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Journal of Medical Internet Research|December 16, 2014
Use of home telemonitoring to support multidisciplinary care of heart failure patients in Finland: randomized controlled trialAnna-Leena Vuorinen, Juha Leppänen, Hannu Kaijanranta, et al.
Frontiers in Cell and Developmental Biology|September 16, 2022
A heterozygous p.S143P mutation in LMNA associates with proteasome dysfunction and enhanced autophagy-mediated degradation of mutant lamins A and CGun West, Minttu Turunen, Anna Aalto, et al.
Annals of Medicine|June 15, 2007
Characterization of familial and sporadic arrhythmogenic right ventricular cardiomyopathy in FinlandMaija Kaartinen, Tiina Heliö, Annukka Lehtonen, et al.
Scientific Reports|April 13, 2019
CMR derived left ventricular septal convexity in carriers of the hypertrophic cardiomyopathy-causing MYBPC3-Q1061X mutationMika Tarkiainen, Petri Sipola, Mikko Jalanko, et al.
Journal of Cardiovascular Magnetic Resonance : Official Journal of the Society for Cardiovascular Magnetic Resonance|June 5, 2016
Cardiovascular magnetic resonance of mitral valve length in hypertrophic cardiomyopathyMika Tarkiainen, Petri Sipola, Mikko Jalanko, et al.
European Journal of Human Genetics : EJHG|March 14, 2003
Genome-wide search in Finnish families with inflammatory bowel disease provides evidence for novel susceptibility lociPaulina Paavola-Sakki, Vesa Ollikainen, Tiina Heliö, et al.
Biomedicines|June 28, 2023
The Junctophilin-2 Mutation p.(Thr161Lys) Is Associated with Hypertrophic Cardiomyopathy Using Patient-Specific iPS Cardiomyocytes and Demonstrates Prolonged Action Potential and Increased ArrhythmogenicityJoona Valtonen, Chandra Prajapati, Reeja Maria Cherian, et al.
European Journal of Heart Failure|January 12, 2005
Hereditary hemochromatosis gene (HFE) mutations C282Y, H63D and S65C in patients with idiopathic dilated cardiomyopathyJokke Hannuksela, Mari Leppilampi, Keijo Peuhkurinen, et al.
BMC Medical Genetics|August 19, 2017
Case reports of two pedigrees with recessive arrhythmogenic right ventricular cardiomyopathy associated with homozygous Thr335Ala variant in DSG2Sami Qadri, Olli Anttonen, Juho Viikilä, et al.
Annals of Medicine|June 2, 2016
Left ventricular mechanical dispersion is associated with nonsustained ventricular tachycardia in hypertrophic cardiomyopathyMikko Jalanko, Mika Tarkiainen, Petri Sipola, et al.
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