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.
139 related articles for article (PubMed ID: 19487412)
21. Hypolipidemic treatment of heterozygous familial hypercholesterolemia: a lifelong challenge. Vuorio AF; Kovanen PT; Gylling H Expert Rev Cardiovasc Ther; 2004 May; 2(3):405-15. PubMed ID: 15151486 [TBL] [Abstract][Full Text] [Related]
22. Comparison of genetic versus clinical diagnosis in familial hypercholesterolemia. Civeira F; Ros E; Jarauta E; Plana N; Zambon D; Puzo J; Martinez de Esteban JP; Ferrando J; Zabala S; Almagro F; Gimeno JA; Masana L; Pocovi M Am J Cardiol; 2008 Nov; 102(9):1187-93, 1193.e1. PubMed ID: 18940289 [TBL] [Abstract][Full Text] [Related]
23. Detection of a known mutation M412T in the LDL receptor in a Chinese Thai FH family. Pongrapeeporn KU; Nuinoon M; Thepsuriyanont P; Kasemsuk B; Charoensuk P; Chantawee R; Wongmanee U; Nuchpramool W Clin Chim Acta; 2006 Mar; 365(1-2):211-6. PubMed ID: 16406299 [TBL] [Abstract][Full Text] [Related]
24. The type of LDLR gene mutation predicts cardiovascular risk in children with familial hypercholesterolemia. Guardamagna O; Restagno G; Rolfo E; Pederiva C; Martini S; Abello F; Baracco V; Pisciotta L; Pino E; Calandra S; Bertolini S J Pediatr; 2009 Aug; 155(2):199-204.e2. PubMed ID: 19446849 [TBL] [Abstract][Full Text] [Related]
25. An apparent inconsistency in parent to offspring transmission of point mutations of LDLR gene in familial hypercholesterolemia. Rabacchi C; Wunsch A; Ghisellini M; Marino M; Pisciotta L; Bertolini S; Calandra S Clin Chim Acta; 2009 Aug; 406(1-2):75-80. PubMed ID: 19467224 [TBL] [Abstract][Full Text] [Related]
26. [Familial hypercholesterolemia in St. Petersburg: diversity of mutations argues against a strong founder effect]. Zakharova FM; Tatishcheva IuA; Golubkov VI; Lipovetskiĭ BM; Konstantinov VO; Denisenko AD; Faergeman O; Vasil'ev VB; Mandel'shtam MIu Genetika; 2007 Sep; 43(9):1255-62. PubMed ID: 17990524 [TBL] [Abstract][Full Text] [Related]
27. Beta-thalassemia is a modifying factor of the clinical expression of familial hypercholesterolemia. Calandra S; Bertolini S; Pes GM; Deiana L; Tarugi P; Pisciotta L; Li Volti S; Li Volti G; Maccarone C Semin Vasc Med; 2004 Aug; 4(3):271-8. PubMed ID: 15630628 [TBL] [Abstract][Full Text] [Related]
28. [Three-year-old boy--a homozygote for familiar hypercholesterolemia]. Dumić M; Uroic AS; Francetić I; Puretić Z; Matisić D; Kes P; Mikecin M; Reiner Z Lijec Vjesn; 2007 May; 129(5):130-3. PubMed ID: 17695192 [TBL] [Abstract][Full Text] [Related]
29. Pathobiology of familial hypercholesterolemic atherosclerosis. Aliev G; Castellani RJ; Petersen RB; Burnstock G; Perry G; Smith MA J Submicrosc Cytol Pathol; 2004; 36(3-4):225-40. PubMed ID: 15906597 [TBL] [Abstract][Full Text] [Related]
31. A novel splice site mutation of the LDL receptor gene in a Tunisian hypercholesterolemic family. Jelassi A; Najah M; Jguirim I; Maatouk F; Lestavel S; Laroussi OS; Rouis M; Boileau C; Rabès JP; Varret M; Slimane MN Clin Chim Acta; 2008 Jun; 392(1-2):25-9. PubMed ID: 18355452 [TBL] [Abstract][Full Text] [Related]
32. A novel method for determining functional LDL receptor activity in familial hypercholesterolemia: application of the CD3/CD28 assay in lymphocytes. Tada H; Kawashiri MA; Noguchi T; Mori M; Tsuchida M; Takata M; Nohara A; Inazu A; Kobayashi J; Yachie A; Mabuchi H; Yamagishi M Clin Chim Acta; 2009 Feb; 400(1-2):42-7. PubMed ID: 19013141 [TBL] [Abstract][Full Text] [Related]
33. Liver transplant combined with heart transplant in severe heterozygous hypercholesterolemia: report of the first case and review of the literature. Alkofer BJ; Chiche L; Khayat A; Deshayes JP; Lepage A; Saloux E; Reznik Y Transplant Proc; 2005 Jun; 37(5):2250-2. PubMed ID: 15964390 [TBL] [Abstract][Full Text] [Related]
34. The patient at risk: who should we be treating? Leitersdorf E Br J Clin Pract Suppl; 1994 Dec; (77):24-7. PubMed ID: 19496269 [TBL] [Abstract][Full Text] [Related]
35. Allelic drop-out in the LDLR gene affects mutation detection in familial hypercholesterolemia. Laios E; Glynou K Clin Biochem; 2008 Jan; 41(1-2):38-40. PubMed ID: 17988659 [TBL] [Abstract][Full Text] [Related]
36. Splice-site mutation c.313+1, G>A in intron 3 of the LDL receptor gene results in transcripts with skipping of exon 3 and inclusion of intron 3. Cameron J; Holla ØL; Kulseth MA; Leren TP; Berge KE Clin Chim Acta; 2009 May; 403(1-2):131-5. PubMed ID: 19361455 [TBL] [Abstract][Full Text] [Related]
37. Diagnosis of heterozygous familial hypercholesterolaemia in children. Nicholls DP; Cather M; Byrne C; Graham CA; Young IS Int J Clin Pract; 2008 Jul; 62(7):990-4. PubMed ID: 18492057 [TBL] [Abstract][Full Text] [Related]
38. Aortic calcifications in familial hypercholesterolemia: potential role of the low-density lipoprotein receptor gene. Alrasadi K; Alwaili K; Awan Z; Valenti D; Couture P; Genest J Am Heart J; 2009 Jan; 157(1):170-6. PubMed ID: 19081415 [TBL] [Abstract][Full Text] [Related]