| scholarly article | Q13442814 |
| P356 | DOI | 10.1002/AJMG.B.30761 |
| P8608 | Fatcat ID | release_uzynqzmrybc2fllmmailrruh4y |
| P698 | PubMed publication ID | 18425766 |
| P2093 | author name string | Liu Zheng | |
| Ye Jing | |||
| Wang Fen | |||
| Dong Xiumin | |||
| Jia Jianping | |||
| Jia Longfei | |||
| Lv Haiyan | |||
| Song Haiqing | |||
| Zhang Xinqing | |||
| P2860 | cites work | “Mini-mental state” | Q25938989 |
| Clinical diagnosis of Alzheimer's disease: report of the NINCDS-ADRDA Work Group under the auspices of Department of Health and Human Services Task Force on Alzheimer's Disease | Q27860795 | ||
| Mutations of the prion protein gene phenotypic spectrum | Q28214069 | ||
| Prion protein: evolution caught en route | Q28776299 | ||
| Frontotemporal lobar degeneration: a consensus on clinical diagnostic criteria | Q29614410 | ||
| Early-onset autosomal dominant Alzheimer disease: prevalence, genetic heterogeneity, and mutation spectrum | Q33870467 | ||
| Huntington disease phenocopy is a familial prion disease | Q34044888 | ||
| High prevalence of pathogenic mutations in patients with early-onset dementia detected by sequence analyses of four different genes | Q34146052 | ||
| Mutant prion proteins in Gerstmann-Sträussler-Scheinker disease with neurofibrillary tangles | Q34539307 | ||
| Prion disease: a deadly disease for protein misfolding. | Q34557081 | ||
| Clinical research criteria for the diagnosis of progressive supranuclear palsy (Steele-Richardson-Olszewski syndrome): report of the NINDS-SPSP international workshop | Q34733901 | ||
| Consensus guidelines for the clinical and pathologic diagnosis of dementia with Lewy bodies (DLB): report of the consortium on DLB international workshop | Q34736093 | ||
| Creutzfeldt-Jakob disease (CJD) with a mutation at codon 148 of prion protein gene: relationship with sporadic CJD. | Q35094470 | ||
| Fatal familial insomnia and familial Creutzfeldt-Jakob disease: different prion proteins determined by a DNA polymorphism | Q35138028 | ||
| Patients with Alzheimer's disease and dementia with Lewy bodies mistaken for Creutzfeldt-Jakob disease | Q35462665 | ||
| Phenotypic variability in familial prion diseases due to the D178N mutation. | Q35484873 | ||
| Mutations causing neurodegenerative tauopathies | Q35992153 | ||
| Overlap between neurodegenerative disorders | Q36117422 | ||
| Prion disease genetics | Q36359872 | ||
| Insertions in the prion protein gene in atypical dementias | Q42614533 | ||
| Disease-associated F198S mutation increases the propensity of the recombinant prion protein for conformational conversion to scrapie-like form | Q44174343 | ||
| A patient with dementia with Lewy bodies and codon 232 mutation of PRNP. | Q44228587 | ||
| Differential diagnosis of 201 possible Creutzfeldt-Jakob disease patients | Q44795783 | ||
| When sporadic disease is not sporadic: the potential for genetic etiology | Q46689019 | ||
| Familial Creutzfeldt-Jakob disease with an R208H-129V haplotype and Kuru plaques | Q46988546 | ||
| A prion-linked psychiatric disorder | Q48041408 | ||
| Novel prion protein gene mutation presenting with subacute PSP-like syndrome. | Q48246405 | ||
| Genetic prion disease: the EUROCJD experience | Q48532612 | ||
| Molecular genetics of human prion diseases in Germany | Q48713992 | ||
| Creutzfeldt-Jakob disease mimicking corticobasal degeneration clinical and MRI data of a case | Q48951730 | ||
| Increased incidence of genetic human prion disease in Hungary. | Q50772959 | ||
| Gerstmann-Sträussler-Scheinker disease with the Q217R mutation mimicking frontotemporal dementia | Q57419080 | ||
| P433 | issue | 6 | |
| P921 | main subject | neurodegeneration | Q1755122 |
| P304 | page(s) | 938-944 | |
| P577 | publication date | 2008-09-01 | |
| P1433 | published in | American Journal of Medical Genetics Part B: Neuropsychiatric Genetics | Q15762380 |
| P1476 | title | PRNP mutations in a series of apparently sporadic neurodegenerative dementias in China | |
| P478 | volume | 147B |
| Q47096801 | A novel prion protein variant in a patient with semantic dementia |
| Q58781975 | Characterization of mutations in (prion) gene and their possible roles in neurodegenerative diseases |
| Q92320503 | Clinical Laboratory Tests Used To Aid in Diagnosis of Human Prion Disease |
| Q46560834 | Genetic PrP Prion Diseases |
| Q39036368 | Genetic prion disease: Experience of a rapidly progressive dementia center in the United States and a review of the literature. |
| Q38871224 | Hereditary Human Prion Diseases: an Update |
| Q47874175 | PSEN1 p.Met233Val in a Complex Neurodegenerative Movement and Neuropsychiatric Disorder |
| Q39605681 | Prion propagation in cells expressing PrP glycosylation mutants |
| Q42882583 | Prospective 10-year surveillance of human prion diseases in Japan. |
| Q36639581 | Quantifying prion disease penetrance using large population control cohorts |
| Q34652909 | Relationships between clinicopathological features and cerebrospinal fluid biomarkers in Japanese patients with genetic prion diseases. |
| Q37364036 | Systematic investigation of predicted effect of nonsynonymous SNPs in human prion protein gene: a molecular modeling and molecular dynamics study |
| Q37705846 | The genetics of prion diseases |
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