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.
177 related articles for article (PubMed ID: 15209474)
1. A boy with autosomal recessive hypercholesterolaemia. Rodenburg J; Wiegman A; Vissers MN; Kastelein JJ; Stalenhoef AF Neth J Med; 2004 Mar; 62(3):89-93. PubMed ID: 15209474 [TBL] [Abstract][Full Text] [Related]
2. Autosomal recessive hypercholesterolaemia: normalization of plasma LDL cholesterol by ezetimibe in combination with statin treatment. Lind S; Olsson AG; Eriksson M; Rudling M; Eggertsen G; Angelin B J Intern Med; 2004 Nov; 256(5):406-12. PubMed ID: 15485476 [TBL] [Abstract][Full Text] [Related]
3. Disruption of autosomal recessive hypercholesterolemia gene shows different phenotype in vitro and in vivo. Harada-Shiba M; Takagi A; Marutsuka K; Moriguchi S; Yagyu H; Ishibashi S; Asada Y; Yokoyama S Circ Res; 2004 Oct; 95(9):945-52. PubMed ID: 15472122 [TBL] [Abstract][Full Text] [Related]
4. Autosomal recessive hypercholesterolaemia: long-term follow up and response to treatment. Naoumova RP; Neuwirth C; Lee P; Miller JP; Taylor KG; Soutar AK Atherosclerosis; 2004 May; 174(1):165-72. PubMed ID: 15135266 [TBL] [Abstract][Full Text] [Related]
5. [Application of gene technology in the diagnosis of familial hypercholesterolemia]. Leren TP; Bakken KS; Rødningen OK; Gundersen KE; Sundvold H; Berg K; Tonstad S; Ose L Tidsskr Nor Laegeforen; 1997 Feb; 117(5):678-81. PubMed ID: 9102960 [TBL] [Abstract][Full Text] [Related]
6. Autosomal recessive hypercholesterolemia in three sisters with phenotypic homozygous familial hypercholesterolemia: diagnostic and therapeutic procedures. Thomas HP; Vogt A; Wilund KR; Schliesser C; Steinhagen-Thiessen E; Kassner U Ther Apher Dial; 2004 Aug; 8(4):275-80. PubMed ID: 15274677 [TBL] [Abstract][Full Text] [Related]
8. Low-density lipoprotein receptor genotype and response to pravastatin in children with familial hypercholesterolemia: substudy of an intima-media thickness trial. Koeijvoets KC; Rodenburg J; Hutten BA; Wiegman A; Kastelein JJ; Sijbrands EJ Circulation; 2005 Nov; 112(20):3168-73. PubMed ID: 16286607 [TBL] [Abstract][Full Text] [Related]
9. Japanese familial hypercholesterolaemia with a 327insC mutation in the LDL receptor gene. Hirota R; Kubo N; Hikiji K; Nakajima K; Hata Y; Sakurabayashi I Ann Clin Biochem; 2002 Sep; 39(Pt 5):526-30. PubMed ID: 12227864 [TBL] [Abstract][Full Text] [Related]
10. Autosomal recessive hypercholesterolaemia: discrimination of ARH protein and LDLR function in the homozygous FH phenotype. Abera AB; Marais AD; Raal FJ; Leisegang F; Jones S; George P; Henderson HE Clin Chim Acta; 2007 Mar; 378(1-2):33-7. PubMed ID: 17150201 [TBL] [Abstract][Full Text] [Related]
11. Use of the denaturing gradient gel electrophoresis (DGGE) method for mutational screening of patients with familial hypercholesterolaemia (FH) and Familial defective apolipoprotein B100 (FDB). Azian M; Hapizah MN; Khalid BA; Khalid Y; Rosli A; Jamal R Malays J Pathol; 2006 Jun; 28(1):7-15. PubMed ID: 17694954 [TBL] [Abstract][Full Text] [Related]
12. Autosomal recessive hypercholesterolaemia in a Morrocan family due to a mutation of the G266C LDL receptor. El Aziz S; Chadli A; El Ghomari H; Farouqi A BMJ Case Rep; 2012 May; 2012():. PubMed ID: 22669020 [TBL] [Abstract][Full Text] [Related]
13. [Identification of a novel mutation at the point of low density lipoprotein receptor gene from a subject with familial hypercholesterolemia]. Liu YR; Tao QM; Chen JZ; Tao M; Guo XG; Shang YP; Zhu JH; Zhang FR; Zheng LR; Wang XX Sheng Li Xue Bao; 2004 Oct; 56(5):566-72. PubMed ID: 15497035 [TBL] [Abstract][Full Text] [Related]
14. New Horizons in the Pathogenesis, Pathophysiology and Treatment of Familial Hypercholesterolaemia. Viigimaa M; Heinsar S; Lovic D; Katsimardou A; Piperidou A; Duishvili D Curr Pharm Des; 2018; 24(31):3599-3604. PubMed ID: 30306860 [TBL] [Abstract][Full Text] [Related]
15. Homozygous familial hypercholesterolemia: current perspectives on diagnosis and treatment. Raal FJ; Santos RD Atherosclerosis; 2012 Aug; 223(2):262-8. PubMed ID: 22398274 [TBL] [Abstract][Full Text] [Related]
16. [Is detection and treatment of familial hypercholesterolemia indicated in children?]. Bakker HD; Wiegman A; Defesche JC; Kastelein JJ Ned Tijdschr Geneeskd; 1997 Dec; 141(52):2548-51. PubMed ID: 9555154 [TBL] [Abstract][Full Text] [Related]
17. [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]
18. Management of a patient with a null low-density lipoprotein receptor mutation: a case report. Kolovou GD; Dedoussis GV; Anagnostopoulou KK; Hatzigeorgiou GCh; Salpea KD; Choumerianou DM; Rammos S; Mikhailidis DP; Cokkinos DV Angiology; 2006 Dec-2007 Jan; 57(6):729-32. PubMed ID: 17235114 [TBL] [Abstract][Full Text] [Related]
19. An 11-year-old boy with familial hypercholesterolemia showing multiple xanthomas and advanced atherosclerosis, who responded to lipid-lowering therapy using statin. Ohshiro T; Mabuchi H; Ohta T J Atheroscler Thromb; 2010 Oct; 17(10):1113. PubMed ID: 20962452 [No Abstract] [Full Text] [Related]
20. Influence of LDL-receptor mutation type on age at first cardiovascular event in patients with familial hypercholesterolaemia. Souverein OW; Defesche JC; Zwinderman AH; Kastelein JJ; Tanck MW Eur Heart J; 2007 Feb; 28(3):299-304. PubMed ID: 17090611 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]