95 related articles for article (PubMed ID: 14755739)
1. Disease penetrance in amyotrophic lateral sclerosis associated with mutations in the SOD1 gene.
Andersen PM; Restagno G; Stewart HG; Chiò A
Ann Neurol; 2004 Feb; 55(2):298-9; author reply 299. PubMed ID: 14755739
[No Abstract] [Full Text] [Related]
2. Compound heterozygosity and variable penetrance in SOD1 amyotrophic lateral sclerosis pedigrees.
Parton MJ; Andersen PM; Broom WJ; Shaw CE
Ann Neurol; 2001 Oct; 50(4):553-4. PubMed ID: 11601511
[No Abstract] [Full Text] [Related]
3. [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]
4. A novel exon 5 mutation (N139H) in the SOD1 gene in a Spanish family associated with incomplete penetrance.
Nogales-Gadea G; Garcia-Arumi E; Andreu AL; Cervera C; Gamez J
J Neurol Sci; 2004 Apr; 219(1-2):1-6. PubMed ID: 15050430
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. How do ALS-associated mutations in superoxide dismutase 1 promote aggregation of the protein?
Shaw BF; Valentine JS
Trends Biochem Sci; 2007 Feb; 32(2):78-85. PubMed ID: 17208444
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. What is the clinical significance of SOD1 mutations in amyotrophic lateral sclerosis?
Orrell RW
J Neurol Neurosurg Psychiatry; 2010 May; 81(5):473. PubMed ID: 20460587
[No Abstract] [Full Text] [Related]
9. Amyotrophic lateral sclerosis and SOD1 gene: an overview.
Ceroni M; Curti D; Alimonti D
Funct Neurol; 2001; 16(4 Suppl):171-80. PubMed ID: 11996514
[No Abstract] [Full Text] [Related]
10. 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]
11. 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]
12. N19S, a new SOD1 mutation in sporadic amyotrophic lateral sclerosis: no evidence for disease causation.
Mayeux V; Corcia P; Besson G; Jafari-Schluep HF; Briolotti V; Camu W
Ann Neurol; 2003 Jun; 53(6):815-8. PubMed ID: 12783432
[TBL] [Abstract][Full Text] [Related]
13. Copper-zinc superoxide dismutase and amyotrophic lateral sclerosis.
Valentine JS; Doucette PA; Zittin Potter S
Annu Rev Biochem; 2005; 74():563-93. PubMed ID: 15952898
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. 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]
16. 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]
17. 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]
18. Genetics of amyotrophic lateral sclerosis.
Robberecht W
J Neurol; 2000 Dec; 247():2-6. PubMed ID: 11200702
[TBL] [Abstract][Full Text] [Related]
19. [Amyotrophic lateral sclerosis associated with mutations in the SOD1 gene].
Aoki M
Rinsho Shinkeigaku; 2010 Nov; 50(11):861. PubMed ID: 21921473
[No Abstract] [Full Text] [Related]
20. Abnormal diffusion tensor in nonsymptomatic familial amyotrophic lateral sclerosis with a causative superoxide dismutase 1 mutation.
Ng MC; Ho JT; Ho SL; Lee R; Li G; Cheng TS; Song YQ; Ho PW; Fong GC; Mak W; Chan KH; Li LS; Luk KD; Hu Y; Ramsden DB; Leong LL
J Magn Reson Imaging; 2008 Jan; 27(1):8-13. PubMed ID: 18022844
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
