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 *

198 related articles for article (PubMed ID: 21247266)

  • 1. A novel L67P SOD1 mutation in an Italian ALS patient.
    del Grande A; Luigetti M; Conte A; Mancuso I; Lattante S; Marangi G; Stipa G; Zollino M; Sabatelli M
    Amyotroph Lateral Scler; 2011 Mar; 12(2):150-2. PubMed ID: 21247266
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A second ALS patient having an L67P mutation in exon 3 of the Cu/Zn superoxide dismutase gene.
    Krieger C; Haase S; Scott P
    Amyotroph Lateral Scler; 2011 Nov; 12(6):466-7. PubMed ID: 21692663
    [No Abstract]   [Full Text] [Related]  

  • 3. A novel exon 1 mutation (G10R) in the SOD1 gene in a patient with familial ALS.
    Ricci C; Benigni M; Battistini S; Greco G; Torzini A; Giannini F
    Amyotroph Lateral Scler; 2010 Oct; 11(5):481-5. PubMed ID: 20331403
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A novel P66S mutation in exon 3 of the SOD1 gene with early onset and rapid progression.
    Keckarević D; Stević Z; Keckarević-Marković M; Kecmanović M; Romac S
    Amyotroph Lateral Scler; 2012 Feb; 13(2):237-40. PubMed ID: 22214314
    [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. 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]  

  • 7. Amyotrophic lateral sclerosis with mutation of the Cu/Zn superoxide dismutase gene (SOD1) in a patient with Down syndrome.
    Marucci G; Morandi L; Bartolomei I; Salvi F; Pession A; Righi A; Lauria G; Foschini MP
    Neuromuscul Disord; 2007 Oct; 17(9-10):673-6. PubMed ID: 17624778
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. 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]  

  • 10. Lack of SOD1 gene mutations and activity alterations in two Italian families with amyotrophic lateral sclerosis.
    Gestri D; Cecchi C; Tedde A; Latorraca S; Orlacchio A; Grassi E; Massaro AM; Liguri G; St George-Hyslop PH; Sorbi S
    Neurosci Lett; 2000 Aug; 289(3):157-60. PubMed ID: 10961653
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A novel T137A SOD1 mutation in an Italian family with two subjects affected by amyotrophic lateral sclerosis.
    Visani M; de Biase D; Bartolomei I; Plasmati R; Morandi L; Cenacchi G; Salvi F; Pession A
    Amyotroph Lateral Scler; 2011 Sep; 12(5):385-8. PubMed ID: 21574856
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. Genetics of ALS in Italian families.
    Gellera C
    Amyotroph Lateral Scler Other Motor Neuron Disord; 2001 Mar; 2 Suppl 1():S43-6. PubMed ID: 11465924
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. [Familial amyotrophic lateral sclerosis and mutations in the Cu/Zn superoxide dismutase gene].
    Nakano R
    Rinsho Shinkeigaku; 1995 Dec; 35(12):1546-8. PubMed ID: 8752459
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A novel p.E121G heterozygous missense mutation of SOD1 in an apparently sporadic ALS case with a 14-year course.
    Canosa A; Calvo A; Moglia C; Barberis M; Brunetti M; Cammarosano S; Manera U; Ilardi A; Restagno G; Chiò A
    Amyotroph Lateral Scler Frontotemporal Degener; 2015 Mar; 16(1-2):127-8. PubMed ID: 25299943
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. A novel exon 3 mutation (D76V) in the SOD1 gene associated with slowly progressive ALS.
    Segovia-Silvestre T; Andreu AL; Vives-Bauza C; Garcia-Arumi E; Cervera C; Gamez J
    Amyotroph Lateral Scler Other Motor Neuron Disord; 2002 Jun; 3(2):69-74. PubMed ID: 12215228
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Identification of two novel mutations in the Cu/Zn superoxide dismutase gene with familial amyotrophic lateral sclerosis: mass spectrometric and genomic analyses.
    Sato T; Yamamoto Y; Nakanishi T; Fukada K; Sugai F; Zhou Z; Okuno T; Nagano S; Hirata S; Shimizu A; Sakoda S
    J Neurol Sci; 2004 Mar; 218(1-2):79-83. PubMed ID: 14759637
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Amyotrophic lateral sclerosis: a new missense mutation in the SOD1 gene.
    Tortelli R; Conforti FL; Cortese R; D'Errico E; Distaso E; Mazzei R; Ungaro C; Magariello A; Gambardella A; Logroscino G; Simone IL
    Neurobiol Aging; 2013 Jun; 34(6):1709.e3-5. PubMed ID: 23182243
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.