Kontula KK - Search Results

1

Effect of apolipoprotein E polymorphism and XbaI polymorphism of apolipoprotein B on response to lovastatin treatment in familial and non-familial hypercholesterolaemia.

Ojala JP, Helve E, Ehnholm C, Aalto-Setälä K, Kontula KK, Tikkanen MJ. Ojala JP, et al. Among authors: kontula kk. J Intern Med. 1991 Nov;230(5):397-405. doi: 10.1111/j.1365-2796.1991.tb00464.x. J Intern Med. 1991. PMID: 1940775 Clinical Trial.

2

Genetic polymorphism of the apolipoprotein B gene locus influences serum LDL cholesterol level in familial hypercholesterolemia.

Aalto-Setälä K, Gylling H, Helve E, Kovanen P, Miettinen TA, Turtola H, Kontula K. Aalto-Setälä K, et al. Hum Genet. 1989 Jul;82(4):305-7. doi: 10.1007/BF00273986. Hum Genet. 1989. PMID: 2567693

3

XbaI and c/g polymorphisms of the apolipoprotein B gene locus are associated with serum cholesterol and LDL-cholesterol levels in Finland.

Aalto-Setälä K, Tikkanen MJ, Taskinen MR, Nieminen M, Holmberg P, Kontula K. Aalto-Setälä K, et al. Atherosclerosis. 1988 Nov;74(1-2):47-54. doi: 10.1016/0021-9150(88)90190-6. Atherosclerosis. 1988. PMID: 2905601

4

Heterozygous familial hypercholesterolaemia: the influence of the mutation type of the low-density-lipoprotein receptor gene and PvuII polymorphism of the normal allele on serum lipid levels and response to lovastatin treatment.

Vuorio AF, Ojala JP, Sarna S, Turtola H, Tikkanen MJ, Kontula K. Vuorio AF, et al. J Intern Med. 1995 Jan;237(1):43-8. doi: 10.1111/j.1365-2796.1995.tb01138.x. J Intern Med. 1995. PMID: 7830029

5

Association of apolipoprotein E and B polymorphisms with serum lipids.

Lehtimäki T, Moilanen T, Aalto-Setälä K, Kontula K, Porkka K, Akerblom HK, Ehnholm C, Rönnemaa T, Viikari J. Lehtimäki T, et al. Ann Med. 1991 Dec;23(6):657-62. doi: 10.3109/07853899109148099. Ann Med. 1991. PMID: 1685655 Free article.

6

Molecular genetics of familial hypercholesterolemia.

Aalto-Setälä K, Kontula K. Aalto-Setälä K, et al. Adv Exp Med Biol. 1991;285:33-7. doi: 10.1007/978-1-4684-5904-3_3. Adv Exp Med Biol. 1991. PMID: 1858564 Review. No abstract available.

7

Serum low density lipoprotein cholesterol level and cholesterol absorption efficiency are influenced by apolipoprotein B and E polymorphism and by the FH-Helsinki mutation of the low density lipoprotein receptor gene in familial hypercholesterolemia.

Gylling H, Aalto-Setälä K, Kontula K, Miettinen TA. Gylling H, et al. Arterioscler Thromb. 1991 Sep-Oct;11(5):1368-75. doi: 10.1161/01.atv.11.5.1368. Arterioscler Thromb. 1991. PMID: 1911722

8

Absence of familial defective apolipoprotein B-100 in Finnish patients with elevated serum cholesterol.

Hämäläinen T, Palotie A, Aalto-Setälä K, Kontula K, Tikkanen MJ. Hämäläinen T, et al. Atherosclerosis. 1990 Jun;82(3):177-83. doi: 10.1016/0021-9150(90)90038-k. Atherosclerosis. 1990. PMID: 2375782

9

Apolipoprotein A-I/C-III/A-IV SstI and apolipoprotein B XbaI polymorphisms and their association with carotid artery intima-media thickness in the Finnish population. The Cardiovascular Risk in Young Finns Study.

Islam MS, Raitakari OT, Juonala M, Kähönen M, Hutri-Kähönen N, Collings A, Aalto-Setälä K, Kontula K, Marniemi J, Viikari JS, Lehtimäki T. Islam MS, et al. Atherosclerosis. 2005 May;180(1):79-86. doi: 10.1016/j.atherosclerosis.2004.10.043. Epub 2005 Jan 1. Atherosclerosis. 2005. PMID: 15823278

10

Direct sequencing of affinity-captured amplified human DNA application to the detection of apolipoprotein E polymorphism.

Syvänen AC, Aalto-Setälä K, Kontula K, Söderlund H. Syvänen AC, et al. FEBS Lett. 1989 Nov 20;258(1):71-4. doi: 10.1016/0014-5793(89)81618-7. FEBS Lett. 1989. PMID: 2591536 Free article.

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