AAAAAA

   
Results: 1-25 | 26-35
Results: 1-25/35
Involvement of the cardiac ryanodine receptor/calcium release channel in catecholaminergic polymorphic ventricular tachycardia
Authors: Marks, AR Priori, S Memmi, M Kontula, K Laitinen, PJ
Citation: Ar. Marks et al., Involvement of the cardiac ryanodine receptor/calcium release channel in catecholaminergic polymorphic ventricular tachycardia, J CELL PHYS, 190(1), 2002, pp. 1-6
Response of the QT interval to mental and physical stress in types LQT1 and LQT2 of the long QT syndrome
Authors: Paavonen, KJ Swan, H Piippo, K Hokkanen, L Laitinen, P Viitasalo, M Toivonen, L Kontula, K
Citation: Kj. Paavonen et al., Response of the QT interval to mental and physical stress in types LQT1 and LQT2 of the long QT syndrome, HEART, 86(1), 2001, pp. 39-44
Genetic analysis in Finnish families with inflammatory bowel disease supports linkage to chromosome 3p21
Authors: Paavola, P Helio, T Kiuru, M Halme, L Turunen, U Terwilliger, J Karvonen, AL Julkunen, R Niemela, S Nurmi, H Farkkila, M Kontula, K
Citation: P. Paavola et al., Genetic analysis in Finnish families with inflammatory bowel disease supports linkage to chromosome 3p21, EUR J HUM G, 9(5), 2001, pp. 328-334
Association of lipoprotein lipase Ser447Ter polymorphism with brain infarction: a population-based neuropathological study
Authors: Myllykangas, L Polvikoski, T Sulkava, R Notkola, IL Rastas, S Verkkoniemi, A Tienari, PJ Niinisto, L Hardy, J Perez-Tur, J Kontula, K Haltia, M
Citation: L. Myllykangas et al., Association of lipoprotein lipase Ser447Ter polymorphism with brain infarction: a population-based neuropathological study, ANN MED, 33(7), 2001, pp. 486-492
Familial hypercholesterolaemia in Finland: common, rare and mild mutationsof the LDL receptor and their clinical consequences
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
A founder mutation of the potassium channel KCNQ1 in long QT syndrome - Implications for estimation of disease prevalence and molecular diagnostics
Authors: Piippo, K Swan, H Pasternack, M Chapman, H Paavonen, K Viitasalo, M Toivonen, L Kontula, K
Citation: K. Piippo et al., A founder mutation of the potassium channel KCNQ1 in long QT syndrome - Implications for estimation of disease prevalence and molecular diagnostics, J AM COL C, 37(2), 2001, pp. 562-568
HFE haemochromatosis gene mutations in liver transplant patients
Authors: Halme, L Melio, T Makinen, J Hockerstedt, K Farkkila, M Piippo, K Krusius, T Kontula, K
Citation: L. Halme et al., HFE haemochromatosis gene mutations in liver transplant patients, SC J GASTR, 36(8), 2001, pp. 881-885
Prevalence of Alzheimer's disease in very elderly people - A prospective neuropathological study
Authors: Polvikoski, T Sulkava, R Myllykangas, L Notkola, IL Niinisto, L Verkkoniemi, A Kainulainen, K Kontula, K Perez-Tur, J Hardy, J Haltia, M
Citation: T. Polvikoski et al., Prevalence of Alzheimer's disease in very elderly people - A prospective neuropathological study, NEUROLOGY, 56(12), 2001, pp. 1690-1696
Mutations of the cardiac ryanodine receptor (RyR2) gene in familial polymorphic ventricular tachycardia
Authors: Laitinen, PJ Brown, KM Piippo, K Swam, H Devaney, JM Brahmbhatt, B Donarum, EA Marino, M Tiso, N Viitasalo, M Toivonen, L Stephan, DA Kontula, K
Citation: Pj. Laitinen et al., Mutations of the cardiac ryanodine receptor (RyR2) gene in familial polymorphic ventricular tachycardia, CIRCULATION, 103(4), 2001, pp. 485-490
Effect of the antimalarial drug Halofantrine in the long QT syndrome due to a mutation of the cardiac sodium channel gene SCN5A
Authors: Piippo, K Holmstrom, S Swan, H Viitasalo, M Raatikka, M Toivonen, L Kontula, K
Citation: K. Piippo et al., Effect of the antimalarial drug Halofantrine in the long QT syndrome due to a mutation of the cardiac sodium channel gene SCN5A, AM J CARD, 87(7), 2001, pp. 909
No evidence for mutations of the leptin or leptin receptor genes in women with polycystic ovary syndrome
Authors: Oksanen, L Tiitinen, A Kaprio, J Koistinen, HA Karonen, SL Kontula, K
Citation: L. Oksanen et al., No evidence for mutations of the leptin or leptin receptor genes in women with polycystic ovary syndrome, MOL HUM REP, 6(10), 2000, pp. 873-876
Stanol ester margarine alone and with simvastatin lowers serum cholesterolin families with familial hypercholesterolemia caused by the FH-North Karelia mutation
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
Apolipoprotein E, cognitive function, and dementia in a general populationaged 85 years and over
Authors: Juva, K Verkkoniemi, A Viramo, P Polvikoski, T Kainulainen, K Kontula, K Sulkava, R
Citation: K. Juva et al., Apolipoprotein E, cognitive function, and dementia in a general populationaged 85 years and over, INT PSYCHOG, 12(3), 2000, pp. 379-387
C282Y mutation and type 2 diabetes - Reply
Authors: Salonen, JT Tuomainen, TP Kontula, K
Citation: Jt. Salonen et al., C282Y mutation and type 2 diabetes - Reply, BR MED J, 321(7271), 2000, pp. 1289-1289
Role of C282Y mutation in haemochromatosis gene in development of type 2 diabetes in healthy men: prospective cohort study
Authors: Salonen, JT Tuomainen, TP Kontula, K
Citation: Jt. Salonen et al., Role of C282Y mutation in haemochromatosis gene in development of type 2 diabetes in healthy men: prospective cohort study, BR MED J, 320(7251), 2000, pp. 1706-1707
The common pentanucleotide polymorphism of the3 '-untranslated region of the leptin receptor gene is associated with serum insulin levels and the risk of type 2 diabetes in non-diabetic men: a prospective case-control study
Authors: Lakka, HM Oksanen, L Tuomainen, TP Kontula, K Salonen, JT
Citation: Hm. Lakka et al., The common pentanucleotide polymorphism of the3 '-untranslated region of the leptin receptor gene is associated with serum insulin levels and the risk of type 2 diabetes in non-diabetic men: a prospective case-control study, J INTERN M, 248(1), 2000, pp. 77-83
Homozygosity for a HERG potassium channel mutation causes a severe form oflong-QT syndrome: Identification of an apparent founder mutation in the Finns
Authors: Piippo, K Laitinen, P Swan, H Toivonen, L Viitasalo, M Pasternack, M Paavonen, K Chapman, H Wann, KT Hirvela, E Sajantila, A Kontula, K
Citation: K. Piippo et al., Homozygosity for a HERG potassium channel mutation causes a severe form oflong-QT syndrome: Identification of an apparent founder mutation in the Finns, J AM COL C, 35(7), 2000, pp. 1919-1925
Cardiovascular risk factors and Alzheimer's disease: a genetic associationstudy in a population aged 85 or over
Authors: Myllykangas, L Polvikoski, T Sulkava, R Verkkoniemi, A Tienari, P Niinisto, L Kontula, K Hardy, J Haltia, M Perez-Tur, J
Citation: L. Myllykangas et al., Cardiovascular risk factors and Alzheimer's disease: a genetic associationstudy in a population aged 85 or over, NEUROSCI L, 292(3), 2000, pp. 195-198
Genome-wide scan of predisposing loci for increased diastolic blood pressure in Finnish siblings
Authors: Perola, M Kainulainen, K Pajukanta, P Terwilliger, JD Hiekkalinna, T Ellonen, P Kaprio, J Koskenvuo, M Kontula, K Peltonen, L
Citation: M. Perola et al., Genome-wide scan of predisposing loci for increased diastolic blood pressure in Finnish siblings, J HYPERTENS, 18(11), 2000, pp. 1579-1585
677 C -> T polymorphism of the methylenetetrahydrofolate reductase gene and preeclampsia
Authors: Laivuori, H Kaaja, R Ylikorkala, O Hiltunen, T Kontula, K
Citation: H. Laivuori et al., 677 C -> T polymorphism of the methylenetetrahydrofolate reductase gene and preeclampsia, OBSTET GYN, 96(2), 2000, pp. 277-280
APOE epsilon 4 does not predict mortality, cognitive decline, or dementia in the oldest old
Authors: Juva, K Verkkoniemi, A Viramo, P Polvikoski, T Kainulainen, K Kontula, K Sulkava, R
Citation: K. Juva et al., APOE epsilon 4 does not predict mortality, cognitive decline, or dementia in the oldest old, NEUROLOGY, 54(2), 2000, pp. 412-415
Genome-wide scan of obesity in Finnish sibpairs reveals linkage to chromosome Xq24
Authors: Ohman, M Oksanen, L Kaprio, J Koskenvuo, M Mustajoki, P Rissanen, A Salmi, J Kontula, K Peltonen, L
Citation: M. Ohman et al., Genome-wide scan of obesity in Finnish sibpairs reveals linkage to chromosome Xq24, J CLIN END, 85(9), 2000, pp. 3183-3190
Genetic polymorphism of platelet glycoprotein IIIa in patients with acute myocardial infarction and acute ischaemic stroke
Authors: Kekomaki, S Hamalainen, L Kauppinen-Makelin, R Palomaki, H Kaste, M Kontula, K
Citation: S. Kekomaki et al., Genetic polymorphism of platelet glycoprotein IIIa in patients with acute myocardial infarction and acute ischaemic stroke, J CARD RISK, 6(1), 1999, pp. 13-17
Testing of human homologues of murine obesity genes as candidate regions in Finnish obese sib pairs
Authors: Ohman, M Oksanen, L Kainulainen, K Janne, OA Kaprio, J Koskenvuo, M Mustajoki, P Kontula, K Peltonen, L
Citation: M. Ohman et al., Testing of human homologues of murine obesity genes as candidate regions in Finnish obese sib pairs, EUR J HUM G, 7(2), 1999, pp. 117-124
Angiotensin converting enzyme gene insertion/deletion polymorphism, angiotensinogen gene polymorphisms, family history of hypertension, and childhoodblood pressure
Authors: Taittonen, L Uhari, M Kontula, K Kainulainen, K Miettinen, H Turtinen, J Nuutinen, M
Citation: L. Taittonen et al., Angiotensin converting enzyme gene insertion/deletion polymorphism, angiotensinogen gene polymorphisms, family history of hypertension, and childhoodblood pressure, AM J HYPERT, 12(9), 1999, pp. 858-866
Risultati: 1-25 | 26-35