These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
348 related articles for article (PubMed ID: 26802983)
1. Cosegregation of serum cholesterol with cholesterol intestinal absorption markers in families with primary hypercholesterolemia without mutations in LDLR, APOB, PCSK9 and APOE genes. Baila-Rueda L; Pérez-Ruiz MR; Jarauta E; Tejedor MT; Mateo-Gallego R; Lamiquiz-Moneo I; de Castro-Orós I; Cenarro A; Civeira F Atherosclerosis; 2016 Mar; 246():202-7. PubMed ID: 26802983 [TBL] [Abstract][Full Text] [Related]
2. Lipid phenotype and heritage pattern in families with genetic hypercholesterolemia not related to LDLR, APOB, PCSK9, or APOE. Jarauta E; Pérez-Ruiz MR; Pérez-Calahorra S; Mateo-Gallego R; Cenarro A; Cofán M; Ros E; Civeira F; Tejedor MT J Clin Lipidol; 2016; 10(6):1397-1405.e2. PubMed ID: 27919357 [TBL] [Abstract][Full Text] [Related]
3. Effect of mutations in LDLR and PCSK9 genes on phenotypic variability in Tunisian familial hypercholesterolemia patients. Slimani A; Jelassi A; Jguirim I; Najah M; Rebhi L; Omezzine A; Maatouk F; Hamda KB; Kacem M; Rabès JP; Abifadel M; Boileau C; Rouis M; Slimane MN; Varret M Atherosclerosis; 2012 May; 222(1):158-66. PubMed ID: 22417841 [TBL] [Abstract][Full Text] [Related]
4. Increased intestinal cholesterol absorption in autosomal dominant hypercholesterolemia and no mutations in the low-density lipoprotein receptor or apolipoprotein B genes. García-Otín AL; Cofán M; Junyent M; Recalde D; Cenarro A; Pocoví M; Ros E; Civeira F J Clin Endocrinol Metab; 2007 Sep; 92(9):3667-73. PubMed ID: 17566095 [TBL] [Abstract][Full Text] [Related]
5. Spectrum of mutations in index patients with familial hypercholesterolemia in Singapore: Single center study. Pek SLT; Dissanayake S; Fong JCW; Lin MX; Chan EZL; Tang JI; Lee CW; Ong HY; Sum CF; Lim SC; Tavintharan S Atherosclerosis; 2018 Feb; 269():106-116. PubMed ID: 29353225 [TBL] [Abstract][Full Text] [Related]
7. Clinical characterization and mutation spectrum of German patients with familial hypercholesterolemia. Grenkowitz T; Kassner U; Wühle-Demuth M; Salewsky B; Rosada A; Zemojtel T; Hopfenmüller W; Isermann B; Borucki K; Heigl F; Laufs U; Wagner S; Kleber ME; Binner P; März W; Steinhagen-Thiessen E; Demuth I Atherosclerosis; 2016 Oct; 253():88-93. PubMed ID: 27596133 [TBL] [Abstract][Full Text] [Related]
8. Reduced penetrance of autosomal dominant hypercholesterolemia in a high percentage of families: importance of genetic testing in the entire family. Garcia-Garcia AB; Ivorra C; Martinez-Hervas S; Blesa S; Fuentes MJ; Puig O; Martín-de-Llano JJ; Carmena R; Real JT; Chaves FJ Atherosclerosis; 2011 Oct; 218(2):423-30. PubMed ID: 21868016 [TBL] [Abstract][Full Text] [Related]
9. Spectrum of mutations in Italian patients with familial hypercholesterolemia: New results from the LIPIGEN study. Pirillo A; Garlaschelli K; Arca M; Averna M; Bertolini S; Calandra S; Tarugi P; Catapano AL; Atheroscler Suppl; 2017 Oct; 29():17-24. PubMed ID: 28965616 [TBL] [Abstract][Full Text] [Related]
10. 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]
11. Diagnostic Yield and Clinical Utility of Sequencing Familial Hypercholesterolemia Genes in Patients With Severe Hypercholesterolemia. Khera AV; Won HH; Peloso GM; Lawson KS; Bartz TM; Deng X; van Leeuwen EM; Natarajan P; Emdin CA; Bick AG; Morrison AC; Brody JA; Gupta N; Nomura A; Kessler T; Duga S; Bis JC; van Duijn CM; Cupples LA; Psaty B; Rader DJ; Danesh J; Schunkert H; McPherson R; Farrall M; Watkins H; Lander E; Wilson JG; Correa A; Boerwinkle E; Merlini PA; Ardissino D; Saleheen D; Gabriel S; Kathiresan S J Am Coll Cardiol; 2016 Jun; 67(22):2578-89. PubMed ID: 27050191 [TBL] [Abstract][Full Text] [Related]
12. Identification of a novel LDLR disease-causing variant using capture-based next-generation sequencing screening of familial hypercholesterolemia patients in Taiwan. Hsiung YC; Lin PC; Chen CS; Tung YC; Yang WS; Chen PL; Su TC Atherosclerosis; 2018 Oct; 277():440-447. PubMed ID: 30270083 [TBL] [Abstract][Full Text] [Related]
15. 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]
16. ABCG5/G8 gene is associated with hypercholesterolemias without mutation in candidate genes and noncholesterol sterols. Lamiquiz-Moneo I; Baila-Rueda L; Bea AM; Mateo-Gallego R; Pérez-Calahorra S; Marco-Benedí V; Martín-Navarro A; Ros E; Cofán M; Rodríguez-Rey JC; Pocovi M; Cenarro A; Civeira F J Clin Lipidol; 2017; 11(6):1432-1440.e4. PubMed ID: 29066094 [TBL] [Abstract][Full Text] [Related]
17. Bile acid synthesis precursors in subjects with genetic hypercholesterolemia negative for LDLR/APOB/PCSK9/APOE mutations. Association with lipids and carotid atherosclerosis. Baila-Rueda L; Cenarro A; Lamiquiz-Moneo I; Mateo-Gallego R; Bea AM; Perez-Calahorra S; Marco-Benedi V; Civeira F J Steroid Biochem Mol Biol; 2017 May; 169():226-233. PubMed ID: 27769814 [TBL] [Abstract][Full Text] [Related]
18. Genetic variation in APOB, PCSK9, and ANGPTL3 in carriers of pathogenic autosomal dominant hypercholesterolemic mutations with unexpected low LDL-Cl Levels. Huijgen R; Sjouke B; Vis K; de Randamie JS; Defesche JC; Kastelein JJ; Hovingh GK; Fouchier SW Hum Mutat; 2012 Feb; 33(2):448-55. PubMed ID: 22095935 [TBL] [Abstract][Full Text] [Related]
19. Effects of familial hypercholesterolemia-associated genes on the phenotype of premature myocardial infarction. Lee C; Cui Y; Song J; Li S; Zhang F; Wu M; Li L; Hu D; Chen H Lipids Health Dis; 2019 Apr; 18(1):95. PubMed ID: 30971288 [TBL] [Abstract][Full Text] [Related]
20. The genetic spectrum of familial hypercholesterolemia in the central south region of China. Xiang R; Fan LL; Lin MJ; Li JJ; Shi XY; Jin JY; Liu YX; Chen YQ; Xia K; Zhao SP Atherosclerosis; 2017 Mar; 258():84-88. PubMed ID: 28235710 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]