Mozas P - Search Results

1

The apolipoprotein B R3500Q gene mutation in Spanish subjects with a clinical diagnosis of familial hypercholesterolemia.

Castillo S, Tejedor D, Mozas P, Reyes G, Civeira F, Alonso R, Ros E, Pocoví M, Mata P. Castillo S, et al. Among authors: mozas p. Atherosclerosis. 2002 Nov;165(1):127-35. doi: 10.1016/s0021-9150(02)00190-9. Atherosclerosis. 2002. PMID: 12208478

2

A mutation (-49C>T) in the promoter of the low density lipoprotein receptor gene associated with familial hypercholesterolemia.

Mozas P, Galetto R, Albajar M, Ros E, Pocoví M, Rodríguez-Rey JC. Mozas P, et al. J Lipid Res. 2002 Jan;43(1):13-8. J Lipid Res. 2002. PMID: 11792717 Free article.

3

Molecular characterization of familial hypercholesterolemia in Spain: identification of 39 novel and 77 recurrent mutations in LDLR.

Mozas P, Castillo S, Tejedor D, Reyes G, Alonso R, Franco M, Saenz P, Fuentes F, Almagro F, Mata P, Pocoví M. Mozas P, et al. Hum Mutat. 2004 Aug;24(2):187. doi: 10.1002/humu.9264. Hum Mutat. 2004. PMID: 15241806

4

Reliable low-density DNA array based on allele-specific probes for detection of 118 mutations causing familial hypercholesterolemia.

Tejedor D, Castillo S, Mozas P, Jiménez E, López M, Tejedor MT, Artieda M, Alonso R, Mata P, Simón L, Martínez A, Pocoví M; Spanish FH Group. Tejedor D, et al. Among authors: mozas p. Clin Chem. 2005 Jul;51(7):1137-44. doi: 10.1373/clinchem.2004.045203. Epub 2005 May 12. Clin Chem. 2005. PMID: 15890894

5

Screening of APOB gene mutations in subjects with clinical diagnosis of familial hypercholesterolemia.

Meriño-Ibarra E, Castillo S, Mozas P, Cenarro A, Martorell E, Díaz JL, Suárez-Tembra M, Alonso R, Civeira F, Mata P, Pocoví M; Spanish Group of Familial Hypercholesterolemia. Meriño-Ibarra E, et al. Among authors: mozas p. Hum Biol. 2005 Oct;77(5):663-73. Hum Biol. 2005. PMID: 16596945

6

Mutation analysis in 36 unrelated Spanish subjects with familial hypercholesterolemia: identification of 3 novel mutations in the LDL receptor gene.

Mozas P, Cenarro A, Civeira F, Castillo S, Ros E, Pocovi M. Mozas P, et al. Hum Mutat. 2000 May;15(5):483-4. doi: 10.1002/(SICI)1098-1004(200005)15:5<483::AID-HUMU19>3.0.CO;2-Q. Hum Mutat. 2000. PMID: 10790219

7

A double mutant [N543H+2393del9] allele in the LDL receptor gene in familial hypercholesterolemia: effect on plasma cholesterol levels and cardiovascular disease.

Castillo S, Reyes G, Tejedor D, Mozas P, Suarez Y, Lasuncion MA, Cenarro A, Civeira F, Alonso R, Mata P, Pocovi M; Spanish Group of FH. Castillo S, et al. Among authors: mozas p. Hum Mutat. 2002 Dec;20(6):477. doi: 10.1002/humu.9087. Hum Mutat. 2002. PMID: 12442279

8

Apolipoprotein E genotype is not associated with cardiovascular disease in heterozygous subjects with familial hypercholesterolemia.

Mozas P, Castillo S, Reyes G, Tejedor D, Civeira F, García-Alvarez I, Puzo J, Cenarro A, Alonso R, Mata P, Pocoví M; Spanish group FH. Mozas P, et al. Am Heart J. 2003 Jun;145(6):999-1005. doi: 10.1016/S0002-8703(02)94788-5. Am Heart J. 2003. PMID: 12796755

9

[Differences in clinical presentation between subjects with a phenotype of familial hypercholesterolemia determined by defects in the LDL-receptor and defects in Apo B-100].

García-Alvarez I, Castillo S, Mozas P, Tejedor D, Reyes G, Artieda M, Cenarro A, Alonso R, Mata P, Pocovi M, Civeira F; Grupo de Estudio de la Hipercolesterolemia Familiar. García-Alvarez I, et al. Among authors: mozas p. Rev Esp Cardiol. 2003 Aug;56(8):769-74. doi: 10.1016/s0300-8932(03)76955-3. Rev Esp Cardiol. 2003. PMID: 12892621 Free article. Spanish.

10

A common variant in the ABCA1 gene is associated with a lower risk for premature coronary heart disease in familial hypercholesterolaemia.

Cenarro A, Artieda M, Castillo S, Mozas P, Reyes G, Tejedor D, Alonso R, Mata P, Pocoví M, Civeira F; Spanish FH group. Cenarro A, et al. Among authors: mozas p. J Med Genet. 2003 Mar;40(3):163-8. doi: 10.1136/jmg.40.3.163. J Med Genet. 2003. PMID: 12624133 Free PMC article.

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