Neurology Specific Literature Search   
 
[home][thesaurus]
    

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 1900 to 1950 of 1974 << Previous Next >>

Clinical & Path Features & Lab Confirmation of Creutzfeldt-Jakob Disease with Pituitary Derived Human Growth Hormone
NEJM 313:734-738, Gibbs,C.J.,et al, 1985

Potential Epidemic of Creutzfeldt-Jakob Disease from Human Growth Hormone Therapy
NEJM 313:728-731, Brown,P.,et al, 1985

Is the Neurologic Examination Becoming Obsolete
Neurol 35:559, Ziegler,D.K., 1985

Relapsing Ophthalmoparesis-Sensory Neuropathy Syndrome
Neurol 35:595-596, Kaplan,J.G.,et al, 1985

Cysticercosis-Review of 230 Patients
Bull Clin Neurosci 50:76-101, McCormick.G.F., 1985

Creutzfeldt-Jakob Disease of Long Duration:Clinicopathological Characteristics
Ann Neurol 16:295-304, Brown,P.,et al, 1984

Creutzfeldt-Jakob Disease:A Case of 16 Years Duration
Ann Neurol 15:107-110, Cutler,N.R.,et al, 1984

Ophthalmoplegic Polyneuropathy:Another Case in Association with Epstein-Barr Virus
Ann Neurol 15:403, Brey,R.L., 1984

Electrophysiologic Studies in Miller Fisher Syndrome
Neurol 34:685-688, Jamal,G.A.,et al, 1984

Classic & Generalized Variants of Pick's Disease, A Clinicopath, Ultrastruc & Immunocyto Study
Ann Neurol 16:467-480, Munoz-Garcia,D.,et al, 1984

Sodium Hydroxide Decontamination of Creutzfeldt-Jacob Disease Virus
NEJM 310:727, Brown,P.,et al, 1984

Miller Fisher Syndrome:Clinical & Electrophysiologic Evidence of Peripheral Origin in 10 Cases
Neurol 34:953-956, Sauron,B.,et al, 1984

Bitemporal Hypometabolism in Creutzfeldt-Jakob Disease Measured by Positron Emission Tomography
J Comput Assist Tomogr 8:978-981, Friedland,R.P.,et al, 1984

The Terminology of Transient Visual Loss Due to Vascular Insufficiency
Stroke 15:907-908, Hedges,T.R., 1984

Clinicopathological Conference
Case 49-1983, Creutzfeldt-Jakob, NEJM 309:1440-1449983., , 1983

The Human Kluver-Bucy Syndrome
Neurol 33:1141-1145, Lilly,R.,et al, 1983

Slowly Progressive Aphasia without Generalized Dementia
Ann Neurol 13:687, Heath,P.D.,et al, 1983

The Effect of Amantadine on Arousal & EEG Patterns of Creutzfeldt-Jakob Disease
Arch Neurol 40:555-559, Terzano,M.G.,et al, 1983

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

Ophthalmoplegic Polyneuropathy Associated with Infectious Mononucleosis
Ann Neurol 13:219-220, Salazar,A.,et al, 1983

New Diagnostic Criteria for Multiple Sclerosis:Guidelines for Research Protocols
Neurol 13:227-231, Poser,C.M.,et al, 1983

Misdiagnosis of Stroke
Lancet 1:328-331, Norris,J.W.&Hachinski,V.C., 1982

Slowly Progressive Aphasia Without Generalized Dementia
Ann Neurol 11:592-598, Mesulam,M.M., 1982

Computed Tomography in Pick's Disease:Findings in a Family Affected in Three Consecutive Generations
J Comput Assist Tomogr 6:907-911, Groen,J.J.,et al, 1982

Chemical Disinfection Of Creutzfeldt-Jakob Disease Virus
NEJM 306:1279-1282, Brown,P.,et al, 1982

Repeated Suppression Of Creutzfeldt-Jakob Disease With Vidarabine
Jr. , et al, Lancet 2:564-56582., Furlow,T.W., 1982

Yersinia Arthritis & Guillain-Barre Syndrome
NEJM 307:755, Faraq,S.S.,et al, 1982

Upward Gaze Paralysis as the Initial Sign of Fisher's Syndrome
Arch Neurol 39:781-782, Keane,J.R.,et al, 1982

Brainstem Encephalitis & The Syndrome Of Miller Fisher
Brain 105:481-495, Al-Din,A.N.,et al, 1982

Biologic Distinction Between Sporadic & Familial Alzheimer Disease by an in vitro Cell Fusion Test
Neurol 31:323-325, Dubois-Moreau,M.C.,et al, 1981

Autonomic Dysfunction in Subacute Spongiform Encephalopathy
Arch Neurol 38:114-117, Khurana,R.K.,et al, 1981

Fisher Syndrome in Childhood
Neurol 31:555-560, Becker,W.J.,et al, 1981

Successful Plasmapheresis in the Miller-Fisher Syndrome
BMJ 282:778, Littlewood,R.,et al, 1981

Fisher's Syndrome Associated With Epstein-Barr Virus
Arch Neurol 38:134-135, Slavick,H.E.,et al, 1981

Kluver-Bucy Syndrome in Pick disease:Clinical & patho-logic Correlations
Neurol 31:1415-1422, Cummings,J.L.,et al, 1981

Amyotrophic Lateral Sclerosis & its Association with Dementia, Parkinsonism & Other Neurological Disorders:A Review
Brain 104:217-247, Hudson,A.J., 1981

Evidence For & Against the Transmissibility of Alzheimer Disease
Neurol 30:945-950, Goudsmit,J.,et al, 1980

Periodic Lateralized Epileptiform Complexes (PLEDs) in Creutzfeldt-Jakob Disease
Neurol 30:611-617, Au,W.J.,et al, 1980

Failure of Interferon to Modify Creutzfeldt-Jakob Disease
BMJ 280:902, Kovanen,J.,et al, 1980

The Not-So-Benign Miller Fisher Syndrome, A Variant of the Guillain-Barre Syndrome
Arch Neurol 37:384-385, Blau,I.,et al, 1980

Transissible Dementias:Current Problems in Tissue Handling
Neurol 30:302-303, Baringer,J.R.,et al, 1980

Serial EEG Findings in 27 Cases of Creutzfeldt-Jakob Disease
Arch Neurol 37:143-145, Chiofalo,N.,et al, 1980

Alzheimer Neurofibrillary Tangles in Diseases Other Than Senile & Presenile Dementia
Ann Neurol 5:288-294, Wisniewski,K.,et al, 1979

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

Clinical Similarity of Alzheimer & Creutzfeldt-Jakob Disease
Ann Neurol 6:368-369, Watson,C.P., 1979

Benign Recurrent Vertigo
JNNP 42:363-367, Slater,R., 1979

Creutzfeldt-Jakob Disease Treated with Amantadine
JNNP 42:960-961, Sanders,W.L., 1979

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

Subacute Spongiform Encephalopathy (Creutzfeldt-Jakob Disease)
Brain 101:333-344, Masters,C.L.,et al, 1978



Showing articles 1900 to 1950 of 1974 << Previous Next >>