90 related articles for article (PubMed ID: 21839474)
1. D11Y SOD1 mutation and benign ALS: a consistent genotype-phenotype correlation.
Del Grande A; Conte A; Lattante S; Luigetti M; Marangi G; Zollino M; Madia F; Bisogni G; Sabatelli M
J Neurol Sci; 2011 Oct; 309(1-2):31-3. PubMed ID: 21839474
[TBL] [Abstract][Full Text] [Related]
2. A novel SOD1 mutation in a young amyotrophic lateral sclerosis patient with a very slowly progressive clinical course.
Georgoulopoulou E; Gellera C; Bragato C; Sola P; Chiari A; Bernabei C; Mandrioli J
Muscle Nerve; 2010 Oct; 42(4):596-7. PubMed ID: 20740631
[TBL] [Abstract][Full Text] [Related]
3. Amyotrophic lateral sclerosis: a new missense mutation in the SOD1 gene.
Tortelli R; Conforti FL; Cortese R; D'Errico E; Distaso E; Mazzei R; Ungaro C; Magariello A; Gambardella A; Logroscino G; Simone IL
Neurobiol Aging; 2013 Jun; 34(6):1709.e3-5. PubMed ID: 23182243
[TBL] [Abstract][Full Text] [Related]
4. Identification of a novel D109Y mutation in Cu/Zn superoxide dismutase (sod1) gene associated with amyotrophic lateral sclerosis.
Naini A; Mehrazin M; Lu J; Gordon P; Mitsumoto H
J Neurol Sci; 2007 Mar; 254(1-2):17-21. PubMed ID: 17257622
[TBL] [Abstract][Full Text] [Related]
5. 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; 79(1):66-72. PubMed ID: 22722621
[TBL] [Abstract][Full Text] [Related]
6. 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; 10(1):58-60. PubMed ID: 18608106
[TBL] [Abstract][Full Text] [Related]
7. Novel SOD1 mutation p.V31A identified with a slowly progressive form of amyotrophic lateral sclerosis.
Dangoumau A; Verschueren A; Hammouche E; Papon MA; Blasco H; Cherpi-Antar C; Pouget J; Corcia P; Andres CR; Vourc'h P
Neurobiol Aging; 2014 Jan; 35(1):266.e1-4. PubMed ID: 23954173
[TBL] [Abstract][Full Text] [Related]
8. Novel SOD1 N86K mutation is associated with a severe phenotype in familial ALS.
Beck M; Sendtner M; Toyka KV
Muscle Nerve; 2007 Jul; 36(1):111-4. PubMed ID: 17299743
[TBL] [Abstract][Full Text] [Related]
9. Clinical heterogeneity in Italian patients with amyotrophic lateral sclerosis.
Piaceri I; Del Mastio M; Tedde A; Bagnoli S; Latorraca S; Massaro F; Paganini M; Corrado A; Sorbi S; Nacmias B
Clin Genet; 2012 Jul; 82(1):83-7. PubMed ID: 21651514
[TBL] [Abstract][Full Text] [Related]
10. SOD1 G93D mutation presenting as paucisymptomatic amyotrophic lateral sclerosis.
Luigetti M; Madia F; Conte A; Marangi G; Zollino M; Del Grande A; Dileone M; Tonali PA; Sabatelli M
Amyotroph Lateral Scler; 2009; 10(5-6):479-82. PubMed ID: 19922144
[TBL] [Abstract][Full Text] [Related]
11. D90A-SOD1 ALS mimicking monoclonal gammopathy-associated ALS.
Synofzik M; Hagen JM; Biskup S; Schöls L
Amyotroph Lateral Scler; 2012 May; 13(3):326-7. PubMed ID: 22409356
[No Abstract] [Full Text] [Related]
12. 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; 247(1):21-8. PubMed ID: 16674979
[TBL] [Abstract][Full Text] [Related]
13. Founder effect hypothesis of D11Y SOD1 mutation in Italian amyotrophic lateral sclerosis patients.
Lattante S; Marangi G; Luigetti M; Conte A; Mandrioli J; Del Grande A; Zollino M; Sabatelli M
Amyotroph Lateral Scler; 2012 Feb; 13(2):241-2. PubMed ID: 22292847
[No Abstract] [Full Text] [Related]
14. 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]
15. A novel T137A SOD1 mutation in an Italian family with two subjects affected by amyotrophic lateral sclerosis.
Visani M; de Biase D; Bartolomei I; Plasmati R; Morandi L; Cenacchi G; Salvi F; Pession A
Amyotroph Lateral Scler; 2011 Sep; 12(5):385-8. PubMed ID: 21574856
[TBL] [Abstract][Full Text] [Related]
16. A novel p.E121G heterozygous missense mutation of SOD1 in an apparently sporadic ALS case with a 14-year course.
Canosa A; Calvo A; Moglia C; Barberis M; Brunetti M; Cammarosano S; Manera U; Ilardi A; Restagno G; Chiò A
Amyotroph Lateral Scler Frontotemporal Degener; 2015 Mar; 16(1-2):127-8. PubMed ID: 25299943
[TBL] [Abstract][Full Text] [Related]
17. Identification of a novel missense (C7W) mutation of SOD1 in a large familial amyotrophic lateral sclerosis pedigree.
Wang Z; Cai W; Cui F; Cai T; Chen Z; Mao F; Teng H; Chen L; Wang J; Sun Z; Huang X; Yu P
Neurobiol Aging; 2014 Mar; 35(3):725.e11-5. PubMed ID: 24094577
[TBL] [Abstract][Full Text] [Related]
18. The p.E22G mutation in the Cu/Zn superoxide-dismutase gene predicts a long survival time: clinical and genetic characterization of a seven-generation ALS1 Spanish pedigree.
Syriani E; Morales M; Gamez J
J Neurol Sci; 2009 Oct; 285(1-2):46-53. PubMed ID: 19524271
[TBL] [Abstract][Full Text] [Related]
19. Genetic analysis and SOD1 mutation screening in Iranian amyotrophic lateral sclerosis patients.
Alavi A; Nafissi S; Rohani M; Zamani B; Sedighi B; Shamshiri H; Fan JB; Ronaghi M; Elahi E
Neurobiol Aging; 2013 May; 34(5):1516.e1-8. PubMed ID: 23062701
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]