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.
121 related articles for article (PubMed ID: 24471417)
1. Amyotrophic lateral sclerosis in pregnancy is associated with a vascular endothelial growth factor promoter genotype. Lunetta C; Sansone VA; Penco S; Mosca L; Tarlarini C; Avemaria F; Maestri E; Melazzini MG; Meola G; Corbo M Eur J Neurol; 2014 Apr; 21(4):594-8. PubMed ID: 24471417 [TBL] [Abstract][Full Text] [Related]
2. An epigenetic analysis of SOD1 and VEGF in ALS. Oates N; Pamphlett R Amyotroph Lateral Scler; 2007 Apr; 8(2):83-6. PubMed ID: 17453634 [TBL] [Abstract][Full Text] [Related]
3. Meta-analysis of vascular endothelial growth factor variations in amyotrophic lateral sclerosis: increased susceptibility in male carriers of the -2578AA genotype. Lambrechts D; Poesen K; Fernández-Santiago R; Al-Chalabi A; Del Bo R; Van Vught PW; Khan S; Marklund SL; Brockington A; van Marion I; Anneser J; Shaw C; Ludolph AC; Leigh NP; Comi GP; Gasser T; Shaw PJ; Morrison KE; Andersen PM; Van den Berg LH; Thijs V; Siddique T; Robberecht W; Carmeliet P J Med Genet; 2009 Dec; 46(12):840-6. PubMed ID: 18413368 [TBL] [Abstract][Full Text] [Related]
4. Genetic analysis and SOD1 mutation screening in Iranian amyotrophic lateral sclerosis patients. Alavi A; Nafissi S; Rohani M; Zamani B; Sedighi B; Shamshiri H; Fan JB; Ronaghi M; Elahi E Neurobiol Aging; 2013 May; 34(5):1516.e1-8. PubMed ID: 23062701 [TBL] [Abstract][Full Text] [Related]
5. 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]
6. 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]
7. Association of polymorphisms in vascular endothelial growth factor gene with the age of onset of amyotrophic lateral sclerosis. Chen D; Shen L; Wang L; Lu A; Zhang H; Zhang X; Zhang Y; Shui W; Li L; Fan D; Zhang J Amyotroph Lateral Scler; 2007 Jun; 8(3):144-9. PubMed ID: 17538775 [TBL] [Abstract][Full Text] [Related]
8. Lack of association between VEGF polymorphisms and ALS in a Dutch population. Van Vught PW; Sutedja NA; Veldink JH; Koeleman BP; Groeneveld GJ; Wijmenga C; Uitdehaag BM; de Jong JM; Baas F; Wokke JH; Van den Berg LH Neurology; 2005 Nov; 65(10):1643-5. PubMed ID: 16301496 [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]
11. Vascular endothelial growth factor prolongs survival in a transgenic mouse model of ALS. Zheng C; Nennesmo I; Fadeel B; Henter JI Ann Neurol; 2004 Oct; 56(4):564-7. PubMed ID: 15389897 [TBL] [Abstract][Full Text] [Related]
12. 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]
13. VEGF delivery with retrogradely transported lentivector prolongs survival in a mouse ALS model. Azzouz M; Ralph GS; Storkebaum E; Walmsley LE; Mitrophanous KA; Kingsman SM; Carmeliet P; Mazarakis ND Nature; 2004 May; 429(6990):413-7. PubMed ID: 15164063 [TBL] [Abstract][Full Text] [Related]
14. Pathological TDP-43 distinguishes sporadic amyotrophic lateral sclerosis from amyotrophic lateral sclerosis with SOD1 mutations. Mackenzie IR; Bigio EH; Ince PG; Geser F; Neumann M; Cairns NJ; Kwong LK; Forman MS; Ravits J; Stewart H; Eisen A; McClusky L; Kretzschmar HA; Monoranu CM; Highley JR; Kirby J; Siddique T; Shaw PJ; Lee VM; Trojanowski JQ Ann Neurol; 2007 May; 61(5):427-34. PubMed ID: 17469116 [TBL] [Abstract][Full Text] [Related]
15. Identify mutation in amyotrophic lateral sclerosis cases using HaloPlex target enrichment system. Liu ZJ; Li HF; Tan GH; Tao QQ; Ni W; Cheng XW; Xiong ZQ; Wu ZY Neurobiol Aging; 2014 Dec; 35(12):2881.e11-2881.e15. PubMed ID: 25109764 [TBL] [Abstract][Full Text] [Related]
16. Expression of hepatocyte growth factor and c-Met in the anterior horn cells of the spinal cord in the patients with amyotrophic lateral sclerosis (ALS): immunohistochemical studies on sporadic ALS and familial ALS with superoxide dismutase 1 gene mutation. Kato S; Funakoshi H; Nakamura T; Kato M; Nakano I; Hirano A; Ohama E Acta Neuropathol; 2003 Aug; 106(2):112-20. PubMed ID: 12707786 [TBL] [Abstract][Full Text] [Related]