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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 250 to 300 of 2929 << Previous Next >>

Pruritus in Creutzfeldt-Jakob Disease
Neurol 46:940-941, Shabtai,H.,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

MR Imaging of Creutzfeldt-Jakob Disease
Radiology 199:793-798, Finkenstaedt,M.,et al, 1996

The Inherited Ataxias and the New Genetics
JNNP 61:327-332, Hammans,S.R., 1996

Clinical and Genetic Abnormalities in Patients with Friedreich's Ataxia
NEJM 335:1169-1175, 12221996., Durr,A.,et al, 1996

Brain Death:MR and MR Angiography
AJNR 17:731-735, Ishii,K.,et al, 1996

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

Accuracy and Reliability of Periodic Sharp Wave Complexes in Creutzfeldt-Jakob Disease
Arch Neurol 53:162-166, Steinhoff,B.J.,et al, 1996

A Case of Creutzfeldt-Jakob Disease (CJD) Started with Monoparesis of the Left Arm
Rinshi Shinkeigaku 36:1245-1248, Obi, T.,et al, 1996

MRI of Creutzfeldt-Jakob Disease:Asymmetric High Signal Intensity of the Basal Ganglia
Neurol 45:1932-1933, Yoon,S.S.,et al, 1995

Creutzfeldt-Jakob Disease after Liver Transplantation
Ann Neurol 38:269-272, Creange,A.,et al, 1995

Management of Acoustic Neuroma
BMJ 311:1141-1144, Wright,A.&Bradford,R., 1995

Human Spongiform Encephalopathy:The NIH Series of 300 Cases of Experimentally Transmitted Disease
Ann Neurol 35:513-529, Brown,P.,et al, 1994

The Apolipoprotein E Alleles as Major Susceptibility Factors for Creutzfeldt-Jakob Disease
Lancet 344:1315-1318, 13101994., Amouyel,P.,et al, 1994

Trinucleotide Repeat Expansion in Neurological Disease
Ann Neurol 36:814-822, LaSpada,A.R.,et al, 1994

MR Diagnosis of Creutzfeldt-Jakob Disease:Significance of High Signal Intensity of the Basal Ganglia
AJR 162:137-140, Barboriak,D.P.,et al, 1994

Iatrogenic Creutzfeldt-Jakob Disease:An Example of the Interplay Between Ancient Genes and Modern Medicine
Neurol 44:291-293, Brown,P.,et al, 1994

Positron Emission Tomographjy and Histopathology in Creutzfeldt-Jakob Disease
Neurol 43:1828-1830, Goldman,S.,et al, 1993

Creutzfeldt-Jakob Disease in a Physician:A Review of the Disorder in Health Care Workers
Neurol 43:205-206, Berger,J.R.&David,N.J., 1993

Inherited Prion Disease (PrP lysine 200) in Britain:Two Case Reports
BMJ 306:301-302, 2881993., Collinge,J.,et al, 1993

Creutzfeldt-Jakob Disease and Blood Transfusion
lancet 341:205-207, Esmonde,T.F.G.,et al, 1993

MRI Abnormalities in Creutzfeldt-Jakob Disease
Neuroradiology 35:584-585, DiRocco,A.,et al, 1993

Creutzfeldt-Jakob Disease in a Recipient of Human Pituitary-Derived Gonadotrophin:A Second Case
JNNP 55:1094-1095, Cochius,J.I.,et al, 1992

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

Drug Induced Creutzfeldt-Jakob Like Syndrome
J Psychiatr Neurosci 17:103-105, Finelli,P.F., 1992

Demonstration of the Transmissible Agent in Tissue From a Pregnant Woman with Creutzfeldt-Jakob Disease
NEJM 327:649, Tamai,Y.,et al, 1992

"Friendly Fire"in Medicine:Hormones, Homografts, and Creutzfeldt-Jakob Disease
Lancet 340:24-27, Brown,P.,et al, 1992

The Use of Magnetic Resonance Imaging in Diagnosing Infantile Neuroaxonal Dystrophy
Neurol 43:110-113, Tanabe,Y.,et al, 1992

Evaluation of Cerebral Biopsies for the Diagnosis of Dementia
Arch Neurol 49:28-31, Hulette,C.M.,et al, 1992

Creutzfeldt-Jakob Disease in a Pathologist
Neurol 42:463, Gorman,D.G.,et al, 1992

Chiari I Malformations:Clinical and Radiologic Reappraisal
Radiology 183:347-353, Elster,A.D.&Chen,M.Y.M., 1992

Protein Processing in Lysosomes:The New Therapeutic Target in Neurodegenerative Disease
Lancet 340:156-159, Mayer,R.J.,et al, 1992

Creutzfeldt-Jakob Disease in Pituitary Growth Hormone Recipients in the United States
JAMA 265:880-884, Fradkin,J.E.,et al, 1991

CT Appearance of Panencephalopathic and Ataxic Type of Creutzfeldt-Jakob Disease
J Comput Assist Tomogr 15:3332-3344, Berciano,J.,et al, 1991

Magnetic Resonance Imaging of Creutzfeldt-Jakob Disease
Ann Neurol 29:438-440, Milton,W.J.,et al, 1991

Ataxia-Telangiectasia:An Interdisciplinary Approach to Pathogenesis
Medicine 70:99-117, Gatti,R.A.,et al, 1991

Dementia Presenting with Aphasia:Clinical Characteristics
JNNP 54:542-545, Mendez,M.F.&Zander,B.A., 1991

Serial MR Imaging in Creutzfeldt-Jakob Disease
Neuroradiology 33:364-367, Uchino,A.,et al, 1991

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

Creutzfeldt-Jakob Disease in a Patient with a Cadaveric Dural Graft
Neurol 41:940-941, Miyashita,K.,et al, 1991

Sarcoidosis of the Nervous System, A Clinical Approach
Arch Int Med 151:1317-1321, Sharma,Om.P.&Sharma,A.D., 1991

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

Mortality, Neoplasia, & Creutzfeldt-Jakob Disease in Patients Treated with Human Pituitary Growth Hormone in the UK
BMJ 302:824-828, Buchanan,C.R.,et al, 1991

Creutzfeldt-Jakob Disease and Other Transmissible Spongiform Encephalopathies
Ed, F. O. Bastian, Mosby Year Book, St. Louis 9:153, Maertens,P.&Quindlen,E.A., 1991

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

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

Rapid Detection of Creutzfeldt-Jakob Disease and Scrapie Prion Porteins
Neurol 40:110-117, Serban,D.,et al, 1990

A Simple & Effective Method for Inactivating Virus Infectivity from Patients with Creutzfeldt-Jakob Disease
Neurol 40:887-890, Brown,P.,et al, 1990

Positron Emission Tomography in Creutzfeldt-Jakob Disease
Arch Neurol 47:1035-1038, Holthodd,V.A.,et al, 1990

Transplanted Infections:Donor-To-Host Transmission with the Allograft
Ann Int Med 110:1001-1016, Gottesdiener,K.M., 1989



Showing articles 250 to 300 of 2929 << Previous Next >>