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Journal Abstract Search
353 related items for PubMed ID: 20472325
1. FUS, TARDBP, and SOD1 mutations in a Taiwanese cohort with familial ALS. Tsai CP, Soong BW, Lin KP, Tu PH, Lin JL, Lee YC. Neurobiol Aging; 2011 Mar; 32(3):553.e13-21. PubMed ID: 20472325 [Abstract] [Full Text] [Related]
2. 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 [Abstract] [Full Text] [Related]
3. SOD1, ANG, TARDBP and FUS mutations in amyotrophic lateral sclerosis: a United States clinical testing lab experience. Brown JA, Min J, Staropoli JF, Collin E, Bi S, Feng X, Barone R, Cao Y, O'Malley L, Xin W, Mullen TE, Sims KB. Amyotroph Lateral Scler; 2012 Feb; 13(2):217-22. PubMed ID: 22292843 [Abstract] [Full Text] [Related]
4. Screening of SOD1, FUS and TARDBP genes in patients with amyotrophic lateral sclerosis in central-southern China. Hou L, Jiao B, Xiao T, Zhou L, Zhou Z, Du J, Yan X, Wang J, Tang B, Shen L. Sci Rep; 2016 Sep 08; 6():32478. PubMed ID: 27604643 [Abstract] [Full Text] [Related]
5. FUS and TARDBP but not SOD1 interact in genetic models of amyotrophic lateral sclerosis. Kabashi E, Bercier V, Lissouba A, Liao M, Brustein E, Rouleau GA, Drapeau P. PLoS Genet; 2011 Aug 08; 7(8):e1002214. PubMed ID: 21829392 [Abstract] [Full Text] [Related]
6. Screening of the SOD1, FUS, TARDBP, ANG, and OPTN mutations in Korean patients with familial and sporadic ALS. Kwon MJ, Baek W, Ki CS, Kim HY, Koh SH, Kim JW, Kim SH. Neurobiol Aging; 2012 May 08; 33(5):1017.e17-23. PubMed ID: 22244934 [Abstract] [Full Text] [Related]
7. 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 08; 49(4):258-63. PubMed ID: 22499346 [Abstract] [Full Text] [Related]
8. Improving the knowledge of amyotrophic lateral sclerosis genetics: novel SOD1 and FUS variants. Bertolin C, D'Ascenzo C, Querin G, Gaiani A, Boaretto F, Salvoro C, Vazza G, Angelini C, Cagnin A, Pegoraro E, Sorarù G, Mostacciuolo ML. Neurobiol Aging; 2014 May 08; 35(5):1212.e7-1212.e10. PubMed ID: 24325798 [Abstract] [Full Text] [Related]
9. De novo truncating FUS gene mutation as a cause of sporadic amyotrophic lateral sclerosis. DeJesus-Hernandez M, Kocerha J, Finch N, Crook R, Baker M, Desaro P, Johnston A, Rutherford N, Wojtas A, Kennelly K, Wszolek ZK, Graff-Radford N, Boylan K, Rademakers R. Hum Mutat; 2010 May 08; 31(5):E1377-89. PubMed ID: 20232451 [Abstract] [Full Text] [Related]
12. 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 31; 75(9):807-14. PubMed ID: 20668259 [Abstract] [Full Text] [Related]
14. Contribution of major amyotrophic lateral sclerosis genes to the etiology of sporadic disease. Lattante S, Conte A, Zollino M, Luigetti M, Del Grande A, Marangi G, Romano A, Marcaccio A, Meleo E, Bisogni G, Rossini PM, Sabatelli M. Neurology; 2012 Jul 03; 79(1):66-72. PubMed ID: 22722621 [Abstract] [Full Text] [Related]
20. FUS-immunoreactive inclusions are a common feature in sporadic and non-SOD1 familial amyotrophic lateral sclerosis. Deng HX, Zhai H, Bigio EH, Yan J, Fecto F, Ajroud K, Mishra M, Ajroud-Driss S, Heller S, Sufit R, Siddique N, Mugnaini E, Siddique T. Ann Neurol; 2010 Jun 03; 67(6):739-48. PubMed ID: 20517935 [Abstract] [Full Text] [Related] Page: [Next] [New Search]