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
head turning
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
roving eye movements
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 250 to 300 of 1972 << Previous Next >>

Diagnosis of Creutzfeldt-Jakob Disease by Western Blot Identification of Marker Protein in Human Brain Tissue
NEJM 314:547-551, Brown,P.,et al, 1986

Abnormal Proteins in the Cerebrospinal Fluid of Patients with Creutzfeldt-Jakob Disease
NEJM 315:279-283, Harrington,M.G.,et al, 1986

Unilateral Creutzfeldt-Jakob Disease
Neurol 36:1517-1520, Yamanouchi,H.,et al, 1986

Creutzfeldt-Jakob Disease:Clinical Analysis of a Consecutive Series of 230 Neuropathologically Verified Cases
Ann Neurol 20:597-602, Brown,P.,et al, 1986

Computed Tomography During Creutzfeldt-Jakob Disease
Neuroradiology 27:362-364, Westphal,K.P.&Schachenmayr,W., 1985

Creutzfeldt-Jakob Disease after Administration of Human Growth Hormone
Lancet 2:244-246, Powell-Jackson,J.,et al, 1985

Human Growth Hormone & Creutzfeldt-Jakob Disease
Ann Int Med 103:288-289, Raiti,S., 1985

Creutzfeldt-Jakob Disease in a Young Adult with Idiopathic Hypopituitarism, Relation to Growth Hormone
NEJM 313:731-733, Koch,T.K.,et al, 1985

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

Subacute Spongiform Encephalopathy (Creutzfeldt-Jakob Disease) with Amyloid Angiopathy
JNNP 48:1175-1178, Keohane,C.,et al, 1985

Cerebral MR & CT Imaging in Creutzfeldt-Jakob Disease
J Comput Assist Tomogr 9:125-128, Kovanen,J.,et al, 1985

Ataxic Creutzfeldt-Jakob Disease:Diagnostic Techniques & Neuropathologic Observations in Early Disease
Neurol 35:254-257, Jones,H.R.,et al, 1985

Creutzfeldt-Jakob Disease Prion Proteins in Human Brains
NEJM 312:73-78, Bockman,J.M.,et al, 1985

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

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

Sodium Hydroxide Decontamination of Creutzfeldt-Jacob Disease Virus
NEJM 310:727, 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

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

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

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

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

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

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

Creutzfeldt-Jakob Disease in a 20-year-old Woman
Neurol 30:492-496, Packer,R.J.,et al, 1980

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

Clin. Path. Conference
Creutzfeldt-Jakob Disease, Ataxic Type, with Kuru Plaques, Case Record 45-1980, NEJM 303:1162-11710., , 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

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

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

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

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

Precautions in Medical Care Handling Matrl. of Patients with Transmissible Virus Dementia (Creutzfeldt-Jakob Disease)
NEJM 297:1253, Gajdusek,C.,et al, 1977

Clinical Pathologic Conference, Creutzfeldt-Jakob Disease, (Case record 43-1977)
NEJM 297:930, Scully,R.E.,et al, 1977

Creutzfeldt-Jakob Disease:Possible Association with Eating Brains
NEJM 296:820, 1977. (Letter), Alter,M.,et al, 1977

Computed Tomography in the Diagnosis of Creutzfeldt-Jakob Disease
J Comput Assist Tomogr 1:211-215, Krishna,C.V.G.,et al, 1977

Viral Infections & Demylinating Diseases
NEJM 288:1103, Weiner,J.,et al, 1973

The Association of Parkinsonism & Motor Neuron Disease
Neurol 22:443, Brait,K., 1972

Progressive Dementia-"Aspects of Diagnosis"
Hospital Physician, Nov 1970, p. 84., , 1970

Neuro CPC of MGH
Jacob-Creutzfeldt Disease, NEJM 264:1359-13641961., , 1961

Clinical Picture in Creutzfeldt-Jakob Disease
Trans of Amer Neuro Assn 5:l47, Fisher,C.M., 1960

A 62-Year-Old Woman with Progressive Spasticity, Weakness,and Gait Instability
Neurol 104:e210290, Voloshyna-Farber, E.Y.,et al, 2025

A 60-Year-Old Man with Weakness and Gait Dysfunction
JAMA Neurol 82:305-306, Jones,F.J.S.,et al, 2025

Severe Myotonic Crisis Resembling Malignant Hyperthermia
Neurol 104:e213497, Wadhwani,A.R.,et al, 2025

Congenital Titinopathy:Comprehensive Characterization of the Most Severe End of the Disease Spectrum
Ann Neurol 97:611-628, Coppens,S.,et al, 2025

A Toddler with Acute-Onset Hypotonia, Areflexia, and Ataxia
Neurol 104:e213593, Pence, K.L. &Clark, R.A., 2025



Showing articles 250 to 300 of 1972 << Previous Next >>