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| Title : Familial hypertriglyceridemia: biochemical, clinical and molecular study in a Moroccan family - Bouabdellah_2015_Ann.Biol.Clin.(Paris)_73_474 |
| Author(s) : Bouabdellah M , Iraqi H , Benlian P , Berqia I , Benchekroun L , Chraibi A , Chabraoui L |
| Ref : Ann Biol Clin (Paris) , 73 :474 , 2015 |
| Abstract : Bouabdellah_2015_Ann.Biol.Clin.(Paris)_73_474 |
| ESTHER : Bouabdellah_2015_Ann.Biol.Clin.(Paris)_73_474 |
| PubMedSearch : Bouabdellah_2015_Ann.Biol.Clin.(Paris)_73_474 |
| PubMedID: 26104879 |
| Title : Combined hyperlipidemia\/hyperalphalipoproteinemia associated with premature spontaneous atherosclerosis in mice lacking hepatic lipase and low density lipoprotein receptor - Barcat_2006_Atherosclerosis_188_347 |
| Author(s) : Barcat D , Amadio A , Palos-Pinto A , Daret D , Benlian P , Darmon M , Berard AM |
| Ref : Atherosclerosis , 188 :347 , 2006 |
| Abstract : Barcat_2006_Atherosclerosis_188_347 |
| ESTHER : Barcat_2006_Atherosclerosis_188_347 |
| PubMedSearch : Barcat_2006_Atherosclerosis_188_347 |
| PubMedID: 16384559 |
| Title : Classical LCAT deficiency resulting from a novel homozygous dinucleotide deletion in exon 4 of the human lecithin: cholesterol acyltransferase gene causing a frameshift and stop codon at residue 144 - Teh_1999_Atherosclerosis_146_141 |
| Author(s) : Teh EM , Chisholm JW , Dolphin PJ , Pouliquen Y , Savoldelli M , De Gennes JL , Benlian P |
| Ref : Atherosclerosis , 146 :141 , 1999 |
| Abstract : Teh_1999_Atherosclerosis_146_141 |
| ESTHER : Teh_1999_Atherosclerosis_146_141 |
| PubMedSearch : Teh_1999_Atherosclerosis_146_141 |
| PubMedID: 10487497 |
| Title : Compound heterozygosity for frameshift mutations in the gene for lipoprotein lipase in a patient with early-onset chylomicronemia - |
| Author(s) : Foubert L , De Gennes JL , Benlian P , Truffert J , Miao L , Hayden MR |
| Ref : Hum Mutat , Suppl 1 :S141 , 1998 |
| PubMedID: 9452069 |
| Title : A single Ser259Arg mutation in the gene for lipoprotein lipase causes chylomicronemia in Moroccans of Berber ancestry - Foubert_1997_Hum.Mutat_10_179 |
| Author(s) : Foubert L , Bruin T , De Gennes JL , Ehrenborg E , Furioli J , Kastelein J , Benlian P , Hayden M |
| Ref : Hum Mutat , 10 :179 , 1997 |
| Abstract : Foubert_1997_Hum.Mutat_10_179 |
| ESTHER : Foubert_1997_Hum.Mutat_10_179 |
| PubMedSearch : Foubert_1997_Hum.Mutat_10_179 |
| PubMedID: 9298816 |
| Gene_locus related to this paper: human-LPL |
| Title : Assessment of French patients with LPL deficiency for French Canadian mutations - Foubert_1997_J.Med.Genet_34_672 |
| Author(s) : Foubert L , De Gennes JL , Lagarde JP , Ehrenborg E , Raisonnier A , Girardet JP , Hayden MR , Benlian P |
| Ref : Journal of Medical Genetics , 34 :672 , 1997 |
| Abstract : Foubert_1997_J.Med.Genet_34_672 |
| ESTHER : Foubert_1997_J.Med.Genet_34_672 |
| PubMedSearch : Foubert_1997_J.Med.Genet_34_672 |
| PubMedID: 9279761 |
| Title : Premature atherosclerosis in patients with familial chylomicronemia caused by mutations in the lipoprotein lipase gene - Benlian_1996_N.Engl.J.Med_335_848 |
| Author(s) : Benlian P , De Gennes JL , Foubert L , Zhang H , Gagne SE , Hayden M |
| Ref : N Engl J Med , 335 :848 , 1996 |
| Abstract : Benlian_1996_N.Engl.J.Med_335_848 |
| ESTHER : Benlian_1996_N.Engl.J.Med_335_848 |
| PubMedSearch : Benlian_1996_N.Engl.J.Med_335_848 |
| PubMedID: 8778602 |
| Gene_locus related to this paper: human-LPL |
| Title : Complete paternal isodisomy for chromosome 8 unmasked by lipoprotein lipase deficiency - Benlian_1996_Am.J.Hum.Genet_59_431 |
| Author(s) : Benlian P , Foubert L , Gagne E , Bernard L , De Gennes JL , Langlois S , Robinson W , Hayden M |
| Ref : American Journal of Human Genetics , 59 :431 , 1996 |
| Abstract : Benlian_1996_Am.J.Hum.Genet_59_431 |
| ESTHER : Benlian_1996_Am.J.Hum.Genet_59_431 |
| PubMedSearch : Benlian_1996_Am.J.Hum.Genet_59_431 |
| PubMedID: 8755931 |
| Gene_locus related to this paper: human-LPL |
| Title : Homozygous deletion of exon 9 causes lipoprotein lipase deficiency: possible intron-Alu recombination - Benlian_1995_J.Lipid.Res_36_356 |
| Author(s) : Benlian P , Etienne J , De Gennes JL , Noe L , Brault D , Raisonnier A , Arnault F , Hamelin J , Foubert L , Chuat JC , et al. |
| Ref : J Lipid Res , 36 :356 , 1995 |
| Abstract : Benlian_1995_J.Lipid.Res_36_356 |
| ESTHER : Benlian_1995_J.Lipid.Res_36_356 |
| PubMedSearch : Benlian_1995_J.Lipid.Res_36_356 |
| PubMedID: 7751824 |
| Title : Recurrent missense mutations at the first and second base of codon Arg243 in human lipoprotein lipase in patients of different ancestries - Ma_1994_Hum.Mutat_3_52 |
| Author(s) : Ma Y , Liu MS , Chitayat D , Bruin T , Beisiegel U , Benlian P , Foubert L , De Gennes JL , Funke H , Forsythe I , Blaichman S , Papanikolaou M , Erkelens DW , Kastelein J , Brunzell JD , Hayden MR |
| Ref : Hum Mutat , 3 :52 , 1994 |
| Abstract : Ma_1994_Hum.Mutat_3_52 |
| ESTHER : Ma_1994_Hum.Mutat_3_52 |
| PubMedSearch : Ma_1994_Hum.Mutat_3_52 |
| PubMedID: 7906986 |