142 related articles for article (PubMed ID: 17636481)
1. Analysis of a genetic defect in the TATA box of the SOD1 gene in a patient with familial amyotrophic lateral sclerosis.
Niemann S; Broom WJ; Brown RH
Muscle Nerve; 2007 Nov; 36(5):704-7. PubMed ID: 17636481
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. 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]
4. 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]
5. [Identification of the mutation of SOD1 gene in a familial amyotrophic lateral sclerosis].
Shi SG; Li LS; Chen KN; Liu X
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Apr; 21(2):149-52. PubMed ID: 15079798
[TBL] [Abstract][Full Text] [Related]
6. An analysis of the entire SOD1 gene in sporadic ALS.
Luquin N; Yu B; Trent RJ; Morahan JM; Pamphlett R
Neuromuscul Disord; 2008 Jul; 18(7):545-52. PubMed ID: 18504130
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. The IVS1 +319 t>a of SOD1 gene is not an ALS causing mutation.
Restagno G; Gomez A; Lombardo F; Cocco E; Calvo A; Ghiglione P; Mutani R; Chiò A
Amyotroph Lateral Scler Other Motor Neuron Disord; 2005 Mar; 6(1):45-9. PubMed ID: 16036425
[TBL] [Abstract][Full Text] [Related]
9. Pathological TDP-43 distinguishes sporadic amyotrophic lateral sclerosis from amyotrophic lateral sclerosis with SOD1 mutations.
Mackenzie IR; Bigio EH; Ince PG; Geser F; Neumann M; Cairns NJ; Kwong LK; Forman MS; Ravits J; Stewart H; Eisen A; McClusky L; Kretzschmar HA; Monoranu CM; Highley JR; Kirby J; Siddique T; Shaw PJ; Lee VM; Trojanowski JQ
Ann Neurol; 2007 May; 61(5):427-34. PubMed ID: 17469116
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. Genetic analysis of the cystatin C gene in familial and sporadic ALS patients.
Watanabe M; Jackson M; Ikeda M; Mizushima K; Amari M; Takatama M; Hirai S; Ikeda Y; Shizuka-Ikeda M; Okamoto K
Brain Res; 2006 Feb; 1073-1074():20-4. PubMed ID: 16443201
[TBL] [Abstract][Full Text] [Related]
12. A novel codon4 mutation (A4F) in the SOD1gene in familial amyotrophic lateral sclerosis.
Baek W; Koh SH; Park JS; Kim YS; Kim HY; Kwon MJ; Ki CS; Kim SH
J Neurol Sci; 2011 Jul; 306(1-2):157-9. PubMed ID: 21496827
[TBL] [Abstract][Full Text] [Related]
13. DNA sequence analysis of the conserved region around the SOD1 gene locus in recessively inherited ALS.
Broom WJ; Johnson DV; Garber M; Andersen PM; Lennon N; Landers J; Nusbaum C; Russ C; Brown RH
Neurosci Lett; 2009 Sep; 463(1):64-9. PubMed ID: 19596401
[TBL] [Abstract][Full Text] [Related]
14. 50bp deletion in the promoter for superoxide dismutase 1 (SOD1) reduces SOD1 expression in vitro and may correlate with increased age of onset of sporadic amyotrophic lateral sclerosis.
Broom WJ; Greenway M; Sadri-Vakili G; Russ C; Auwarter KE; Glajch KE; Dupre N; Swingler RJ; Purcell S; Hayward C; Sapp PC; McKenna-Yasek D; Valdmanis PN; Bouchard JP; Meininger V; Hosler BA; Glass JD; Polack M; Rouleau GA; Cha JH; Hardiman O; Brown RH
Amyotroph Lateral Scler; 2008 Aug; 9(4):229-37. PubMed ID: 18608091
[TBL] [Abstract][Full Text] [Related]
15. Genetics of amyotrophic lateral sclerosis.
Robberecht W
J Neurol; 2000 Dec; 247 Suppl 6():VI/2-6. PubMed ID: 19714405
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. Amyotrophic lateral sclerosis: copper/zinc superoxide dismutase (SOD1) gene mutations.
Orrell RW
Neuromuscul Disord; 2000 Jan; 10(1):63-8. PubMed ID: 10677867
[TBL] [Abstract][Full Text] [Related]
18. Slowly progressing amyotrophic lateral sclerosis caused by H46R SOD1 mutation.
Holmøy T; Bjørgo K; Roos PM
Eur Neurol; 2007; 58(1):57-8. PubMed ID: 17483589
[No Abstract] [Full Text] [Related]
19. Genetics of amyotrophic lateral sclerosis.
Robberecht W
J Neurol; 2000 Dec; 247():2-6. PubMed ID: 11200702
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]