97 related articles for article (PubMed ID: 7607414)
1. Segregation analysis of plasma lipoprotein(a) levels in pedigrees with molecularly defined familial hypercholesterolemia.
Friedlander Y; Leitersdorf E
Genet Epidemiol; 1995; 12(2):129-43. PubMed ID: 7607414
[TBL] [Abstract][Full Text] [Related]
2. Concentrations of the atherogenic Lp(a) are elevated in FH.
Lingenhel A; Kraft HG; Kotze M; Peeters AV; Kronenberg F; Kruse R; Utermann G
Eur J Hum Genet; 1998 Jan; 6(1):50-60. PubMed ID: 9781014
[TBL] [Abstract][Full Text] [Related]
3. Influence of apolipoprotein E genotypes on plasma lipid and lipoprotein concentrations: results from a segregation analysis in pedigrees with molecularly defined familial hypercholesterolemia.
Friedlander Y; Leitersdorf E
Genet Epidemiol; 1996; 13(2):159-77. PubMed ID: 8722744
[TBL] [Abstract][Full Text] [Related]
4. Relationship between apolipoprotein(a) phenotype, lipoprotein(a) concentration in plasma, and low density lipoprotein receptor function in a large kindred with familial hypercholesterolemia due to the pro664----leu mutation in the LDL receptor gene.
Soutar AK; McCarthy SN; Seed M; Knight BL
J Clin Invest; 1991 Aug; 88(2):483-92. PubMed ID: 1830890
[TBL] [Abstract][Full Text] [Related]
5. [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]
6. Diverse effect of ethnicity on plasma lipoprotein[a] levels in heterozygote patients with familial hypercholesterolemia.
Leitersdorf E; Friedlander Y; Bard JM; Fruchart JC; Eisenberg S; Stein Y
J Lipid Res; 1991 Sep; 32(9):1513-9. PubMed ID: 1836489
[TBL] [Abstract][Full Text] [Related]
7. Plasma Lp(a) values in familial hypercholesterolemia and its relation to coronary heart disease.
Real JT; Ascaso JF; Chaves FJ; Tenés S; Priego MA; Puig O; Armengod ME; Carmena R
Nutr Metab Cardiovasc Dis; 1999 Feb; 9(1):41-4. PubMed ID: 10726108
[TBL] [Abstract][Full Text] [Related]
8. Lipoprotein(a) levels in familial hypercholesterolemia: an important predictor of cardiovascular disease independent of the type of LDL receptor mutation.
Alonso R; Andres E; Mata N; Fuentes-Jiménez F; Badimón L; López-Miranda J; Padró T; Muñiz O; Díaz-Díaz JL; Mauri M; Ordovás JM; Mata P;
J Am Coll Cardiol; 2014 May; 63(19):1982-9. PubMed ID: 24632281
[TBL] [Abstract][Full Text] [Related]
9. Lipoprotein(a) in homozygous familial hypercholesterolemia.
Kraft HG; Lingenhel A; Raal FJ; Hohenegger M; Utermann G
Arterioscler Thromb Vasc Biol; 2000 Feb; 20(2):522-8. PubMed ID: 10669652
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. [Lipoprotein(a) in heterozygote familial hypercholesterolemia].
Ochoa Sosa CA; Zamora González J; González Hermosillo JA; Ize Lema I; Cardoso Saldaña G; Posadas Romero C
Arch Inst Cardiol Mex; 1994; 64(6):549-55. PubMed ID: 7726691
[TBL] [Abstract][Full Text] [Related]
12. Influence of lipoprotein (a) levels and isoforms on fibrinolytic activity--study in families with high lipoprotein (a) levels.
Falcó C; Estellés A; Dalmau J; España F; Aznar J
Thromb Haemost; 1998 Apr; 79(4):818-23. PubMed ID: 9580386
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Detection of the Pro664-Leu mutation in the low-density lipoprotein receptor and its relation to lipoprotein(a) levels in patients with familial hypercholesterolemia of Dutch ancestry from The Netherlands and Canada.
Defesche JC; van de Ree MA; Kastelein JJ; van Diermen DE; Janssens NW; van Doormaal JJ; Hayden MR
Clin Genet; 1992 Dec; 42(6):273-80. PubMed ID: 1493640
[TBL] [Abstract][Full Text] [Related]
15. [Relationship between lipoprotein A, apolipoprotein A and their isoforms in parents and children].
Ferrer Lorente B; Dalmau Serra J; Falcó Couchoud C; Estellés Cortés A; España Furió F; Aznar Lucea J
An Esp Pediatr; 1998 Jun; 48(6):587-92. PubMed ID: 9662841
[TBL] [Abstract][Full Text] [Related]
16. Lp(a) levels and atherosclerotic vascular disease in a sample of patients with familial hypercholesterolemia sharing the same gene defect.
Carmena R; Lussier-Cacan S; Roy M; Minnich A; Lingenhel A; Kronenberg F; Davignon J
Arterioscler Thromb Vasc Biol; 1996 Jan; 16(1):129-36. PubMed ID: 8548413
[TBL] [Abstract][Full Text] [Related]
17. HDL cholesterol levels in patients with molecularly defined familial hypercholesterolemia.
Miltiadous G; Cariolou MA; Elisaf M
Ann Clin Lab Sci; 2002; 32(1):50-4. PubMed ID: 11848618
[TBL] [Abstract][Full Text] [Related]
18. Sib-pair analysis detects elevated Lp(a) levels and large variation of Lp(a) concentration in subjects with familial defective ApoB.
van der Hoek YY; Lingenhel A; Kraft HG; Defesche JC; Kastelein JJ; Utermann G
J Clin Invest; 1997 May; 99(9):2269-73. PubMed ID: 9151801
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. A novel LDLR mutation, H190Y, in a Utah kindred with familial hypercholesterolemia.
Hopkins PN; Wu LL; Stephenson SH; Xin Y; Katsumata H; Nobe Y; Nakajima T; Hirayama T; Emi M; Williams RR
J Hum Genet; 1999; 44(6):364-7. PubMed ID: 10570905
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
