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Differential
(Click to cross reference)
akinetic mute
alternating rapid movement, impaired
anorexia
ataxia
ataxia, cerebellar
ataxia, progressive
ataxia, truncal
ataxic gait
atypical
basal ganglia, lesion, bilateral
behavioral disorder
brain biopsy
CAT scan, abnormal
cerebellar lesion
cerebellum, disease of
Clinical Pathologic Conference(C.P.C.)
cognition, slowed
confusion
Creutzfeldt-Jakob disease, genetic
deep gray nuclei
dementia
dementia, familial
dementia, rapidly progressive
difficulty climbing stairs
diplopia
dizziness
dysarthria
dysdiadochokinesia
dysmetria
eye movement, disorders of
falling
familial
finger nose finger test
gait disorder
gait, apraxic
genetic neurologic disorders
genetic testing
grasp reflex
handwriting
heel-knee-shin test
hypophonia
imbalance
immunohistochemistry
incoordination
insomnia
intellectual deterioration
Jakob-Creutzfeldt disease
Jakob-Creutzfeldt disease, cerebellar variant
Jakob-Creutzfeldt disease, variant
Jakob-Creutzfeldt disease, young adult
kuru plaques
memory, defect of recent
memory, impairment of
MRI
MRI, abnormal
MRI, diffusion weighted
MRI, false negative
MRI, high signal intensity of basal ganglia
MRI, negative
MRI, punctate pattern
mutism
myoclonic jerks
myoclonus
neurologic disease, diagnoses of
neuropathology
pathologic reflex
prion disease
progressive neurologic disorder
pursuit eye movements, abnormal
rapidly progressing neurologic illness
real-time quaking-induced conversion
release phenomena
Romberg's sign
rooting reflex
saccadic eye movements, abnormal
seizure
snout reflex
square wave jerks
startle myoclonus
startle reaction
symmetric brain lesions
tandem gait, ataxic
tau protein
thalamus, lesion of-bilateral
tremor, intention
viral infection, CNS
vision, blurred
walking frame
walking, difficulty with
weight loss
wheelchair
wide based gait
workup
Showing articles 200 to 250 of 2929 << Previous Next >>

Carbamazepine Encephalopathy Masquerading as Creutzfeldt-Jakob Disease
Neurol 65:650-651, Horvath,J.,et al, 2005

Clinicopath Conf, Prion Disease (Sporadic Creutzfeldt-Jakob Disease)
NEJM 353:1042-1050, Case 27-2005, 2005

Unusual Variants of Alexander's Disease
Ann Neurol 57:327-338, van der Knaap,M.S., et al, 2005

Psychiatric Manifestations of Creutzfeldt-Jakob Disease: A 25-Year Analysis
J Neuropsychiatry Clin Neurosci 17:489-495, Wall,C.A.,et al, 2005

CJD--A Case of Mistaken Identity
Lancet 364:2068, Campbell,S.,et al, 2004

Sporadic Creutzfeldt-Jakob Disease
Neurol 63:450-456,410, Meissner,B.,et al, 2004

White Matter Lesions in Panencephalopathic Type of Creutzfeldt-Jakob Disease: MR Imaging and Pathologic Correlation
AJNR 25:910-918,905, Matsusue,E.,et al, 2004

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

Antivonvulsants for Creutzfeldt-Jakob Disease?
Lancet 361:224, Fioel,A.,et al, 2003

Thalamic Involvement in Sporadic Creutzfeldt-Jakob Disease: A Diffusion-Weighted MR Imaging Study
AJNR 24:908-915, Tschampa,H.J.,et al, 2003

14-3-3 Protein in the CSF of Patients with Rapidly Progressive Dementia
Neurol 61:354-357, Huang,N.,et al, 2003

Extraneural Pathologic Prion Protein in Sporadic Creutzfeldt-Jakob Disease
NEJM 349:1812-1820, Glatzel,M.,et al, 2003

Generalized Convulsive Status Epilepticus in Creutzfeldt-Jakob Disease
Seizure 12:403-406, Neufeld,M.Y.,et al, 2003

Correlation of Diffusion-Weighted Magnetic Resonance Imaging With Neuropathology in Creutzfeldt-Jakob Disease
Arch Neurol 59:128-134, Mittal,S.,et al, 2002

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

Emerging Patterns of Diffusion-Weighted MR Imaging in Creutzfeldt-Jakob Disease: Case Report and Review of the Literature
AJNR 23:550-556, Mao-Draayer,Y.,et al, 2002

Sporadic Creutzfeldt-Jakob Disease and Surgery
Neurol 59:543-548, Ward,H.J.T.,et al, 2002

Spontaneous Intracerebral Hemorrhage
NEJM 344:1450-1460, Qureshi,A.I.,et al, 2001

Alexander Disease: Diagnosis with MR Imaging
AJNR 22:541-552, van der Knaap,M.S.,et al, 2001

Creutzfeldt-Jakob Disease: Serial Changes on Diffusion-Weighted MRI
J Comput Assist Tomogr 25:274-277, Matoba,M.,et al, 2001

14-3-3 Protein Cerebrspinal Fluid Detection in Human Growth Hormone-Treated Creutzfeldt-Jakob Disease Patients
Ann Neurol 49:257-260, Brandel,J.,et al, 2001

Magnetic Resonance Imaging in the Clinical Diagnosis of Creutzfeldt-Jakob Disease
Arch Neurol 57:1751-1757, Schroter,A.,et al, 2000

Diffusion-Weighted MR Imaging of the Brain
Radiology 217:331-345, Schaefer,P.W.,et al, 2000

Misleading Results With the 14-3-3 Assay for the Diagnosis of Creutzfeldt-Jakob Disease
Neurol 55:1396-1397, Chapman,T.,et al, 2000

Iatrogenic Creutzfeldt-Jakob Disease at the Millenium
Neurol 55:1075-1081, Brown,P.,et al, 2000

Evolution of Sporadic Olivopontocerebellar Atrophy Into Multiple System Atrophy
Neurol 55:527-532, Gilman,S. et al, 2000

Risk of Acquiring Creutzfeldt-Jakob Disease from Blood Transfusions: Systematic Review of Case-Control Studies
BMJ 321:17-19, Wilson,K. et al, 2000

FLAIR MRI in sporadic Creutzfeldt-Jakob Disease
Neurol 55:147-148, Vrancken,A.F.J.E. et al, 2000

Alien Hand Sign in Creutzfeldt-Jakob Disease
JNNP 68:103-104, Inzelberg,R.,et al, 2000

Surgical Treatment and Risk of Sporadic Creutzfeldt-Jakob Disease:A Case-Control Study
Lancet 353:693-697, Collins,S.,et al, 1999

Hashimoto's Encephalitis as a Differential Diagnosis of Creutzfeldt-Jakob Disease
JNNP 66:172-176, Seipelt,M.,et al, 1999

Progressive Aphasia with Rapidly Progressive Dementia in a 49 Year Old Woman
JNNP 66:238-243, Greene,J.D.W.,et al,, 1999

Infantile Neuroaxonal Dystrophy,Clinical Spectrum and Diagnostic Criteria
Neurol 52:1472-1478, Nardocci,N.,et al, 1999

Clinical and Neuroradiological Features of Intracranial Vertebrobasilar Artery Dissection
Stroke 30:1083-1090, Hosoya,T.,et al, 1999

Seizures and Creutzfeldt-Jakob Disease
NCMJ 60:108-109, Cokgor,I.,et al, 1999

Creutzfeldt-Jakob Disease Presenting as Complex Partial Status Epilepticus: A Report of Two Cases
JNNP 66:406-407, Rees,J.H.,et al, 1999

Incidence of Dominant Spinocerebellar and Friedreich Triplet Repeats Among 361 Ataxic Families
Neurol 51:1666-1671, Moseley,M.L.,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 (CJD) after Blood Product Transfusion From a Donor with CJD
Neurol 50:1872-1873, Patryk,D.,et al, 1998

Clinical Usefulness of Magnetic Resonance Imaging in Multiple System Atrophy
JNNP 65:65-71, Schrag,A.,et al, 1998

Consequences of the Delayed Diagnosis of Ataxia-Telangiectasia
Pediatrics 102:98-100, Cabana,M.D.,et al, 1998

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

Transmission ofr Creutzfeldt-Jakob Disease in Corneal Grafts, Exclusion Criteria Ensure Risk is Small
BMJ 315:1553-1554, Allan,B.&Tuft,S., 1997

Creutzfeldt-Jakob Disease after Extracranial Dura Mater Embolization for a Nasopharyngeal Angiofibroma
Neurol 48:1451-1453, Antoine,J.C.,et al, 1997

Creutzfeldt-Jakob Dis after Embolization of Intercostal Arteries with Cadaveric Dura Suggest a Syst Trans of Prion Agent
Neurol 48:1470-1471, Defebvre,L.,et al, 1997

Peripheral NEuropathy in Creutzfeldt-Jakob Disease
Neurol 48:784, Esiri,M.M.,et al, 1997

Autoantibodies to Glutamic Acid Decarboxylase in Three Patients With Cerebellar Ataxia, Late-Onset Insulin-Dependent Diabetes Mellitus, and Polyendocrine Autoimmunity
Neurol 49:1026-1030, Saiz,A.,et al, 1997

Apolipoprotein E Phenotype Freq & CSF Concentra are not Assoc with Creutzfeldt-Jakob Disease
Arch Neurol 53:1233-1238, Zerr,I.,et al, 1996

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

Creutzfeldt-Jakob Disease from Contaminated Growth Hormone Extracts in France
Neurol 47:690-695, Billette de Villemeur,T.,et al, 1996



Showing articles 200 to 250 of 2929 << Previous Next >>