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 *

267 related articles for article (PubMed ID: 18608106)

  • 1. Further evidence that D90A-SOD1 mutation is recessively inherited in ALS patients in Italy.
    Luisa Conforti F; Sprovieri T; Mazzei R; Patitucci A; Ungaro C; Zoccolella S; Magariello A; Bella VL; Tessitore A; Tedeschi G; Simone IL; Majorana G; Valentino P; Citrigno L; Gabriele A; Bono F; Monsurrò MR; Muglia M; Quattrone A
    Amyotroph Lateral Scler; 2009 Feb; 10(1):58-60. PubMed ID: 18608106
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. DNA sequence analysis of the conserved region around the SOD1 gene locus in recessively inherited ALS.
    Broom WJ; Johnson DV; Garber M; Andersen PM; Lennon N; Landers J; Nusbaum C; Russ C; Brown RH
    Neurosci Lett; 2009 Sep; 463(1):64-9. PubMed ID: 19596401
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. 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]  

  • 6. Variants in candidate ALS modifier genes linked to Cu/Zn superoxide dismutase do not explain divergent survival phenotypes.
    Broom WJ; Russ C; Sapp PC; McKenna-Yasek D; Hosler BA; Andersen PM; Brown RH
    Neurosci Lett; 2006 Jan; 392(1-2):52-7. PubMed ID: 16174551
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Mutational analysis of the Cu/Zn superoxide dismutase gene in 23 familial and 69 sporadic cases of amyotrophic lateral sclerosis in Belgium.
    Aguirre T; Matthijs G; Robberecht W; Tilkin P; Cassiman JJ
    Eur J Hum Genet; 1999 Jul; 7(5):599-602. PubMed ID: 10439968
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Clinical heterogeneity in Italian patients with amyotrophic lateral sclerosis.
    Piaceri I; Del Mastio M; Tedde A; Bagnoli S; Latorraca S; Massaro F; Paganini M; Corrado A; Sorbi S; Nacmias B
    Clin Genet; 2012 Jul; 82(1):83-7. PubMed ID: 21651514
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Recessively inherited amyotrophic lateral sclerosis: a Germany family with the D90A CuZn-SOD mutation.
    Winter SM; Claus A; Oberwittler C; Völkel H; Wenzler S; Ludolph AC
    J Neurol; 2000 Oct; 247(10):783-6. PubMed ID: 11127534
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Preserved slow conducting corticomotoneuronal projections in amyotrophic lateral sclerosis with autosomal recessive D90A CuZn-superoxide dismutase mutation.
    Weber M; Eisen A; Stewart HG; Andersen PM
    Brain; 2000 Jul; 123 ( Pt 7)():1505-15. PubMed ID: 10869061
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. 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]  

  • 14. Four familial ALS pedigrees discordant for two SOD1 mutations: are all SOD1 mutations pathogenic?
    Felbecker A; Camu W; Valdmanis PN; Sperfeld AD; Waibel S; Steinbach P; Rouleau GA; Ludolph AC; Andersen PM
    J Neurol Neurosurg Psychiatry; 2010 May; 81(5):572-7. PubMed ID: 20460594
    [TBL] [Abstract][Full Text] [Related]  

  • 15. D90A-SOD1 mediated amyotrophic lateral sclerosis: a single founder for all cases with evidence for a Cis-acting disease modifier in the recessive haplotype.
    Parton MJ; Broom W; Andersen PM; Al-Chalabi A; Nigel Leigh P; Powell JF; Shaw CE;
    Hum Mutat; 2002 Dec; 20(6):473. PubMed ID: 12442272
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Phenotype difference between ALS patients with expanded repeats in C9ORF72 and patients with mutations in other ALS-related genes.
    Millecamps S; Boillée S; Le Ber I; Seilhean D; Teyssou E; Giraudeau M; Moigneu C; Vandenberghe N; Danel-Brunaud V; Corcia P; Pradat PF; Le Forestier N; Lacomblez L; Bruneteau G; Camu W; Brice A; Cazeneuve C; Leguern E; Meininger V; Salachas F
    J Med Genet; 2012 Apr; 49(4):258-63. PubMed ID: 22499346
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Superoxide dismutase in amyotrophic lateral sclerosis patients homozygous for the D90A mutation.
    Jonsson PA; Graffmo KS; Andersen PM; Marklund SL; Brännström T
    Neurobiol Dis; 2009 Dec; 36(3):421-4. PubMed ID: 19703565
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. Distinct cerebral lesions in sporadic and 'D90A' SOD1 ALS: studies with [11C]flumazenil PET.
    Turner MR; Hammers A; Al-Chalabi A; Shaw CE; Andersen PM; Brooks DJ; Leigh PN
    Brain; 2005 Jun; 128(Pt 6):1323-9. PubMed ID: 15843422
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Compound heterozygous D90A and D96N SOD1 mutations in a recessive amyotrophic lateral sclerosis family.
    Hand CK; Mayeux-Portas V; Khoris J; Briolotti V; Clavelou P; Camu W; Rouleau GA
    Ann Neurol; 2001 Feb; 49(2):267-71. PubMed ID: 11220750
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 14.