Neudle.com: "pulvinar sign"

Differential
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abscess, intracerebral

abscess, intracranial

abulia

acetaminophen

acute disseminated encephalomyelitis

adverse drug reaction

alcohol

alcohol, neurologic complications with

alcoholism

ammonia

angiography, cerebral

angiography, cerebral, false negative

angiography, cerebral, negative

animal exposure

anorexia

anterior horn cell disease

anti MAG antibodies

antibodies to measles

autonomic dysfunction

Babinski sign

bacterial infection

basal ganglia

basal ganglia, lesion of

basal ganglia, lesion, bilateral

Behcet's syndrome

blood transfusion

border zone infarct, cortical

carbon monoxide poisoning

CAT scan

CAT scan, abnormal

CAT scan, abscess, cerebral

CAT scan, false negative

CAT scan, ring sign

caudate nucleus

caudate nucleus, atrophy

central artery of Percheron

central nervous system, infection of

central pontine myelinolysis

cerebellar atrophy, secondary

cerebellar lesion

cerebellum

cerebral cortex

cerebral cortical atrophy

cerebral cortical encephaliis

cerebral edema

cerebral edema, cytotoxic

cerebral edema, vasogenic

cerebral vasculature

cerebral veins

cerebral venous infarction

cerebral venous thrombosis

cerebral venous thrombosis, deep

cerebrospinal fluid

cerebrospinal fluid, abnormal

cerebrospinal fluid, cell count

cerebrospinal fluid, elevated protein of

cerebrospinal fluid, oligoclonal IgG in

cerebrovascular accident

cerebrovascular accident, women

Clinical Pathologic Conference(C.P.C.)

cognition

coma

concentration, impaired

confusion

conus medullaris, lesion of

corpus callosum

corpus callosum, lesion of

degenerative diseases of CNS

delay in diagnosis

dementia

dementia, presenile

dementia, rapidly progressive

dementia, reversible

dementia, transmissible

demyelinating disease

depression

developmental milestones, loss of

developmental retardation

diagnostic criteria

differential diagnosis

disability rating scale, neurological

disability, neurological

drooling

dropped head syndrome

drowsiness

drug overdose

dural sinus thrombosis

dysarthria

electroencephalogram, abnormalities of

electroencephalogram, periodic complexes

encephalitis

encephalitis, eastern equine

encephalitis, sequelae in

encephalitis, viral

encephalopathy

encephalopathy, metabolic

encephalopathy, neonatal

endemic area

enzyme, defect

epidemiology of neurology

escherichia coli

Europe

eye movement, disorders of

Fabry's disease

facial asymmetry

facial weakness

facial weakness, central

facial weakness, central, emotional

familial

fatal familial insomnia

fatigue

fever

fistula, arterio-venous, dural

fistula, arterio-venous, pulmonary

flaccid paralysis

flavivirus

frontal lobe, pathologic signs of

fundus, abnormality of

funduscopic exam

gadolinium

gangliosidosis GM2

gastrectomy, neurologic complications following

gastric partitioning

gastritis

genetic neurologic disorders

genetic testing

gliosis

globus pallidus

globus pallidus, lesion of

globus pallidus, lesion of, bilateral

hearing loss, bilateral

hearing loss, sudden, bilateral

hemiparesis

hemisensory loss

hemolytic-uremic syndrome

hemorrhage, thalamic

hepatic encephalopathy

hepatic encephalopathy, acute

hepatic failure

hepatic failure, acute

heralding manifestation

hyperammonemic encephalopathy

hypoglycemia, newborn and infant

hypomyelination

hyponatremia

hypoxia, newborn

hypoxic encephalopathy

iatrogenic neurologic disorders

imbalance

immunohistochemistry

immunosuppressive agents

incidence

inclusion bodies

inclusion bodies, eosinophilic intranuclear

insular cortex, lesion

insular cortex, lesion, bilateral

intellectual deficit

intellectual deterioration

internal capsule

iron, brain

Jakob-Creutzfeldt disease

Jakob-Creutzfeldt disease, medical precaution with

Jakob-Creutzfeldt disease, variant

Jewish

laminar necrosis, cortical

Leigh's disease

lenticular nucleus, lesion of

lenticular nucleus, lesion of, bilateral

lentiform fork sign

leukocytosis

leukoencephalopathy

level of consciousness, decreased

limbic encephalitis

linear lesion

lipid storage disorder of CNS

liver disease

liver function enzymes

lymphadenopathy

lymphoma

lymphoma involving CNS

lysosomal storage disease

malaise

mammillary bodies

medulla oblongata, lesion of

MELAS syndrome

memory, impairment of

meningeal enhancement

mental status, abnormal

metabolic acidosis

microangiopathy, brain

microangiopathy, retina

microhemorrhage, intracerebral

microinfarcts

midbrain

midbrain, infarction of

midbrain, lesion of

middle cerebellar peduncle, lesion

middle cerebellar peduncle, lesion, bilateral

misdiagnosis

mitochondrial disease

MRI, abnormal, seizure causing

MRI, angiography

MRI, CAT scan compared to

MRI, contrast enhanced

MRI, diffusion weighted

MRI, disappearing lesion on

MRI, false negative

MRI, false positive

MRI, FLAIR

MRI, high signal foci on

MRI, high signal intensity of basal ganglia

MRI, hypointense signal foci on

MRI, intravascular enhancement

MRI, mass effect on

MRI, negative

MRI, nodular enhancement

multiple sclerosis, misdiagnosis

multiple sclerosis, plaque

myelinolysis, extrapontine

myelitis

myelitis, longitudinal

myelitis, transverse

myoclonus

nausea and vomiting

nerve conduction studies

neurologic complications of, surgery

neurologic complications of, systemic disease

neurologic disease

neurologic disease, diagnoses of

neurologic signs

neurologic symptoms

neuromuscular disease, electrodiagnosis of

neuromyelitis optica (Devic's disease)

neuromyelitis optica spectrum disorder

neuromyelitis optica, IgG

neuronopathy, sensory

neurons

neuroophthalmology

neuropathology

neuropathology, brain

neuroradiology

neurotoxin

next-generation sequencing

nutritional deficiency

nystagmus

nystagmus, gaze-evoked

old age, neurology of

ophthalmoplegia

optic neuritis

optic neuritis, bilateral

optic neuritis, recurrent

optical coherence tomography

overlap syndrome

owl's eye sign of spinal cord

pain, leg

papilledema

pediatric neurology

periaqueductal lesion

pleocytosis of cerebrospinal fluid

POLG1 gene

poliomyelitis-like illness

preclinical

pregnancy, neurologic complications in

prion disease

prognosis

progressive neurologic disorder

protein 14-3-3, cerebrospinal fluid

pseudobulbar palsy

psychiatric disorder

psychiatric problems in neurologic disorders

pulvinar

pulvinar sign

putamen, lesion of, bilateral

pyramidal tract dysfunction

quadriplegia

rapidly fatal neurologic illness

rapidly progressing neurologic illness

rash

recurrent

remote effect of cancer on the nervous system

renal failure

respiratory failure

retinal artery occlusion

retinal branch artery occlusion

retinal infarction

retinopathy

reversible neurologic disorder

sensorineural hearing loss

serologic testing

serologic testing of cerebrospinal fluid

Shiga toxin

Sjogren's syndrome

Sjogren's syndrome, neurologic manifestations of

sleep pathology and physiology

spinal cord, lesion of

splenium of corpus callosum

startle reaction

status epilepticus

steroid therapy, CNS treatment and complications with

straight sinus

subacute sclerosing panencephalitis(S.S.P.E.)Dawson's disease

substantia nigra

superior colliculus

Susac's syndrome

symmetric brain lesions

temporal lobe, lesion

temporal lobe, status

thalamic ataxia syndrome

thalamus

thalamus L-sign

thalamus, infarction of

thalamus, infarction, bilateral

thalamus, lesion of

thalamus, lesion of-bilateral

third ventricle, wall

tick bite

tick-borne encephalitis

tinnitus

tinnitus, pulsatile

tone, muscle, increased

tonsil biopsy

treatment of neurologic disorder

tremor

tremor, thalamic

uremia

uremic encephalopathy

visuospatial disturbance

walking, difficulty with

water channel antibodies

Wernicke's encephalopathy

West Nile fever

wheelchair

white matter disease

Showing articles 0 to 50 of 2529 Next >>

Atypical Presentation of HLA-B51 Positive Neuro-Bechet Disease in a 27-Year-Old Patient, The Waterfall Sign
Neurol 104:e210257, AbuAlrob,M.A., 2025

Acute and Progressive Cognitive Decline in a 38-Year-Old Man
Neurol 105: e213871, Wu,L.,et al, 2025

Validation of the 2023 International Diagnostic Criteria for MOGAD in a Selected Cohort of Adults and Children
Neurol 103:e209321, Varley,J.A.,et al, 2024

Slowly rogressive Cerebellar Ataxia in a 55-Year-Old Female Patient
JAMA Neurol 80:107-108, Bernaola,M.T.,et al, 2023

Thalamus L-Sign: A Potential Biomarker of Neonatal Partial, Prolonged Hypoxic-Ischemic Brain Injury or Hypoglycemic Encephalopathy
AJNR 43:919-925, Misser, S.K.,et al, 2022

Lentiform Fork Sign in Metabolic Acidosis
Ann Neurol 89:188-189, Kumar, N. & Kumar, D., 2021

Ictal Pulvinar Hyperperfusion Sign
Ann Neurol 89:190-191, Renard, D.,et al, 2021

Nonalcoholic Wernicke Encephalopathy
Neurol 97:e1541-e1542, Hansen, G.,et al, 2021

Clinical and Neuroimaging Findings in MOGAD-MRI and OCT
Clin Exp Immunol 206:266-281, Bartels,F.,et al, 2021

Pediatric Leigh Syndrome
Ann Neurol 88:218-232, Alves, C.A.P.F.,et al, 2020

A 68-year-old Man with Rapid Cognitive Decline
Neurol 93:315-318, Berth, S.H.,et al, 2019

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

Clinicopathologic Conference, Tay-Sacks Disease (GM2, Gangliosidosis)
NEJM 370:1830-1841, Case 14-2014, 2014

Subacute Sclerosing Panencephalitis
www.MedLink.com, February, Auwaeter,P.G.&Johnson,R.T., 2013

Diffusion-Weighted Imaging in Acute Hyperammonemic Encephalopathy
Neurohosp 3:125-130, Rosario, M.,et al, 2013

Imaging Findings in Tick-Borne Encephalitis with Differential Diagnostic Considerations
AJR 199:420-427, Horger, M.,et al, 2012

Neurologic Manifestations of E Coli infection - induced Hemolytic-Uremic Syndrome in Adults
Neurol 79:1466-1473, Weissenborn, K.,et al, 2012

Hyperammonemic Encephalopathy
Neurol 78:600-601, Capizzano,A.A.,et al, 2012

Brain Abnormalities in Neuromyelitis Optica Spectrum Disorder
Multiple Sclerosis International ID 735486, Kim, W.,et al, 2012

Diagnosing variant Creutzfeldt-Jakob disease: a retrospective analysis of the first 150 cases in the UK
JNNP 82:646-651, Heath, C.A.,et al, 2011

Acute Hyperammonemic Encephalopathy in Adults: Imaging Findings
AJNR 32:413-418, U-King-Im,J.M.,et al, 2010

Acute Hepatic Encephalopathy: Diffusion-Weighted and Fluid-Attenuated Inversion Recovery Findings, and Correlation With Plasma Ammonia Level and Clinical Outcome
AJNR 31:1471-1479, McKinney,A.M.,et al, 2010

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

MR Imaging in Novel Influenza A(H1N1)-Associated Meningoencephalitis
AJNR 31:394-395, 393, Haktanir,A., 2010

MRI Lesion Profiles in Sporadic Creutzfeldt-Jakob Disease
Neurol 72:1994-2001, Meissner,B.,et al, 2009

MR Imaging Findings in 56 Patients with Wernicke Encephalopathy: Nonalcoholics May Differ from Alcoholics
AJNR 30:171-176, Zuccoli,Z.,et al, 2009

MR Imaging, Diffusion-Weighted Imaging and MR Spectroscopy Findings in Acute Rapidly Progressive Subacute Sclerosing Panencephalitis
Brain Dev 29:306-311, Oguz, K.K.,et al, 2007

Gray Matter Involvement in Multiple Sclerosis
Neurol 68:634-642, Pirko,I.,et al, 2007

Neuroimaging Findings in Human Prion Disease
JNNP 78:664-670, Macfarlane,R.G.,et al, 2007

West Nile Virus Neuroinvasive Disease
Ann Neurol 60:286-300, Davis,L.E.,et al, 2006

Clinical Presentation and Pre-Mortem Diagnosis of Variant Creutzfeldt-Jakob Disease Associated With Blood Transfusion: A Case Report
Lancet 368:2061-2067, Wroe,S.J.,et al, 2006

Wernicke Encephalopathy After Bariatric Surgery: Losing More Than Just Weight
Neurol 65:1987,1847, Foster,D.,et al, 2005

The "Pulvinar Sign" in a Case of Paraneoplastic Limbic Encephalitis Associated with Non-Hodgkins Lymphoma
JNNP 76:882-884, Mihara,M.,et al, 2005

Diffusion-weighted and Perfusion MRI Demonstrates Parenchymal Changes in Complex Partial Status Epilepticus
Brain 128:1369-1376, Szabo, K.,et al, 2005

False-Positive Pulvinar Sign on MRI in Sporadic Creutzfeldt-Jakob Disease
Neurol 62:1235-1236, Petzold,G.C.,et al, 2004

Diagnosing Variant Creutzfeldt-Jakob Disease with the Pulvinar Sign:"MR Imaging Findings in 86 Neuropathologically Confirmed Cases
AJNR 24:1560-1569, Collie,D.A.,et al, 2003

Sporadic CJD Clinically Mimicking Variant CJD With Bilateral Increased Signal in the Pulvinar
Neurol 58:148-149, Haik,S.,et al, 2002

Acute Hepatic Encephalopathy with Diffuse Cortical Lesions
Neuroradiology 43:551-554, Arnold, S.M.,et al, 2001

Diffusion-Weighted MR Imaging in Biopsy-Proven Creutzfeldt-Jakob Disease
Korean J Radiol 2:192-196, Kim,H-C.,et al, 2001

The Magnetic Resonance Imaging Appearances of the Brain in Acute Carbon Monoxide Poisoning
Clin Radiol 55:273-280, O'Donnell,P.,et al, 2000

The Pulvinar Sign on Magnetic Resonance Imaging in Variant Creutzfeldt-Jakob Disease
Lancet 355:1412-1418,1384, Zeidler,M.,et al, 2000

Diagnosis of New Variant Creutzfeldt-Jakob Disease
Ann Neurol 47:575-582, Will,R.G.,et al, 2000

Volitional and Emotional Supranuclear Facial Weakness
NEJM 338:1515, Ross,R.T.&Mathiesen,R., 1998

Retinocochleocerebral Vasculopathy
Medicine 77:12-40, Petty,G.W.,et al, 1998

Clinical and Neuroradiographic Manifestations of Eastern Equine Encephalitis
NEJM 336:1867-1874, Deresiewicz,R.L.,et al, 1997

Thrombosis of the Deep Venous Drainage of Brain in Adults:Analysis of Seven Cases with Review of Literature
Arch Neurol 52:1101-1108, Crawford,S.C.,et al, 1995

The Thalamic Ataxia Syndrome
Neurol 44:810-814, Solomon,D.H.,et al, 1994

Pontine and Extrapontine Myelinolysis:A Neurologic Disorder Following Rapid Correction of Hyponatremia
Medicine 72:359-373, Karp,B.I.&Laureno,R., 1993

Fatal Familial Insomnia:Clinical and Pathologic Study of Five New Cases
Neurol 42:312-319, Manetto,V.,et al, 1992

Showing articles 0 to 50 of 2529 Next >>