141 related articles for article (PubMed ID: 28430294)
1. GRN mutation in a patient with a behavioral variant of frontotemporal lobar degeneration (bvFTD).
Walczysková S; Ressner P; Hilscherová Š; Kotlas J; Konrád J; Svobodová V
Folia Neuropathol; 2017; 55(1):67-72. PubMed ID: 28430294
[No Abstract] [Full Text] [Related]
2. Genetic and clinical features of progranulin-associated frontotemporal lobar degeneration.
Chen-Plotkin AS; Martinez-Lage M; Sleiman PM; Hu W; Greene R; Wood EM; Bing S; Grossman M; Schellenberg GD; Hatanpaa KJ; Weiner MF; White CL; Brooks WS; Halliday GM; Kril JJ; Gearing M; Beach TG; Graff-Radford NR; Dickson DW; Rademakers R; Boeve BF; Pickering-Brown SM; Snowden J; van Swieten JC; Heutink P; Seelaar H; Murrell JR; Ghetti B; Spina S; Grafman J; Kaye JA; Woltjer RL; Mesulam M; Bigio E; Lladó A; Miller BL; Alzualde A; Moreno F; Rohrer JD; Mackenzie IR; Feldman HH; Hamilton RL; Cruts M; Engelborghs S; De Deyn PP; Van Broeckhoven C; Bird TD; Cairns NJ; Goate A; Frosch MP; Riederer PF; Bogdanovic N; Lee VM; Trojanowski JQ; Van Deerlin VM
Arch Neurol; 2011 Apr; 68(4):488-97. PubMed ID: 21482928
[TBL] [Abstract][Full Text] [Related]
3. A distinct clinical, neuropsychological and radiological phenotype is associated with progranulin gene mutations in a large UK series.
Beck J; Rohrer JD; Campbell T; Isaacs A; Morrison KE; Goodall EF; Warrington EK; Stevens J; Revesz T; Holton J; Al-Sarraj S; King A; Scahill R; Warren JD; Fox NC; Rossor MN; Collinge J; Mead S
Brain; 2008 Mar; 131(Pt 3):706-20. PubMed ID: 18234697
[TBL] [Abstract][Full Text] [Related]
4. A Novel Loss-of-Function GRN Mutation p.(Tyr229*): Clinical and Neuropathological Features.
Kuuluvainen L; Pöyhönen M; Pasanen P; Siitonen M; Rummukainen J; Tienari PJ; Paetau A; Myllykangas L
J Alzheimers Dis; 2017; 55(3):1167-1174. PubMed ID: 27767988
[TBL] [Abstract][Full Text] [Related]
5. A novel frameshift GRN mutation results in frontotemporal lobar degeneration with a distinct clinical phenotype in two siblings: case report and literature review.
Hosaka T; Ishii K; Miura T; Mezaki N; Kasuga K; Ikeuchi T; Tamaoka A
BMC Neurol; 2017 Sep; 17(1):182. PubMed ID: 28915852
[TBL] [Abstract][Full Text] [Related]
6. Rare exonic variant affects GRN splicing and contributes to frontotemporal lobar degeneration.
Wauters E; Gossye H; Frydas A; Sieben A; Van Broeckhoven C
Neurobiol Aging; 2023 Oct; 130():61-69. PubMed ID: 37459659
[TBL] [Abstract][Full Text] [Related]
7. A mutation in the 5'-UTR of GRN gene associated with frontotemporal lobar degeneration: phenotypic variability and possible pathogenetic mechanisms.
Puoti G; Lerza MC; Ferretti MG; Bugiani O; Tagliavini F; Rossi G
J Alzheimers Dis; 2014; 42(3):939-47. PubMed ID: 25024321
[TBL] [Abstract][Full Text] [Related]
8. Understanding phenotype variability in frontotemporal lobar degeneration due to granulin mutation.
Bonvicini C; Milanesi E; Pilotto A; Cattane N; Premi E; Archetti S; Padovani A; Gennarelli M; Borroni B
Neurobiol Aging; 2014 May; 35(5):1206-11. PubMed ID: 24368088
[TBL] [Abstract][Full Text] [Related]
9. A novel GRN mutation (GRN c.708+6_+9delTGAG) in frontotemporal lobar degeneration with TDP-43-positive inclusions: clinicopathologic report of 6 cases.
Bit-Ivan EN; Suh E; Shim HS; Weintraub S; Hyman BT; Arnold SE; McCarty-Wood E; Van Deerlin VM; Schneider JA; Trojanowski JQ; Frosch MP; Baker MC; Rademakers R; Mesulam M; Bigio EH
J Neuropathol Exp Neurol; 2014 May; 73(5):467-73. PubMed ID: 24709683
[TBL] [Abstract][Full Text] [Related]
10. Brain progranulin expression in GRN-associated frontotemporal lobar degeneration.
Chen-Plotkin AS; Xiao J; Geser F; Martinez-Lage M; Grossman M; Unger T; Wood EM; Van Deerlin VM; Trojanowski JQ; Lee VM
Acta Neuropathol; 2010 Jan; 119(1):111-22. PubMed ID: 19649643
[TBL] [Abstract][Full Text] [Related]
11. Expression of TMEM106B, the frontotemporal lobar degeneration-associated protein, in normal and diseased human brain.
Busch JI; Martinez-Lage M; Ashbridge E; Grossman M; Van Deerlin VM; Hu F; Lee VM; Trojanowski JQ; Chen-Plotkin AS
Acta Neuropathol Commun; 2013 Jul; 1():36. PubMed ID: 24252750
[TBL] [Abstract][Full Text] [Related]
12. Distinct profiles of brain atrophy in frontotemporal lobar degeneration caused by progranulin and tau mutations.
Rohrer JD; Ridgway GR; Modat M; Ourselin S; Mead S; Fox NC; Rossor MN; Warren JD
Neuroimage; 2010 Nov; 53(3):1070-6. PubMed ID: 20045477
[TBL] [Abstract][Full Text] [Related]
13. The neuroimaging signature of frontotemporal lobar degeneration associated with Granulin mutations: an effective connectivity study.
Premi E; Grassi M; Gazzina S; Paghera B; Pepe D; Archetti S; Padovani A; Borroni B
J Nucl Med; 2013 Jul; 54(7):1066-71. PubMed ID: 23687363
[TBL] [Abstract][Full Text] [Related]
14. Development and validation of pedigree classification criteria for frontotemporal lobar degeneration.
Wood EM; Falcone D; Suh E; Irwin DJ; Chen-Plotkin AS; Lee EB; Xie SX; Van Deerlin VM; Grossman M
JAMA Neurol; 2013 Nov; 70(11):1411-7. PubMed ID: 24081456
[TBL] [Abstract][Full Text] [Related]
15. Autosomal Dominant Frontotemporal Lobar Degeneration in a Filipino Family with Progranulin Mutation.
Dominguez J; Ng A; Yu J; Guevarra AC; Daroy ML; Alfon A; Catindig JA; Dizon M; Santiago J; Del Moral MC; Yu J; Jamerlan A; Ligsay A; Bagyinszky E; An SS; Kim S
Dement Geriatr Cogn Disord; 2020; 49(6):557-564. PubMed ID: 33486486
[TBL] [Abstract][Full Text] [Related]
16. Partial deletions of the GRN gene are a cause of frontotemporal lobar degeneration.
Clot F; Rovelet-Lecrux A; Lamari F; Noël S; Keren B; Camuzat A; Michon A; Jornea L; Laudier B; de Septenville A; Caroppo P; Campion D; Cazeneuve C; Brice A; LeGuern E; Le Ber I;
Neurogenetics; 2014 May; 15(2):95-100. PubMed ID: 24469240
[TBL] [Abstract][Full Text] [Related]
17. Progranulin gene (GRN) promoter methylation is increased in patients with sporadic frontotemporal lobar degeneration.
Galimberti D; D'Addario C; Dell'osso B; Fenoglio C; Marcone A; Cerami C; Cappa SF; Palazzo MC; Arosio B; Mari D; Maccarrone M; Bresolin N; Altamura AC; Scarpini E
Neurol Sci; 2013 Jun; 34(6):899-903. PubMed ID: 22797721
[TBL] [Abstract][Full Text] [Related]
18. Missense mutations in progranulin gene associated with frontotemporal lobar degeneration: study of pathogenetic features.
Karch CM; Ezerskiy L; Redaelli V; Giovagnoli AR; Tiraboschi P; Pelliccioni G; Pelliccioni P; Kapetis D; D'Amato I; Piccoli E; Ferretti MG; Tagliavini F; Rossi G
Neurobiol Aging; 2016 Feb; 38():215.e1-215.e12. PubMed ID: 26652843
[TBL] [Abstract][Full Text] [Related]
19. Extended FTLD pedigree segregating a Belgian GRN-null mutation: neuropathological heterogeneity in one family.
Sieben A; Van Mossevelde S; Wauters E; Engelborghs S; van der Zee J; Van Langenhove T; Santens P; Praet M; Boon P; Miatton M; Van Hoecke S; Vandenbulcke M; Vandenberghe R; Cras P; Cruts M; De Deyn PP; Van Broeckhoven C; Martin JJ
Alzheimers Res Ther; 2018 Jan; 10(1):7. PubMed ID: 29370838
[TBL] [Abstract][Full Text] [Related]
20. Novel progranulin mutations with reduced serum-progranulin levels in frontotemporal lobar degeneration.
Chiang HH; Forsell C; Lilius L; Öijerstedt L; Thordardottir S; Shanmugarajan K; Westerlund M; Nennesmo I; Thonberg H; Graff C
Eur J Hum Genet; 2013 Nov; 21(11):1260-5. PubMed ID: 23463024
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
