Miettinen H - Search Results

1

Two different allelic mutations in a Finnish family with lecithin:cholesterol acyltransferase deficiency.

Miettinen H, Gylling H, Ulmanen I, Miettinen TA, Kontula K. Miettinen H, et al. Among authors: miettinen ta. Arterioscler Thromb Vasc Biol. 1995 Apr;15(4):460-7. doi: 10.1161/01.atv.15.4.460. Arterioscler Thromb Vasc Biol. 1995. PMID: 7749857

2

[The Finnish genes of coronary heart disease].

Kontula K, Koivisto UM, Miettinen H, Vuorio A. Kontula K, et al. Among authors: miettinen h. Duodecim. 1994;110(7):721-9. Duodecim. 1994. PMID: 8542827 Review. Finnish. No abstract available.

3

The use of PCR in diagnosing lipoprotein disorders.

Kontula K, Koivisto UM, Miettinen H. Kontula K, et al. Among authors: miettinen h. Ann Med. 1992 Jun;24(3):195-9. doi: 10.3109/07853899209147821. Ann Med. 1992. PMID: 1627316 Review. No abstract available.

4

Arg506Gln factor V mutation (factor V Leiden) in patients with ischaemic cerebrovascular disease and survivors of myocardial infarction.

Kontula K, Ylikorkala A, Miettinen H, Vuorio A, Kauppinen-Mäkelin R, Hämäläinen L, Palomäki H, Kaste M. Kontula K, et al. Among authors: miettinen h. Thromb Haemost. 1995 Apr;73(4):558-60. Thromb Haemost. 1995. PMID: 7495058

5

Genetic risk factors and ischaemic cerebrovascular disease: role of common variation of the genes encoding apolipoproteins and angiotensin-converting enzyme.

Aalto-Setälä K, Palomäki H, Miettinen H, Vuorio A, Kuusi T, Raininko R, Salonen O, Kaste M, Kontula K. Aalto-Setälä K, et al. Among authors: miettinen h. Ann Med. 1998 Apr;30(2):224-33. doi: 10.3109/07853899808999408. Ann Med. 1998. PMID: 9667803

6

Linkage of the long QT syndrome to the short arm of chromosome 11: use of five highly polymorphic markers towards more detailed localization of the mutant gene.

Kainulainen K, Swan H, Miettinen H, Viitasalo M, Rovamo L, Toivonen L, Kontula K. Kainulainen K, et al. Among authors: miettinen h. Hum Genet. 1995 Oct;96(4):395-400. doi: 10.1007/BF00191795. Hum Genet. 1995. PMID: 7557959

7

Angiotensin converting enzyme gene insertion/deletion polymorphism, angiotensinogen gene polymorphisms, family history of hypertension, and childhood blood pressure.

Taittonen L, Uhari M, Kontula K, Kainulainen K, Miettinen H, Turtinen J, Nuutinen M. Taittonen L, et al. Among authors: miettinen h. Am J Hypertens. 1999 Sep;12(9 Pt 1):858-66. doi: 10.1016/s0895-7061(99)00060-6. Am J Hypertens. 1999. PMID: 10509542

8

Lack of association of apolipoprotein E allele epsilon 4 with late-onset Alzheimer's disease among Finnish centenarians.

Sobel E, Louhija J, Sulkava R, Davanipour Z, Kontula K, Miettinen H, Tikkanen M, Kainulainen K, Tilvis R. Sobel E, et al. Among authors: miettinen h. Neurology. 1995 May;45(5):903-7. doi: 10.1212/wnl.45.5.903. Neurology. 1995. PMID: 7746404

9

Insulin resistance syndrome predicts the risk of coronary heart disease and stroke in healthy middle-aged men: the 22-year follow-up results of the Helsinki Policemen Study.

Pyörälä M, Miettinen H, Halonen P, Laakso M, Pyörälä K. Pyörälä M, et al. Among authors: miettinen h. Arterioscler Thromb Vasc Biol. 2000 Feb;20(2):538-44. doi: 10.1161/01.atv.20.2.538. Arterioscler Thromb Vasc Biol. 2000. PMID: 10669654

10

Serum cholesterol and high density lipoprotein cholesterol distributions in patients with acute myocardial infarction and in the general population of Kuopio province, eastern Finland.

Lehto S, Palomäki P, Miettinen H, Penttilä I, Salomaa V, Tuomilehto J, Jauhiainen M, Pyörälä K. Lehto S, et al. Among authors: miettinen h. J Intern Med. 1993 Feb;233(2):179-85. doi: 10.1111/j.1365-2796.1993.tb00671.x. J Intern Med. 1993. PMID: 8433079

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