Mata P - Search Results

1

Autosomal Recessive Hypercholesterolemia: Long-Term Cardiovascular Outcomes.

D'Erasmo L, Minicocci I, Nicolucci A, Pintus P, Roeters Van Lennep JE, Masana L, Mata P, Sánchez-Hernández RM, Prieto-Matos P, Real JT, Ascaso JF, Lafuente EE, Pocovi M, Fuentes FJ, Muntoni S, Bertolini S, Sirtori C, Calabresi L, Pavanello C, Averna M, Cefalu AB, Noto D, Pacifico AA, Pes GM, Harada-Shiba M, Manzato E, Zambon S, Zambon A, Vogt A, Scardapane M, Sjouke B, Fellin R, Arca M. D'Erasmo L, et al. Among authors: mata p. J Am Coll Cardiol. 2018 Jan 23;71(3):279-288. doi: 10.1016/j.jacc.2017.11.028. J Am Coll Cardiol. 2018. PMID: 29348020 Free article.

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

5

Efficacy and safety of ezetimibe added to ongoing statin therapy for treatment of patients with primary hypercholesterolemia.

Gagné C, Bays HE, Weiss SR, Mata P, Quinto K, Melino M, Cho M, Musliner TA, Gumbiner B; Ezetimibe Study Group. Gagné C, et al. Among authors: mata p. Am J Cardiol. 2002 Nov 15;90(10):1084-91. doi: 10.1016/s0002-9149(02)02774-1. Am J Cardiol. 2002. PMID: 12423708 Clinical Trial.

6

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: mata p. Hum Mutat. 2002 Dec;20(6):477. doi: 10.1002/humu.9087. Hum Mutat. 2002. PMID: 12442279

7

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

8

[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: mata 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.

9

Familial hypercholesterolemia in Spain: case-finding program, clinical and genetic aspects.

Pocovi M, Civeira F, Alonso R, Mata P. Pocovi M, et al. Among authors: mata p. Semin Vasc Med. 2004 Feb;4(1):67-74. doi: 10.1055/s-2004-822988. Semin Vasc Med. 2004. PMID: 15199435 Review.

10

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: mata p. Hum Mutat. 2004 Aug;24(2):187. doi: 10.1002/humu.9264. Hum Mutat. 2004. PMID: 15241806

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