Castillo S - Search Results

1

Cardiovascular disease in familial hypercholesterolaemia: influence of low-density lipoprotein receptor mutation type and classic risk factors.

Alonso R, Mata N, Castillo S, Fuentes F, Saenz P, Muñiz O, Galiana J, Figueras R, Diaz JL, Gomez-Enterría P, Mauri M, Piedecausa M, Irigoyen L, Aguado R, Mata P; Spanish Familial Hypercholesterolaemia Group. Alonso R, et al. Among authors: castillo s. Atherosclerosis. 2008 Oct;200(2):315-21. doi: 10.1016/j.atherosclerosis.2007.12.024. Epub 2008 Feb 20. Atherosclerosis. 2008. PMID: 18243212

2

MEDPED and the Spanish Familial Hypercholesterolemia Foundation.

Mata P, Alonso R, Castillo S, Pocovi M; Spanish Group of Familial Hypercholesterolemia. Mata P, et al. Among authors: castillo s. Atheroscler Suppl. 2002 Mar;2(3):9-11. doi: 10.1016/s1567-5688(01)00014-9. Atheroscler Suppl. 2002. PMID: 11923123

3

[Heterozygous familial hypercholesterolemia in Spain. Description of 819 non related cases].

Alonso R, Castillo S, Civeira F, Puzo J, de la Cruz JJ, Pocoví M, Mata P. Alonso R, et al. Among authors: castillo s. Med Clin (Barc). 2002 Apr 13;118(13):487-92. doi: 10.1016/s0025-7753(02)72428-7. Med Clin (Barc). 2002. PMID: 11975885 Spanish.

4

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. Atherosclerosis. 2002 Nov;165(1):127-35. doi: 10.1016/s0021-9150(02)00190-9. Atherosclerosis. 2002. PMID: 12208478

5

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. Among authors: castillo s. Hum Mutat. 2004 Aug;24(2):187. doi: 10.1002/humu.9264. Hum Mutat. 2004. PMID: 15241806

6

Tendon xanthomas in familial hypercholesterolemia are associated with cardiovascular risk independently of the low-density lipoprotein receptor gene mutation.

Civeira F, Castillo S, Alonso R, Meriño-Ibarra E, Cenarro A, Artied M, Martín-Fuentes P, Ros E, Pocoví M, Mata P; Spanish Familial Hypercholesterolemia Group. Civeira F, et al. Among authors: castillo s. Arterioscler Thromb Vasc Biol. 2005 Sep;25(9):1960-5. doi: 10.1161/01.ATV.0000177811.14176.2b. Epub 2005 Jul 14. Arterioscler Thromb Vasc Biol. 2005. PMID: 16020744

7

Genetic diagnosis of familial hypercholesterolemia using a DNA-array based platform.

Alonso R, Defesche JC, Tejedor D, Castillo S, Stef M, Mata N, Gomez-Enterria P, Martinez-Faedo C, Forga L, Mata P. Alonso R, et al. Among authors: castillo s. Clin Biochem. 2009 Jun;42(9):899-903. doi: 10.1016/j.clinbiochem.2009.01.017. Epub 2009 Feb 6. Clin Biochem. 2009. PMID: 19318025

8

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: castillo s. 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.

9

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. Among authors: castillo s. Am Heart J. 2003 Jun;145(6):999-1005. doi: 10.1016/S0002-8703(02)94788-5. Am Heart J. 2003. PMID: 12796755

10

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: castillo s. Clin Chem. 2005 Jul;51(7):1137-44. doi: 10.1373/clinchem.2004.045203. Epub 2005 May 12. Clin Chem. 2005. PMID: 15890894

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