302 related articles for article (PubMed ID: 21877919)
1. Recurrent G41S mutation in Cu/Zn superoxide dismutase gene (SOD1) causing familial amyotrophic lateral sclerosis in a large Polish family.
Berdyński M; Kuźma-Kozakiewicz M; Ricci C; Kubiszewska J; Millecamps S; Salachas F; Łusakowska A; Carrera P; Meininger V; Battistini S; Kwieciński H; Zekanowski C
Amyotroph Lateral Scler; 2012 Jan; 13(1):132-6. PubMed ID: 21877919
[TBL] [Abstract][Full Text] [Related]
2. G41S SOD1 mutation: A common ancestor for six ALS Italian families with an aggressive phenotype.
Battistini S; Ricci C; Giannini F; Calzavara S; Greco G; Del Corona A; Mancuso M; Battistini N; Siciliano G; Carrera P
Amyotroph Lateral Scler; 2010; 11(1-2):210-5. PubMed ID: 19488901
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. A novel SOD1 mutation in amyotrophic lateral sclerosis with a distinct clinical phenotype.
Hu J; Chen K; Ni B; Li L; Chen G; Shi S
Amyotroph Lateral Scler; 2012 Jan; 13(1):149-54. PubMed ID: 22185396
[TBL] [Abstract][Full Text] [Related]
5. Molecular analysis of the superoxide dismutase 1 gene in Spanish patients with sporadic or familial amyotrophic lateral sclerosis.
García-Redondo A; Bustos F; Juan Y Seva B; Del Hoyo P; Jiménez S; Campos Y; Martín MA; Rubio JC; Cañadillas F; Arenas J; Esteban J
Muscle Nerve; 2002 Aug; 26(2):274-8. PubMed ID: 12210393
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. SOD1 mutations in amyotrophic lateral sclerosis. Results from a multicenter Italian study.
Battistini S; Giannini F; Greco G; Bibbò G; Ferrera L; Marini V; Causarano R; Casula M; Lando G; Patrosso MC; Caponnetto C; Origone P; Marocchi A; Del Corona A; Siciliano G; Carrera P; Mascia V; Giagheddu M; Carcassi C; Orrù S; Garrè C; Penco S
J Neurol; 2005 Jul; 252(7):782-8. PubMed ID: 15789135
[TBL] [Abstract][Full Text] [Related]
8. Clinical characteristics of familial amyotrophic lateral sclerosis with a Phe20Cys mutation in the SOD1 gene in a Korean family.
Kim HY; Ki CS; Koh SH; Park KH; Sunwoo IN; Kim SH
Amyotroph Lateral Scler; 2007 Apr; 8(2):73-8. PubMed ID: 17453632
[TBL] [Abstract][Full Text] [Related]
9. ALS with variable phenotypes in a six-generation family caused by leu144phe mutation in the SOD1 gene.
Masè G; Ros S; Gemma A; Bonfigli L; Carraro N; Cazzato G; Rolfo M; Zanconati F; Sepcic J; Jurjevic A; Pirulli D; Boniotto M; Zezlina S; Crovella S; Amoroso A
J Neurol Sci; 2001 Oct; 191(1-2):11-8. PubMed ID: 11676987
[TBL] [Abstract][Full Text] [Related]
10. A novel L67P SOD1 mutation in an Italian ALS patient.
del Grande A; Luigetti M; Conte A; Mancuso I; Lattante S; Marangi G; Stipa G; Zollino M; Sabatelli M
Amyotroph Lateral Scler; 2011 Mar; 12(2):150-2. PubMed ID: 21247266
[TBL] [Abstract][Full Text] [Related]
11. 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]
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. Familial ALS in Germany: origin of the R115G SOD1 mutation by a founder effect.
Niemann S; Joos H; Meyer T; Vielhaber S; Reuner U; Gleichmann M; Dengler R; Müller U
J Neurol Neurosurg Psychiatry; 2004 Aug; 75(8):1186-8. PubMed ID: 15258228
[TBL] [Abstract][Full Text] [Related]
14. A novel exon 3 mutation (D76V) in the SOD1 gene associated with slowly progressive ALS.
Segovia-Silvestre T; Andreu AL; Vives-Bauza C; Garcia-Arumi E; Cervera C; Gamez J
Amyotroph Lateral Scler Other Motor Neuron Disord; 2002 Jun; 3(2):69-74. PubMed ID: 12215228
[TBL] [Abstract][Full Text] [Related]
15. Severe familial ALS with a novel exon 4 mutation (L106F) in the SOD1 gene.
Battistini S; Ricci C; Lotti EM; Benigni M; Gagliardi S; Zucco R; Bondavalli M; Marcello N; Ceroni M; Cereda C
J Neurol Sci; 2010 Jun; 293(1-2):112-5. PubMed ID: 20385392
[TBL] [Abstract][Full Text] [Related]
16. Respiratory onset in an ALS family with L144F SOD1 mutation.
Corcia P; Petiot P; Stevic Z; Vourc'h P; Morales R; Gordon PH; Pageot N; Andres C; Camu W
J Neurol Neurosurg Psychiatry; 2011 Jul; 82(7):747-9. PubMed ID: 20562451
[TBL] [Abstract][Full Text] [Related]
17. Amyotrophic lateral sclerosis with mutation of the Cu/Zn superoxide dismutase gene (SOD1) in a patient with Down syndrome.
Marucci G; Morandi L; Bartolomei I; Salvi F; Pession A; Righi A; Lauria G; Foschini MP
Neuromuscul Disord; 2007 Oct; 17(9-10):673-6. PubMed ID: 17624778
[TBL] [Abstract][Full Text] [Related]
18. I112M SOD1 mutation causes ALS with rapid progression and reduced penetrance in four Mediterranean families.
Gamez J; Caponnetto C; Ferrera L; Syriani E; Marini V; Morales M; Bordo D; Pirro C; Garre C; Origone P
Amyotroph Lateral Scler; 2011 Jan; 12(1):70-5. PubMed ID: 20515426
[TBL] [Abstract][Full Text] [Related]
19. Four familial ALS pedigrees discordant for two SOD1 mutations: are all SOD1 mutations pathogenic?
Felbecker A; Camu W; Valdmanis PN; Sperfeld AD; Waibel S; Steinbach P; Rouleau GA; Ludolph AC; Andersen PM
J Neurol Neurosurg Psychiatry; 2010 May; 81(5):572-7. PubMed ID: 20460594
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
