BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

90 related articles for article (PubMed ID: 21839474)

  • 21. A screening for superoxide dismutase-1 D90A mutation in Italian patients with sporadic amyotrophic lateral sclerosis.
    Mancuso M; Filosto M; Naini A; Rocchi A; Del Corona A; Sartucci F; Siciliano G; Murri L
    Amyotroph Lateral Scler Other Motor Neuron Disord; 2002 Dec; 3(4):215-8. PubMed ID: 12710511
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Cerebrospinal fluid neurofilament light levels in amyotrophic lateral sclerosis: impact of SOD1 genotype.
    Zetterberg H; Jacobsson J; Rosengren L; Blennow K; Andersen PM
    Eur J Neurol; 2007 Dec; 14(12):1329-33. PubMed ID: 17903209
    [TBL] [Abstract][Full Text] [Related]  

  • 23. No association of the SOD1 locus and disease susceptibility or phenotype in sporadic ALS.
    Broom WJ; Parton MJ; Vance CA; Russ C; Andersen PM; Hansen V; Leigh PN; Powell JF; Al-Chalabi A; Shaw CE
    Neurology; 2004 Dec; 63(12):2419-22. PubMed ID: 15623718
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Recurrent G41S mutation in Cu/Zn superoxide dismutase gene (SOD1) causing familial amyotrophic lateral sclerosis in a large Polish family.
    Berdyński M; Kuźma-Kozakiewicz M; Ricci C; Kubiszewska J; Millecamps S; Salachas F; Łusakowska A; Carrera P; Meininger V; Battistini S; Kwieciński H; Zekanowski C
    Amyotroph Lateral Scler; 2012 Jan; 13(1):132-6. PubMed ID: 21877919
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Genotype-phenotype correlation and evidence for a common ancestor in two Italian ALS patients with the D124G
    Ricci C; Giannini F; Intini E; Battistini S
    Amyotroph Lateral Scler Frontotemporal Degener; 2019 Nov; 20(7-8):611-614. PubMed ID: 31170830
    [No Abstract]   [Full Text] [Related]  

  • 26. A4V superoxide dismutase mutation in apparently sporadic ALS resembling neuralgic amyotrophy.
    Weiss MD; Ravits JM; Schuman N; Carter GT
    Amyotroph Lateral Scler; 2006 Mar; 7(1):61-3. PubMed ID: 16546761
    [TBL] [Abstract][Full Text] [Related]  

  • 27. 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]  

  • 28. Misfolded superoxide dismutase-1 in CSF from amyotrophic lateral sclerosis patients.
    Zetterström P; Andersen PM; Brännström T; Marklund SL
    J Neurochem; 2011 Apr; 117(1):91-9. PubMed ID: 21226712
    [TBL] [Abstract][Full Text] [Related]  

  • 29. 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]  

  • 30. 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]  

  • 31. An ALS case with a novel D90N-SOD1 heterozygous missense mutation.
    Calvo A; Ilardi A; Moglia C; Canosa A; Carrara G; Valentini C; Ossola I; Brunetti M; Restagno G; Chiò A
    Amyotroph Lateral Scler; 2012 Jun; 13(4):393-5. PubMed ID: 22632444
    [TBL] [Abstract][Full Text] [Related]  

  • 32. ALS patients with mutations in the SOD1 gene have an unique metabolomic profile in the cerebrospinal fluid compared with ALS patients without mutations.
    Wuolikainen A; Andersen PM; Moritz T; Marklund SL; Antti H
    Mol Genet Metab; 2012 Mar; 105(3):472-8. PubMed ID: 22264771
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Severe familial ALS with a novel exon 4 mutation (L106F) in the SOD1 gene.
    Battistini S; Ricci C; Lotti EM; Benigni M; Gagliardi S; Zucco R; Bondavalli M; Marcello N; Ceroni M; Cereda C
    J Neurol Sci; 2010 Jun; 293(1-2):112-5. PubMed ID: 20385392
    [TBL] [Abstract][Full Text] [Related]  

  • 34. CuZn-superoxide dismutase gene in sporadic amyotrophic lateral sclerosis patients from Russia: Asp90Ala (D90A) mutation and novel rare polymorphism IVS3+35 A>C.
    Slominsky PA; Shadrina MI; Kondratyeva EA; Tupitsina TV; Levitsky GN; Skvortsova VI; Limborska SA
    Hum Mutat; 2000 Sep; 16(3):277-8. PubMed ID: 10980551
    [No Abstract]   [Full Text] [Related]  

  • 35. Combined fulminant frontotemporal dementia and amyotrophic lateral sclerosis associated with an I113T SOD1 mutation.
    Katz JS; Katzberg HD; Woolley SC; Marklund SL; Andersen PM
    Amyotroph Lateral Scler; 2012 Oct; 13(6):567-9. PubMed ID: 22670877
    [TBL] [Abstract][Full Text] [Related]  

  • 36. A novel codon4 mutation (A4F) in the SOD1gene in familial amyotrophic lateral sclerosis.
    Baek W; Koh SH; Park JS; Kim YS; Kim HY; Kwon MJ; Ki CS; Kim SH
    J Neurol Sci; 2011 Jul; 306(1-2):157-9. PubMed ID: 21496827
    [TBL] [Abstract][Full Text] [Related]  

  • 37. D90A-SOD1 mutation in ALS: The first report of heterozygous Italian patients and unusual findings.
    Giannini F; Battistini S; Mancuso M; Greco G; Ricci C; Volpi N; Del Corona A; Piazza S; Siciliano G
    Amyotroph Lateral Scler; 2010; 11(1-2):216-9. PubMed ID: 20184519
    [TBL] [Abstract][Full Text] [Related]  

  • 38. A novel p.E121G SOD1 mutation in slowly progressive form of amyotrophic lateral sclerosis induces cytoplasmic aggregates in cultured motor neurons and reduces cell viability.
    Dangoumau A; Deschamps R; Veyrat-Durebex C; Pettmann B; Corcia P; Andres CR; Vourc'h P
    Amyotroph Lateral Scler Frontotemporal Degener; 2015 Mar; 16(1-2):131-4. PubMed ID: 25336041
    [TBL] [Abstract][Full Text] [Related]  

  • 39. 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]  

  • 40. SOD1 (A4V)-mediated ALS presenting with lower motor neuron facial diplegia and unilateral vocal cord paralysis.
    Salameh JS; Atassi N; David WS
    Muscle Nerve; 2009 Nov; 40(5):880-2. PubMed ID: 19618436
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 5.