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.
72 related articles for article (PubMed ID: 19714537)
1. Enlarging clinical spectrum of FALS with TARDBP gene mutations: S393L variant in an Italian family showing phenotypic variability and relevance for genetic counselling. Origone P; Caponnetto C; Bandettini Di Poggio M; Ghiglione E; Bellone E; Ferrandes G; Mancardi GL; Mandich P Amyotroph Lateral Scler; 2010; 11(1-2):223-7. PubMed ID: 19714537 [TBL] [Abstract][Full Text] [Related]
2. Co-occurrence of progressive anarthria with an S393L TARDBP mutation and ALS within a family. Praline J; Vourc'h P; Guennoc AM; Veyrat-Durebex C; Corcia P Amyotroph Lateral Scler; 2012 Jan; 13(1):155-7. PubMed ID: 21830990 [TBL] [Abstract][Full Text] [Related]
3. High frequency of TARDBP gene mutations in Italian patients with amyotrophic lateral sclerosis. Corrado L; Ratti A; Gellera C; Buratti E; Castellotti B; Carlomagno Y; Ticozzi N; Mazzini L; Testa L; Taroni F; Baralle FE; Silani V; D'Alfonso S Hum Mutat; 2009 Apr; 30(4):688-94. PubMed ID: 19224587 [TBL] [Abstract][Full Text] [Related]
4. A novel TARDBP insertion/deletion mutation in the flail arm variant of amyotrophic lateral sclerosis. Solski JA; Yang S; Nicholson GA; Luquin N; Williams KL; Fernando R; Pamphlett R; Blair IP Amyotroph Lateral Scler; 2012 Sep; 13(5):465-70. PubMed ID: 22424122 [TBL] [Abstract][Full Text] [Related]
5. 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]
6. TARDBP (TDP-43) sequence analysis in patients with familial and sporadic ALS: identification of two novel mutations. Del Bo R; Ghezzi S; Corti S; Pandolfo M; Ranieri M; Santoro D; Ghione I; Prelle A; Orsetti V; Mancuso M; Sorarù G; Briani C; Angelini C; Siciliano G; Bresolin N; Comi GP Eur J Neurol; 2009 Jun; 16(6):727-32. PubMed ID: 19236453 [TBL] [Abstract][Full Text] [Related]
7. High frequency of the TARDBP p.Ala382Thr mutation in Sardinian patients with amyotrophic lateral sclerosis. Orrù S; Manolakos E; Orrù N; Kokotas H; Mascia V; Carcassi C; Petersen MB Clin Genet; 2012 Feb; 81(2):172-8. PubMed ID: 21418058 [TBL] [Abstract][Full Text] [Related]
8. Association between novel TARDBP mutations and Chinese patients with amyotrophic lateral sclerosis. Xiong HL; Wang JY; Sun YM; Wu JJ; Chen Y; Qiao K; Zheng QJ; Zhao GX; Wu ZY BMC Med Genet; 2010 Jan; 11():8. PubMed ID: 20082726 [TBL] [Abstract][Full Text] [Related]
9. Phenotypes in Swiss patients with familial ALS carrying TARDBP mutations. Czell D; Andersen PM; Morita M; Neuwirth C; Perren F; Weber M Neurodegener Dis; 2013; 12(3):150-5. PubMed ID: 23327806 [TBL] [Abstract][Full Text] [Related]
10. SOD1, ANG, VAPB, TARDBP, and FUS mutations in familial amyotrophic lateral sclerosis: genotype-phenotype correlations. Millecamps S; Salachas F; Cazeneuve C; Gordon P; Bricka B; Camuzat A; Guillot-Noël L; Russaouen O; Bruneteau G; Pradat PF; Le Forestier N; Vandenberghe N; Danel-Brunaud V; Guy N; Thauvin-Robinet C; Lacomblez L; Couratier P; Hannequin D; Seilhean D; Le Ber I; Corcia P; Camu W; Brice A; Rouleau G; LeGuern E; Meininger V J Med Genet; 2010 Aug; 47(8):554-60. PubMed ID: 20577002 [TBL] [Abstract][Full Text] [Related]
13. Different clinical and neuropathologic phenotypes of familial ALS with A315E TARDBP mutation. Fujita Y; Ikeda M; Yanagisawa T; Senoo Y; Okamoto K Neurology; 2011 Oct; 77(15):1427-31. PubMed ID: 21956716 [TBL] [Abstract][Full Text] [Related]
15. Evaluating the contribution of the gene TARDBP in Italian patients with amyotrophic lateral sclerosis. Lattante S; Sabatelli M; Bisogni G; Marangi G; Doronzio PN; Martello F; Renzi AG; Del Giudice E; Leon A; Cimbolli P; Marchione D; Costantino U; Lucioli G; Bernardo D; Meleo E; Patanella AK; Romano A; Zollino M; Conte A Eur J Neurol; 2023 May; 30(5):1246-1255. PubMed ID: 36732882 [TBL] [Abstract][Full Text] [Related]
16. A rare Cu/Zn superoxide dismutase mutation causing familial amyotrophic lateral sclerosis with variable age of onset and incomplete penetrance in China. Zhang H; Zhao H; Lu M; Zhang Y; Wang L; Zhang J; Ma D; Fan D Amyotroph Lateral Scler Other Motor Neuron Disord; 2005 Dec; 6(4):234-8. PubMed ID: 16319027 [TBL] [Abstract][Full Text] [Related]
17. Genetic variants in the promoter of TARDBP in sporadic amyotrophic lateral sclerosis. Luquin N; Yu B; Saunderson RB; Trent RJ; Pamphlett R Neuromuscul Disord; 2009 Oct; 19(10):696-700. PubMed ID: 19695877 [TBL] [Abstract][Full Text] [Related]
18. Large-scale screening of TARDBP mutation in amyotrophic lateral sclerosis in Japanese. Iida A; Kamei T; Sano M; Oshima S; Tokuda T; Nakamura Y; Ikegawa S Neurobiol Aging; 2012 Apr; 33(4):786-90. PubMed ID: 20675015 [TBL] [Abstract][Full Text] [Related]
19. Contribution of TARDBP mutations to sporadic amyotrophic lateral sclerosis. Daoud H; Valdmanis PN; Kabashi E; Dion P; Dupré N; Camu W; Meininger V; Rouleau GA J Med Genet; 2009 Feb; 46(2):112-4. PubMed ID: 18931000 [TBL] [Abstract][Full Text] [Related]
20. Targeted high-throughput sequencing identifies a TARDBP mutation as a cause of early-onset FTD without motor neuron disease. Synofzik M; Born C; Rominger A; Lummel N; Schöls L; Biskup S; Schüle C; Grasshoff U; Klopstock T; Adamczyk C Neurobiol Aging; 2014 May; 35(5):1212.e1-5. PubMed ID: 24300238 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]