These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

118 related articles for article (PubMed ID: 9455983)

  • 1. Prominent sensory and autonomic disturbances in familial amyotrophic lateral sclerosis with a Gly93Ser mutation in the SOD1 gene.
    Kawata A; Kato S; Hayashi H; Hirai S
    J Neurol Sci; 1997 Dec; 153(1):82-5. PubMed ID: 9455983
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Familial amyotrophic lateral sclerosis with Gly93Ser mutation in Cu/Zn superoxide dismutase: a clinical and neuropathological study.
    Suzuki M; Irie T; Watanabe T; Mikami H; Yamazaki T; Oyanagi K; Ono S
    J Neurol Sci; 2008 May; 268(1-2):140-4. PubMed ID: 18191946
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. 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]  

  • 5. 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]  

  • 6. Cu/Zn superoxide dismutase activity in familial and sporadic amyotrophic lateral sclerosis.
    Robberecht W; Sapp P; Viaene MK; Rosen D; McKenna-Yasek D; Haines J; Horvitz R; Theys P; Brown R
    J Neurochem; 1994 Jan; 62(1):384-7. PubMed ID: 8263541
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A SOD1 gene mutation in a patient with slowly progressing familial ALS.
    Penco S; Schenone A; Bordo D; Bolognesi M; Abbruzzese M; Bugiani O; Ajmar F; Garrè C
    Neurology; 1999 Jul; 53(2):404-6. PubMed ID: 10430435
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. [Clinical features and neuropathological findings of familial amyotrophic lateral sclerosis with an H43R mutation in Cu/Zn superoxide dismutase].
    Mochizuki Y; Mizutani T; Nakano R; Fukushima T; Honma T; Nemoto N; Takei K
    Rinsho Shinkeigaku; 2003 Aug; 43(8):491-5. PubMed ID: 14658402
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Different clinical phenotypes of siblings with familial amyotrophic lateral sclerosis showing Cys146Arg point mutation of superoxide dismutase 1 gene].
    Ito K; Uchiyama T; Fukutake T; Arai K; Kanesaka T; Hattori T
    Rinsho Shinkeigaku; 2002 Feb; 42(2):175-7. PubMed ID: 12424972
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Large-scale SOD1 mutation screening provides evidence for genetic heterogeneity in amyotrophic lateral sclerosis.
    van Es MA; Dahlberg C; Birve A; Veldink JH; van den Berg LH; Andersen PM
    J Neurol Neurosurg Psychiatry; 2010 May; 81(5):562-6. PubMed ID: 19965850
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Instability of mutant Cu/Zn superoxide dismutase (Ala4Thr) associated with familial amyotrophic lateral sclerosis.
    Nakano R; Inuzuka T; Kikugawa K; Takahashi H; Sakimura K; Fujii J; Taniguchi N; Tsuji S
    Neurosci Lett; 1996 Jun; 211(2):129-31. PubMed ID: 8830861
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Clinical and pathological studies of familial amyotrophic lateral sclerosis (FALS) with SOD1 H46R mutation in large Japanese families.
    Arisato T; Okubo R; Arata H; Abe K; Fukada K; Sakoda S; Shimizu A; Qin XH; Izumo S; Osame M; Nakagawa M
    Acta Neuropathol; 2003 Dec; 106(6):561-8. PubMed ID: 14517684
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. 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]  

  • 16. 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]  

  • 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. 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]  

  • 19. A frequent ala 4 to val superoxide dismutase-1 mutation is associated with a rapidly progressive familial amyotrophic lateral sclerosis.
    Rosen DR; Bowling AC; Patterson D; Usdin TB; Sapp P; Mezey E; McKenna-Yasek D; O'Regan J; Rahmani Z; Ferrante RJ
    Hum Mol Genet; 1994 Jun; 3(6):981-7. PubMed ID: 7951249
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Japanese familial amyotrophic lateral sclerosis family with a two-base deletion in the superoxide dismutase-1 gene.
    Watanabe Y; Adachi Y; Nakashima K
    Neuropathology; 2001 Mar; 21(1):61-6. PubMed ID: 11304044
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.