These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
122 related articles for article (PubMed ID: 38228392)
1. Liu C; Dong L; Wang J; Li J; Huang X; Lei D; Mao C; Chu S; Sha L; Xu Q; Peng B; Cui L; Gao J J Med Genet; 2024 May; 61(6):543-548. PubMed ID: 38228392 [TBL] [Abstract][Full Text] [Related]
2. Genetic Spectrum and Clinical Heterogeneity of Chinese Frontotemporal Dementia Patients: Data from PUMCH Dementia Cohort. Dong L; Wang J; Liu C; Li J; Mao C; Huang X; Chu S; Peng B; Cui L; Gao J J Alzheimers Dis; 2022; 89(3):893-901. PubMed ID: 35964197 [TBL] [Abstract][Full Text] [Related]
3. Analyses MAPT, GRN, and C9orf72 mutations in Chinese patients with frontotemporal dementia. Tang M; Gu X; Wei J; Jiao B; Zhou L; Zhou Y; Weng L; Yan X; Tang B; Xu J; Shen L Neurobiol Aging; 2016 Oct; 46():235.e11-5. PubMed ID: 27311648 [TBL] [Abstract][Full Text] [Related]
5. Progranulin Gene Mutations in Chinese Patients with Frontotemporal Dementia: A Case Report and Literature Review. Chu M; Nan H; Jiang D; Liu L; Huang A; Wang Y; Wu L J Alzheimers Dis; 2023; 93(1):225-234. PubMed ID: 36970912 [TBL] [Abstract][Full Text] [Related]
6. The spectrum of mutations in progranulin: a collaborative study screening 545 cases of neurodegeneration. Yu CE; Bird TD; Bekris LM; Montine TJ; Leverenz JB; Steinbart E; Galloway NM; Feldman H; Woltjer R; Miller CA; Wood EM; Grossman M; McCluskey L; Clark CM; Neumann M; Danek A; Galasko DR; Arnold SE; Chen-Plotkin A; Karydas A; Miller BL; Trojanowski JQ; Lee VM; Schellenberg GD; Van Deerlin VM Arch Neurol; 2010 Feb; 67(2):161-70. PubMed ID: 20142524 [TBL] [Abstract][Full Text] [Related]
7. Genetic Features of MAPT, GRN, C9orf72 and CHCHD10 Gene Mutations in Chinese Patients with Frontotemporal Dementia. Che XQ; Zhao QH; Huang Y; Li X; Ren RJ; Chen SD; Wang G; Guo QH Curr Alzheimer Res; 2017; 14(10):1102-1108. PubMed ID: 28462717 [TBL] [Abstract][Full Text] [Related]
8. Rates of Brain Atrophy Across Disease Stages in Familial Frontotemporal Dementia Associated With MAPT, GRN, and C9orf72 Pathogenic Variants. Staffaroni AM; Goh SM; Cobigo Y; Ong E; Lee SE; Casaletto KB; Wolf A; Forsberg LK; Ghoshal N; Graff-Radford NR; Grossman M; Heuer HW; Hsiung GR; Kantarci K; Knopman DS; Kremers WK; Mackenzie IR; Miller BL; Pedraza O; Rascovsky K; Tartaglia MC; Wszolek ZK; Kramer JH; Kornak J; Boeve BF; Boxer AL; Rosen HJ; JAMA Netw Open; 2020 Oct; 3(10):e2022847. PubMed ID: 33112398 [TBL] [Abstract][Full Text] [Related]
9. Frontotemporal dementia-related gene mutations in clinical dementia patients from a Chinese population. Shi Z; Liu S; Xiang L; Wang Y; Liu M; Liu S; Han T; Zhou Y; Wang J; Cai L; Gao S; Ji Y J Hum Genet; 2016 Dec; 61(12):1003-1008. PubMed ID: 27439681 [TBL] [Abstract][Full Text] [Related]
10. Cerebrospinal Fluid YKL-40 and Chitotriosidase Levels in Frontotemporal Dementia Vary by Clinical, Genetic and Pathological Subtype. Woollacott IOC; Nicholas JM; Heller C; Foiani MS; Moore KM; Russell LL; Paterson RW; Keshavan A; Schott JM; Warren JD; Heslegrave A; Zetterberg H; Rohrer JD Dement Geriatr Cogn Disord; 2020; 49(1):56-76. PubMed ID: 32344399 [TBL] [Abstract][Full Text] [Related]
11. Distinct clinical and pathological phenotypes in frontotemporal dementia associated with MAPT, PGRN and C9orf72 mutations. Snowden JS; Adams J; Harris J; Thompson JC; Rollinson S; Richardson A; Jones M; Neary D; Mann DM; Pickering-Brown S Amyotroph Lateral Scler Frontotemporal Degener; 2015; 16(7-8):497-505. PubMed ID: 26473392 [TBL] [Abstract][Full Text] [Related]
12. Age at symptom onset and death and disease duration in genetic frontotemporal dementia: an international retrospective cohort study. Moore KM; Nicholas J; Grossman M; McMillan CT; Irwin DJ; Massimo L; Van Deerlin VM; Warren JD; Fox NC; Rossor MN; Mead S; Bocchetta M; Boeve BF; Knopman DS; Graff-Radford NR; Forsberg LK; Rademakers R; Wszolek ZK; van Swieten JC; Jiskoot LC; Meeter LH; Dopper EG; Papma JM; Snowden JS; Saxon J; Jones M; Pickering-Brown S; Le Ber I; Camuzat A; Brice A; Caroppo P; Ghidoni R; Pievani M; Benussi L; Binetti G; Dickerson BC; Lucente D; Krivensky S; Graff C; Öijerstedt L; Fallström M; Thonberg H; Ghoshal N; Morris JC; Borroni B; Benussi A; Padovani A; Galimberti D; Scarpini E; Fumagalli GG; Mackenzie IR; Hsiung GR; Sengdy P; Boxer AL; Rosen H; Taylor JB; Synofzik M; Wilke C; Sulzer P; Hodges JR; Halliday G; Kwok J; Sanchez-Valle R; Lladó A; Borrego-Ecija S; Santana I; Almeida MR; Tábuas-Pereira M; Moreno F; Barandiaran M; Indakoetxea B; Levin J; Danek A; Rowe JB; Cope TE; Otto M; Anderl-Straub S; de Mendonça A; Maruta C; Masellis M; Black SE; Couratier P; Lautrette G; Huey ED; Sorbi S; Nacmias B; Laforce R; Tremblay ML; Vandenberghe R; Damme PV; Rogalski EJ; Weintraub S; Gerhard A; Onyike CU; Ducharme S; Papageorgiou SG; Ng ASL; Brodtmann A; Finger E; Guerreiro R; Bras J; Rohrer JD; Lancet Neurol; 2020 Feb; 19(2):145-156. PubMed ID: 31810826 [TBL] [Abstract][Full Text] [Related]
13. Identification and functional characterization of novel variants of MAPT and GRN in Chinese patients with frontotemporal dementia. Cheng HR; Lin RR; Li HL; Xue YY; Gao PR; Chen DF; Tao QQ; Wu ZY Neurobiol Aging; 2023 Mar; 123():233-243. PubMed ID: 36641371 [TBL] [Abstract][Full Text] [Related]
14. Phenotype Heterogeneity and Genotype Correlation of MAPT Mutations in a Chinese PUMCH Cohort. Mao C; Dong L; Li J; Huang X; Lei D; Wang J; Chu S; Liu C; Peng B; Cui L; Gao J J Mol Neurosci; 2021 May; 71(5):1015-1022. PubMed ID: 33006106 [TBL] [Abstract][Full Text] [Related]
16. Targeted exome sequencing reveals homozygous TREM2 R47C mutation presenting with behavioral variant frontotemporal dementia without bone involvement. Ng ASL; Tan YJ; Yi Z; Tandiono M; Chew E; Dominguez J; Macas M; Ng E; Hameed S; Ting S; Tan EK; Foo JN; Kandiah N Neurobiol Aging; 2018 Aug; 68():160.e15-160.e19. PubMed ID: 29748150 [TBL] [Abstract][Full Text] [Related]
17. Genetic and clinical landscape of Chinese frontotemporal dementia: dominance of TBK1 and OPTN mutations. Nan H; Kim YJ; Chu M; Li D; Li J; Jiang D; Wu Y; Ohtsuka T; Wu L Alzheimers Res Ther; 2024 Jun; 16(1):127. PubMed ID: 38872230 [TBL] [Abstract][Full Text] [Related]
18. The unexpected co-occurrence of GRN and MAPT p.A152T in Basque families: Clinical and pathological characteristics. Moreno F; Indakoetxea B; Barandiaran M; Caballero MC; Gorostidi A; Calafell F; Gabilondo A; Tainta M; Zulaica M; Martí Massó JF; López de Munain A; Sánchez-Juan P; Lee SE PLoS One; 2017; 12(6):e0178093. PubMed ID: 28594853 [TBL] [Abstract][Full Text] [Related]
19. Genetic screen in a large series of patients with primary progressive aphasia. Ramos EM; Dokuru DR; Van Berlo V; Wojta K; Wang Q; Huang AY; Miller ZA; Karydas AM; Bigio EH; Rogalski E; Weintraub S; Rader B; Miller BL; Gorno-Tempini ML; Mesulam MM; Coppola G Alzheimers Dement; 2019 Apr; 15(4):553-560. PubMed ID: 30599136 [TBL] [Abstract][Full Text] [Related]
20. C9orf72 expansions are the most common cause of genetic frontotemporal dementia in a Southeast Asian cohort. Tan YJ; Yong ACW; Foo JN; Lian MM; Lim WK; Dominguez J; Fong ZH; Narasimhalu K; Chiew HJ; Ng KP; Ting SKS; Kandiah N; Ng ASL Ann Clin Transl Neurol; 2023 Apr; 10(4):568-578. PubMed ID: 36799407 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]