Ribalta J - Search Results

1

Familial hypercholesterolemia in Morocco: first report of mutations in the LDL receptor gene.

El Messal M, Aït Chihab K, Chater R, Vallvé JC, Bennis F, Hafidi A, Ribalta J, Varret M, Loutfi M, Rabès JP, Kettani A, Boileau C, Masana L, Adlouni A. El Messal M, et al. Among authors: ribalta j. J Hum Genet. 2003;48(4):199-203. doi: 10.1007/s10038-003-0010-x. Epub 2003 Mar 18. J Hum Genet. 2003. PMID: 12730724

2

Familial hypercholesterolemia associated with severe hypoalphalipoproteinemia in a Moroccan family.

Ait Chihab K, Chater R, Cenarro A, Kettani A, Castillo S, Loutfi M, Ribalta J, Adlouni A, Pocovi M, El Messal M. Ait Chihab K, et al. Among authors: ribalta j. J Genet. 2007 Aug;86(2):159-63. doi: 10.1007/s12041-007-0020-0. J Genet. 2007. PMID: 17968143 No abstract available.

3

Exon 4, and in particular codon 152 of the LDL receptor gene, is a hot spot for point mutations.

Vallvé JC, Alonso-Villaverde C, Ribalta J, Pérez-Jiménez F, Masana L. Vallvé JC, et al. Among authors: ribalta j. Atherosclerosis. 1998 Sep;140(1):191-2. doi: 10.1016/s0021-9150(98)00140-3. Atherosclerosis. 1998. PMID: 9733232 No abstract available.

4

A variation in the apolipoprotein C-III gene is associated with an increased number of circulating VLDL and IDL particles in familial combined hyperlipidemia.

Ribalta J, La Ville AE, Vallvé JC, Humphries S, Turner PR, Masana L. Ribalta J, et al. J Lipid Res. 1997 Jun;38(6):1061-9. J Lipid Res. 1997. PMID: 9215535 Free article.

5

Low plasma vitamin A concentrations in familial combined hyperlipidemia.

Ribalta J, LaVille AE, Girona J, Vallvé JC, Masana L. Ribalta J, et al. Clin Chem. 1997 Dec;43(12):2379-83. Clin Chem. 1997. PMID: 9439457

6

Evidence against alterations in Lecithin:cholesterol acyltransferase (LCAT) activity in familial combined hyperlipidemia.

Ribalta J, La Ville AE, Vallvé JC, Girona J, Masana L. Ribalta J, et al. Atherosclerosis. 1998 Jun;138(2):383-9. doi: 10.1016/s0021-9150(98)00043-4. Atherosclerosis. 1998. PMID: 9690923

7

Vitamin A is linked to the expression of the AI-CIII-AIV gene cluster in familial combined hyperlipidemia.

Ribalta J, Girona J, Vallvé JC, La Ville AE, Heras M, Masana L. Ribalta J, et al. J Lipid Res. 1999 Mar;40(3):426-31. J Lipid Res. 1999. PMID: 10064730 Free article.

8

[Familial combined hyperlipidemia: detection and characterisation of the hyperlipidemic profile among children and adolescents].

Ribalta J, La Ville AE, Heras M, Plana N, Masana L. Ribalta J, et al. Med Clin (Barc). 1997 Jun 28;109(5):161-4. Med Clin (Barc). 1997. PMID: 9289537 Spanish.

9

2,4-Decadienal downregulates TNF-alpha gene expression in THP-1 human macrophages.

Girona J, Vallvé JC, Ribalta J, Heras M, Olivé S, Masana L. Girona J, et al. Among authors: ribalta j. Atherosclerosis. 2001 Sep;158(1):95-101. doi: 10.1016/s0021-9150(01)00419-1. Atherosclerosis. 2001. PMID: 11500179

10

Polymorphisms in LPL, CETP, and HL protect HIV-infected patients from atherogenic dyslipidemia in an allele-dose-dependent manner.

Guardiola M, Echeverria P, González M, Vallvé JC, Puig J, Clotet B, Ribalta J, Negredo E. Guardiola M, et al. Among authors: ribalta j. AIDS Res Hum Retroviruses. 2015 Sep;31(9):882-8. doi: 10.1089/AID.2015.0061. Epub 2015 Jul 20. AIDS Res Hum Retroviruses. 2015. PMID: 26101956

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