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.
60 related articles for article (PubMed ID: 20192886)
1. G127R: A novel SOD1 mutation associated with rapidly evolving ALS and severe pain syndrome. Holmøy T; Wilson JA; von der Lippe C; Andersen PM; Berg-Hansen P Amyotroph Lateral Scler; 2010 Oct; 11(5):478-80. PubMed ID: 20192886 [TBL] [Abstract][Full Text] [Related]
2. SOD1 G93D mutation presenting as paucisymptomatic amyotrophic lateral sclerosis. Luigetti M; Madia F; Conte A; Marangi G; Zollino M; Del Grande A; Dileone M; Tonali PA; Sabatelli M Amyotroph Lateral Scler; 2009; 10(5-6):479-82. PubMed ID: 19922144 [TBL] [Abstract][Full Text] [Related]
3. 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]
4. 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]
5. 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]
6. Fast course ALS presenting with vocal cord paralysis: clinical features, bioinformatic and modelling analysis of the novel SOD1 Gly147Ser mutation. Origone P; Caponnetto C; Mantero V; Cichero E; Fossa P; Geroldi A; Verdiani S; Bellone E; Mancardi G; Mandich P Amyotroph Lateral Scler; 2012 Jan; 13(1):144-8. PubMed ID: 21929355 [TBL] [Abstract][Full Text] [Related]
7. Identification of a novel D109Y mutation in Cu/Zn superoxide dismutase (sod1) gene associated with amyotrophic lateral sclerosis. Naini A; Mehrazin M; Lu J; Gordon P; Mitsumoto H J Neurol Sci; 2007 Mar; 254(1-2):17-21. PubMed ID: 17257622 [TBL] [Abstract][Full Text] [Related]
8. 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]
9. 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]
10. 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]
11. Novel SOD1 N86K mutation is associated with a severe phenotype in familial ALS. Beck M; Sendtner M; Toyka KV Muscle Nerve; 2007 Jul; 36(1):111-4. PubMed ID: 17299743 [TBL] [Abstract][Full Text] [Related]
12. Heterozygous SOD1 D90A mutation presenting as slowly progressive predominant upper motor neuron amyotrophic lateral sclerosis. Luigetti M; Conte A; Madia F; Marangi G; Zollino M; Mancuso I; Dileone M; Del Grande A; Di Lazzaro V; Tonali PA; Sabatelli M Neurol Sci; 2009 Dec; 30(6):517-20. PubMed ID: 19685200 [TBL] [Abstract][Full Text] [Related]
13. 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]
14. 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]
15. G41S SOD1 mutation: A common ancestor for six ALS Italian families with an aggressive phenotype. Battistini S; Ricci C; Giannini F; Calzavara S; Greco G; Del Corona A; Mancuso M; Battistini N; Siciliano G; Carrera P Amyotroph Lateral Scler; 2010; 11(1-2):210-5. PubMed ID: 19488901 [TBL] [Abstract][Full Text] [Related]
16. Limited corticospinal tract involvement in amyotrophic lateral sclerosis subjects with the A4V mutation in the copper/zinc superoxide dismutase gene. Cudkowicz ME; McKenna-Yasek D; Chen C; Hedley-Whyte ET; Brown RH Ann Neurol; 1998 Jun; 43(6):703-10. PubMed ID: 9629839 [TBL] [Abstract][Full Text] [Related]
17. 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]
18. 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]
19. 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]
20. H46R SOD1 mutation is consistently associated with a relatively benign form of amyotrophic lateral sclerosis with slow progression. Zou ZY; Liu MS; Li XG; Cui LY Amyotroph Lateral Scler Frontotemporal Degener; 2016; 17(7-8):610-613. PubMed ID: 27348463 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]