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 *

220 related articles for article (PubMed ID: 12402272)

  • 1. "True" sporadic ALS associated with a novel SOD-1 mutation.
    Alexander MD; Traynor BJ; Miller N; Corr B; Frost E; McQuaid S; Brett FM; Green A; Hardiman O
    Ann Neurol; 2002 Nov; 52(5):680-3. PubMed ID: 12402272
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. A novel SOD1 mutation in a young amyotrophic lateral sclerosis patient with a very slowly progressive clinical course.
    Georgoulopoulou E; Gellera C; Bragato C; Sola P; Chiari A; Bernabei C; Mandrioli J
    Muscle Nerve; 2010 Oct; 42(4):596-7. PubMed ID: 20740631
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. Sporadic ALS associated with the D90A Cu,Zn superoxide dismutase mutation in Russia.
    Skvortsova VI; Limborska SA; Slominsky PA; Levitskaya NI; Levitsky GN; Shadrina MI; Kondratyeva EA
    Eur J Neurol; 2001 Mar; 8(2):167-72. PubMed ID: 11284995
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Coexistence of dominant and recessive familial amyotrophic lateral sclerosis with the D90A Cu,Zn superoxide dismutase mutation within the same country.
    Khoris J; Moulard B; Briolotti V; Hayer M; Durieux A; Clavelou P; Malafosse A; Rouleau GA; Camu W
    Eur J Neurol; 2000 Mar; 7(2):207-11. PubMed ID: 10809943
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Cortical hyperexcitability may precede the onset of familial amyotrophic lateral sclerosis.
    Vucic S; Nicholson GA; Kiernan MC
    Brain; 2008 Jun; 131(Pt 6):1540-50. PubMed ID: 18469020
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. Early onset of severe familial amyotrophic lateral sclerosis with a SOD-1 mutation: potential impact of CNTF as a candidate modifier gene.
    Giess R; Holtmann B; Braga M; Grimm T; Müller-Myhsok B; Toyka KV; Sendtner M
    Am J Hum Genet; 2002 May; 70(5):1277-86. PubMed ID: 11951178
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Molecular analyses of the Cu/Zn superoxide dismutase gene in patients with familial amyotrophic lateral sclerosis (ALS) in Japan.
    Aoki M; Abe K; Itoyama Y
    Cell Mol Neurobiol; 1998 Dec; 18(6):639-47. PubMed ID: 9876871
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Superoxide dismutase-1 (SOD-1) gene mutation-dependent mechanisms of neural degeneration in amyotrophic lateral sclerosis].
    Iłzecka J
    Neurol Neurochir Pol; 2001; 35(3):461-9. PubMed ID: 11732268
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. 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]  

  • 14. 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]  

  • 15. The human G93A SOD1 phenotype closely resembles sporadic amyotrophic lateral sclerosis.
    Synofzik M; Fernández-Santiago R; Maetzler W; Schöls L; Andersen PM
    J Neurol Neurosurg Psychiatry; 2010 Jul; 81(7):764-7. PubMed ID: 20176600
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. Mutations in all five exons of SOD-1 may cause ALS.
    Shaw CE; Enayat ZE; Chioza BA; Al-Chalabi A; Radunovic A; Powell JF; Leigh PN
    Ann Neurol; 1998 Mar; 43(3):390-4. PubMed ID: 9506558
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. An unusual case of familial ALS and cerebellar ataxia.
    Yasser S; Fecto F; Siddique T; Sheikh KA; Athar P
    Amyotroph Lateral Scler; 2010 Dec; 11(6):568-70. PubMed ID: 20540686
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Expression of hepatocyte growth factor and c-Met in the anterior horn cells of the spinal cord in the patients with amyotrophic lateral sclerosis (ALS): immunohistochemical studies on sporadic ALS and familial ALS with superoxide dismutase 1 gene mutation.
    Kato S; Funakoshi H; Nakamura T; Kato M; Nakano I; Hirano A; Ohama E
    Acta Neuropathol; 2003 Aug; 106(2):112-20. PubMed ID: 12707786
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.