Mafalda Vieira da Rocha Peixoto e Bourbon de Sampaio Pimentel


AuthID: R-000-KH5

Publicações a aguardar confirmação

51
TÍTULO: MOLECULAR ASPECTS OF HOMOZYGOUS FAMILIAL HYPERCHOLESTEROLEMIA IN IBERO-AMERICAN COUNTRIES  Full Text
AUTORES: Alves, AC; Alonso, R; Cuevas, A; Medeiros Margarida, AM; Pereira, CA; Jannes, EC; Krieger, EJ; Arroyo, R; Schreier, L; Corral, P; Banares, GV; Araujo, M; Asenjo, S; Stoll, M; Dell'Oca, N; Reyes, X; Ressia, A; Campo, R; Merchan, A; Magana Torres T Teresa; Vasques Cardenas, NA; Mata, P; Santos, R; Bourbon, M; ...Mais
PUBLICAÇÃO: 2019, FONTE: 87th Congress of the European-Atherosclerosis-Society (EAS) in ATHEROSCLEROSIS, VOLUME: 287
INDEXADO EM: WOS
52
TÍTULO: FH PHENOTYPE: MONOGENIC, POLYGENIC OR OTHER CAUSES?  Full Text
AUTORES: Mariano, C; Alves, AC; Medeiros, AM; Chora, JR; Futema, M; Humphries, SE; Bourbon, M;
PUBLICAÇÃO: 2019, FONTE: 87th Congress of the European-Atherosclerosis-Society (EAS) in ATHEROSCLEROSIS, VOLUME: 287
INDEXADO EM: WOS
53
TÍTULO: HIGH LIPOPROTEIN(A) CHOLESTEROL IN PATIENTS WITH FAMILIAL HYPERCHOLESTEROLEMIA  Full Text
AUTORES: Medeiros, AM; Alves, AC; Bourbon, M;
PUBLICAÇÃO: 2019, FONTE: 87th Congress of the European-Atherosclerosis-Society (EAS) in ATHEROSCLEROSIS, VOLUME: 287
INDEXADO EM: WOS
54
TÍTULO: FUNCTIONAL GENOMICS IN A COHORT OF FH MUTATION NEGATIVE PATIENTS  Full Text
AUTORES: Rossi, N; Graca, R; Medeiros, AM; Abrantes, L; Alves, AC; Zimon, M; Rausch, T; Benes, V; Pepperkok, R; Bourbon, M;
PUBLICAÇÃO: 2019, FONTE: 87th Congress of the European-Atherosclerosis-Society (EAS) in ATHEROSCLEROSIS, VOLUME: 287
INDEXADO EM: WOS
55
TÍTULO: Functional Analysis of LDLR (Low-Density Lipoprotein Receptor) Variants in Patient Lymphocytes to Assess the Effect of Evinacumab in Homozygous Familial Hypercholesterolemia Patients With a Spectrum of LDLR Activity
AUTORES: Banerjee, P; Chan, KC; Tarabocchia, M; Benito Vicente, A; Alves, AC; Uribe, KB; Bourbon, M; Skiba, PJ; Pordy, R; Gipe, DA; Gaudet, D; Martin, C;
PUBLICAÇÃO: 2019, FONTE: ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, VOLUME: 39, NÚMERO: 11
INDEXADO EM: Scopus WOS CrossRef: 61
NO MEU: ORCID
56
TÍTULO: Clinical Genetic Testing for Familial Hypercholesterolemia: JACC Scientific Expert Panel
AUTORES: Sturm, AC; Knowles, JW; Gidding, SS; Ahmad, ZS; Ahmed, CD; Ballantyne, CM; Baum, SJ; Bourbon, M; Carrié, A; Cuchel, M; de Ferranti, SD; Defesche, JC; Freiberger, T; Hershberger, RE; Hovingh, GK; Karayan, L; Kastelein, JJP; Kindt, I; Lane, SR; Leigh, SE; Linton, MF; Mata, P; Neal, WA; Nordestgaard, BG; Santos, RD; Harada Shiba, M; Sijbrands, EJ; Stitziel, NO; Yamashita, S; Wilemon, KA; Ledbetter, DH; Rader, DJ; ...Mais
PUBLICAÇÃO: 2018, FONTE: Journal of the American College of Cardiology, VOLUME: 72, NÚMERO: 6
INDEXADO EM: Scopus
NO MEU: ORCID
57
TÍTULO: Clinical Genetic Testing for Familial Hypercholesterolemia
AUTORES: Sturm, AC; Knowles, JW; Gidding, SS; Ahmad, ZS; Ahmed, CD; Ballantyne, CM; Baum, SJ; Bourbon, M; Carrie, A; Cuchel, M; de Ferranti, SD; Defesche, JC; Freiberger, T; Hershberger, RE; Hovingh, GK; Karayan, L; Kastelein, JJP; Kindt, I; Lane, SR; Leigh, SE; Linton, MF; Mata, P; Neal, WA; Nordestgaard, BG; Santos, RD; Harada Shiba, M; Sijbrands, EJ; Stitziel, NO; Yamashita, S; Wilemon, KA; Ledbetter, DH; Rader, DJ; ...Mais
PUBLICAÇÃO: 2018, FONTE: JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, VOLUME: 72, NÚMERO: 6
INDEXADO EM: WOS CrossRef: 402
NO MEU: ORCID
58
TÍTULO: Further evidence of novel APOB mutations as a cause of familial hypercholesterolaemia
AUTORES: Alves, AC; Benito Vicente, A; Medeiros, AM; Reeves, K; Martin, C; Bourbon, M;
PUBLICAÇÃO: 2018, FONTE: ATHEROSCLEROSIS, VOLUME: 277
INDEXADO EM: Scopus WOS CrossRef: 22 Handle
NO MEU: ORCID
59
TÍTULO: Overview of the current status of familial hypercholesterolaemia care in over 60 countries - The EAS Familial Hypercholesterolaemia Studies Collaboration (FHSC)
AUTORES: Vallejo Vaz, AJ; De Marco, M; Stevens, CAT; Akram, A; Freiberger, T; Hovingh, GK; Kastelein, JJP; Mata, P; Raal, FJ; Santos, RD; Soran, H; Watts, GF; Abifadel, M; Aguilar Salinas, CA; Al Khnifsawi, M; AlKindi, FA; Alnouri, F; Alonso, R; Al Rasadi, K; Al Sarraf, A; Ashavaid, TF; Binder, CJ; Bogsrud, MP; Bourbon, M; Bruckert, E; Chlebus, K; Corral, P; Descamps, O; Durst, R; Ezhov, M; Fras, Z; Genest, J; Groselj, U; Harada Shiba, M; Kayikcioglu, M; Lalic, K; Lam, CSP; Latkovskis, G; Laufs, U; Liberopoulos, E; Lin, J; Maher, V; Majano, N; Marais, AD; Marz, W; Mirrakhimov, E; Miserez, AR; Mitchenko, O; Nawawi, HM; Nordestgaard, BG; Paragh, G; Petrulioniene, Z; Pojskic, B; Postadzhiyan, A; Reda, A; Reiner, Z; Sadoh, WE; Sahebkar, A; Shehab, A; Shek, AB; Stoll, M; Su, TC; Subramaniam, T; Susekov, AV; Symeonides, P; Tilney, M; Tomlinson, B; Truong, TH; Tselepis, AD; Tybjaerg Hansenb, A; Vazquez Cardenas, A; Viigimaa, M; Vohnout, B; Widen, E; Yamashita, S; Banach, M; Gaita, D; Jiang, LX; Nilsson, L; Santos, LE; Schunkert, H; Tokgozoglu, L; Car, J; Catapano, AL; Ray, KK; ...Mais
PUBLICAÇÃO: 2018, FONTE: ATHEROSCLEROSIS, VOLUME: 277
INDEXADO EM: Scopus WOS CrossRef: 153 Handle
NO MEU: ORCID
60
TÍTULO: Clinical utility of the polygenic LDL-C SNP score in familial hypercholesterolemia
AUTORES: Futema, M; Bourbon, M; Williams, M; Humphries, SE;
PUBLICAÇÃO: 2018, FONTE: ATHEROSCLEROSIS, VOLUME: 277
INDEXADO EM: Scopus WOS CrossRef: 40 Handle
NO MEU: ORCID
Página 6 de 12. Total de resultados: 118.

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