| Title : Autoantibodies against GPIHBP1 as a Cause of Hypertriglyceridemia - Beigneux_2017_N.Engl.J.Med_376_1647 |
| Author(s) : Beigneux AP , Miyashita K , Ploug M , Blom DJ , Ai M , Linton MF , Khovidhunkit W , Dufour R , Garg A , McMahon MA , Pullinger CR , Sandoval NP , Hu X , Allan CM , Larsson M , Machida T , Murakami M , Reue K , Tontonoz P , Goldberg IJ , Moulin P , Charriere S , Fong LG , Nakajima K , Young SG |
| Ref : N Engl J Med , 376 :1647 , 2017 |
| Abstract : |
| PubMedSearch : Beigneux_2017_N.Engl.J.Med_376_1647 |
| PubMedID: 28402248 |
| Title : Autoantibodies against GPIHBP1 as a Cause of Hypertriglyceridemia - Beigneux_2017_N.Engl.J.Med_376_1647 |
| Author(s) : Beigneux AP , Miyashita K , Ploug M , Blom DJ , Ai M , Linton MF , Khovidhunkit W , Dufour R , Garg A , McMahon MA , Pullinger CR , Sandoval NP , Hu X , Allan CM , Larsson M , Machida T , Murakami M , Reue K , Tontonoz P , Goldberg IJ , Moulin P , Charriere S , Fong LG , Nakajima K , Young SG |
| Ref : N Engl J Med , 376 :1647 , 2017 |
| Abstract : |
| PubMedSearch : Beigneux_2017_N.Engl.J.Med_376_1647 |
| PubMedID: 28402248 |
| Title : Autoantibodies against GPIHBP1 as a Cause of Hypertriglyceridemia - Beigneux_2017_N.Engl.J.Med_376_1647 |
| Author(s) : Beigneux AP , Miyashita K , Ploug M , Blom DJ , Ai M , Linton MF , Khovidhunkit W , Dufour R , Garg A , McMahon MA , Pullinger CR , Sandoval NP , Hu X , Allan CM , Larsson M , Machida T , Murakami M , Reue K , Tontonoz P , Goldberg IJ , Moulin P , Charriere S , Fong LG , Nakajima K , Young SG |
| Ref : N Engl J Med , 376 :1647 , 2017 |
| Abstract : |
| PubMedSearch : Beigneux_2017_N.Engl.J.Med_376_1647 |
| PubMedID: 28402248 |
| Title : Characterization of a new LCAT mutation causing familial LCAT deficiency (FLD) and the role of APOE as a modifier gene of the FLD phenotype - Baass_2009_Atherosclerosis_207_452 |
| Author(s) : Baass A , Wassef H , Tremblay M , Bernier L , Dufour R , Davignon J |
| Ref : Atherosclerosis , 207 :452 , 2009 |
| Abstract : |
| PubMedSearch : Baass_2009_Atherosclerosis_207_452 |
| PubMedID: 19515369 |
| Title : Characterization of a new LCAT mutation causing familial LCAT deficiency (FLD) and the role of APOE as a modifier gene of the FLD phenotype - Baass_2009_Atherosclerosis_207_452 |
| Author(s) : Baass A , Wassef H , Tremblay M , Bernier L , Dufour R , Davignon J |
| Ref : Atherosclerosis , 207 :452 , 2009 |
| Abstract : |
| PubMedSearch : Baass_2009_Atherosclerosis_207_452 |
| PubMedID: 19515369 |
| Title : Characterization of a new LCAT mutation causing familial LCAT deficiency (FLD) and the role of APOE as a modifier gene of the FLD phenotype - Baass_2009_Atherosclerosis_207_452 |
| Author(s) : Baass A , Wassef H , Tremblay M , Bernier L , Dufour R , Davignon J |
| Ref : Atherosclerosis , 207 :452 , 2009 |
| Abstract : |
| PubMedSearch : Baass_2009_Atherosclerosis_207_452 |
| PubMedID: 19515369 |
| Title : Severe oily ichthyosis in monozygotic twins mimicking Chanarin-Dorfman syndrome but not associated with a mutation of the CGI58 gene - |
| Author(s) : Solomon C , Bernier L , Germain L , Dufour R , Davignon J |
| Ref : Arch Dermatol , 142 :402 , 2006 |
| PubMedID: 16549731 |
| Gene_locus related to this paper: human-ABHD5 |
| Title : Severe oily ichthyosis in monozygotic twins mimicking Chanarin-Dorfman syndrome but not associated with a mutation of the CGI58 gene - |
| Author(s) : Solomon C , Bernier L , Germain L , Dufour R , Davignon J |
| Ref : Arch Dermatol , 142 :402 , 2006 |
| PubMedID: 16549731 |
| Gene_locus related to this paper: human-ABHD5 |
| Title : Severe oily ichthyosis in monozygotic twins mimicking Chanarin-Dorfman syndrome but not associated with a mutation of the CGI58 gene - |
| Author(s) : Solomon C , Bernier L , Germain L , Dufour R , Davignon J |
| Ref : Arch Dermatol , 142 :402 , 2006 |
| PubMedID: 16549731 |
| Gene_locus related to this paper: human-ABHD5 |