211 related articles for article (PubMed ID: 30528349)
1. Frontotemporal dementia spectrum: first genetic screen in a Greek cohort.
Ramos EM; Koros C; Dokuru DR; Van Berlo V; Kroupis C; Wojta K; Wang Q; Andronas N; Matsi S; Beratis IN; Huang AY; Lee SE; Bonakis A; Florou-Hatziyiannidou C; Fragkiadaki S; Kontaxopoulou D; Agiomyrgiannakis D; Kamtsadeli V; Tsinia N; Papastefanopoulou V; Stamelou M; Miller BL; Stefanis L; Papatriantafyllou JD; Papageorgiou SG; Coppola G
Neurobiol Aging; 2019 Mar; 75():224.e1-224.e8. PubMed ID: 30528349
[TBL] [Abstract][Full Text] [Related]
2. Screening for the C9ORF72 repeat expansion in a greek frontotemporal dementia cohort.
Kartanou C; Karadima G; Koutsis G; Breza M; Papageorgiou SG; Paraskevas GP; Kapaki E; Panas M
Amyotroph Lateral Scler Frontotemporal Degener; 2018 Feb; 19(1-2):152-154. PubMed ID: 29166782
[TBL] [Abstract][Full Text] [Related]
3. Identification of C9orf72 repeat expansions in patients with amyotrophic lateral sclerosis and frontotemporal dementia in mainland China.
Jiao B; Tang B; Liu X; Yan X; Zhou L; Yang Y; Wang J; Xia K; Shen L
Neurobiol Aging; 2014 Apr; 35(4):936.e19-22. PubMed ID: 24269022
[TBL] [Abstract][Full Text] [Related]
4. Clinical and genetic analysis of MAPT, GRN, and C9orf72 genes in Korean patients with frontotemporal dementia.
Kim EJ; Kwon JC; Park KH; Park KW; Lee JH; Choi SH; Jeong JH; Kim BC; Yoon SJ; Yoon YC; Kim S; Park KC; Choi BO; Na DL; Ki CS; Kim SH
Neurobiol Aging; 2014 May; 35(5):1213.e13-7. PubMed ID: 24387985
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. 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]
7. Mutation spectrum of chinese amyotrophic lateral sclerosis patients with frontotemporal dementia.
Yang X; Sun X; Liu Q; Liu L; Li J; Cai Z; Zhang K; Liu S; He D; Shen D; Liu M; Cui L; Zhang X
Orphanet J Rare Dis; 2022 Nov; 17(1):404. PubMed ID: 36345033
[TBL] [Abstract][Full Text] [Related]
8. The frequency of the C9orf72 expansion in a Brazilian population.
Cintra VP; Bonadia LC; Andrade HMT; de Albuquerque M; Eusébio MF; de Oliveira DS; Claudino R; Gonçalves MVM; Teixeira AL; de Godoy Rousseff Prado L; de Souza LC; Dourado MET; Oliveira ASB; Tumas V; França MC; Marques W
Neurobiol Aging; 2018 Jun; 66():179.e1-179.e4. PubMed ID: 29449030
[TBL] [Abstract][Full Text] [Related]
9. Genetic screening of a large series of North American sporadic and familial frontotemporal dementia cases.
Ramos EM; Dokuru DR; Van Berlo V; Wojta K; Wang Q; Huang AY; Deverasetty S; Qin Y; van Blitterswijk M; Jackson J; Appleby B; Bordelon Y; Brannelly P; Brushaber DE; Dickerson B; Dickinson S; Domoto-Reilly K; Faber K; Fields J; Fong J; Foroud T; Forsberg LK; Gavrilova R; Ghoshal N; Goldman J; Graff-Radford J; Graff-Radford N; Grant I; Grossman M; Heuer HW; Hsiung GR; Huey E; Irwin D; Kantarci K; Karydas A; Kaufer D; Kerwin D; Knopman D; Kornak J; Kramer JH; Kremers W; Kukull W; Litvan I; Ljubenkov P; Lungu C; Mackenzie I; Mendez MF; Miller BL; Onyike C; Pantelyat A; Pearlman R; Petrucelli L; Potter M; Rankin KP; Rascovsky K; Roberson ED; Rogalski E; Shaw L; Syrjanen J; Tartaglia MC; Tatton N; Taylor J; Toga A; Trojanowski JQ; Weintraub S; Wong B; Wszolek Z; Rademakers R; Boeve BF; Rosen HJ; Boxer AL; ; Coppola G
Alzheimers Dement; 2020 Jan; 16(1):118-130. PubMed ID: 31914217
[TBL] [Abstract][Full Text] [Related]
10. Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study.
Majounie E; Renton AE; Mok K; Dopper EG; Waite A; Rollinson S; Chiò A; Restagno G; Nicolaou N; Simon-Sanchez J; van Swieten JC; Abramzon Y; Johnson JO; Sendtner M; Pamphlett R; Orrell RW; Mead S; Sidle KC; Houlden H; Rohrer JD; Morrison KE; Pall H; Talbot K; Ansorge O; ; ; ; Hernandez DG; Arepalli S; Sabatelli M; Mora G; Corbo M; Giannini F; Calvo A; Englund E; Borghero G; Floris GL; Remes AM; Laaksovirta H; McCluskey L; Trojanowski JQ; Van Deerlin VM; Schellenberg GD; Nalls MA; Drory VE; Lu CS; Yeh TH; Ishiura H; Takahashi Y; Tsuji S; Le Ber I; Brice A; Drepper C; Williams N; Kirby J; Shaw P; Hardy J; Tienari PJ; Heutink P; Morris HR; Pickering-Brown S; Traynor BJ
Lancet Neurol; 2012 Apr; 11(4):323-30. PubMed ID: 22406228
[TBL] [Abstract][Full Text] [Related]
11. Multiple variants in families with amyotrophic lateral sclerosis and frontotemporal dementia related to C9orf72 repeat expansion: further observations on their oligogenic nature.
Giannoccaro MP; Bartoletti-Stella A; Piras S; Pession A; De Massis P; Oppi F; Stanzani-Maserati M; Pasini E; Baiardi S; Avoni P; Parchi P; Liguori R; Capellari S
J Neurol; 2017 Jul; 264(7):1426-1433. PubMed ID: 28620717
[TBL] [Abstract][Full Text] [Related]
12. Targeted next-generation sequencing study in familial ALS-FTD Portuguese patients negative for C9orf72 HRE.
Gromicho M; Coutinho AM; Pronto-Laborinho AC; Raposeiro R; Tavares J; Antunes D; de Carvalho M
J Neurol; 2020 Dec; 267(12):3578-3592. PubMed ID: 32638105
[TBL] [Abstract][Full Text] [Related]
13. Expanding the spectrum of C9ORF72-related neurodegenerative disorders in the Greek population.
Kartanou C; Kontogeorgiou Z; Rentzos M; Potagas C; Aristeidou S; Kapaki E; Paraskevas GP; Constantinides VC; Stefanis L; Papageorgiou SG; Houlden H; Panas M; Koutsis G; Karadima G
J Neurol Sci; 2022 Nov; 442():120450. PubMed ID: 36252286
[TBL] [Abstract][Full Text] [Related]
14. OPTN p.Met468Arg and ATXN2 intermediate length polyQ extension in families with C9orf72 mediated amyotrophic lateral sclerosis and frontotemporal dementia.
Farhan SMK; Gendron TF; Petrucelli L; Hegele RA; Strong MJ
Am J Med Genet B Neuropsychiatr Genet; 2018 Jan; 177(1):75-85. PubMed ID: 29080331
[TBL] [Abstract][Full Text] [Related]
15. Frontotemporal dementia with amyotrophic lateral sclerosis: a clinical comparison of patients with and without repeat expansions in C9orf72.
Snowden JS; Harris J; Richardson A; Rollinson S; Thompson JC; Neary D; Mann DM; Pickering-Brown S
Amyotroph Lateral Scler Frontotemporal Degener; 2013 Apr; 14(3):172-6. PubMed ID: 23421625
[TBL] [Abstract][Full Text] [Related]
16. [C9orf72 in Japanese amyotrophic lateral sclerosis (ALS)].
Tomiyama H
Rinsho Shinkeigaku; 2013; 53(11):1074-6. PubMed ID: 24291883
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. The wide genetic landscape of clinical frontotemporal dementia: systematic combined sequencing of 121 consecutive subjects.
Blauwendraat C; Wilke C; Simón-Sánchez J; Jansen IE; Reifschneider A; Capell A; Haass C; Castillo-Lizardo M; Biskup S; Maetzler W; Rizzu P; Heutink P; Synofzik M
Genet Med; 2018 Feb; 20(2):240-249. PubMed ID: 28749476
[TBL] [Abstract][Full Text] [Related]
19. Analysis of C9orf72 in patients with frontotemporal dementia and amyotrophic lateral sclerosis from Argentina.
Itzcovich T; Xi Z; Martinetto H; Chrem-Méndez P; Russo MJ; de Ambrosi B; Uchitel OD; Nogués M; Silva E; Rojas G; Bagnatti P; Amengual A; Campos J; Rogaeva E; St George-Hyslop P; Allegri R; Sevlever G; Surace EI
Neurobiol Aging; 2016 Apr; 40():192.e13-192.e15. PubMed ID: 26925510
[TBL] [Abstract][Full Text] [Related]
20. Investigating the Genetic Profile of the Amyotrophic Lateral Sclerosis/Frontotemporal Dementia (ALS-FTD) Continuum in Patients of Diverse Race, Ethnicity and Ancestry.
Mesaros M; Lenz S; Lim W; Brown J; Drury L; Roggenbuck J
Genes (Basel); 2021 Dec; 13(1):. PubMed ID: 35052416
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
