Civeira F - Search Results

1

A third major locus for autosomal dominant hypercholesterolemia maps to 1p34.1-p32.

Varret M, Rabès JP, Saint-Jore B, Cenarro A, Marinoni JC, Civeira F, Devillers M, Krempf M, Coulon M, Thiart R, Kotze MJ, Schmidt H, Buzzi JC, Kostner GM, Bertolini S, Pocovi M, Rosa A, Farnier M, Martinez M, Junien C, Boileau C. Varret M, et al. Among authors: civeira f. Am J Hum Genet. 1999 May;64(5):1378-87. doi: 10.1086/302370. Am J Hum Genet. 1999. PMID: 10205269 Free PMC article.

2

[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.

3

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

4

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.

5

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.

6

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

7

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

8

Beta-glucocerebrosidase gene locus as a link for Gaucher's disease and familial hypo-alpha-lipoproteinaemia.

Pocovi M, Cenarro A, Civeira F, Torralba MA, Perez-Calvo JI, Mozas P, Giraldo P, Giralt M, Myers RH, Cupples LA, Ordovas JM. Pocovi M, et al. Among authors: civeira f. Lancet. 1998 Jun 27;351(9120):1919-23. doi: 10.1016/S0140-6736(97)09490-7. Lancet. 1998. PMID: 9654259 Free article.

9

Identification of recurrent and novel mutations in the LDL receptor gene in Spanish patients with familial hypercholesterolemia. Mutations in brief no. 135. Online.

Cenarro A, Jensen HK, Casao E, Civeira F, González-Bonillo J, Rodríguez-Rey JC, Gregersen N, Pocoví M. Cenarro A, et al. Among authors: civeira f. Hum Mutat. 1998;11(5):413. doi: 10.1002/(SICI)1098-1004(1998)11:5<413::AID-HUMU16>3.0.CO;2-I. Hum Mutat. 1998. PMID: 10206683

10

P1A1/A2 polymorphism of platelet glycoprotein IIIa and risk of acute coronary syndromes in heterozygous familial hypercholesterolemia.

Cenarro A, Casao E, Civeira F, Jensen HK, Faergeman O, Pocoví M. Cenarro A, et al. Among authors: civeira f. Atherosclerosis. 1999 Mar;143(1):99-104. doi: 10.1016/s0021-9150(98)00283-4. Atherosclerosis. 1999. PMID: 10208484

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