Mafalda Vieira da Rocha Peixoto e Bourbon de Sampaio Pimentel
AuthID: R-000-KH5
111
TITLE: PCSK9 gene analysis in Portuguese patients with familial hypercholesterolemia Full Text
AUTHORS: Alves, AC; Rato, Q; Furtado, A; Bourbon, M;
PUBLISHED: 2007, SOURCE: 76th Congress of the European-Atherosclerosis-Society in ATHEROSCLEROSIS SUPPLEMENTS, VOLUME: 8, ISSUE: 1
AUTHORS: Alves, AC; Rato, Q; Furtado, A; Bourbon, M;
PUBLISHED: 2007, SOURCE: 76th Congress of the European-Atherosclerosis-Society in ATHEROSCLEROSIS SUPPLEMENTS, VOLUME: 8, ISSUE: 1
INDEXED IN: 
WOS 
CrossRef
WOS CrossRef112
TITLE: A rare polymorphism in the low density lipoprotein (LDL) gene that affects mRNA splicing Full Text
AUTHORS: Bourbon, M; Sun, XM; Soutar, AK;
PUBLISHED: 2007, SOURCE: Atherosclerosis, VOLUME: 195, ISSUE: 1
AUTHORS: Bourbon, M; Sun, XM; Soutar, AK;
PUBLISHED: 2007, SOURCE: Atherosclerosis, VOLUME: 195, ISSUE: 1
113
TITLE: Molecular study of familial hypercholesterolemia in Portugal Full Text
AUTHORS: Bourbon, M; Alves, AC; Medeiros, AM; Silva, S; Soutar, AK;
PUBLISHED: 2006, SOURCE: 14th Meeting of the International-Society-of-Atherosclerosis in ATHEROSCLEROSIS SUPPLEMENTS, VOLUME: 7, ISSUE: 3
AUTHORS: Bourbon, M; Alves, AC; Medeiros, AM; Silva, S; Soutar, AK;
PUBLISHED: 2006, SOURCE: 14th Meeting of the International-Society-of-Atherosclerosis in ATHEROSCLEROSIS SUPPLEMENTS, VOLUME: 7, ISSUE: 3
INDEXED IN: WOS CrossRef
WOS CrossRef114
TITLE: Mutation detection in LDLR gene by DHPLC and sequencing Full Text
AUTHORS: Alves, AC; Soutar, AK; Bourbon, M;
PUBLISHED: 2006, SOURCE: 14th Meeting of the International-Society-of-Atherosclerosis in ATHEROSCLEROSIS SUPPLEMENTS, VOLUME: 7, ISSUE: 3
AUTHORS: Alves, AC; Soutar, AK; Bourbon, M;
PUBLISHED: 2006, SOURCE: 14th Meeting of the International-Society-of-Atherosclerosis in ATHEROSCLEROSIS SUPPLEMENTS, VOLUME: 7, ISSUE: 3
INDEXED IN: WOS CrossRef
WOS CrossRef115
TITLE: Clinical characteristics of Portuguese patients with a clinical diagnosis of familial hypercholesterolaemia Full Text
AUTHORS: Bourbon, M; Alves, AC; Silva, JM; Rato, Q; Silva, PM; Azevedo, I; Furtado, A; Naoumova, RP;
PUBLISHED: 2006, SOURCE: 14th Meeting of the International-Society-of-Atherosclerosis in ATHEROSCLEROSIS SUPPLEMENTS, VOLUME: 7, ISSUE: 3
AUTHORS: Bourbon, M; Alves, AC; Silva, JM; Rato, Q; Silva, PM; Azevedo, I; Furtado, A; Naoumova, RP;
PUBLISHED: 2006, SOURCE: 14th Meeting of the International-Society-of-Atherosclerosis in ATHEROSCLEROSIS SUPPLEMENTS, VOLUME: 7, ISSUE: 3
INDEXED IN: WOS CrossRef
WOS CrossRef116
TITLE: Determinants of variable response to statin treatment in patients with refractory familial hypercholesterolemia
AUTHORS: O'Neill, FH; Patel, DD; Knight, BL; Neuwirth, CKY; Bourbon, M; Soutar, AK; Taylor, GW; Thompson, GR; Naoumova, RP;
PUBLISHED: 2001, SOURCE: Arteriosclerosis, Thrombosis, and Vascular Biology, VOLUME: 21, ISSUE: 5
AUTHORS: O'Neill, FH; Patel, DD; Knight, BL; Neuwirth, CKY; Bourbon, M; Soutar, AK; Taylor, GW; Thompson, GR; Naoumova, RP;
PUBLISHED: 2001, SOURCE: Arteriosclerosis, Thrombosis, and Vascular Biology, VOLUME: 21, ISSUE: 5
INDEXED IN: 
Scopus
Scopus IN MY: 
ORCID
ORCID117
TITLE: Characterization of a novel cellular defect in patients with phenotypic homozygous familial hypercholesterolemia
AUTHORS: Norman, D; Sun, XM; Bourbon, M; Knight, BL; Naoumova, RP; Soutar, AK;
PUBLISHED: 1999, SOURCE: Journal of Clinical Investigation, VOLUME: 104, ISSUE: 5
AUTHORS: Norman, D; Sun, XM; Bourbon, M; Knight, BL; Naoumova, RP; Soutar, AK;
PUBLISHED: 1999, SOURCE: Journal of Clinical Investigation, VOLUME: 104, ISSUE: 5
INDEXED IN: Scopus
Scopus IN MY: ORCID
ORCID118
TITLE: Inheritance of two different alleles of the low-density lipoprotein (LDL)-receptor gene carrying the recurrent Pro664Leu mutation in a patient with homozygous familial hypercholesterolaemia Full Text
AUTHORS: Bourbon, M; Fowler, AM; Sun, XM; Soutar, AK;
PUBLISHED: 1999, SOURCE: Clinical Genetics, VOLUME: 56, ISSUE: 3
AUTHORS: Bourbon, M; Fowler, AM; Sun, XM; Soutar, AK;
PUBLISHED: 1999, SOURCE: Clinical Genetics, VOLUME: 56, ISSUE: 3
