164 related articles for article (PubMed ID: 19596401)
1. 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]
2. 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]
3. 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]
4. 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]
5. 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]
6. 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]
7. Recessive amyotrophic lateral sclerosis families with the D90A SOD1 mutation share a common founder: evidence for a linked protective factor.
Al-Chalabi A; Andersen PM; Chioza B; Shaw C; Sham PC; Robberecht W; Matthijs G; Camu W; Marklund SL; Forsgren L; Rouleau G; Laing NG; Hurse PV; Siddique T; Leigh PN; Powell JF
Hum Mol Genet; 1998 Dec; 7(13):2045-50. PubMed ID: 9817920
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. 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]
10. 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]
11. 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]
12. 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]
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. 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]
15. 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]
16. 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]
17. 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]
18. 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]
19. CuZn-superoxide dismutase in D90A heterozygotes from recessive and dominant ALS pedigrees.
Jonsson PA; Bäckstrand A; Andersen PM; Jacobsson J; Parton M; Shaw C; Swingler R; Shaw PJ; Robberecht W; Ludolph AC; Siddique T; Skvortsova VI; Marklund SL
Neurobiol Dis; 2002 Aug; 10(3):327-33. PubMed ID: 12270693
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
