertigo
BMJ 359:j5165, ODay, J. & Bhatt, P., 2017

Should Patients with Ischemic Stroke or Transient Ischemic Attack with Atrial Fibrillation and Microbleeds be Anticoagulated?
Stroke 48:3408-3412, Shoamanesh, A.,et al, 2017

Imaging Characteristics of Venous Parenchymal Abnormalities
Stroke 48:3258-3265, Arnoux, A.,et al, 2017

Paraneoplastic and Autoimmune Encephalitis
UptoDate July, Dalmau, J.,et al, 2017

The Useless Hand of Oppenheim
Pract Neurol 17:464-468, Wiblin, L. & Guadagno, J., 2017

Clinicopathologic Conference, Biotinthiamine-Responsive Basal Ganglia Disease Due to Mutation SLC19A3
NEJM 377:2376-2385, Case 38-2017, 2017

Redefining the Pulvinar Sign in Fabry Disease
AJNR 38:2264-2269, Cocozza, S.,et al, 2017

Neuroimaging Changes in Menkes Disease, Part 1
AJNR 38:1850-1857, Manara, R.,et al, 2017

Basal Ganglia T1 Hyperintensity in Hereditary Hemorrhagic Telangiectasia
AJNR 38:1929-1933, Parvinian, A.,et al, 2017

Computed Tomographic Perfusion to Predict Response to Recanalization in Ischemic Stroke
Ann Neurol 81:849-856, Lansberg, M.G.,et al, 2017

Brain Imaging in Myotonic Dystrophy Type 1
Neurol 89:960-969, Okkersen, K.,et al, 2017

Syringomyelia
BMJ 358:j3811, Takada, T.,et al, 2017

Intrathecal 2-hydroxypropyl-�-cyclodextrin Decreases Neurological Disease Progression in Niemann-Pick disease, type C1: a non-randomised, open-label, phase 1-2 trial
Lancet 390:1758-1768, Ory, D.S.,et al, 2017

A 46-year-old man with Persistent Hiccups, Cognitive Dysfunction, and Imbalance
Neurol 89:e193-e196, Lamb, C.J.,et al, 2017

My Weeping Patient
Neurol 89:e202, Peters, J.,et al, 2017

MR Neurography for the Diagnosis of Hypertrophic Neuropathies
Neurol 89:e201, Sgobbi de Souza, P.V.,et al, 2017

Clinicopathologic Conference, Eosinophilic Granulomatosis with Polyangiitis
NEJM 377:1569-1578, Case 32-2017, 2017

T2*-Based MR imaging of hyperglycemia-induced hemichorea-hemiballism
J Neuroradiol 44:31-37, Yu, F.,et al, 2017

Hypoglossal Nerve Palsy due to Basilar Invagination
Neurol 89:e214-e215, Bakhsheshian, J.,et al, 2017

Island Sign - An Imaging Predictor for Early Hematoma Expansion and Poor Outcome in Patients with Intracerebral Hemorrhage
Stroke 48:3019-3025, Li, Q.,et al, 2017

A Case of Ataxia, Seizure, and Choreoathetosis in a 34-year-old Woman
Neurol 89:e220-e223, Xiao, F. & Wang, X.F., 2017

A Returning Traveler with Epilepsy
BMJ 359:J4664, Bandi, H.,et al, 2017

Effects of Spaceflight on Astronaut Brain Structure as Indicated on MRI
NEJM 377:1746-1753, Roberts, D.R.,et al, 2017

Maternal Use of antiepileptic Agents During Pregnancy and Major Congenital Malformations in Children
JAMA 318:1700-1701, Bromley, R.L.,et al, 2017



Showing articles 1800 to 1850 of 13819 << Previous Next >>