X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (19) 19
index medicus (19) 19
creutzfeldt-jakob disease (13) 13
middle aged (12) 12
aged (11) 11
female (11) 11
male (11) 11
neurosciences (11) 11
clinical neurology (8) 8
creutzfeldt-jakob syndrome - genetics (8) 8
mutation (8) 8
aged, 80 and over (7) 7
creutzfeldt-jakob-disease (7) 7
case-control studies (6) 6
genotype (6) 6
nervous system diseases (6) 6
prion protein (6) 6
prions - genetics (6) 6
protein (6) 6
adult (5) 5
brain - pathology (5) 5
bse (5) 5
prion diseases (5) 5
prion proteins (5) 5
risk (5) 5
creutzfeldt-jakob syndrome - diagnosis (4) 4
epidemiology (4) 4
mental disorders (4) 4
neurology (4) 4
risk factors (4) 4
surveillance (4) 4
abridged index medicus (3) 3
age (3) 3
alzheimer disease - genetics (3) 3
alzheimer's disease (3) 3
animal diseases (3) 3
animals (3) 3
classification (3) 3
creutzfeldt-jakob syndrome - cerebrospinal fluid (3) 3
creutzfeldt-jakob syndrome - mortality (3) 3
creutzfeldt-jakob syndrome - pathology (3) 3
dementia (3) 3
diagnosis (3) 3
europe (3) 3
genetic aspects (3) 3
genetic predisposition to disease (3) 3
genetics (3) 3
multidisciplinary sciences (3) 3
pathology (3) 3
point mutation (3) 3
polymorphism (3) 3
polymorphism, single nucleotide (3) 3
prions (3) 3
prnp (3) 3
proteins (3) 3
prp (3) 3
psychiatry (3) 3
research (3) 3
sensitivity and specificity (3) 3
alpha-synuclein (2) 2
alzheimers-disease (2) 2
amyloid precursor protein (2) 2
analysis (2) 2
apoe genotype (2) 2
article (2) 2
arvicolinae (2) 2
biology (2) 2
brain chemistry (2) 2
cell biology (2) 2
codon 129 (2) 2
cohort studies (2) 2
frontotemporal dementia (2) 2
genes (2) 2
genetics & heredity (2) 2
genomes (2) 2
genomics (2) 2
gerstmann-straussler-scheinker disease - genetics (2) 2
haplotypes (2) 2
heterogeneity (2) 2
identification (2) 2
infectious diseases (2) 2
internal medicine (2) 2
italy (2) 2
mortality (2) 2
neurodegenerative diseases (2) 2
original research article (2) 2
pathogenesis (2) 2
patients (2) 2
phenotype (2) 2
prion (2) 2
prion protein gene (2) 2
prion protein polymorphism (2) 2
prion proteins - genetics (2) 2
prions - chemistry (2) 2
prnp gene (2) 2
protein folding (2) 2
prpsc proteins - analysis (2) 2
prpsc proteins - genetics (2) 2
recombinant proteins - chemistry (2) 2
research article (2) 2
more...
Library Location Library Location
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Journal of Neurology, Neurosurgery & Psychiatry, ISSN 0022-3050, 12/2018, Volume 89, Issue 12, pp. 1243 - 1249
ObjectivesThe Glu to Lys change at codon 200 (E200K) of the PRNP gene is the most frequent mutation associated to genetic Creutzfeldt-Jakob disease (CJD) and... 
GWA study | Creutzfeldt-Jakob disease | PATHOGENESIS | SYSTEM | SURGERY | SOLUBLE EPOXIDE HYDROLASE | SCRAPIE | RISK-FACTORS | INHIBITION | PSYCHIATRY | MOUSE | CLINICAL NEUROLOGY | GENOME-WIDE ASSOCIATION | Cytochrome | Neurosciences | BSE | Pathogenesis | Genes | Population | Genomes | Mutation | Age
Journal Article
Science Translational Medicine, ISSN 1946-6234, 01/2016, Volume 8, Issue 322, pp. 322ra9 - 322ra9
Journal Article
Acta neuropathologica communications, ISSN 2051-5960, 03/2019, Volume 7, Issue 1, pp. 47 - 47
First-degree family members refused genetic examination. [...]the case reported here differs from previously described cases because of the presence of a rapid... 
Prion diseases | R208H | Mutation | Neuropathology | Genetic Creutzfeldt-Jakob disease | Dementia | HAPLOTYPE | NEUROSCIENCES | Creutzfeldt-Jakob disease | Haplotypes | Proteins | Genotype & phenotype | Insomnia | BSE | Patients | Polymorphism
Journal Article
PLoS ONE, ISSN 1932-6203, 04/2015, Volume 10, Issue 4, pp. e0123654 - e0123654
Journal Article
Journal Article
Science translational medicine, ISSN 1946-6234, 1/2016, Volume 8, Issue 322, pp. 322ra9 - 322ra9
More than 100,000 genetic variants are reported to cause Mendelian disease in humans, but the penetrance - the probability that a carrier of the purported... 
Journal Article