Neurology Specific Literature Search   
 
[home][thesaurus]
    

Differential
(Click to cross reference)
akinetic mute
alternating rapid movement, impaired
Alzheimer's disease
Alzheimer's disease, familial
amyloid plaques
aneuploidy
animal exposure
arm weakness
ataxia
ataxia, cerebellar
ataxia, progressive
ataxic gait
atypical
basal ganglia
basal ganglia, lesion of
basal ganglia, lesion, bilateral
behavioral disorder
blood transfusion
bovine spongiform encephalopathy
brain biopsy
central nervous system, infection of
cerebellar lesion
cerebral cortex
cerebrospinal fluid, abnormal
cerebrospinal fluid, protein of
chorea
choreoathetosis
chromosomal abnormality
chromosome 20
cingulate gyrus
Clinical Pathologic Conference(C.P.C.)
cognition, slowed
corneal transplant
Creutzfeldt-Jakob disease, genetic
deep gray nuclei
degenerative diseases of CNS
dementia
dementia, familial
dementia, presenile
dementia, rapidly progressive
dementia, transmissible
diet
difficulty climbing stairs
dizziness
dysarthria
dysdiadochokinesia
dysmetria
electroencephalogram
electroencephalogram, abnormalities of
electroencephalogram, periodic complexes
encephalopathy
epidemiology of neurology
eye movement, disorders of
falling
familial
fasciculation
fatal familial insomnia
finger nose finger test
gait disorder
gaze palsy
gaze palsy, supranuclear
gaze palsy, vertical
gene
gene mutation
genetic counselling
genetic linkage
genetic neurologic disorders
genetic testing
Gerstmann-Straussler-Scheinker disease
growth hormone
hallucination
handwriting
heel-knee-shin test
hockey stick sign
iatrogenic neurologic disorders
imbalance
insomnia
intellectual deterioration
Jakob-Creutzfeldt disease
Jakob-Creutzfeldt disease, cerebellar variant
Jakob-Creutzfeldt disease, conjugal
Jakob-Creutzfeldt disease, medical precaution with
Jakob-Creutzfeldt disease, variant
Jakob-Creutzfeldt disease, young adult
kuru
life expectancy
linear lesion
lymphoma involving CNS
molecular genetics
mongolism
monoparesis
mortality
motor cortex
MRI
MRI, abnormal
MRI, diffusion weighted
MRI, FLAIR
MRI, indications for
MRI, negative
MRI, punctate pattern
MRI, susceptibility weighted
mutism
myoclonic jerks
myoclonus
myoclonus, cortical
myoclonus, stimulus sensitive
neurologic disease, diagnoses of
neurologic signs
neuropathology
nystagmus
occupational neurologic disorders
pituitary, hormones of
polymerase chain reaction
prion disease
prognosis
progressive neurologic disorder
protein 14-3-3, cerebrospinal fluid
psychosis
psychotic behavior
pulvinar sign
rapidly progressing neurologic illness
real-time quaking-induced conversion
review article
risk factors
Romberg's sign
scrapie
seizure
skin, biopsy
sleep pathology and physiology
slow virus infection of CNS
spongy degeneration of brain
startle myoclonus
striatum, lesion of
striatum, lesion of, bilateral
symmetric brain lesions
tandem gait, ataxic
thalamus, lesion of
thalamus, lesion of-bilateral
trauma
tremor
upgaze, paralysis of
urinary incontinence
viral infection, CNS
walking frame
walking, difficulty with
weakness, acute
weakness, focal
wheelchair
wide based gait
workup
Showing articles 0 to 50 of 1937 Next >>

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

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

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

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

MR Imaging of Familial Creutzfeldt-Jakob Disease: A Blinded and Controlled Study
AJNR 29:1638-1643, Fulbright,R.K.,et al, 2008

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

Creutzfeldt-Jacob Disease in a Husband and Wife
Neurol 50:684-688, Brown,P.,et al, 1998

Case-Control Study of Risk Factors of Creutzfeldt-Jacob Disease in Europe During 1993-95
Lancet 351:1081-1085, Van Duijn,C.M.,et al, 1998

Creutzfeldt-Jakob Disease and Related Transmissible Spongiform Encephalopathies
NEJM 339:1994-2004, Johnson,R.T. & Gibbs,Jr.,C.J., 1998

Fatal Insomnia in a Case of Familial Creutzfeldt-Jakob Disease with the Codon 200Lys Mutation
Neurol 46:758-761, Chapman,J.,et al, 1996

Risk Factors for Creutzfeldt-Jakob Disease:A Reanalysis of Case-Control Studies
Neurol 46:1287-1291, Wientjens,D.P.W.M.,et al, 1996

Creutzfeldt-Jakob Disease in a Young Woman
Lancet 347:945-948, Tabrizi,S.J.,et al, 1996

Human Prion Diseases
Ann Neurol 35:385-395, Prusiner,S.B.&Hsiao,K.K., 1994

Familial Creutzfeldt-Jakob Disease (Codon 200 Mutation) with Supranuclear Palsy
Bertoni. J. M. , et al, JAMA 268:2413-2415., , 1992

Genetic Predisposition to Iatrogenic Creutzfeldt-Jakob Disease
Lancet 337:1441-1442, Collinge,J.,et al, 1991

Mutation of the Prion Protein in Libyan Jews with Creutzfeldt-Jakob Disease
NEJM 324:1091-1097, Hsiao,K.,et al, 1991

The Spongiform Encephalopathies, Editorial
JNNP 54:761-763, Will,R.G., 1991

Inherited Human Prion Diseases
Neurol 40:1820-1827, Hsiao,K.&Prusiner,S.B., 1990

Familial Creutzfeldt-Jakob Disease without Periodic EEG Activity
Ann Neurol 28:585-588, Tietjen,G.E.&Drury,I., 1990

Supranuclear Gaze Palsy in Familial Creutzfeldt-Jakob Disease
Arch Neurol 40:618-622, Bertoni,J.M.,et al, 1983

Creutzfeldt-Jakob Disease:Patterns of Worldwide Occurrence & the Significance of Familial & Sporadic Clustering
Ann Neurol 5:177-188, Masters,C.L.,et al, 1979

Studies in Aging of the Brain:IV. Familial Alzheimer Dis. :Relat. to Transmiss. Demetia, Aneuploidy, & Microtubular Defects
Neurol 29:1402, Book,R.H.,et al, 1979

Precautions in Familial Transmissible Dementia
Arch Neurol 35:697-698, Cook,R.,et al, 1978

Spastic Pseudosclerosis (Creutzfeldt-Jakob Dis) Van Rossum A. , In:Vinken, P. J.
Handbk of Clin Neurol Vol 6 North-Holland Publ. Amster 1968 Ch 28, p 726., Bruyn,G.W., 1968

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

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

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

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

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

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

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

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

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

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

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

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



Showing articles 0 to 50 of 1937 Next >>