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Differential
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abscess, intracerebral

acquired immunodeficiency syndrome

adenine arabinoside

advances in neurology

adverse drug reaction

Alice in Wonderland syndrome

alien hand syndrome

alternating rapid movement, impaired

Alzheimer's disease

Alzheimer's disease, familial

Alzheimer's disease, rapidly progressive

Alzheimer's disease, rate of clinical decline

Alzheimer's disease, visual variant

amantadine

ammonia

AMPA receptor antibodies

amyloid angiopathy, cerebral

amyloid plaques

amyotrophic lateral sclerosis

amyotrophic lateral sclerosis, childhood

amyotrophic lateral sclerosis, familial

amyotrophic lateral sclerosis, guamian type of

amyotrophic lateral sclerosis, Parkinson-dementia-complex

amyotrophic lateral sclerosis, post-encephalitic

anatomy of

aneuploidy

angiitis, isolated of CNS

anticonvulsants, untoward effects of

antithyroid antibodies

aphasia, transcortical

aphasia, transcortical-sensory

autonomic dysfunction

basal ganglia, lesion of

basal ganglia, lesion, bilateral

basilar artery occlusion

bovine spongiform encephalopathy

bradykinesia

bradyphrenia

brain biopsy

brain biopsy, complications of

brain biopsy, false negative

brain biopsy, indication

brain biopsy, negative

brain scan

carbamazepine

carbamazepine, toxicity

carbon monoxide poisoning

carcinoma

carcinoma of breast

cardiac transplantation

CAT scan

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CAT scan, emission

CAT scan, emission, abnormal

CAT scan, false negative

caudate nucleus, lesion of

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cell fusion test

central nervous system, infection of

central pontine myelinolysis

cerebellar atrophy, primary

cerebellar atrophy, secondary

cerebellar degeneration

cerebellar lesion

cerebellum, disease of

cerebral cortex

cerebral cortical atrophy

cerebral glucose metabolism

cerebral infarction

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cerebral venous thrombosis, deep

cerebrospinal fluid

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cerebrovascular accident

cerebrovascular accident, mimics

cerebrovascular accident, misdiagnosis

Charles Bonnet's syndrome

children

chorea

choreoathetosis

chromosomal abnormality

chromosome 20

cingulate gyrus

Clinical Pathologic Conference(C.P.C.)

cognition

cognition, slowed

cogwheel rigidty

color vision, impaired

coma

comorbidities

complications

concentration, impaired

confusion

contactin associated protein like 2 antibodies

controversies in neurology

corneal transplant

cortical blindness

cortical infarction

cortical-basal ganglionic degeneration

Creutzfeldt-Jakob disease, genetic

deep gray nuclei

degenerative diseases of CNS

dementia, diagnostic evaluation of

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dementia, familial

dementia, frontotemporal

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dementia, prevention of

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dementia, reversible

dementia, screening for

dementia, transmissible

dementia, treatment of

demyelinating disease

denial of blindness(Antons syndrome)

differential diagnosis

difficulty climbing stairs

diplopia

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dissociated sensory loss

dizziness

driving

drug induced neurologic disorders

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dural graft, cadaveric

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electrophoretic pattern, CSF

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emotional lability

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epidemiology of neurology

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episodic disorders

experimental allergic encephalitis

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Fabry's disease

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fatigue

fever

fibrillations

finger nose finger test

Fisher C.M.

flavivirus

flu-like illness

follicle stimulating hormone

frontal lobe, anatomy and physiology

frontal lobe, pathologic signs of

gait disorder

gait, apraxic

gamma amino butyric acid receptor antibody

gaze palsy

gaze palsy, supranuclear

genetic neurologic disorders

genetic testing

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Gerstmann-Straussler-Scheinker disease

glioma

gliosis

glycine receptor antibodies

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hemianopia, homonymous

hemiparesis

hepatolenticular degeneration(Wilson's disease)

heralding manifestation

herpes simplex encephalitis

herpes simplex virus

herpes virus infection

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human immunodeficiency virus type 1

Huntington's chorea

hydrocephalus

hydrocephalus, normal pressure

hypoxic encephalopathy

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intellectual deterioration

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interobserver agreement

intracerebral hemorrhage

Jakob-Creutzfeldt disease

Jakob-Creutzfeldt disease, cerebellar variant

Jakob-Creutzfeldt disease, conjugal

Jakob-Creutzfeldt disease, Heidenhain variant

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Jakob-Creutzfeldt disease, unilateral

Jakob-Creutzfeldt disease, variant

Jakob-Creutzfeldt disease, young adult

jocularity

kuru

kuru plaques

laminar necrosis, cortical

laughing, pathologic

lead poisoning

Leigh's disease

leucine rich glioma inactivated 1 antibodies

leukoencephalitis, acute necrotizing hemorrhagic

Lewy body disease, diffuse

life expectancy

limbic encephalitis

linear lesion

lipid storage disorder of CNS

lithium

liver disease

liver transplantation

lobar atrophy

lymphoma

lymphoma involving CNS

lymphoma, primary of CNS

memory, defect of recent

memory, impairment of

meningitis

meningoencephalitis

mental status, abnormal

Mini Mental Status Examination

misdiagnosis

mitochondrial disease

Morvan's fibrillary chorea

motor cortex

motor neuron disease

movement disorder

movement disorder, drug induced

movement disorder, extrapyramidal

MRI

MRI pattern

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MRI, abnormal, seizure causing

MRI, ADC maps

MRI, artifacts

MRI, CAT scan compared to

MRI, cerebrovascular disease

MRI, demyelinating disease

MRI, diffusion tensor

MRI, diffusion weighted

MRI, diffusion weighted, pattern

MRI, early changes in CVA

MRI, high signal foci on

MRI, high signal intensity of basal ganglia

MRI, punctate pattern

MRI, serial

MRI, spinal cord

MRI, susceptibility weighted

MRI, T1 weighted high signal foci

multiple sclerosis

multiple system atrophy

myelitis, longitudinal

myoclonus, differential diagnosis of

myoclonus, stimulus sensitive

nasal brushings

negative

neoplasm, intracranial

neoplasm, metastatic to CNS

neoplasm, pituitary

neoplasm, primary intracerebral

neoplasm, primary of CNS

nerve conduction studies

neurofibrillary degeneration

neurofibromatosis 1

neurologic complications of, surgery

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neurologic signs

neurologic testing

neuron specific enolase

neuronal cell surface antigen

neuronal ceroid-lipofuscinosis

neuropathology

neuropathology, brain

nucleus basalis of Meynert

nystagmus

nystagmus, periodic alternating

occipital cortex

occipital lobe

occipital lobe, lesion of

occupational neurologic disorders

ocular motility, disorders of

old age, neurology of

organ transplantation

osmotic demyelination syndrome

pain

pain, leg

paranoia

parietal lobe, lesion of

parietal lobe, syndromes of

Parkinson disease

Parkinson disease, motor neuron disease with

Parkinson disease, postencephalitic

Parkinsonism plus syndrome

Parkinsonism syndrome

PAS positive

PAS positive material in the brain

pathognomonic

pathologic reflex

peduncular hallucinosis

perseveration

personality change

pituitary, hormones of

PLEDs

PLEDs, bilateral independent

pleocytosis of cerebrospinal fluid

polymerase chain reaction

polyneuropathy

polyneuropathy, chronic inflammatory demyelinating

polysomnogram

pons, lesion of

posterior cortical atrophy

posterior leukoencephalopathy syndrome

postictal encephalopathy

potassium channel antibodies

practice guidelines

preclinical

pregnancy, neurologic complications in

prevention of neurologic disorders

prion disease

prognosis

progressive infantile poliodystrophy

progressive multifocal leucoencephalopathy

progressive neurologic disorder

proprioception

prosopagnosia

protein 14-3-3, cerebrospinal fluid

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

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

pruritus

psychiatric disorder

psychiatric problems in neurologic disorders

psychomotor retardation

psychosis

psychotic behavior

pulvinar sign

pursuit eye movements, abnormal

putamen, lesion of

putamen, lesion of, bilateral

pyramidal tract

pyramidal tract dysfunction

rapidly fatal neurologic illness

rapidly progressing neurologic illness

real-time quaking-induced conversion

release phenomena

remote effect of cancer on the nervous system

reversible cerebral vasoconstrictive syndromes

reversible neurologic disorder

review article

rigidity

risk factors

risk-benefit assessment

Romberg's sign

rooting reflex

roving eye movements

saccadic eye movements, abnormal

seizure, nonconvulsive

single photon emission computed tomography

skin, biopsy

sleep

sleep pathology and physiology

slow virus infection of CNS

spinal cord, lesion of

spongy degeneration of brain

status epilepticus, nonconvulsive

steroid

steroid therapy, CNS treatment and complications with

striatum, lesion of

striatum, lesion of, bilateral

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

symmetric brain lesions

temporal lobe, status

thalamic tumors

thalamic tumors, bilateral

thalamus

thalamus, infarction of

thalamus, infarction, bilateral

thalamus, lesion of

thalamus, lesion of-bilateral

treatment of neurologic disorder

visual acuity, decreased

visual loss, progressive

walking frame

walking, difficulty with

Wallerian degeneration

Wernicke's encephalopathy

West Nile fever

Western immunoblot test

Showing articles 0 to 50 of 291 Next >>

Punctate Diffuse Cortex Signals in Creutzfeldt-Jakob Disease
JAMA Neurol 81:291-292, Chen,Z.,et al, 2024

Roving Eye and Head in a Patient with Genetic Creutzfeldt-Jakob Disease
Neurol 102:e209385, Nishida,K.,, 2024

Clinicopathologic Conference, Genetic Creutzfeldt-Jakob Disease
NEJM 386;674-687, Case 5-2022, 2022

Laboratory Diagnosis of Creutzfeldt-Jakob Disease
NEJM 386:1345-1350, Zerr, I., 2022

More Than a Little Unsteady
NEJM 387:e9, Kraft, A.W.,et al, 2022

Complete Evaluation of Dementia: PET and MRI Correlation and Diagnosis for the Neuroradiologist
AJNR 42:998-1007, Oldan, J.D.,et al, 2021

Sporadic Creutzfeldt-Jakob Disease in a Very Young Person
Neurol 97:813-816,801, Appleby, B.S.,et al, 2021

Homonymous Hemianopia with Normal Magnetic Resonance Imaging
JAMA Ophthalmol doi:10.1001/JAMAOphthalmol.2020.0447, Cai, S.,et al, 2020

Rapid Progression of Prion Disease Associated with Transverse Myelitis
Neurol 94:e1670-e1672, Hussein, O.,et al, 2020

Long Survival Sporadic Creutzfeldt-Jakob Disease
Neurol 95:87-88, Liu, X.Y.,et al, 2020

A 57-Year-Old Woman with Progressive Ataxia and Falls
Neurol 95:650-656, Badahdah, A., 2020

Bornavirus Encephalitis Shows a Characteristic Magnetic Resonance Phenotype in Humans
Ann Neurol 88:723-735, Finck, T.,et al, 2020

Dressing Apraxia as Initial Manifestation of Creutzfeldt-Jakob Disease
Tremor and Other Hyperkinetic Movements 10:1-3, Heckmann, J.G.,et al, 2020

Variant Creutzfeldt-Jakob Disease Diagnosed 7.5 Years after Occupational Exposure
NEJM 383:83-85, Brandel, J.P.,et al, 2020

An Atypical Presentation of Creutzfeldt-Jakob Disease with a Heidenhain Variant and Balints Syndrome
Cureus DOI:10.7759/cureus,8608, Gupta,A. & Dhingra,A., 2020

RT-QuIC: A New Test for Sporadic CJD
Pract Neurol 19:49-55, Green, A.J.E., 2019

Clinicopathologic Conference, Creutzfeldt-Jakob Disease
NEJM 381:1569-1578, Case 32-2019, 2019

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

Diagnosis of Human Prion Disease Using Real-Time Quaking-Induced Conversion Testing of Olfactory Mucosa and Cerebrospinal Fluid Samples
JAMA Neurol 74:155-162,144, Bongianni, M.,et al, 2017

Precipitous Deterioration of Motor Function, Cognition, and Behavior
JAMA Neurol 74:591-596, Fernandez-Fournier, M.,et al, 2017

Creutzfeldt-Jakob Disease and Hashimotos Thyroiditis: A Case Report Illustrating Prion-Induced Encephalitis
J Neuroinfect D 7:1-6, Dabul, L.,et al, 2016

Distinguishing Neuroimaging Features in Patients Presenting with Visual Hallucinations
AJNR 37:774-781, Winton-Brown, T.T.,et al, 2016

Cerebrospinal Fluid Real-Time Quaking-Induced Conversion is a Robust and Reliable Test for Sporadic Creutzfeldt-Jakob Disease: An International Study
Ann Neurol 80:160-165, McGuire, L.I.,et al, 2016

Diffusion-Weighted MRI Abnormalities Antedate the Onset of Sporadic Creutzfeldt-Jakob Disease
Neurol 87:843, Suzuki, K.,et al, 2016

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

A 64-year-old Man with Visual Distortions
Neurol 87:e252-e256, McGrath, E.R.,et al, 2016

Rapid and Sensitive RT-QuIC Detection of Human Creutzfeldt-Jakob Disease Using Cerebrospinal Fluid
mBio 6:e02451-14, Orru,C.D.,et al, 2015

Unilateral Cortical Hyperintensity in Diffusion-Weighted MRI;New Criteria for Early Sporadic Creutzfeldt-Jakob Disease
Iran J Neurol 14:108-109, Tabrizi,N.,&Abedini,M, 2015

Limbic Encephalitis Associated with Anti-Voltage-Gated Potassium Channel Complex Antibodies Mimicking Creutzfeldt-Jakob Disease
JAMA Neurol 71:79-82, Yoo,J.Y. & Hirsch, L.J., 2014

A Test for Creutzfeldt-Jakob Disease Using Nasal Brushings
NEJM 371:519-529, Orru, C.D.,et al, 2014

Serial Magnetic Resonance Imaging Changes in Sporadic Creutzfeldt-Jakob Disease with Valine Homozygosity at Codon 129 of the Prion Protein Gene
JAMA Neurol 71:1186-1187, Furukawa, F.,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

A Creutzfeldt-Jakob Disease Case Presenting with Psychiatric Symptoms
JNBS doi:10.5455/JNBS.1386249156, Aslan,A.A.,et al, 2014

Sporadic Creutzfeldt-Jakob Disease with Focal Findings: Caveats to Current Diagnostic Criteria
Neurol Internat 5:1-5, Mader, E.C.,et al, 2013

A Comparison of Tau and 14-3-3 Protein in the Diagosis of Creutzfeldt-Jakob Disease
Neurol 79:547-552, Hamlin, C.,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

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

Cerebral White Matter Disruption in Creutzfeldt-Jakob Disease
AJNR 33:1945-1950, Lee,H.,et al, 2012

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

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

Differential Diagnosis of Bilateral Abnormalities of the Basal Ganglia and Thalamus
RadioGraphics 31:5-30, Hegde,A.N.,et al, 2011

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

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

Encephalitis and antibodies to synaptic and neuronal cell surface proteins
Neurol 77:179-189, Lancaster, E.,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

Open Biopsy in Patients With Acute Progressive Neurologic Decline and Absence of Mass Lesion
Neurol 75:419-424, Schuette,A.J., et al, 2010

Sporadic Creutzfeldt-Jakob Disease Mimicking Nonconvulsive Status Epilepticus
Neurol 74:1995-1999, Lapergue,B., et al, 2010

Showing articles 0 to 50 of 291 Next >>