Neudle.com: MRI rapid

Differential
(Click to cross reference)

abdominal reflex, absent

abulia

acetylcysteine

acute ataxia of childhood

acute cerebellar ataxia

adenovirus infection

adenylate kinase 5 autoantibodies

adrenal lesion

adrenoleukodystrophy

adrenoleukodystrophy, adult onset

adult-onset leukodystrophy, with neuroaxonal spheroids

advances in neurology

adverse drug reaction

affect, flat

agitation

akinetic mute

Alberta Stroke Program Early CT score

algorithm

alien hand syndrome

alternating rapid movement

alternating rapid movement, impaired

Alzheimer's disease

amnesia

amyloid angiopathy, cerebral

amyloid angiopathy, cerebral, inflammatory type

aneurysm, intracranial

angiitis, isolated of CNS

angiitis, isolated of CNS, tumefactive

angiography, cerebral, beaded vessels

angiography, cerebral

angiography, cerebral, false negative

angiography, cerebral, negative

ankle edema

anorexia

anterior cerebral artery, occlusion of

anterior temporal branch of posterior cerebral artery

anti IgLON5

anti Yo antibody

antibodies to voltage-gated calcium channels

antithyroid antibodies

arteriovenous malformation

arteriovenous malformation, cerebral

arteritides

arthritis

artificial intelligence

ascites

asterixis

ataxia

ataxia telangiectasia

autoimmune encephalopathy

autoimmune meningitis

automobile accidents

autonomic cardiovascular reflexes

autonomic dysfunction

basal ganglia, lesion of

basal ganglia, lesion, bilateral

brain biopsy, false negative

brain biopsy, indication

brain biopsy, negative

brainstem, atrophy

brainstem, lesion of

brucellosis

brucellosis, nervous system involvement with

calcification, intracranial

carcinoma

carcinoma of breast

carotid artery disease, noninvasive evaluation of

carotid artery occlusion, intracranial

carotid artery stenosis

CAT scan

CAT scan, abnormal

CAT scan, angiography

CAT scan, angiography, false negative

CAT scan, angiography, false positive

CAT scan, complication with

CAT scan, contrast enhanced

CAT scan, dense artery sign

CAT scan, early changes in CVA

CAT scan, emission

CAT scan, emission, abnormal

CAT scan, false negative

CAT scan, false positive

CAT scan, indications for

CAT scan, mismatch between cerebral blood volume/flow

CAT scan, mismatch between perfusion/diffusion

CAT scan, perfusion

CAT scan, venography

cataracts

cauda equina, enhancement

caudate nucleus, lesion of, bilateral

cavernous sinus, syndrome

CD4 counts

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 autosomal dominate arteriopathy with subcortical infarction and leukoencephalopathy

cerebral autosomal recessive arteriopathy with subcortical infarction and leukoencephalopathy

cerebral blood flow

cerebral cortex

cerebral cortical atrophy

cerebral death

cerebral edema

cerebral edema, vasogenic

cerebral embolism

cerebral embolism, cardiac origin

cerebral embolism, mechanical extraction

cerebral infarction

cerebral infarction, hemorrhagic

cerebral infarction, subcortical

cerebral ischemia

cerebral palsy, work up

cerebral venous infarction

cerebral venous thrombosis

cerebral venous thrombosis, deep

cerebroretinal microangiopathy with calcifications and cysts

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, beta-D-glucan

cerebrospinal fluid, cytology

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, lactic acid concentration

cerebrospinal fluid, oligoclonal IgG in

cerebrospinal fluid, red cells in

cerebrospinal fluid, xanthochromia of

cerebrovascular accident

cerebrovascular accident, acute management of

cerebrovascular accident, age of lesion

cerebrovascular accident, arterial occlusion, location

cerebrovascular accident, awakening with

cerebrovascular accident, bilateral

cerebrovascular accident, delay in treatment

cerebrovascular accident, mimics

cerebrovascular accident, misdiagnosis

cerebrovascular accident, multiple

cerebrovascular accident, non atherosclerotic cause of

cerebrovascular accident, nonvascular territory

cerebrovascular accident, prognosis in

cerebrovascular accident, severity

cerebrovascular accident, surgical treatment of

cerebrovascular accident, three territory involvement

cerebrovascular accident, thrombolytic agents in treatment

cerebrovascular accident, time of onset

cerebrovascular accident, time of presentation

cerebrovascular accident, time to treatment

cerebrovascular accident, topographic pattern

cerebrovascular accident, unknown time of onset

cerebrovascular accident, vascular territory involved

cerebrovascular accident, volume

cerebrovascular accident, work up for

cerebrovascular accident, young adult

cerebrovascular disease

cerebrovascular disease, noninvasive evaluation of

choroid plexus, enhancement

chromosomal abnormality

chromosome 20

cingulate island sign

clinical mismatch

Clinical Pathologic Conference(C.P.C.)

clot retrieval

cognition

cognition, slowed

collateral circulation

concentration, impaired

confusion

constipation

contrast agent

contrast agents, neurotoxicity of

controversies in neurology

corneal transplant

corpus callosum, lesion of

cortical blindness

cortical infarction

cortical infarction, small

cortical-basal ganglionic degeneration

cranial nerve enhancement

cranial nerve palsies

cranial nerve palsies, bilateral

cranial neuropathy

cranial neuropathy, multiple

creatinine, elevated

Creutzfeldt-Jakob disease, genetic

cryptococcal meningitis

degenerative diseases of CNS

dementia, age at onset

dementia, autoimmune

dementia, cerebrovascular disease causing

dementia, diagnostic evaluation of

dementia, differential diagnosis of

dementia, familial

dementia, frontotemporal

dementia, presenile

dementia, rapidly progressive

dementia, reversible

dementia, screening for

dementia, thalamic

dementia, transmissible

dementia, treatment of

demyelinating disease

denial of blindness(Antons syndrome)

dense middle cerebral artery sign

dense posterior cerebral artery sign

dentate nuclei, lesion of

differential diagnosis

difficulty climbing stairs

diplopia

disability rating scale, neurological

disorientation

dizziness

down-beat nystagmus

down-beat nystagmus, primary position of gaze

DPPX

DPPX, antibodies, encephalitis

driving

drooling

dural arteriovenous malformation

dural sinus thrombosis

EDTA(ehtylenediamine tetraacetic acid)

efficacy

electroencephalogram

electroencephalogram, abnormalities of

electroencephalogram, focal delta activity

electroencephalogram, periodic complexes

electromyogram

electron microscopy

ELISA

emergencies, neurologic

emergency room, treatment of stroke

emergent neuroimaging

encephalitis

encephalitis, acanthamoeba

encephalitis, amebic

encephalitis, autoimmune

encephalitis, bornavirus

encephalitis, brainstem

encephalitis, viral

encephalomyelitis, postinfectious

encephalopathy

encephalopathy, Hashimoto's

encephalopathy, metabolic

encephalopathy, progressive

endemic area

endovascular therapy

endovascular therapy, futile interhospital transfer

endovascular therapy, late time window

endovascular therapy, selection criteria

endovascular therapy, time window

enolase

ependymitis

episodic disorders

episodic neurologic deficits

episodic unconsciousness

Epstein-Barr virus

esophageal varices

executive dysfunction

exercise intolerance

EXTEND trial

extralimbic encephalitis

eye movement, disorders of

Fabry's disease

facial expression abnormality

facial nerve palsy, bilateral

facial pain

facial weakness

faciobrachial dystonic seizure

fibrinolytic agents, intra-arterial local infusion

fibrinolytic therapy, selection criteria

fibrinolytic therapy, timing of administration

fine motor function, impaired

finger nose finger test

finger numbness

fistula, arterio-venous

fistula, arterio-venous, dural

fourth ventricle, floor

Friedreich's ataxia

frontal lobe, anatomy and physiology

frontal lobe, atrophy

frontal lobe, pathologic signs of

fundus, abnormality of

gadolinium

gait disorder

gait, apraxic

gammaglobulin therapy, intravenous

gaze palsy

gaze palsy, supranuclear

genetic neurologic disorders

genetic testing

genu of corpus callosum

Gerstmann-Straussler-Scheinker disease

hallucination, visual

headache, sudden onset of

hearing loss

hearing loss, bilateral

hearing loss, rapidly progressive

hearing loss, sudden, bilateral

heel-knee-shin test

hematuria, microscopic

hemianopia

hemianopia, homonymous

hemidystonia

hemimyoclonic jerks

hemiparesis

hemiparesis, recurrent

hemiplegia

hemorrhage, thalamic

hemosiderosis of CNS, superficial

hepatic encephalopathy

hepatic failure

hepatolenticular degeneration(Wilson's disease)

hepatolenticular degeneration(Wilson's disease), presymptomatic

heralding manifestation

herniation syndromes, intracranial

herpes simplex encephalitis

hiccoughs

hiccoughs, intractable

highly active antiretroviral therapy

hippocampal atrophy

hippocampal infarction

hippocampus

hippocampus, hyperintense

HIV CSF viral escape syndrome

hoarseness

human immunodeficiency virus type 1

hypertensive encephalopathy

hypertensive encephalopathy, venous

hypertrophic intracranial pachymeningitis

iatrogenic neurologic disorders

immunosuppressive agents

infectious mononucleosis

infectious mononucleosis, neurologic findings with

inferior olivary nucleus

insomnia

intellectual deficit

intellectual deterioration

internal auditory canal

interobserver agreement

intracerebral hemorrhage

intracerebral hemorrhage, awakening with

intracerebral hemorrhage, lobar

intracranial pressure, increased

ischemic core

ischemic penumbra

Jakob-Creutzfeldt disease

Jakob-Creutzfeldt disease, cerebellar variant

Jakob-Creutzfeldt disease, Heidenhain variant

Jakob-Creutzfeldt disease, unilateral

Jakob-Creutzfeldt disease, variant

Jakob-Creutzfeldt disease, young adult

Kayser-Fleischer ring

Kernig's sign

lactate

lactic acidemia

lactic dehydrogenase(LDH)

lacunar infarction

laminar necrosis, cortical

lateropulsion

L-dopa

leg weakness, bilateral

lesions too numerous to count

lethargy

leucine rich glioma inactivated 1 antibodies

leukoencephalopathy, adult onset, sporadic

leukopenia

level of consciousness, decreased

Lewy body

Lewy body disease, diffuse

life expectancy

limbic encephalitis

linear lesion

listeria monocytogenes

listeriosis, CNS

liver disease

liver function enzymes

lobar atrophy

logopenia

lumbar puncture

lumbar puncture, complications of

lymphoma

lymphoma involving CNS

lymphoma, primary of CNS

lymphomatosis cerebri

malformation, vascular

malformation, vascular, cerebral

malformation, vascular, treatment of

manganese intoxication

Marburg's disease

masked facies

medulla oblongata, lesion of

melanocytoma, meningeal

MELAS syndrome

memory, defect of recent

memory, impairment of

memory, recent

meningeal biopsy

meningeal enhancement

meningeal enhancement, nodular

meningismus

meningitis

meningitis, aseptic

meningitis, bacterial

meningitis, carcinomatous

meningitis, chronic

meningitis, fungal

meningitis, helminthic

meningitis, listeria monocytogenes

meningitis, neutrophilic

meningitis, noninfectious

meningitis, parameningeal

meningitis, parasitic

meningitis, TB

meningitis, treatment of

meningitis, treatment of, empirical

meningitis, viral etiology in

meningitis-encephalitis PCR panel

meningoencephalitis

meningoencephalitis, amoebic

mental status, abnormal

mesial temporal lobe

microangiopathy, brain

micrographia

microhemorrhage, intracerebral

microsurgery

midbrain, atrophy

middle cerebral artery territory infarction

middle cerebral artery, occlusion of

middle cerebral artery, stenosis of

Middle east

migraine

mild cognitive impairment

mimics

Mini Mental Status Examination

misdiagnosis

mitochondrial disease

mitochondrial encephalomyopathy

molecular genetics

monoclonal antibodies

motor neuron disease, misdiagnosis

movement disorder

movement disorder, extrapyramidal

MRI, angiography, contrast enhanced

MRI, angiography, false negative

MRI, brain tumors

MRI, CAT scan compared to

MRI, cerebrovascular disease

MRI, contrast enhanced

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, early changes in CVA

MRI, false negative

MRI, fast

MRI, FLAIR

MRI, flow void, blood

MRI, functional

MRI, gradient-echo

MRI, high signal foci on

MRI, high signal intensity of basal ganglia

MRI, indications for

MRI, lesion burden

MRI, linear enhancement

MRI, mass effect on

MRI, mismatch between DWI/FLAIR

MRI, mismatch between perfusion/diffusion

MRI, negative

MRI, nodular enhancement

MRI, punctate pattern

MRI, sulcal hyperintensity

MRI, susceptibility weighted

MRI, T1 weighted high signal foci

MRI, venography

MRI, volumetry

MRS

multimodal neuroimaging

multinucleated giant cell

multiple sclerosis

multiple sclerosis, acute

multiple sclerosis, aggressive

multiple sclerosis, differential diagnosis of

multiple sclerosis, misdiagnosis

multiple system atrophy

muscle biopsy

muscle pain

muscle wasting, diffuse

muscle weakness

muscle weakness, proximal

mutism

myelinolysis, extrapontine

myelitis

myelitis, longitudinal

myoclonus, stimulus sensitive

myopathy

myopathy, mitochondrial

nausea and vomiting

neck pain

neoplasm, intracranial

neoplasm, metastatic

neoplasm, metastatic to CNS

neoplasm, metastatic to CNS-miliary

neoplasm, metastatic to eye

neoplasm, primary intracerebral

neoplasm, primary intracranial

neoplasm, primary of CNS

neoplastic angioendotheliosis

nerve conduction studies

nerve root biopsy

nerve root enhancement

neuroaxonal dystrophy

neuroaxonal leukodystrophy

neurocutaneous disease

neurocutaneous melanosis

neuroleptic

neurologic complications of, systemic disease

neurologic disease, diagnoses of

neurologic disease, multifocal

neurologic disease, tempo

neurologic examination, focal

neuron specific enolase

neuroophthalmology

neuropathology

neuropathology, brain

neuropathy

neuropathy, sensory

neuroradiology

next-generation sequencing

night sweats

NIH stroke scale

number needed to treat

numbness, generalized

nystagmus

nystagmus, primary position of gaze

occipital cortex

occipital lobe, infarction

occipital lobe, lesion of

old age, neurology of

olivary degeneration, hypertrophic

ophthalmoplegia

ophthalmoplegia, painful

ophthalmoplegia, progressive external

ophthalmoplegia, total

opportunistic infection

opportunistic infection, CNS

organ transplantation

osmotic demyelination syndrome

otitis, neurologic complications with

paralysis, acute areflexic

paraneoplastic cerebellar degeneration

paraparesis

paraphasias

parasitic infection

parasitic infection, CNS

paresthesias

paresthesias, hands

parietal lobe, atrophy

parietal lobe, lesion of

parietal lobe, syndromes of

Parkinson disease

Parkinson disease, atypical

Parkinson disease, dementia with

Parkinson disease, differential diagnosis of

Parkinson disease, L-dopa nonresponsive

Parkinson disease, rapid progression

Parkinson disease, treatment of

Parkinson disease, tremor, absence of

Parkinsonism multiple-system atrophy

Parkinsonism syndrome

paroxysmal neurologic deficits

PLEDs, bilateral independent

PLEDs, etiology of

pleocytosis of cerebrospinal fluid

pleocytosis of cerebrospinal fluid, neutrophilic

polymerase chain reaction

polymerase chain reaction, false negative

polyneuropathy, chronic inflammatory demyelinating

pons, lesion of

positional head-hanging test

positive sharp waves

post infectious cerebellar ataxia

posterior cerebral artery

posterior cerebral artery embolism

posterior cerebral artery territory infarction

posterior cerebral artery, fetal type

posterior circulation stroke

posterior cortical atrophy

postinfectious

postural abnormality

potassium channel antibodies

practice guidelines

preclinical

pregnancy, neurologic complications in

prion disease

prion protein gene

prognosis

progressive ataxia and palatal tremor

progressive neurologic disorder

progressive supranuclear palsy

proptosis

prosopagnosia

protein 14-3-3, cerebrospinal fluid

protein 14-3-3, cerebrospinal fluid, false negative

protein 14-3-3, cerebrospinal fluid, false positive

proteinuria

protozoan infection

pseudobulbar palsy

pseudomonas aeruginosa

pseudoxanthoma elasticum

psychiatric disorder

psychiatric problems in neurologic disorders

psychomotor retardation

pupil, dilated and fixed, bilateral

pursuit eye movements, abnormal

quality of life

radiation therapy, stereotactic

Rankin score

RAPID CT perfusion maps

rapid onset dystonia parkinsonism

rapidly fatal neurologic illness

rapidly progressing neurologic illness

reading disorder, acquired

real-time quaking-induced conversion

recanalization, arterial

REM sleep behavior disorder

remote effect of cancer on the nervous system

revascularization, surgical

reversible cerebral vasoconstrictive syndromes

reversible neurologic disorder

risk-benefit assessment

rituximab

Romberg's sign

rooting reflex

saccadic eye movements, abnormal

safety

salivation, excessive

sarcoidosis

sarcoidosis, CNS

screening

sedimentation rate, elevated

seizure

seizure, focal

seizure, psychomotor-temporal lobe

sensorineural hearing loss

short stature

simultanagnosia

single photon emission computed tomography

skin, biopsy

skin, lesions in neurologic disorders

sleep pathology and physiology

slit lamp examination

slurred speech

small vessel disease

small vessel vasculitis

speech disorder, non aphasic

speech, pressured

spinal cord

spinal cord, compression of

spinal cord, lesion of

spinal cord, neoplasm, extramedullary

spinal cord, neoplasm, extramedullary intradural

splenium of corpus callosum

splenomegaly

spongy degeneration of brain

spontaneous remission

steroid therapy, CNS treatment and complications with

stop working

straight sinus

stroke center

stroke disability scale

stroke protocol

stroke, progression of

strokelike episodes

subarachnoid hemorrhage

subarachnoid hemorrhage, cerebral convexity

subcortical hemorrhage

swallow evaluation

sweating

SWIFT PRIME Trials

symmetric brain lesions

temporal lobe, lesion

temporal lobe, lesion, bilateral

thalamus, infarction of

thalamus, infarction, bilateral

thalamus, lesion of

thalamus, lesion of-bilateral

thrombolysis, mechanical

tissue plasminogen activator, intravenous

titubation

toxic encephalopathy

transient neurologic deficit

transport of patient

treatment of neurologic disorder

trientine dihydrochloride

trigeminal neuropathy

trigeminal neuropathy, bilateral

uncal herniation

unconsciousness

unconsciousness, episodic

unconsciousness, transient

very long chain fatty acids

vestibulopathy

vibratory sensation, abnormal

visual acuity, decreased

visual field defect

visual loss

visual loss, progressive

visuospatial disturbance

vitamin E deficiency

vocalizations

voice, abnormality of

WAKE-UP trial

walking frame

walking, difficulty with

weakness

weakness, acute

weakness, focal

weakness, generalized

weakness, progressive

weakness, rapidly progressive

white matter disease, subcortical

Showing articles 50 to 100 of 6668 << Previous Next >>

Use of Imaging to Select Patients for Late Window Endovascular Therapy
Stroke 49:2256-2260, Albers, G.W., 2018

Atypical Parkinsonian Syndromes: A General Neurologists Perspective
Eur J Neurol 25:41-58, Deutschlander, A.B.,et al, 2018

Endovascular Stroke Therapy in the Late Time Window
Stroke 49:2559-2561, Schellinger, P.D. & Demaerschalk, B.M., 2018

Clinical Reasoning: A 49-year-old man with Progressive Numbness, Weakness, and Evidence of Leptomeningeal Enhancement
Neurol 90:e90-e93, Lovett, A.,et al, 2018

Thrombectomy 6 to 24 Hours after Stroke with a Mismatch between Deficit and Infarct
NEJM 378:11-22,81, Nogueira, R.G.,et al, 2018

Enlightenment and Challenges Offered by DAWN Trial (DWI or CTP Assessment with Clinical Mismatch in the Triage of Wake Up and Late Presenting Strokes Undergoing Neurointervention with Trevo)
Stroke 49:498-500, Saposnik, G.,et al, 2018

Thrombectomy for Stroke at 6 to 16 Hours with Selection by Perfusion Imaging
NEJM 378:708-718, Albers, G.W.,et al, 2018

Clinical Imaging Factors Associated with Infarct Progression in Patients with Ischemic Stroke During Transfer for Mechanical Thrombectomy
JAMA Neurol 74:1361-1367,1298, Boulouis, G.,et al, 2017

A 27-year-old man with Acute-Onset Ataxia
Neurol 88:e207-e211, Risco, J. & Weiss, M., 2017

Cerebral Amyloid Angiopathy-Related Inflammation Presenting with Isolated Leptomeningitis
Neurol 89:e66-e67, Kang, P.,et al, 2017

DAWN: Thrombectomy Effective Up to 24 Hours after Stroke
Medscape May, Hughes, S., 2017

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

Clinical Pathologic Conference, West Nile Virus Encephalitis
NEJM 377:1878-1886, Case 34-2017, 2017

Endovascular Treatment for Patients with Acute Stroke Who Have a Large Ischemic Core and Large Mismatch Imaging Profile
JAMA Neurol 74:34-40, Rebello, L.C.,et al, 2017

Clinicopathologic Conference, Granulomatous Amebic Encephalitis and Sarcoidosis (Inactive)
NEJM 376:368-379, Case 3-2017, 2017

Cerebellar Ataxia and Hearing Impairment
JAMA Neurol 74:243-244, Lin, C.Y. & Kuo, S.H., 2017

Characteristics in Limbic Encephalitis with Anti-Adenylate Kinase 5 Autoantibodies
Neurol 88:514-524,508, Do, L. & Chanson, E., 2017

Intracranial Dural Arteriovenous Fistulae
Stroke 48:1424-1431, Reynolds, M.R.,et al, 2017

Primary Angiitis of the Central Nervous System
Stroke 48:1248-1255, Boulouis, G.,et al, 2017

Clinicopathologic Conference, MELAS (mitochondrial encephalopathy, lactic acidosis, and stroke like episodes)
NEJM 376:1668-1678, CASE 13-2017, 2017

Long-Term Preclinical Magnetic Resonance Imaging Alterations in Sporadic Creutzfeldt-Jakob Disease
Ann Neurol 80:629-632, Zanusso, G.,et al, 2016

Validation of Clinicoradiological Criteria for the Diagnosis of Cerebral Amyloid Angiopathy-Related Inflammation
JAMA Neurol 73:197-202, Auriel, E.,et al, 2016

A 71-year-old Man with Rapidly Progressive Dementia
Neurol 86:e89-e92, Niemann, N.,et al, 2016

Non-Alzheimers Dementia 2 Lewy Body Dementias
Lancet 386:1683-1697, Walker, Z.,et al, 2015

Clinical Reasoning: An Unusual Case of Subacute Encephalopathy
Neurol 84:e33-e37, Parikh, N.,et al, 2015

Endovascular Therapy for Ischemic Stroke with Perfusion-Imaging Selection
NEJM 372:1009-1018, Campbell, B.C.V.,et al, 2015

Marburgs Variant of Multiple Sclerosis with Extensive Brain Lesions
Int J Neurol Neurother doi:10.23937/2378-3001/2/1/1027, Ludwig, A.,et al, 2015

A Case of Early-Onset Rapidly Progressive Dementia
JAMA Neurol 71:1445-1449, Cachia, D.,et al, 2014

Progressive Neuropsychiatric Symptoms and Motor Impairment
JAMA Neurol 71:794-798, Ghadiri, M.,et al, 2014

A 72-year-old Man with Rapid Cognitive Decline and Unilateral Muscle Jerks
Neurol 82:e194-e197, Duncan, M.,et al, 2014

Effect of Rituximab in Patients with Leucine-Rich, Glioma-Inactivated 1 Antibody-Associated Encephalopathy
JAMA Neurol 71:896-900, Irani, S.R.,et al, 2014

IgG4-Related Leptomeningitis: A Reversible Cause of Rapidly Progressive Cognitive Decline
Neurol 82:540-542, Mehta, S.H.,et al, 2014

Viral Infections of the Nervous System, Chronic Meningitis, and Prior Diseases, Creutzfeldt-Jakob Disease (Subacute Spongiform Encephalopathy)
Adams & Victors Principles of Neurology, Chp 33, pg 769, Ropper, A.H.,et al, 2014

Clinicopathologic Conference, Acute Infectious Mononucleosis due to Epstein-Barr Virus Infection, Complicated by Acute Otitis Media and Postinfectious Cerebellitis
NEJM 369:1253-1261, Case 30-2013, 2013

The Autosomal Recessive Cerebellar Ataxias
NEJM 366:636-646, Anheim,M.,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

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

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

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

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

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

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

Cost-Effectiveness of Multimodal CT for Evaluation Acute Stroke
Neurol 75:1678-1685, Young,K.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

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

Showing articles 50 to 100 of 6668 << Previous Next >>