149 related articles for article (PubMed ID: 21120636)
1. Phenotypic heterogeneity in a SOD1 G93D Italian ALS family: an example of human model to study a complex disease.
Penco S; Lunetta C; Mosca L; Maestri E; Avemaria F; Tarlarini C; Patrosso MC; Marocchi A; Corbo M
J Mol Neurosci; 2011 May; 44(1):25-30. PubMed ID: 21120636
[TBL] [Abstract][Full Text] [Related]
2. SOD1 G93D sporadic amyotrophic lateral sclerosis (SALS) patient with rapid progression and concomitant novel ANG variant.
Luigetti M; Lattante S; Zollino M; Conte A; Marangi G; Del Grande A; Sabatelli M
Neurobiol Aging; 2011 Oct; 32(10):1924.e15-8. PubMed ID: 21621297
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. 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]
5. 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]
6. ALS with variable phenotypes in a six-generation family caused by leu144phe mutation in the SOD1 gene.
Masè G; Ros S; Gemma A; Bonfigli L; Carraro N; Cazzato G; Rolfo M; Zanconati F; Sepcic J; Jurjevic A; Pirulli D; Boniotto M; Zezlina S; Crovella S; Amoroso A
J Neurol Sci; 2001 Oct; 191(1-2):11-8. PubMed ID: 11676987
[TBL] [Abstract][Full Text] [Related]
7. Increase in DNA methylation in patients with amyotrophic lateral sclerosis carriers of not fully penetrant SOD1 mutations.
Coppedè F; Stoccoro A; Mosca L; Gallo R; Tarlarini C; Lunetta C; Marocchi A; Migliore L; Penco S
Amyotroph Lateral Scler Frontotemporal Degener; 2018 Feb; 19(1-2):93-101. PubMed ID: 28859526
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. 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]
10. Identification of a novel missense (C7W) mutation of SOD1 in a large familial amyotrophic lateral sclerosis pedigree.
Wang Z; Cai W; Cui F; Cai T; Chen Z; Mao F; Teng H; Chen L; Wang J; Sun Z; Huang X; Yu P
Neurobiol Aging; 2014 Mar; 35(3):725.e11-5. PubMed ID: 24094577
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. 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]
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 SOD1 gene mutation in a patient with slowly progressing familial ALS.
Penco S; Schenone A; Bordo D; Bolognesi M; Abbruzzese M; Bugiani O; Ajmar F; Garrè C
Neurology; 1999 Jul; 53(2):404-6. PubMed ID: 10430435
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. 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]
17. 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]
18. 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]
19. SOD1, ANG, VAPB, TARDBP, and FUS mutations in familial amyotrophic lateral sclerosis: genotype-phenotype correlations.
Millecamps S; Salachas F; Cazeneuve C; Gordon P; Bricka B; Camuzat A; Guillot-Noël L; Russaouen O; Bruneteau G; Pradat PF; Le Forestier N; Vandenberghe N; Danel-Brunaud V; Guy N; Thauvin-Robinet C; Lacomblez L; Couratier P; Hannequin D; Seilhean D; Le Ber I; Corcia P; Camu W; Brice A; Rouleau G; LeGuern E; Meininger V
J Med Genet; 2010 Aug; 47(8):554-60. PubMed ID: 20577002
[TBL] [Abstract][Full Text] [Related]
20. Clustering of ALS patients in central Italy due to the occurrence of the L84F SOD1 gene mutation.
Ceroni M; Malaspina A; Poloni TE; Alimonti D; Rognoni F; Habgood J; Imbesi F; Antonelli P; Alfonsi E; Curti D; deBelleroche J
Neurology; 1999 Sep; 53(5):1064-71. PubMed ID: 10496267
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
