Dermaut et al., 2000 - Google Patents
Familial Creutzfeldt-Jakob disease in a patient carrying both a presenilin 1 missense substitution and a prion protein gene insertionDermaut et al., 2000
View PDF- Document ID
- 18437169139473666717
- Author
- Dermaut B
- Cruts M
- Backhovens H
- Lübcke U
- Van Everbroeck B
- Sciot R
- Dom R
- Martin J
- Van Broeckhoven C
- Cras P
- Publication year
- Publication venue
- Journal of neurology
External Links
Snippet
We describe a patient who was clinically diagnosed with familial early-onset Alzheimer disease (AD) carrying both the E318G substitution in presenilin 1 (PSEN1) and an insertion of 7 octapeptide coding repeats in the prion protein gene (PRNP). Neuropathological …
- 238000003780 insertion 0 title abstract description 21
Classifications
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12Q—MEASURING OR TESTING PROCESSES INVOLVING ENZYMES OR MICRO-ORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
- C12Q1/00—Measuring or testing processes involving enzymes, nucleic acids or micro-organisms; Compositions therefor; Processes of preparing such compositions
- C12Q1/68—Measuring or testing processes involving enzymes, nucleic acids or micro-organisms; Compositions therefor; Processes of preparing such compositions involving nucleic acids
- C12Q1/6876—Hybridisation probes
- C12Q1/6883—Hybridisation probes for diseases caused by alterations of genetic material
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12Q—MEASURING OR TESTING PROCESSES INVOLVING ENZYMES OR MICRO-ORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
- C12Q2600/00—Oligonucleotides characterized by their use
- C12Q2600/156—Polymorphic or mutational markers
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N2800/00—Detection or diagnosis of diseases
- G01N2800/28—Neurological disorders
- G01N2800/2814—Dementia; Cognitive disorders
- G01N2800/2821—Alzheimer
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| Lendon et al. | Hereditary dysphasic disinhibition dementia A frontotemporal dementia linked to 17 q21‐‐22 | |
| Prasher et al. | Molecular mapping of Alzheimer‐type dementia in Down's syndrome | |
| US5571671A (en) | Method for detecting alzheimer's disease | |
| Webb et al. | Phenotypic heterogeneity and genetic modification of P102L inherited prion disease in an international series | |
| Wu et al. | Early-onset familial Alzheimer's disease (EOFAD) | |
| Zubenko et al. | Association of the apolipoprotein E ϵ4 allele with clinical subtypes of autopsy‐confirmed Alzheimer's disease | |
| Ripoll et al. | A new point mutation in the prion protein gene at codon 210 in Creutzfeldt‐Jakob disease | |
| Dermaut et al. | Familial Creutzfeldt-Jakob disease in a patient carrying both a presenilin 1 missense substitution and a prion protein gene insertion | |
| Capellari et al. | Familial prion disease with a novel 144-bp insertion in the prion protein gene in a Basque family | |
| Heffernan et al. | Temporal cortex synaptophysin mRNA is reduced in Alzheimer's disease and is negatively correlated with the severity of dementia | |
| Le et al. | Cotton wool plaques in non-familial late-onset Alzheimer disease | |
| Reitz et al. | Endophenotypes in normal brain morphology and Alzheimer's disease: a review | |
| Yokota et al. | NACP/α-Synuclein, NAC, and β-amyloid pathology of familial Alzheimer's disease with the E184D presenilin-1 mutation: a clinicopathological study of two autopsy cases | |
| Arai et al. | Apolipoprotein E genotyping and cerebrospinal fluid tau protein: implications for the clinical diagnosis of Alzheimer's disease | |
| Ringman | What the study of persons at risk for familial Alzheimer's disease can tell us about the earliest stages of the disorder: a review | |
| Swartz et al. | Apolipoproteine and Alzheimer's disease: A genetic, molecular and neuroimaging review | |
| Doğan et al. | Clinical and molecular findings in a Turkish family who had a (c. 869-1G> A) splicing variant in PSEN1 gene with a rare condition: the variant alzheimer's disease with spastic paraparesis | |
| Skworc et al. | Familial Creutzfeldt‐Jakob disease with a novel 120‐bp insertion in the prion protein gene | |
| Sleegers et al. | Alzheimer’s disease: genes, pathogenesis and risk prediction | |
| Jimenez‐Escrig et al. | New V272A presenilin 1 mutation with very early onset subcortical dementia and parkinsonism | |
| Bornebroek et al. | Hereditary cerebral hemorrhage with amyloidosis-Dutch type (HCHWA-D): a review of the variety in phenotypic expression | |
| Bertoli Avella et al. | A novel presenilin 1 mutation (L174 M) in a large Cuban family with early onset Alzheimer disease | |
| Martikainen et al. | Brain pathology in three subjects from the same pedigree with presenilin‐1 (PSEN1) P264L mutation | |
| Vöglein et al. | Identification of a rare presenilin 1 single amino acid deletion mutation (F175del) with unusual amyloid-β processing effects | |
| Tiedt et al. | Phenotypic variability in autosomal dominant familial Alzheimer disease due to the S170F mutation of Presenilin-1 |