Neurology Specific Literature Search   
 
[home][thesaurus]
    

Differential
(Click to cross reference)
abscess, intracerebral
abscess, intracerebral, multiple
achilles tendon, enlarged
acute ataxia of childhood
acute cerebellar ataxia
adolescent medicine
adult-onset leukodystrophy, with neuroaxonal spheroids
advances in neurology
adverse drug reaction
affect, flat
agitation
akathisia
alcohol intolerance
alpha-synuclein
alternating hemiplegia
alternating hemiplegia of childhood
alternating rapid movement
alternating rapid movement, impaired
Alzheimer's disease, misdiagnosis
amphetamines
amyotrophic lateral sclerosis
anemia
angiography, cerebral
animal exposure
ankle edema
anorexia
anosmia
anti IgLON5
anti Tr antibodies
anti Yo antibody
antidepressant
aphasia
aphonia
apnea
areflexia
ascites
ataxia
ataxia telangiectasia
ataxia, acute onset
ataxia, cerebellar
ataxia, progressive
ataxia, sensory
ataxia, truncal
ataxic gait
ATP1A3 gene
atypical
autoantibodies
autoimmune cerebellar ataxia
autoimmune disease
autoimmune encephalopathy
automatic behavior
automobile accidents
autonomic dysfunction
axonal spheroid
B 12 deficiency
B12
Babinski sign
basal ganglia, lesion of
basal ganglia, lesion, bilateral
behavioral disorder
Benedikt's syndrome
biologic markers
bovine spongiform encephalopathy
bradykinesia
bradyphrenia
brain atrophy
brain biopsy
brainstem, atrophy
brainstem, lesion of
brainstem, syndrome
bulbar palsy
burning paresthesia
C0ORF72
CAG repeats
carbon monoxide poisoning
carcinoma
carcinoma of breast
CAT scan, abnormal
CAT scan, angiography
CAT scan, angiography, false negative
CAT scan, emission, abnormal
CAT scan, venography
catalepsy
cataplexy
cataracts
cauda equina, enhancement
caudate nucleus, lesion of, bilateral
central nervous system, infection of
cerebellar ataxia, autosomal recessive
cerebellar ataxia, hereditary
cerebellar ataxia, neuropathy and vestibular areflexia syndrome
cerebellar atrophy, primary
cerebellar atrophy, secondary
cerebellar cognitive affective syndrome
cerebellar degeneration
cerebellar lesion
cerebellitis
cerebellitis, autoimmune
cerebellum, disease of
cerebral cortex
cerebral cortical atrophy
cerebral edema
cerebrospinal fluid, abnormal
cerebrospinal fluid, oligoclonal IgG in
cerebrospinal fluid, protein of
cerebrovascular accident, mimics
ceruloplasmin, serum
chewing movements
children
chills
choking
chorea
choreoathetosis
chromosomal abnormality
cingulate island sign
Claude's syndrome
Clinical Pathologic Conference(C.P.C.)
clonus
cognition
cognition, slowed
cogwheel rigidty
coma
coma, episodic
complications
confabulation
confusion
constipation
controversies in neurology
conversion reaction
corpus callosum, lesion of
cough
cranial nerve enhancement
cranial neuropathy
cranial neuropathy, multiple
Creutzfeldt-Jakob disease, genetic
crying, pathologic
cystatin C mutation
deep gray nuclei
degenerative diseases of CNS
delay in diagnosis
delusion
dementia
dementia, age at onset
dementia, familial
dementia, frontal lobe type
dementia, frontotemporal
dementia, presenile
dementia, rapidly progressive
dementia, reversible
dementia, thalamic
dementia, transmissible
dementia, treatment of
depression
developmental retardation
diabetes mellitus
diagnostic criteria
diarrhea
diet
differential diagnosis
difficulty climbing stairs
diplopia
disability, neurological
dizziness
dopa responsive dystonia
down-beat nystagmus
DPPX
DPPX, antibodies, encephalitis
driving
drooling
drowsiness
dural arteriovenous malformation
dysarthria
dysdiadochokinesia
dyskinesia
dysmetria
dysphagia
dystonia
dystonia, face
dystonia, focal
ear, pain in
edema, pedal
efficacy
electroencephalogram, periodic complexes
electromyogram
encephalitis
encephalitis, acanthamoeba
encephalitis, amebic
encephalitis, autoimmune
encephalomyelitis, postinfectious
encephalopathy
encephalopathy, delayed
encephalopathy, progressive
enolase
epidemiology of neurology
episodic disorders
episodic neurologic deficits
episodic unconsciousness
Epstein-Barr virus
Erdheim-Chester disease
escherichia coli
esophageal varices
executive dysfunction
exercise intolerance
eye movement, disorders of
facial expression abnormality
faciobrachial dystonic seizure
falling
false negative
familial
fasciculation
fatal familial insomnia
fatigue
fever
fine motor function, impaired
finger nose finger test
finger numbness
fingerprint bodies
Fisher C.M.
fistula, arterio-venous, dural
fluency
foam cells
foot numbness
Friedreich's ataxia
frontal lobe, anatomy and physiology
frontal lobe, atrophy
frontotemporal dementia, behavioral variant
gait disorder
gait, festinating
gamma amino butyric acid
gammaglobulin therapy, intravenous
gaze palsy, horizontal
gene
gene mutation
genetic counselling
genetic neurologic disorders
genetic testing
genu of corpus callosum
granular osmiphilic material
growth hormone
gyrus, abnormal
hallucination
hallucination, hypnagogic
hallucination, visual
hand weakness
hands, fisted
handwriting
head nodding
headache
hearing loss
heel swelling
heel-knee-shin test
hemidystonia
hemimyoclonic jerks
hemiparesis
hemorrhage, thalamic
hepatic encephalopathy
hepatic failure
hepatolenticular degeneration(Wilson's disease)
hepatolenticular degeneration(Wilson's disease), presymptomatic
heralding manifestation
herniation syndromes, intracranial
histiocytosis
HLA
hoarseness
hyperesthesia
hyperosmolality
hyperreflexia
hypersomnia
hypersomnia, idiopathic
hypoalbuminemia
hypocretin
hypoglycemia
hypometric saccades
hyponatremia
hypophonia
hyposmia
hypothalamus
hypotonia
iatrogenic neurologic disorders
imbalance
imbalance, postural
immunocompetent
immunohistochemistry
immunologic disease
immunomodulation
immunosuppression
immunotherapy
impulsivity
inattention
inclusion bodies
inclusion bodies, eosinophilic cytoplasmic
inclusion bodies, intranuclear
incontinence, fecal
incoordination
infectious mononucleosis
infectious mononucleosis, neurologic findings with
inferior olivary nucleus
insight, loss
insomnia
intellectual deficit
intellectual deterioration
intracranial hypertension, benign
intracranial pressure, increased
Jakob-Creutzfeldt disease
Jakob-Creutzfeldt disease, cerebellar variant
Jakob-Creutzfeldt disease, variant
Jakob-Creutzfeldt disease, young adult
Kayser-Fleischer ring
lactic acidemia
lateropulsion
laughing, pathologic
L-dopa
leg weakness, bilateral
lesions too numerous to count
leucine rich glioma inactivated 1 antibodies
leukocytosis
leukodystrophy
leukoencephalopathy
leukoencephalopathy, adult onset, sporadic
leukopenia
Lewy body
Lewy body disease, diffuse
limbic encephalitis
liver disease
liver function enzymes
lobar atrophy
logopenia
lumbar puncture, complications of
lymphoma
lymphoma involving CNS
lymphoma, primary of CNS
masked facies
MELAS syndrome
memory, defect of recent
memory, impairment of
meningeal enhancement
meningitis
meningitis, acinetobacter calcoaceticus var.antitratus
meningitis, carcinomatous
meningoencephalitis
meningoencephalitis, amoebic
mental status, abnormal
microcephaly
microhemorrhage, intracerebral
midbrain
midbrain, atrophy
midbrain, infarction of
midbrain, lesion of
middle cerebellar peduncle, lesion
migraine
mild cognitive impairment
mimics
misdiagnosis
mitochondrial disease
mitochondrial encephalomyopathy
modafinil
molecular genetics
monoclonal antibodies
mood change
mortality
motor neuron disease
motor neuron disease, misdiagnosis
movement disorder
movement disorder, extrapyramidal
movement disorder, hyperkinetic
MRI
MRI, abnormal
MRI, angiography
MRI, angiography, false negative
MRI, contrast enhanced
MRI, diffusion weighted
MRI, disappearing lesion on
MRI, false negative
MRI, fast
MRI, negative
MRI, perfusion
MRI, punctate pattern
MRI, venography
multiple sclerosis
multiple sclerosis, differential diagnosis of
multiple sclerosis, misdiagnosis
multiple sleep latency test
multiple system atrophy
muscle biopsy
muscle weakness, proximal
mutism
myasthenia gravis
myelinolysis, extrapontine
myelomalacia
myoclonic jerks
myoclonus
myoclonus, epilepsy
myopathy
myopathy, mitochondrial
myxedema, neurologic manifestations of
narcolepsy
nausea and vomiting
negative
nerve conduction studies
nerve root biopsy
neuroaxonal dystrophy
neuroaxonal leukodystrophy
neuroleptic
neuroleptic sensitivity
neurologic complications of, systemic disease
neurologic disease, diagnoses of
neurologic examination, focal
neurologic signs
neuron specific enolase
neuronal ceroid-lipofuscinosis
neuronal intranuclear inclusion disease
neuronal loss
neuronopathy, sensory
neuropathology
neuropathology, brain
neuropathy
neuropathy, sensory
next-generation sequencing
night sweats
Nothnagel's syndrome
numbness, generalized
nutritional deficiency
nystagmus
nystagmus, monocular
nystagmus, primary position of gaze
old age, neurology of
olivary degeneration, hypertrophic
ophthalmoplegia
ophthalmoplegia, progressive external
opportunistic infection
opportunistic infection, CNS
optic atrophy
orthostatic hypotension
osmotic demyelination syndrome
otitis, neurologic complications with
palatal myoclonus
paraneoplastic cerebellar degeneration
parasitic infection
parasitic infection, CNS
paresthesias
paresthesias, hands
parietal lobe, atrophy
Parkinson disease
Parkinson disease, dementia with
Parkinson disease, dystonia with
Parkinson disease, juvenile
Parkinson disease, L-dopa nonresponsive
Parkinson disease, nonmotor problems of
Parkinson disease, presymptomatic detection
Parkinsonism syndrome
paroxysmal hemiplegia
paroxysmal neurologic deficits
PAS positive
PAS positive material in the brain
pathologic reflex
penicillamine
perseveration
personality change
pituitary, hormones of
pleocytosis of cerebrospinal fluid
pleocytosis of cerebrospinal fluid, neutrophilic
POLG1 gene
polymerase chain reaction
polyneuropathy, chronic inflammatory demyelinating
polysomnogram
pons, lesion of
positional head-hanging test
post infectious cerebellar ataxia
posterior cortical atrophy
postinfectious
postural abnormality
potassium channel antibodies
practice guidelines
precipitating factors
pregnancy, neurologic complications in
prion disease
PRKN gene
prognosis
progressive ataxia and palatal tremor
progressive neurologic disorder
protein 14-3-3, cerebrospinal fluid
protein 14-3-3, cerebrospinal fluid, false negative
proteinuria
protozoan infection
pseudobulbar palsy
psychiatric disorder
psychiatric problems in neurologic disorders
psychomotor retardation
psychosis
psychosis, acute
ptosis
ptosis, bilateral
pull test
pupil, dilated and fixed, bilateral
pursuit eye movements, abnormal
rapid onset dystonia parkinsonism
rapidly fatal neurologic illness
rapidly progressing neurologic illness
reading disorder, acquired
real-time quaking-induced conversion
recurrent
regional cerebral blood flow
rehabilitation for neurologic disorders
release phenomena
REM sleep
REM sleep behavior disorder
remote effect of cancer on the nervous system
renal failure
renal stones
retropulsion
review article
RFC1 gene
rigidity
ritalin
rituximab
Romberg's sign
saccadic eye movements, abnormal
safety
salivation, excessive
sarcoidosis
schizophrenia
seizure
seizure, psychomotor-temporal lobe
selective serotonin reuptake inhibitors
sensorineural hearing loss
sensory loss, leg
sexual intercourse
short stature
sinemet
single photon emission computed tomography
sleep
sleep apnea
sleep offset paralysis
sleep onset paralysis
sleep paralysis
sleep pathology and physiology
slit lamp examination
slurred speech
smell
snoring
somnolence
spasticity
speech disorder
speech disorder, non aphasic
spinocerebellar ataxia
spinocerebellar ataxia type 7
splenomegaly
spongy degeneration of brain
spontaneous remission
square wave jerks
staggering
startle myoclonus
startle reaction
status epilepticus
stimulant drugs
storage disease of CNS
strokelike episodes
stuttering
suicide
swallow evaluation
sweating
symmetric brain lesions
synucleinopathy
systemic illness
tandem gait, ataxic
tau protein
tauopathy
temporal lobe, atrophy
temporal lobe, lesion
temporal lobe, lesion, bilateral
thalamus, lesion of
thalamus, lesion of-bilateral
third nerve palsy
third nerve palsy, bilateral
thrombocytopenia
titubation
tongue, fasciculations of
tonic foot response
treatment of neurologic disorder
tremor
tremor, cerebellar
tremor, intention
tremor, postural
trientine dihydrochloride
trinucleotide repeats
uncal herniation
unconsciousness
unconsciousness, episodic
unconsciousness, transient
undiagnosed
upgaze, paralysis of
urinary incontinence
vegetarianism
venous hypertension
venous ischemia
vertigo
vestibular areflexia
vestibulopathy
vibratory sensation, abnormal
viral infection
viral infection, CNS
vision, blurred
visual acuity, decreased
visuospatial disturbance
vitamin deficiency
vitamin E deficiency
vitiligo
vocalizations
voice, abnormality of
walking frame
walking, difficulty with
walking, difficulty with in dark
weakness
weakness, generalized
weakness, progressive
weight gain
weight loss
wheelchair
white matter disease
wide based gait
work loss
workup
zinc
Showing articles 400 to 450 of 1850 << Previous Next >>

Delayed Onset of Progressive Chorea After Acute Basal Ganglia Injury
Mov Disord 28:585-587, Virmani, T.,et al, 2013

The Frequency of Autoimmune N-Methyl-D-Aspartate Receptor Encephalitis Surpasses That of Individual Viral Etiologies in Young Individuals Enrolled in the California Encephalitis Project
Clin Inf Dis 54:899-904, Gable, M.S.,et al, 2012

Evidence-based Guideline: Diagnostic accuracy of CSF 14-3-3 Protein in Sporadic Creutzfeldt-Jakob Disease
Neurol 79:1499-1506, Muayqil, T.,et al, 2012

Dropped Head Syndrome: Report of Three Cases During Treatment with a Mek Inhibitor
Neurol 79:1929-1932, Chen, X.,et al, 2012

Alemtuzumab for Multiples Sclerosis: Who and When to treat?
Lancet 380:1795-1797, 1792, Springer, T. & Kappos, L., 2012

Adult-Onset Opsoclonus-Myoclonus Syndrome
Arch Neurol 69:1598-1607, Klaas, J.,et al, 2012

Differential Diagnosis of Jakob-Creutzfeldt Disease
Arch Neurol 69:1578-1582,1554, Paterson, R.,et al, 2012

CAG Repeat Expansion in Huntington Disease Determines Age at Onset in a Fully Dominant Fashion
Neurol 78:690-695, Lee,J.M.,et al, 2012

Clinical Reasoning: A 13-year-old Boy Presenting with Dystonia,Myoclonus,and Anxiety
Neurol 78:e72-e76, Blackburn,J.S. and Cirillo,M.L., 2012

Progressive Weakness with Respiratory Failure in a Patient with Sarcoidosis
Arch Neurol 69:534-537, Chaudhry,P.,et al, 2012

Acute Stroke Imaging: What is Sufficient for Triage to Endovascular Therapies?
AJNR 33:790-792, Lev, M.H., 2012

Acute Stroke Imaging: CT with CT Angiography and CT Perfusion before Management Decisions
AJNR 33:792-794, Fox, A.J.,et al, 2012

Development of a Suspicion Index to Aid Diagnosis of Niemann-Pick Disease Type C
Neurol 78:1560-1567,1546, Wijburg, F.A.,et al, 2012

A Musicians Dystonia
Lancet 379:2116, Vecchio, M.,et al, 2012

Clinicopathologic Conference, Villaret Syndrome (Ipsilateral Cranial Nerves and Cervical Sympathetic Fibers) due to a Carotid-Artery Dissection and an Associated Aneurysm
NEJM 366:2306-2313, Case 18-2012, 2012

Immunotherapy-Responsive Chorea as the Presenting Feature of LGI1-Antibody Encephalitis
Neurol 79:195-196, Tofaris,G.K.,et al, 2012

Evidence-Based Guideline: Pharmacologic Treatment of Chorea in Huntington Disease
Neurol 79:597-603, Armstrong, M.J. & Miyasaki, J.M., 2012

Acquired Neurosyphilis Presenting as Movement Disorders
Mov Disord 27:690-695, Shah, B.B. & Lang, A.E., 2012

Ipsilateral Stroke in a Patient with Horizontal Gaze Palsy with Progressive Scoliosis and a Subcortical Infarct
Stroke 42:e1-e3, Ng, A.S.L.,et al, 2011

Cortical Restricted Diffusion as the Predominant MRI Finding in Sporadic Creutzfeldt-Jakob Disease
Acta Radiologica 52:336-339, Talbott,S.D.,et al, 2011

Clinicopathologic Conference, Thymoma with Paraneoplastic Myasthenia Gravis, Polymyositis and Myocarditis, and Brain Stem Encephalitis
NEJM 365:2413-2422, Case 39-2011, 2011

Epstein-Barr Virus Infections of the Nervous System
www.medlink.com, Nov, Amlie-Lefond,C., 2011

PANDAS
www.medlink.com,Feb, Erfe,M.C.B., 2011

Trigger Factors and Their Attributable Risk for Rupture of Intracranial Aneurysms A Case-Crossover Study
Stroke 42:1878-1882, Vlak, M.H.M.,et al, 2011

Movement Disorders Emergencies Part 2 Hyperkinetic Disorders
Arch Neurol 68:719-724, Robottom, B.J.,et al, 2011

A Sleeping Giant
NEJM 365:72-77, Morris, A.,et al, 2011

Advanced Brain Imaging Studies Should Be Performed in Patients With Suspected Stroke Presenting Within 4.5 Hours of Symptom Onset
Stroke 42-2666-2667,2670, Parsons, M.W., 2011

Advanced Brain Imaging Studies Should Not Be Performed in Patients With Suspected Stroke Presenting Within 4.5 Hours of Symptom Onset
Stroke 42:2668-2669,2670, Lyden, P.D., 2011

Paraneoplastic Upbeat Nystagmus
Neurol 77:691-693, Wray, S.H.,et al, 2011

Rapidly Progressive Alzheimer Disease
Arch Neurol 68:1124-1130, Schmidt, C.,et al, 2011

Treatable Neurological Disorders Misdiagnosed as Creutzfeldt-Jakob Disease
Ann Neurol 70:437-444, Chitravas, N.,et al, 2011

Treatment of Severe Neurological Deficits with IgG Depletion through Immunoadsorption in Patients with Escherichia coli O104:H4-Associated Haemolytic Uraemic Syndrome: A Prospective Trial
Lancet 378:1166-1173,1120, Greinacher, A.,et al, 2011

GFAP Mutations, Age at Onset, and Clinical Subtypes in Alexander Disease
Neurol 77:1287-1294, Prust, M.,et al, 2011

An Embolic Bow Hunters Stroke Associated with Anomaly of Cervical Spine
Neurol 77:1403-1404, Sakamoto, Y.,et al, 2011

Evidence-based guideline update: Treatment of Essential Tremor
Neurol 77:1752-1755, Zesiewicz, T.A.,et al, 2011

Vertebral Artery Dissection Leading to Stroke Caused by Violent Neck Tics of Tourette Syndrome
Neurol 77:1706-1707, Lehman, L.L.,et al, 2011

Epidemic Profile of Shiga-Toxin-Producing Escherichia coli O104:H4 Outbreak in Germany
NEJM 365:1771-1780, Frank, C.,et al, 2011

Diagnosis and Treatment of Psychogenic Parkinsonism
JNNP 82:1300-1303, Jankovic, J., 2011

Acutely Injured Patients on Dabigatran
NEJM 365:2039-2040, Cotton, B.A.,et al, 2011

Cerebral Blood Flow is the Optimal CT Perfusion Parameter for Assessing Infarct Core
Stroke 42:3435-3440, Campbell, B.C.V.,et al, 2011

Clinicopathologic Conference, Cystoisospora Belli Enteritis and HIV Infection
NEJM 365:2306-2316, Case 38-2011, 2011

Autoimmune Encephalopathy
Semin Neurol 31:144-157, Flanagan, E.,et al, 2011

Intravenous Thrombolytic Therapy for Acute Ischemic Stroke
NEJM 364:22, Wechsler, L.R., 2011

The Evaluation of Rapidly Progressive Dementia
The Neurologist 17:67-74, Rosenbloom,M.H. &Atri,A., 2011

Multimodal Imaging Does Not Delay Intravenous Thrombolytic Therapy in Acute Stroke
AJNR 32:864-68, Salottolo, K.M.,et al, 2011

Diffusion-weighted MRI hyperintensity patterns differentiate CJD from other rapid dementias
Neurol 76:1711-1719, Vitali, P.,et al, 2011

Movement Disorders Emergencies Part 1
, Robottom, B.J., et al, 2011

A Case of Hashimoto Encephalopathy Clinical Manifestation, Imaging, Pathology, Treatment, and Prognosis
The Neurologist 17:141-143, Zhao, W.,et al, 2011

Myasthenia Gravis as a Cause of Head Drop in Parkinson Disease
The Neurologist 17:144-146, Uludag, I.F.,et al, 2011

Rapidly Progressive Corticobasal Degeneration Syndrome
Case Rep Neurol 3:185-190, Herrero Valverde, A.,et al, 2011



Showing articles 400 to 450 of 1850 << Previous Next >>