BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

244 related articles for article (PubMed ID: 29356704)

  • 1. Familial hypercholesterolemia: experience from the French-Canadian population.
    Paquette M; Genest J; Baass A
    Curr Opin Lipidol; 2018 Apr; 29(2):59-64. PubMed ID: 29356704
    [TBL] [Abstract][Full Text] [Related]  

  • 2. The molecular genetic basis and diagnosis of familial hypercholesterolemia in Denmark.
    Jensen HK
    Dan Med Bull; 2002 Nov; 49(4):318-45. PubMed ID: 12553167
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Familial hypercholesterolemia: molecular, biochemical, and clinical characterization of a French-Canadian pediatric population.
    Assouline L; Levy E; Feoli-Fonseca JC; Godbout C; Lambert M
    Pediatrics; 1995 Aug; 96(2 Pt 1):239-46. PubMed ID: 7630677
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Familial hypercholesterolemia: experience from France.
    Rabès JP; Béliard S; Carrié A
    Curr Opin Lipidol; 2018 Apr; 29(2):65-71. PubMed ID: 29389714
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Familial hypercholesterolemia: A largely underestimated cardiovascular risk].
    Ferrières J; Bruckert É; Béliard S; Rabès JP; Farnier M; Krempf M; Cariou B; Danchin N
    Ann Cardiol Angeiol (Paris); 2018 Feb; 67(1):1-8. PubMed ID: 28576280
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Familial hypercholesterolemia: is it time to separate monogenic from polygenic familial hypercholesterolemia?
    Brandts J; Dharmayat KI; Ray KK; Vallejo-Vaz AJ
    Curr Opin Lipidol; 2020 Jun; 31(3):111-118. PubMed ID: 32332432
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Predicting cardiovascular disease in familial hypercholesterolemia.
    Paquette M; Baass A
    Curr Opin Lipidol; 2018 Aug; 29(4):299-306. PubMed ID: 29708923
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Homozygous Familial Hypercholesterolemia in Spain: Prevalence and Phenotype-Genotype Relationship.
    Sánchez-Hernández RM; Civeira F; Stef M; Perez-Calahorra S; Almagro F; Plana N; Novoa FJ; Sáenz-Aranzubía P; Mosquera D; Soler C; Fuentes FJ; Brito-Casillas Y; Real JT; Blanco-Vaca F; Ascaso JF; Pocovi M
    Circ Cardiovasc Genet; 2016 Dec; 9(6):504-510. PubMed ID: 27784735
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Population specific genetic heterogeneity of familial hypercholesterolemia in South Africa.
    Smyth N; Ramsay M; Raal FJ
    Curr Opin Lipidol; 2018 Apr; 29(2):72-79. PubMed ID: 29369830
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Severe heterozygous familial hypercholesterolemia and risk for cardiovascular disease: a study of a cohort of 14,000 mutation carriers.
    Besseling J; Kindt I; Hof M; Kastelein JJ; Hutten BA; Hovingh GK
    Atherosclerosis; 2014 Mar; 233(1):219-23. PubMed ID: 24529147
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A systematic review of current studies in patients with familial hypercholesterolemia by use of national familial hypercholesterolemia registries.
    Mundal L; Retterstøl K
    Curr Opin Lipidol; 2016 Aug; 27(4):388-97. PubMed ID: 27070076
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Phenotype vs. genotype in severe familial hypercholesterolemia: what matters most for the clinician?
    Santos RD
    Curr Opin Lipidol; 2017 Apr; 28(2):130-135. PubMed ID: 28059950
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Atherosclerotic cardiovascular disease risk assessment in familial hypercholesterolemia: does one size fit all?
    Mata P; Alonso R; Pérez de Isla L
    Curr Opin Lipidol; 2018 Dec; 29(6):445-452. PubMed ID: 30382952
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Identifying familial hypercholesterolemia in acute coronary syndrome.
    Gencer B; Nanchen D
    Curr Opin Lipidol; 2016 Aug; 27(4):375-81. PubMed ID: 27092769
    [TBL] [Abstract][Full Text] [Related]  

  • 15. The role of registries and genetic databases in familial hypercholesterolemia.
    Kindt I; Mata P; Knowles JW
    Curr Opin Lipidol; 2017 Apr; 28(2):152-160. PubMed ID: 28169870
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Low density lipoprotein receptor (LDLR) gene mutations in Canadian subjects with familial hypercholesterolemia, but not of French descent.
    Wang J; Huff E; Janecka L; Hegele RA
    Hum Mutat; 2001 Oct; 18(4):359. PubMed ID: 11668627
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Homozygous familial hypercholesterolemia among French Canadians in Québec Province.
    Moorjani S; Roy M; Gagné C; Davignon J; Brun D; Toussaint M; Lambert M; Campeau L; Blaichman S; Lupien P
    Arteriosclerosis; 1989; 9(2):211-6. PubMed ID: 2923577
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Causative mutations and premature cardiovascular disease in patients with heterozygous familial hypercholesterolaemia.
    Rubba P; Gentile M; Marotta G; Iannuzzi A; Sodano M; De Simone B; Jossa F; Iannuzzo G; Giacobbe C; Di Taranto MD; Fortunato G
    Eur J Prev Cardiol; 2017 Jul; 24(10):1051-1059. PubMed ID: 28353356
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Simplified Canadian Definition for Familial Hypercholesterolemia.
    Ruel I; Brisson D; Aljenedil S; Awan Z; Baass A; Bélanger A; Bergeron J; Bewick D; Brophy JM; Brunham LR; Couture P; Dufour R; Francis GA; Frohlich J; Gagné C; Gaudet D; Grégoire JC; Gupta M; Hegele RA; Mancini GBJ; McCrindle BW; Pang J; Raggi P; Tu JV; Watts GF; Genest J
    Can J Cardiol; 2018 Sep; 34(9):1210-1214. PubMed ID: 30093300
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Common low-density lipoprotein receptor mutations in the French Canadian population.
    Leitersdorf E; Tobin EJ; Davignon J; Hobbs HH
    J Clin Invest; 1990 Apr; 85(4):1014-23. PubMed ID: 2318961
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.