182 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]
7. LDL-receptor mutations in Europe.
Dedoussis GV; Schmidt H; Genschel J
Hum Mutat; 2004 Dec; 24(6):443-59. PubMed ID: 15523646
[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]