95 related articles for article (PubMed ID: 9691807)
1. [Molecular biology in the diagnosis of cardiovascular diseases].
Berg K
Tidsskr Nor Laegeforen; 1998 Jun; 118(15):2370-4. PubMed ID: 9691807
[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. Update of the molecular basis of familial hypercholesterolemia in The Netherlands.
Fouchier SW; Kastelein JJ; Defesche JC
Hum Mutat; 2005 Dec; 26(6):550-6. PubMed ID: 16250003
[TBL] [Abstract][Full Text] [Related]
4. Review of risk factors for cardiovascular diseases.
Wu LL
Ann Clin Lab Sci; 1999; 29(2):127-33. PubMed ID: 10219700
[TBL] [Abstract][Full Text] [Related]
5. Angiotensin-converting enzyme gene polymorphism, lipids, and apolipoproteins in menopausal women on hormone replacement therapy.
Cubrilo-Turek M; Sertić J; Duraković Z
Acta Med Croatica; 2001; 55(4-5):161-7. PubMed ID: 12398019
[TBL] [Abstract][Full Text] [Related]
6. Portuguese Familial Hypercholesterolemia Study: presentation of the study and preliminary results.
Bourbon M; Rato Q;
Rev Port Cardiol; 2006 Nov; 25(11):999-1013. PubMed ID: 17274457
[TBL] [Abstract][Full Text] [Related]
7. Characterization and geographic distribution of the low density lipoprotein receptor (LDLR) gene mutations in northwestern Greece.
Miltiadous G; Elisaf M; Bairaktari H; Xenophontos SL; Manoli P; Cariolou MA
Hum Mutat; 2001 May; 17(5):432-3. PubMed ID: 11317361
[TBL] [Abstract][Full Text] [Related]
8. [The genetic contribution to coronary disease. The genetic factors related to lipid metabolism].
da Silva PM
Rev Port Cardiol; 1999; 18(7-8):735-47. PubMed ID: 10466375
[TBL] [Abstract][Full Text] [Related]
9. [Familial hypercholesterolemia and plasma Lp(a) levels: 2 cardiovascular risk factors].
Real JT; Romero G; Priego MA; Chaves FJ; Ascaso JF; Carmena R
An Med Interna; 1999 Feb; 16(2):69-72. PubMed ID: 10192997
[TBL] [Abstract][Full Text] [Related]
10. Frequency of low-density lipoprotein receptor gene mutations in patients with a clinical diagnosis of familial combined hyperlipidemia in a clinical setting.
Civeira F; Jarauta E; Cenarro A; García-Otín AL; Tejedor D; Zambón D; Mallen M; Ros E; Pocoví M
J Am Coll Cardiol; 2008 Nov; 52(19):1546-53. PubMed ID: 19007590
[TBL] [Abstract][Full Text] [Related]
11. [Identification of a novel splice mutation of low density lipoprotein receptor gene in a Chinese family with familial hypercholesterolemia].
Lin J; Wang LY; Liu S; Pan XD; Du LP; Shi FR; Qin YW; Zhao Q; Guo HY
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Feb; 21(1):14-8. PubMed ID: 14767901
[TBL] [Abstract][Full Text] [Related]
12. The application of molecular biology techniques to the diagnosis of hyperlipidaemia and other risk factors for cardio-vascular disease.
Humphries SE
Ann Biol Clin (Paris); 1994; 52(1):67-75. PubMed ID: 8210077
[No Abstract] [Full Text] [Related]
13. [Interaction of ApoE and LDL-R gene polymorphisms and alcohol drinking and smoking on coronary heart disease].
Wang CH; Zhou X; Zhou GD; Han DF; Zheng F
Zhonghua Yi Xue Za Zhi; 2004 Apr; 84(7):554-8. PubMed ID: 15144588
[TBL] [Abstract][Full Text] [Related]
14. Usefulness of genetic polymorphisms and conventional risk factors to predict coronary heart disease in patients with familial hypercholesterolemia.
van der Net JB; Janssens AC; Defesche JC; Kastelein JJ; Sijbrands EJ; Steyerberg EW
Am J Cardiol; 2009 Feb; 103(3):375-80. PubMed ID: 19166692
[TBL] [Abstract][Full Text] [Related]
15. Low-density lipoprotein receptor gene mutation analysis and clinical correlation in Belgian hypercholesterolaemics.
Van Gaal LF; Peeters AV; De Block CE; de Leeuw IH; Thiart R; Kotze MJ
Mol Cell Probes; 2001 Dec; 15(6):329-36. PubMed ID: 11851376
[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. Molecular variation at functional genes and the history of human populations--data on candidate genes for cardiovascular risk in the Mediterranean.
Moral P; Valveny N; López-Alomar A; Calo C; Kandil M; Harich N; González-Pérez E; Via M; Esteban E; Dugoujon JM; Vona G
Coll Antropol; 2003 Dec; 27(2):523-36. PubMed ID: 14746139
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. A Chinese homozygote of familial hypercholesterolemia: identification of a novel C263R mutation in the LDL receptor gene.
Wang D; Wu B; Li Y; Heng W; Zhong H; Mu Y; Wang J
J Hum Genet; 2001; 46(3):152-4. PubMed ID: 11310584
[TBL] [Abstract][Full Text] [Related]
20. The emerging risk factors for cardiovascular disease: a review of the epidemiologic evidence for lipoprotein(a), homocysteine, and fibrinogen.
Catena C; Cavarape A; Dotto L; Colussi G; Novehllo M; De Marchi S; Sechi LA
Adv Clin Path; 2003 Jan; 7(1):3-11. PubMed ID: 19774732
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]