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 *

131 related articles for article (PubMed ID: 22853691)

  • 1. Identification of Tau and SOD1 gene mutation in a small Chinese Han pedigree of adult amyotrophic lateral sclerosis.
    Xu R; Shao B; Wu C; Yang Y; Wang H; Yang R; Zhang X; Yi J; Liu J
    Neurocase; 2013; 19(5):497-504. PubMed ID: 22853691
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Familial amyotrophic lateral sclerosis with a novel G85S mutation of superoxide dismutase 1 gene: clinical features of lower motor neuron disease.
    Takazawa T; Ikeda K; Hirayama T; Kawabe K; Nakamura Y; Ito H; Kano O; Yoshii Y; Tanaka F; Sobue G; Iwasaki Y
    Intern Med; 2010; 49(2):183-6. PubMed ID: 20075587
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Identification of a novel Cys146X mutation of SOD1 in familial amyotrophic lateral sclerosis by whole-exome sequencing.
    Wu J; Shen E; Shi D; Sun Z; Cai T
    Genet Med; 2012 Sep; 14(9):823-6. PubMed ID: 22595939
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [To screen for SQSTM1/p62 gene in Chinese patients with familial amyotrophic lateral sclerosis carrying superoxide dismutase 1 mutation].
    Yang Y; Fan D
    Zhonghua Nei Ke Za Zhi; 2014 Dec; 53(12):957-60. PubMed ID: 25623562
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Clinical phenotypes of a large Chinese multigenerational kindred with autosomal dominant familial ALS due to Ile149Thr SOD1 gene mutation.
    Fong GC; Kwok KH; Song YQ; Cheng TS; Ho PW; Chu AC; Kung MH; Chan KH; Mak W; Cheung RT; Ramsden DB; Ho SL
    Amyotroph Lateral Scler; 2006 Sep; 7(3):142-9. PubMed ID: 16963403
    [TBL] [Abstract][Full Text] [Related]  

  • 7. An Italian kindred with FALS due to c.149T>C mutation in the SOD1 gene: case report of an affected family member.
    Trojsi F; Piccirillo G; Femiano C; Damiano R; Rosaria Monsurrò M
    Acta Myol; 2013 May; 32(1):23-6. PubMed ID: 23853506
    [TBL] [Abstract][Full Text] [Related]  

  • 8. New mutation in the SOD1 (copper/zinc superoxide dismutase-1) gene in a Chinese amyotrophic lateral sclerosis (ALS) patient.
    Cui F; Cai W; Wang Z; Ren Y; Li M; Sun Z; Huang X
    Amyotroph Lateral Scler Frontotemporal Degener; 2013 Dec; 14(7-8):635-7. PubMed ID: 23889606
    [TBL] [Abstract][Full Text] [Related]  

  • 9. SOD1 mutations in amyotrophic lateral sclerosis. Results from a multicenter Italian study.
    Battistini S; Giannini F; Greco G; Bibbò G; Ferrera L; Marini V; Causarano R; Casula M; Lando G; Patrosso MC; Caponnetto C; Origone P; Marocchi A; Del Corona A; Siciliano G; Carrera P; Mascia V; Giagheddu M; Carcassi C; Orrù S; Garrè C; Penco S
    J Neurol; 2005 Jul; 252(7):782-8. PubMed ID: 15789135
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The p.E22G mutation in the Cu/Zn superoxide-dismutase gene predicts a long survival time: clinical and genetic characterization of a seven-generation ALS1 Spanish pedigree.
    Syriani E; Morales M; Gamez J
    J Neurol Sci; 2009 Oct; 285(1-2):46-53. PubMed ID: 19524271
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. A novel 10-base pair insertion mutation in exon 5 of the SOD1 gene in a Chinese family with amyotrophic lateral sclerosis.
    Chen S; Li M; Zhu W; Mao F; Wang J; Sun Z; Huang X
    Neurobiol Aging; 2016 Sep; 45():212.e1-212.e4. PubMed ID: 27297615
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. A combined clinical and computational approach to understand the SOD1
    Diker S; Gelener P; Teralı K; Ergoren MC; Tunca C; Başak AN; Tan E
    Acta Neurol Belg; 2022 Aug; 122(4):955-960. PubMed ID: 33420941
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Recurrent K3E mutation in Cu/Zn superoxide dismutase gene associated with amyotrophic lateral sclerosis.
    Kuźma-Kozakiewicz M; Berdyński M; Morita M; Takahashi Y; Kawata A; Kaida K; Kaźmierczak B; Lusakowska A; Goto J; Tsuji S; Zekanowski C; Kwieciński H
    Amyotroph Lateral Scler Frontotemporal Degener; 2013 Dec; 14(7-8):608-14. PubMed ID: 23898858
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Clinical features and Cu/Zn superoxide dismutase gene mutations in two mainland Chinese families with amyotrophic lateral sclerosis.
    Zhao G; Yin X; Wu D; Mao S; Yin H; Zhang B
    Int J Neurosci; 2011 Apr; 121(4):191-5. PubMed ID: 21329474
    [TBL] [Abstract][Full Text] [Related]  

  • 17. An Italian dominant FALS Leu144Phe SOD1 mutation: genotype-phenotype correlation.
    Ferrera L; Caponnetto C; Marini V; Rizzi D; Bordo D; Penco S; Amoroso A; Origone P; Garrè C
    Amyotroph Lateral Scler Other Motor Neuron Disord; 2003 Sep; 4(3):167-70. PubMed ID: 13129804
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [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]  

  • 19. Slow progression of amyotrophic lateral sclerosis in a Chinese patient carrying SOD1 p.S135T mutation.
    Fu H; Zhang K; Yang X; Li L; Cui L
    Amyotroph Lateral Scler Frontotemporal Degener; 2022 Feb; 23(1-2):143-145. PubMed ID: 33860706
    [TBL] [Abstract][Full Text] [Related]  

  • 20. SOD1A4V-mediated ALS: absence of a closely linked modifier gene and origination in Asia.
    Broom WJ; Johnson DV; Auwarter KE; Iafrate AJ; Russ C; Al-Chalabi A; Sapp PC; McKenna-Yasek D; Andersen PM; Brown RH
    Neurosci Lett; 2008 Jan; 430(3):241-5. PubMed ID: 18055113
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.