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advances in neurology
agnosia
agnosia, visual
akinetic mute
alexia
algorithm
alternating rapid movement, impaired
Alzheimer's disease
Alzheimer's disease, rapidly progressive
Alzheimer's disease, rate of clinical decline
Alzheimer's disease, visual variant
AMPA receptor antibodies
amyloid angiopathy, cerebral
amyloid plaques
amyotrophic lateral sclerosis
angiitis, isolated of CNS
animal exposure
anorexia
anxiety
aphasia, transcortical
aphasia, transcortical-sensory
asymptomatic
ataxia
ataxia, cerebellar
ataxia, progressive
ataxia, truncal
ataxic gait
atypical
autoantibodies
autoimmune disease
axonal degeneration
Balint's syndrome
basal ganglia
basal ganglia, lesion of
basal ganglia, lesion, bilateral
behavioral disorder
biologic markers
blood transfusion
bovine spongiform encephalopathy
brain biopsy
brain biopsy, complications of
brain biopsy, indication
brain biopsy, negative
carcinoma
CAT scan, abnormal
CAT scan, emission, abnormal
caudate nucleus, lesion of
caudate nucleus, lesion of, bilateral
central nervous system, infection of
cerebellar lesion
cerebellum, disease of
cerebral cortex
cerebrospinal fluid
cerebrospinal fluid, abnormal
cerebrospinal fluid, enzymes in
cerebrospinal fluid, protein of
cerebrovascular accident, mimics
cerebrovascular accident, misdiagnosis
Charles Bonnet's syndrome
children
choreoathetosis
chromosome 20
cingulate gyrus
Clinical Pathologic Conference(C.P.C.)
cognition, slowed
comorbidities
complications
concentration, impaired
confusion
contactin associated protein like 2 antibodies
controversies in neurology
cortical blindness
Creutzfeldt-Jakob disease, genetic
deep gray nuclei
degenerative diseases of CNS
delay in diagnosis
delirium
delusion
dementia
dementia, diagnostic evaluation of
dementia, familial
dementia, frontotemporal
dementia, prevention of
dementia, rapidly progressive
dementia, reversible
dementia, screening for
dementia, transmissible
dementia, treatment of
denial of blindness(Antons syndrome)
depression
diabetes mellitus
diagnostic criteria
diet
differential diagnosis
difficulty climbing stairs
diplopia
dizziness
drug withdrawal
dural graft, cadaveric
dysarthria
dysdiadochokinesia
dysmetria
efficacy
electroencephalogram
electroencephalogram, abnormalities of
electroencephalogram, periodic complexes
electron microscopy
electrophoretic pattern, CSF
electrophoretic pattern, serum
encephalitis
encephalitis, autoimmune
encephalitis, paraneoplastic
encephalitis, viral
encephalopathy
encephalopathy, Hashimoto's
encephalopathy, metabolic
endoscopy
enolase
epidemic
epidemiology of neurology
epilepsia partialis continua
episodic disorders
executive dysfunction
eye movement, disorders of
falling
false negative
false positive
familial
farmer
fatal familial insomnia
finger nose finger test
frontal lobe, anatomy and physiology
gait disorder
gait, apraxic
gamma amino butyric acid receptor antibody
gene mutation
genetic counselling
genetic neurologic disorders
genetic testing
Gerstmann syndrome
Gerstmann-Straussler-Scheinker disease
gliosis
glycine receptor antibodies
grasp reflex
growth hormone
hallucination
hallucination, visual
hallucination, visual, benign
handwriting
headache
headache, episodic
heel-knee-shin test
hemianopia, homonymous
hemiparesis
heralding manifestation
hockey stick sign
Huntington's chorea
hyperosmia
hypogeusia
hypophonia
iatrogenic neurologic disorders
imbalance
immunocompetent
immunodeficiency
immunohistochemistry
immunologic disease
immunosuppressive agents
incidence
incoordination
incubation period
insomnia
insular cortex
intellectual deterioration
irritability
Jakob-Creutzfeldt disease
Jakob-Creutzfeldt disease, cerebellar variant
Jakob-Creutzfeldt disease, Heidenhain variant
Jakob-Creutzfeldt disease, medical precaution with
Jakob-Creutzfeldt disease, variant
Jakob-Creutzfeldt disease, young adult
kuru
kuru plaques
leg numbness
leucine rich glioma inactivated 1 antibodies
Lewy body disease, diffuse
life expectancy
limbic encephalitis
lobar atrophy
lymphoma
lymphoma involving CNS
lymphoma, primary of CNS
malignancy screen
memory, defect of recent
memory, impairment of
mental status, abnormal
migraine
mimics
Mini Mental Status Examination
misdiagnosis
molecular genetics
monoparesis
mortality
Morvan's fibrillary chorea
movement disorder
MRI
MRI pattern
MRI, abnormal
MRI, ADC maps
MRI, diffusion weighted
MRI, diffusion weighted, pattern
MRI, false negative
MRI, false positive
MRI, FLAIR
MRI, functional
MRI, high signal foci on
MRI, high signal intensity of basal ganglia
MRI, indications for
MRI, negative
MRI, proton density
MRI, punctate pattern
MRI, serial
multiple sclerosis
multiple system atrophy
mutism
myoclonic jerks
myoclonus
nasal brushings
negative
neoplasm, primary of CNS
neurologic complications of, surgery
neurologic disease
neurologic disease, diagnoses of
neurologic examination, focal
neurologic signs
neurologic testing
neuron specific enolase
neuronal cell surface antigen
neuropathology
neuropathology, brain
neuropathy
NMDA antagonists
normal
nystagmus
occipital cortex
occipital lobe
occipital lobe, lesion of
occupational neurologic disorders
old age, neurology of
olfactory biopsy
olfactory bulb
olfactory cortex
olfactory mucosa
olfactory pathway
olfactory tract
pain
pain, leg
palmomental response
Parkinson disease
Parkinsonism plus syndrome
Parkinsonism syndrome
pathognomonic
pathologic reflex
peduncular hallucinosis
personality change
pituitary, hormones of
posterior cortical atrophy
posterior leukoencephalopathy syndrome
potassium channel antibodies
practice guidelines
preclinical
prevention of neurologic disorders
prion disease
prognosis
progressive neurologic disorder
protein 14-3-3, cerebrospinal fluid
protein 14-3-3, cerebrospinal fluid, false negative
protein 14-3-3, cerebrospinal fluid, false positive
psychiatric disorder
psychiatric problems in neurologic disorders
psychosis
pulvinar sign
pursuit eye movements, abnormal
putamen, lesion of
putamen, lesion of, bilateral
rapidly progressing neurologic illness
real-time quaking-induced conversion
release phenomena
remote effect of cancer on the nervous system
reversible cerebral vasoconstrictive syndromes
review article
risk factors
risk-benefit assessment
Romberg's sign
rooting reflex
saccadic eye movements, abnormal
sarcoidosis, CNS
scrapie
screening
seizure
senile plaques
sensory symptoms
serum S100 protein
simultanagnosia
single photon emission computed tomography
skin, biopsy
smell
snout reflex
spongy degeneration of brain
square wave jerks
startle myoclonus
startle reaction
stiff legs
striatum, lesion of
striatum, lesion of, bilateral
symmetric brain lesions
tandem gait, ataxic
taste
tau protein
tauopathy
thalamus, lesion of
thalamus, lesion of-bilateral
thyroiditis
tone, muscle
tonsil biopsy
toxic encephalopathy
treatment of neurologic disorder
tremor, intention
vasculitides
vertigo
vertigo, episodic
viral infection, CNS
vision, blurred
visual cortex
visual impairment
visual loss
visual loss, progressive
walking frame
walking, difficulty with
weight loss
West Nile fever
Western immunoblot test
wheelchair
wide based gait
workup
Showing articles 250 to 300 of 1974 << Previous Next >>

Precautions in Handling Tissues
Fluids, & Other Contam Materials from Patients with Documented or Suspected Creutzfeldt-Jakob Diseas, , Aeurol 19:75-77,1986., 1986

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

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

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

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

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

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

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

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

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

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

Imaging Findings in Giant Cell Arteritis:Dont Turn a Blind Eye to the Obvious!
AJNR 46:457-464, Bathla,G.,et al, 2025

A 56-Year-Old Woman with New-Onset Hoarsement and Dysphagia
Neurol 104:e213363, McAree,M. & Frontera, J.A., 2025

A 32 Year-Old Woman with Recurrent Intracerebral Hemorrhages
Neurol 104:e213422, Hindsholm,M.F.,et al, 2025

Clinical Presentation, Investigation Findings, and Outcomes of IgG4-Related Pachymeningitis,A Systematic Review
JAMA Neurol 82:193-199, Terrim,S.,et al, 2025

Clinicopathological Conference, Eosinophilic meningitis due to Angiostrongylus cantonensis infection
NEJM 392:699-709, Case 5-2025, 2025



Showing articles 250 to 300 of 1974 << Previous Next >>