Civeira F - Search Results

1

Autosomal recessive hypercholesterolemia in Spain.

Sánchez-Hernández RM, Prieto-Matos P, Civeira F, Lafuente EE, Vargas MF, Real JT, Goicoechea FG, Fuentes FJ, Pocovi M, Boronat M, Wägner AM, Masana L. Sánchez-Hernández RM, et al. Among authors: civeira f. Atherosclerosis. 2018 Feb;269:1-5. doi: 10.1016/j.atherosclerosis.2017.12.006. Epub 2017 Dec 6. Atherosclerosis. 2018. PMID: 29245109

2

The MspI restriction fragment length polymorphism 3' to the apolipoprotein A-II gene: relationships with lipids, apolipoproteins, and premature coronary artery disease.

Civeira F, Genest J, Pocovi M, Salem DN, Herbert PN, Wilson PW, Schaefer EJ, Ordovas JM. Civeira F, et al. Atherosclerosis. 1992 Feb;92(2-3):165-76. doi: 10.1016/0021-9150(92)90275-l. Atherosclerosis. 1992. PMID: 1352975

3

[Factors associated with hypoalphalipoproteinemia].

Civeira F, Blasco M, Murillo J, Moreda A, Alamillo JA, Pocovi M. Civeira F, et al. Med Clin (Barc). 1992 Oct 17;99(12):450-3. Med Clin (Barc). 1992. PMID: 1460896 Spanish.

4

[Hyperlipoproteinemia type III: genetic basis and environmental factors, diagnosis, and treatment].

Pocoví M, Garcés C, Casao E, Cenarro A, Civeira F. Pocoví M, et al. Among authors: civeira f. Rev Clin Esp. 1992 Nov;191(8):444-50. Rev Clin Esp. 1992. PMID: 1488520 Review. Spanish. No abstract available.

5

Restriction fragment length polymorphisms of the apolipoprotein A-I, C-III, A-IV gene locus. Relationships with lipids, apolipoproteins, and premature coronary artery disease.

Ordovas JM, Civeira F, Genest J Jr, Craig S, Robbins AH, Meade T, Pocovi M, Frossard PM, Masharani U, Wilson PW, et al. Ordovas JM, et al. Among authors: civeira f. Atherosclerosis. 1991 Mar;87(1):75-86. doi: 10.1016/0021-9150(91)90234-t. Atherosclerosis. 1991. PMID: 1678604 Free article.

6

Adenine for guanine substitution -78 base pairs 5' to the apolipoprotein (APO) A-I gene: relation with high density lipoprotein cholesterol and APO A-I concentrations.

Civeira F, Pocovi M, Cenarro A, Garces C, Ordovas JM. Civeira F, et al. Clin Genet. 1993 Dec;44(6):307-12. doi: 10.1111/j.1399-0004.1993.tb03906.x. Clin Genet. 1993. PMID: 8131302

7

Identification of a novel mutation in exon 13 of the LDL receptor gene causing familial hypercholesterolemia in two Spanish families.

Cenarro A, Jensen HK, Casao E, Civeira F, Gonzàlez-Bonillo J, Pocoví M, Gregersen N. Cenarro A, et al. Among authors: civeira f. Biochim Biophys Acta. 1996 May 24;1316(1):1-4. doi: 10.1016/0925-4439(96)00006-3. Biochim Biophys Acta. 1996. PMID: 8634338 Free article.

8

Incomplete dominance of type III hyperlipoproteinemia is associated with the rare apolipoprotein E2 (Arg136-->Ser) variant in multigenerational pedigree studies.

Pocovi M, Cenarro A, Civeira F, Myers RH, Casao E, Esteban M, Ordovas JM. Pocovi M, et al. Among authors: civeira f. Atherosclerosis. 1996 Apr 26;122(1):33-46. doi: 10.1016/0021-9150(95)06745-0. Atherosclerosis. 1996. PMID: 8724110 Free article.

9

Two novel mutations in the LDL receptor gene: common causes of familial hypercholesterolemia in a Spanish population.

Cenarro A, Jensen HK, Civeira F, Casao E, Ferrando J, González-Bonillo J, Pocoví M, Gregersen N. Cenarro A, et al. Among authors: civeira f. Clin Genet. 1996 Apr;49(4):180-5. doi: 10.1111/j.1399-0004.1996.tb03283.x. Clin Genet. 1996. PMID: 8828982

10

Apo E variants in patients with type III hyperlipoproteinemia.

Civeira F, Pocoví M, Cenarro A, Casao E, Vilella E, Joven J, González J, Garcia-Otín AL, Ordovás JM. Civeira F, et al. Atherosclerosis. 1996 Dec 20;127(2):273-82. doi: 10.1016/s0021-9150(96)05969-2. Atherosclerosis. 1996. PMID: 9125318

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