León Sanz, Miguel
Manual de recomendaciones nutricionales al alta hospitalaria [libro] - Barcelona: You&Us, 2001. - 309 p. ; 30 cm.
Formato Vancouver:
León Sanz M, Celaya Pérez, S, editores. Manual de recomendaciones nutricionales al alta hospitalaria. barcelona. You&Us; 2001.
Background: Some epidemiological, genetic, and experimental data suggest a possible role of vitamin D in the pathogenesis of multiple sclerosis (MS) and in experimental autoimmune encephalomyelitis. Data on the possible contribution of several single nucleotide polymorphisms (SNP) in the vitamin D receptor (VDR) gene to the risk for MS are controversial. Several studies suggested an interaction between some SNPs in the VDR gene and HLADRB1*1501 in the risk for MS. Objectives: The aim of this study was to investigate a possible influence of the SNPs rs2228570 and rs731236 in the VDR gene in the risk for MS. A secondary objective was to address the possible interactions between VDR genes and HLADRB1*1501. Methods: We analyzed the allelic and genotype frequency of VDR rs2228570, rs731236, and HLADRB1*1501 (rs3135388) in 303 patients with
Manual de recomendaciones nutricionales al alta hospitalaria [libro] - Barcelona: You&Us, 2001. - 309 p. ; 30 cm.
Formato Vancouver:
León Sanz M, Celaya Pérez, S, editores. Manual de recomendaciones nutricionales al alta hospitalaria. barcelona. You&Us; 2001.
Background: Some epidemiological, genetic, and experimental data suggest a possible role of vitamin D in the pathogenesis of multiple sclerosis (MS) and in experimental autoimmune encephalomyelitis. Data on the possible contribution of several single nucleotide polymorphisms (SNP) in the vitamin D receptor (VDR) gene to the risk for MS are controversial. Several studies suggested an interaction between some SNPs in the VDR gene and HLADRB1*1501 in the risk for MS. Objectives: The aim of this study was to investigate a possible influence of the SNPs rs2228570 and rs731236 in the VDR gene in the risk for MS. A secondary objective was to address the possible interactions between VDR genes and HLADRB1*1501. Methods: We analyzed the allelic and genotype frequency of VDR rs2228570, rs731236, and HLADRB1*1501 (rs3135388) in 303 patients with
