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2. Identification of two novel mutations in the Cu/Zn superoxide dismutase gene with familial amyotrophic lateral sclerosis: mass spectrometric and genomic analyses. Sato T, Yamamoto Y, Nakanishi T, Fukada K, Sugai F, Zhou Z, Okuno T, Nagano S, Hirata S, Shimizu A, Sakoda S. J Neurol Sci; 2004 Mar 15; 218(1-2):79-83. PubMed ID: 14759637 [Abstract] [Full Text] [Related]
3. Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis. Rosen DR, Siddique T, Patterson D, Figlewicz DA, Sapp P, Hentati A, Donaldson D, Goto J, O'Regan JP, Deng HX. Nature; 1993 Mar 04; 362(6415):59-62. PubMed ID: 8446170 [Abstract] [Full Text] [Related]
4. [Familial amyotrophic lateral sclerosis and mutations in the Cu/Zn superoxide dismutase gene]. Nakano R. Rinsho Shinkeigaku; 1995 Dec 04; 35(12):1546-8. PubMed ID: 8752459 [Abstract] [Full Text] [Related]
5. Variants in candidate ALS modifier genes linked to Cu/Zn superoxide dismutase do not explain divergent survival phenotypes. Broom WJ, Russ C, Sapp PC, McKenna-Yasek D, Hosler BA, Andersen PM, Brown RH. Neurosci Lett; 2006 Jan 09; 392(1-2):52-7. PubMed ID: 16174551 [Abstract] [Full Text] [Related]
6. Copper/zinc superoxide dismutase 1 and sporadic amyotrophic lateral sclerosis: analysis of 155 cases and identification of a novel insertion mutation. Jackson M, Al-Chalabi A, Enayat ZE, Chioza B, Leigh PN, Morrison KE. Ann Neurol; 1997 Nov 09; 42(5):803-7. PubMed ID: 9392581 [Abstract] [Full Text] [Related]
11. Limited corticospinal tract involvement in amyotrophic lateral sclerosis subjects with the A4V mutation in the copper/zinc superoxide dismutase gene. Cudkowicz ME, McKenna-Yasek D, Chen C, Hedley-Whyte ET, Brown RH. Ann Neurol; 1998 Jun 09; 43(6):703-10. PubMed ID: 9629839 [Abstract] [Full Text] [Related]
12. D90A-SOD1 mediated amyotrophic lateral sclerosis: a single founder for all cases with evidence for a Cis-acting disease modifier in the recessive haplotype. Parton MJ, Broom W, Andersen PM, Al-Chalabi A, Nigel Leigh P, Powell JF, Shaw CE, D90A SOD1 ALS Consortium. Hum Mutat; 2002 Dec 09; 20(6):473. PubMed ID: 12442272 [Abstract] [Full Text] [Related]
13. [From gene to disease: amyotrophic lateral sclerosis]. van Vught PW, Veldink JH, Baas F, van Muiswinkel FL, van den Berg LH. Ned Tijdschr Geneeskd; 2004 Oct 23; 148(43):2125-7. PubMed ID: 15553356 [Abstract] [Full Text] [Related]
14. Identification of three mutations in the Cu,Zn-superoxide dismutase (Cu,Zn-SOD) gene with familial amyotrophic lateral sclerosis: transduction of human Cu,Zn-SOD into PC12 cells by HIV-1 TAT protein basic domain. Chou CM, Huang CJ, Shih CM, Chen YP, Liu TP, Chen CT. Ann N Y Acad Sci; 2005 May 23; 1042():303-13. PubMed ID: 15965076 [Abstract] [Full Text] [Related]
18. SOD1 mutation is associated with accumulation of neurofilaments in amyotrophic lateral sclerosis. Rouleau GA, Clark AW, Rooke K, Pramatarova A, Krizus A, Suchowersky O, Julien JP, Figlewicz D. Ann Neurol; 1996 Jan 23; 39(1):128-31. PubMed ID: 8572658 [Abstract] [Full Text] [Related]
19. Mutational analysis of the Cu/Zn superoxide dismutase gene in a Catalan ALS population: should all sporadic ALS cases also be screened for SOD1? Gamez J, Corbera-Bellalta M, Nogales G, Raguer N, García-Arumí E, Badia-Canto M, Lladó-Carbó E, Alvarez-Sabín J. J Neurol Sci; 2006 Aug 15; 247(1):21-8. PubMed ID: 16674979 [Abstract] [Full Text] [Related]
20. Further evidence that D90A-SOD1 mutation is recessively inherited in ALS patients in Italy. Luisa Conforti F, Sprovieri T, Mazzei R, Patitucci A, Ungaro C, Zoccolella S, Magariello A, Bella VL, Tessitore A, Tedeschi G, Simone IL, Majorana G, Valentino P, Citrigno L, Gabriele A, Bono F, Monsurrò MR, Muglia M, Quattrone A. Amyotroph Lateral Scler; 2009 Feb 15; 10(1):58-60. PubMed ID: 18608106 [Abstract] [Full Text] [Related] Page: [Next] [New Search]