Report for Huttunen JK

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References (3)

Title : Molecular genetic study of Finns with hypoalphalipoproteinemia and hyperalphalipoproteinemia: a novel Gly230 Arg mutation (LCAT[Fin]) of lecithin:cholesterol acyltransferase (LCAT) accounts for 5\% of cases with very low serum HDL cholesterol levels - Miettinen_1998_Arterioscler.Thromb.Vasc.Biol_18_591
Author(s) : Miettinen HE , Gylling H , Tenhunen J , Virtamo J , Jauhiainen M , Huttunen JK , Kantola I , Miettinen TA , Kontula K
Ref : Arterioscler Thromb Vasc Biol , 18 :591 , 1998
Abstract : Miettinen_1998_Arterioscler.Thromb.Vasc.Biol_18_591
ESTHER : Miettinen_1998_Arterioscler.Thromb.Vasc.Biol_18_591
PubMedSearch : Miettinen_1998_Arterioscler.Thromb.Vasc.Biol_18_591
PubMedID: 9555865

Title : Heterogeneity of primary lipoprotein lipase deficiency -
Author(s) : Brunzell JD , Chait A , Nikkila EA , Ehnholm C , Huttunen JK , Steiner G
Ref : Metabolism , 29 :624 , 1980
PubMedID: 7382827

Title : Effect of clofibrate on postheparin plasma triglyceride lipase activities in patients with hypertriglyceridemia - Nikkila_1977_Metabolism_26_179
Author(s) : Nikkila EA , Huttunen JK , Ehnholm C
Ref : Metabolism , 26 :179 , 1977
Abstract : Nikkila_1977_Metabolism_26_179
ESTHER : Nikkila_1977_Metabolism_26_179
PubMedSearch : Nikkila_1977_Metabolism_26_179
PubMedID: 834151