137 related articles for article (PubMed ID: 12039658)
1. Identification of a novel mutation in Cu/Zn superoxide dismutase gene associated with familial amyotrophic lateral sclerosis.
Naini A; Musumeci O; Hayes L; Pallotti F; Del Bene M; Mitsumoto H
J Neurol Sci; 2002 Jun; 198(1-2):17-9. PubMed ID: 12039658
[TBL] [Abstract][Full Text] [Related]
2. A novel mutation (Cys6Gly) in the Cu/Zn superoxide dismutase gene associated with rapidly progressive familial amyotrophic lateral sclerosis.
Kohno S; Takahashi Y; Miyajima H; Serizawa M; Mizoguchi K
Neurosci Lett; 1999 Dec; 276(2):135-7. PubMed ID: 10624810
[TBL] [Abstract][Full Text] [Related]
3. Superoxide dismutase gene mutations in Italian patients with familial and sporadic amyotrophic lateral sclerosis: identification of three novel missense mutations.
Gellera C; Castellotti B; Riggio MC; Silani V; Morandi L; Testa D; Casali C; Taroni F; Di Donato S; Zeviani M; Mariotti C
Neuromuscul Disord; 2001 May; 11(4):404-10. PubMed ID: 11369193
[TBL] [Abstract][Full Text] [Related]
4. Marked reduction of the Cu/Zn superoxide dismutase polypeptide in a case of familial amyotrophic lateral sclerosis with the homozygous mutation.
Kato M; Aoki M; Ohta M; Nagai M; Ishizaki F; Nakamura S; Itoyama Y
Neurosci Lett; 2001 Oct; 312(3):165-8. PubMed ID: 11602336
[TBL] [Abstract][Full Text] [Related]
5. Familial amyotrophic lateral sclerosis (ALS) in Japan associated with H46R mutation in Cu/Zn superoxide dismutase gene: a possible new subtype of familial ALS.
Aoki M; Ogasawara M; Matsubara Y; Narisawa K; Nakamura S; Itoyama Y; Abe K
J Neurol Sci; 1994 Oct; 126(1):77-83. PubMed ID: 7836951
[TBL] [Abstract][Full Text] [Related]
6. Superoxide dismutase concentration and activity in familial amyotrophic lateral sclerosis.
Bowling AC; Barkowski EE; McKenna-Yasek D; Sapp P; Horvitz HR; Beal MF; Brown RH
J Neurochem; 1995 May; 64(5):2366-9. PubMed ID: 7722523
[TBL] [Abstract][Full Text] [Related]
7. Amyotrophic lateral sclerosis and structural defects in Cu,Zn superoxide dismutase.
Deng HX; Hentati A; Tainer JA; Iqbal Z; Cayabyab A; Hung WY; Getzoff ED; Hu P; Herzfeldt B; Roos RP
Science; 1993 Aug; 261(5124):1047-51. PubMed ID: 8351519
[TBL] [Abstract][Full Text] [Related]
8. A novel mutation in Cu/Zn superoxide dismutase gene in Japanese familial amyotrophic lateral sclerosis.
Nakano R; Sato S; Inuzuka T; Sakimura K; Mishina M; Takahashi H; Ikuta F; Honma Y; Fujii J; Taniguchi N
Biochem Biophys Res Commun; 1994 Apr; 200(2):695-703. PubMed ID: 8179602
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Identification of new mutations in the Cu/Zn superoxide dismutase gene of patients with familial amyotrophic lateral sclerosis.
Pramatarova A; Figlewicz DA; Krizus A; Han FY; Ceballos-Picot I; Nicole A; Dib M; Meininger V; Brown RH; Rouleau GA
Am J Hum Genet; 1995 Mar; 56(3):592-6. PubMed ID: 7887412
[TBL] [Abstract][Full Text] [Related]
11. Variance of age at onset in a Japanese family with amyotrophic lateral sclerosis associated with a novel Cu/Zn superoxide dismutase mutation.
Aoki M; Abe K; Houi K; Ogasawara M; Matsubara Y; Kobayashi T; Mochio S; Narisawa K; Itoyama Y
Ann Neurol; 1995 May; 37(5):676-9. PubMed ID: 7755363
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. Oxidative stress and metal content in blood and cerebrospinal fluid of amyotrophic lateral sclerosis patients with and without a Cu, Zn-superoxide dismutase mutation.
Ihara Y; Nobukuni K; Takata H; Hayabara T
Neurol Res; 2005 Jan; 27(1):105-8. PubMed ID: 15829169
[TBL] [Abstract][Full Text] [Related]
14. Variable clinical symptoms in familial amyotrophic lateral sclerosis with a novel point mutation in the Cu/Zn superoxide dismutase gene.
Ikeda M; Abe K; Aoki M; Sahara M; Watanabe M; Shoji M; St George-Hyslop PH; Hirai S; Itoyama Y
Neurology; 1995 Nov; 45(11):2038-42. PubMed ID: 7501156
[TBL] [Abstract][Full Text] [Related]
15. Clinical characteristics of familial amyotrophic lateral sclerosis with Cu/Zn superoxide dismutase gene mutations.
Abe K; Aoki M; Ikeda M; Watanabe M; Hirai S; Itoyama Y
J Neurol Sci; 1996 Mar; 136(1-2):108-16. PubMed ID: 8815157
[TBL] [Abstract][Full Text] [Related]
16. Familial amyotrophic lateral sclerosis with a mutation in the Cu/Zn superoxide dismutase gene.
Takahashi H; Makifuchi T; Nakano R; Sato S; Inuzuka T; Sakimura K; Mishina M; Honma Y; Tsuji S; Ikuta F
Acta Neuropathol; 1994; 88(2):185-8. PubMed ID: 7985500
[TBL] [Abstract][Full Text] [Related]
17. Identification of six novel SOD1 gene mutations in familial amyotrophic lateral sclerosis.
Boukaftane Y; Khoris J; Moulard B; Salachas F; Meininger V; Malafosse A; Camu W; Rouleau GA
Can J Neurol Sci; 1998 Aug; 25(3):192-6. PubMed ID: 9706719
[TBL] [Abstract][Full Text] [Related]
18. Amyotrophic lateral sclerosis associated with homozygosity for an Asp90Ala mutation in CuZn-superoxide dismutase.
Andersen PM; Nilsson P; Ala-Hurula V; Keränen ML; Tarvainen I; Haltia T; Nilsson L; Binzer M; Forsgren L; Marklund SL
Nat Genet; 1995 May; 10(1):61-6. PubMed ID: 7647793
[TBL] [Abstract][Full Text] [Related]
19. [Familial amyotrophic lateral sclerosis associated with mutant Cu/Zn superoxide dismutase as a conformational disease].
Koide T; Igarashi S; Kikugawa K; Nakano R; Inuzuka T; Tsuji S; Yamada M; Takahashi H
Rinsho Shinkeigaku; 1999 Dec; 39(12):1283-4. PubMed ID: 10791098
[TBL] [Abstract][Full Text] [Related]
20. Glycation proceeds faster in mutated Cu, Zn-superoxide dismutases related to familial amyotrophic lateral sclerosis.
Takamiya R; Takahashi M; Myint T; Park YS; Miyazawa N; Endo T; Fujiwara N; Sakiyama H; Misonou Y; Miyamoto Y; Fujii J; Taniguchi N
FASEB J; 2003 May; 17(8):938-40. PubMed ID: 12626432
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]