327 related articles for article (PubMed ID: 20660363)
1. Novel missense and truncating mutations in FUS/TLS in familial ALS.
Waibel S; Neumann M; Rabe M; Meyer T; Ludolph AC
Neurology; 2010 Aug; 75(9):815-7. PubMed ID: 20660363
[TBL] [Abstract][Full Text] [Related]
2. De novo FUS gene mutations are associated with juvenile-onset sporadic amyotrophic lateral sclerosis in China.
Zou ZY; Cui LY; Sun Q; Li XG; Liu MS; Xu Y; Zhou Y; Yang XZ
Neurobiol Aging; 2013 Apr; 34(4):1312.e1-8. PubMed ID: 23046859
[TBL] [Abstract][Full Text] [Related]
3. C-terminal FUS/TLS mutations in familial and sporadic ALS in Germany.
Drepper C; Herrmann T; Wessig C; Beck M; Sendtner M
Neurobiol Aging; 2011 Mar; 32(3):548.e1-4. PubMed ID: 20018407
[TBL] [Abstract][Full Text] [Related]
4. Identification of novel FUS mutations in sporadic cases of amyotrophic lateral sclerosis.
Belzil VV; Daoud H; St-Onge J; Desjarlais A; Bouchard JP; Dupre N; Lacomblez L; Salachas F; Pradat PF; Meininger V; Camu W; Dion PA; Rouleau GA
Amyotroph Lateral Scler; 2011 Mar; 12(2):113-7. PubMed ID: 21261515
[TBL] [Abstract][Full Text] [Related]
5. FUS/TLS gene mutations are the second most frequent cause of familial ALS in the Spanish population.
Syriani E; Morales M; Gamez J
Amyotroph Lateral Scler; 2011 Mar; 12(2):118-23. PubMed ID: 21128870
[TBL] [Abstract][Full Text] [Related]
6. Truncating mutations in FUS/TLS give rise to a more aggressive ALS-phenotype than missense mutations: a clinico-genetic study in Germany.
Waibel S; Neumann M; Rosenbohm A; Birve A; Volk AE; Weishaupt JH; Meyer T; Müller U; Andersen PM; Ludolph AC
Eur J Neurol; 2013 Mar; 20(3):540-546. PubMed ID: 23217123
[TBL] [Abstract][Full Text] [Related]
7. FUS mutations in frontotemporal lobar degeneration with amyotrophic lateral sclerosis.
Broustal O; Camuzat A; Guillot-Noël L; Guy N; Millecamps S; Deffond D; Lacomblez L; Golfier V; Hannequin D; Salachas F; Camu W; Didic M; Dubois B; Meininger V; Le Ber I; Brice A;
J Alzheimers Dis; 2010; 22(3):765-9. PubMed ID: 21158017
[TBL] [Abstract][Full Text] [Related]
8. Identification of a FUS splicing mutation in a large family with amyotrophic lateral sclerosis.
Belzil VV; St-Onge J; Daoud H; Desjarlais A; Bouchard JP; Dupré N; Camu W; Dion PA; Rouleau GA
J Hum Genet; 2011 Mar; 56(3):247-9. PubMed ID: 21160488
[TBL] [Abstract][Full Text] [Related]
9. FUS mutations in familial amyotrophic lateral sclerosis in the Netherlands.
Groen EJ; van Es MA; van Vught PW; Spliet WG; van Engelen-Lee J; de Visser M; Wokke JH; Schelhaas HJ; Ophoff RA; Fumoto K; Pasterkamp RJ; Dooijes D; Cuppen E; Veldink JH; van den Berg LH
Arch Neurol; 2010 Feb; 67(2):224-30. PubMed ID: 20142531
[TBL] [Abstract][Full Text] [Related]
10. FUS mutations in sporadic amyotrophic lateral sclerosis: clinical and genetic analysis.
Sproviero W; La Bella V; Mazzei R; Valentino P; Rodolico C; Simone IL; Logroscino G; Ungaro C; Magariello A; Patitucci A; Tedeschi G; Spataro R; Condino F; Bono F; Citrigno L; Monsurrò MR; Muglia M; Gambardella A; Quattrone A; Conforti FL
Neurobiol Aging; 2012 Apr; 33(4):837.e1-5. PubMed ID: 22055719
[TBL] [Abstract][Full Text] [Related]
11. Novel FUS/TLS mutations and pathology in familial and sporadic amyotrophic lateral sclerosis.
Hewitt C; Kirby J; Highley JR; Hartley JA; Hibberd R; Hollinger HC; Williams TL; Ince PG; McDermott CJ; Shaw PJ
Arch Neurol; 2010 Apr; 67(4):455-61. PubMed ID: 20385912
[TBL] [Abstract][Full Text] [Related]
12. Evidence for an oligogenic basis of amyotrophic lateral sclerosis.
van Blitterswijk M; van Es MA; Hennekam EA; Dooijes D; van Rheenen W; Medic J; Bourque PR; Schelhaas HJ; van der Kooi AJ; de Visser M; de Bakker PI; Veldink JH; van den Berg LH
Hum Mol Genet; 2012 Sep; 21(17):3776-84. PubMed ID: 22645277
[TBL] [Abstract][Full Text] [Related]
13. FUS/TLS-immunoreactive neuronal and glial cell inclusions increase with disease duration in familial amyotrophic lateral sclerosis with an R521C FUS/TLS mutation.
Suzuki N; Kato S; Kato M; Warita H; Mizuno H; Kato M; Shimakura N; Akiyama H; Kobayashi Z; Konno H; Aoki M
J Neuropathol Exp Neurol; 2012 Sep; 71(9):779-88. PubMed ID: 22878663
[TBL] [Abstract][Full Text] [Related]
14. Novel optineurin mutations in sporadic amyotrophic lateral sclerosis patients.
van Blitterswijk M; van Vught PW; van Es MA; Schelhaas HJ; van der Kooi AJ; de Visser M; Veldink JH; van den Berg LH
Neurobiol Aging; 2012 May; 33(5):1016.e1-7. PubMed ID: 21802176
[TBL] [Abstract][Full Text] [Related]
15. Screening of the FUS gene in familial and sporadic amyotrophic lateral sclerosis patients of Chinese origin.
Zou ZY; Peng Y; Feng XH; Wang XN; Sun Q; Liu MS; Li XG; Cui LY
Eur J Neurol; 2012 Jul; 19(7):977-83. PubMed ID: 22340366
[TBL] [Abstract][Full Text] [Related]
16. Frameshift and novel mutations in FUS in familial amyotrophic lateral sclerosis and ALS/dementia.
Yan J; Deng HX; Siddique N; Fecto F; Chen W; Yang Y; Liu E; Donkervoort S; Zheng JG; Shi Y; Ahmeti KB; Brooks B; Engel WK; Siddique T
Neurology; 2010 Aug; 75(9):807-14. PubMed ID: 20668259
[TBL] [Abstract][Full Text] [Related]
17. Novel FUS mutations identified through molecular screening in a large cohort of familial and sporadic amyotrophic lateral sclerosis.
Tarlarini C; Lunetta C; Mosca L; Avemaria F; Riva N; Mantero V; Maestri E; Quattrini A; Corbo M; Melazzini MG; Penco S
Eur J Neurol; 2015 Nov; 22(11):1474-81. PubMed ID: 26176978
[TBL] [Abstract][Full Text] [Related]
18. The occurrence of mutations in FUS in a Belgian cohort of patients with familial ALS.
Damme PV; Goris A; Race V; Hersmus N; Dubois B; Bosch LV; Matthijs G; Robberecht W
Eur J Neurol; 2010 May; 17(5):754-6. PubMed ID: 19922450
[TBL] [Abstract][Full Text] [Related]
19. Nuclear transport impairment of amyotrophic lateral sclerosis-linked mutations in FUS/TLS.
Ito D; Seki M; Tsunoda Y; Uchiyama H; Suzuki N
Ann Neurol; 2011 Jan; 69(1):152-62. PubMed ID: 21280085
[TBL] [Abstract][Full Text] [Related]
20. Phenotype difference between ALS patients with expanded repeats in C9ORF72 and patients with mutations in other ALS-related genes.
Millecamps S; Boillée S; Le Ber I; Seilhean D; Teyssou E; Giraudeau M; Moigneu C; Vandenberghe N; Danel-Brunaud V; Corcia P; Pradat PF; Le Forestier N; Lacomblez L; Bruneteau G; Camu W; Brice A; Cazeneuve C; Leguern E; Meininger V; Salachas F
J Med Genet; 2012 Apr; 49(4):258-63. PubMed ID: 22499346
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]