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Results: 1-5 |
Results: 5

Authors: Vuorio, AF Aalto-Setala, K Koivisto, UM Turtola, H Nissen, H Kovanen, PT Miettinen, TA Gylling, H Oksanen, H Kontula, K
Citation: Af. Vuorio et al., Familial hypercholesterolaemia in Finland: common, rare and mild mutationsof the LDL receptor and their clinical consequences, ANN MED, 33(6), 2001, pp. 410-421

Authors: Vuorio, AF Gylling, H Turtola, H Kontula, K Ketonen, P Miettinen, TA
Citation: Af. Vuorio et al., Stanol ester margarine alone and with simvastatin lowers serum cholesterolin families with familial hypercholesterolemia caused by the FH-North Karelia mutation, ART THROM V, 20(2), 2000, pp. 500-506

Authors: Vuorio, AF Paulin, L Saltevo, J Kontula, K
Citation: Af. Vuorio et al., Single-nucleotide polymorphisms may cause erroneous results in primer-introduced restriction enzyme analyses: a case of molecular misdiagnosis of homozygous vs heterozygous familial hypercholesterolemia, MOL CELL PR, 13(6), 1999, pp. 421-424

Authors: Kuismanen, K Savontaus, ML Kozlov, A Vuorio, AF Sajantila, A
Citation: K. Kuismanen et al., Coagulation factor V Leiden mutation in sudden fatal pulmonary embolism and in a general northern European population sample, FOREN SCI I, 106(2), 1999, pp. 71-75

Authors: Vuorio, AF Kontula, K Turtola, H Sajantila, A
Citation: Af. Vuorio et al., Post mortem molecularly defined familial hypercholesterolemia and sudden cardiac death of young men, FOREN SCI I, 106(2), 1999, pp. 87-92
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