References
- TosunDSchuffNRabinoviciGDDiagnostic utility of ASL-MRI and FDG-PET in the behavioral variant of FTD and ADAnn Clin Transl Neurol201631074075127752510
- OlszewskaDALonerganRFallonEMLynchTGenetics of frontotemporal dementiaCurr Neurol Neurosci Rep2016161210727878525
- GuoQHZhouBZhaoQHWangBHongZMemory and Executive Screening (MES): a brief cognitive test for detecting mild cognitive impairmentBMC Neurol20121211923050770
- KasugaKKikuchiMTokutakeTSystematic review and meta-analysis of Japanese familial Alzheimer’s disease and FTDP-17J Hum Genet201560528128325694106
- OgakiKLiYTakanashiMIshikawaKAnalyses of the MAPT, PGRN, and C9orf72 mutations in Japanese patients with FTLD, PSP, and CBSParkinsonism Relat Disord2013191152022818528
- KimEJKwonJCParkKHClinical and genetic analysis of MAPT, GRN, and C9orf72 genes in Korean patients with frontotemporal dementiaNeurobiol Aging20143551213.e1317
- TangMGuXWeiJAnalyses MAPT, GRN, and C9orf72 mutations in Chinese patients with frontotemporal dementiaNeurobiol Aging201646235.e1115
- ShiZLiuSXiangLFrontotemporal dementia-related gene mutations in clinical dementia patients from a Chinese populationJ Hum Genet201661121003100827439681
- CheXQZhaoQHHuangYGenetic features of MAPT, GRN, C9orf72 and CHCHD10 gene mutations in Chinese patients with frontotemporal dementiaCurr Alzheimer Res201714101102110828462717
- LinHCLinCHChenPLChengSJChenPHIntrafamilial phenotypic heterogeneity in a Taiwanese family with a MAPT p.R5H mutation: a case report and literature reviewBMC Neurol201717118628923025
- YangYTangBSWengLGenetic identification is critical for the diagnosis of parkinsonism: a Chinese pedigree with early onset of parkinsonismPLoS One2015108e013624526295349
- WuLYFengXYLiHZClinical and neuroimaging features of frontotemporal dementia with parkinsonism linked to chromosome 17China J Neurol20175011116
- SunLChenKLiXXiaoSRapidly progressive frontotemporal dementia associated with MAPT mutation G389RJ Alzheimers Dis201755277778527802239
- SiudaJFujiokaSWszolekZKParkinsonian syndrome in familial frontotemporal dementiaParkinsonism Relat Disord201420995796424998994
- SitekEJNarozanskaEBarczakAAgraphia in patients with frontotemporal dementia and parkinsonism linked to chromosome 17 with P301L MAPT mutation: dysexecutive, aphasic, apraxic or spatial phenomenon?Neurocase2014201698623121543
- IshizukaTNakamuraMIchibaMSanoAFamilial semantic dementia with P301L mutation in the Tau geneDement Geriatr Cogn Disord201131533434021555888
- KodamaKOkadaSIsekiEFamilial frontotemporal dementia with a P301L tau mutation in JapanJ Neurol Sci20001761576410865093
- Borrego-ÉcijaSMorgadoJPalencia-MadridLFrontotemporal Dementia Caused by the P301L Mutation in the MAPT Gene: Clinicopathological Features of 13 Cases from the Same Geographical Origin in Barcelona, SpainDement Geriatr Cogn Disord2017443–421322128934750
- VerfaillieSCAdriaanseSMBinnewijzendMACerebral perfusion and glucose metabolism in Alzheimer’s disease and frontotemporal dementia: two sides of the same coin?Eur Radiol201525103050305925899416