المؤلفون: FinHCM Study Grp, Jääskeläinen, Pertti, Vangipurapu, Jagadish, Raivo, Joose, Kuulasmaa, Teemu, Helio, Tiina, Aalto-Setala, Katriina, Kaartinen, Maija, Ilveskoski, Erkki, Vanninen, Sari, Hämäläinen, Liisa, Melin, John, Kokkonen, Jorma, Nieminen, Markku S., Laakso, Markku, Kuusisto, Johanna, Kervinen, Helena, Mustonen, Juha, Juvonen, Jukka, Niemi, Mari, Uusimaa, Paavo, Junttila, Juhani, Kotila, Matti, Pietila, Mikko, Jyrkila, Heini, Mahonen, Ilkka, Vartia, Paula

المساهمون: Department of Medicine, Clinicum, Kardiologian yksikkö, HUS Heart and Lung Center

مصطلحات موضوعية: Hypertrophic cardiomyopathy, Genetics, Targeted sequencing, Mutation, Mortality, Outcome, HEAVY-CHAIN GENE, ALPHA-TROPOMYOSIN, ASP175ASN MUTATION, MAGNETIC-RESONANCE, FOUNDER MUTATIONS, DISEASE, IMPAIRMENT, INSIGHTS, General medicine, internal medicine and other clinical medicine

وصف الملف: application/pdf

العلاقة: This work was supported by the Academy of Finland, the Finnish Foundation for Cardiovascular Research, and the Kuopio University Hospital (EVO grants to J.K.).; FinHCM Study Grp , Jääskeläinen , P , Vangipurapu , J , Raivo , J , Kuulasmaa , T , Helio , T , Aalto-Setala , K , Kaartinen , M , Ilveskoski , E , Vanninen , S , Hämäläinen , L , Melin , J , Kokkonen , J , Nieminen , M S , Laakso , M , Kuusisto , J , Kervinen , H , Mustonen , J , Juvonen , J , Niemi , M , Uusimaa , P , Junttila , J , Kotila , M , Pietila , M , Jyrkila , H , Mahonen , I & Vartia , P 2019 , ' Genetic basis and outcome in a nationwide study of Finnish patients with hypertrophic cardiomyopathy ' , ESC Heart Failure , vol. 6 , no. 2 , pp. 436-445 . https://doi.org/10.1002/ehf2.12420Test; http://hdl.handle.net/10138/301568Test; 6c52151a-8d97-45ef-81df-a35df5289500; 000464451900023

الإتاحة: http://hdl.handle.net/10138/301568Test

المؤلفون: Helena Kervinen, Paavo Uusimaa, Juhani Junttila, Tiina Heliö, Mari Niemi, Joose Raivo, Maija Kaartinen, John Melin, Ilkka Mahonen, Markku Laakso, Johanna Kuusisto, Liisa Hämäläinen, Heini Jyrkila, Matti Kotila, Paula Vartia, Markku S. Nieminen, Erkki Ilveskoski, Mikko Pietilä, Teemu Kuulasmaa, Jukka Juvonen, Pertti Jääskeläinen, FinHCM Study Grp, Jagadish Vangipurapu, Juha Mustonen, Sari U. M. Vanninen, Jorma Kokkonen, Katriina Aalto-Setälä

المساهمون: Department of Medicine, Clinicum, Kardiologian yksikkö, HUS Heart and Lung Center

المصدر: ESC Heart Failure

مصطلحات موضوعية: Male, medicine.medical_treatment, DNA Mutational Analysis, ASP175ASN MUTATION, TPM1, 030204 cardiovascular system & hematology, DISEASE, 0302 clinical medicine, FOUNDER MUTATIONS, Original Research Articles, MAGNETIC-RESONANCE, Original Research Article, Registries, 030212 general & internal medicine, Finland, Outcome, education.field_of_study, Hazard ratio, Hypertrophic cardiomyopathy, IMPAIRMENT, Implantable cardioverter-defibrillator, Pedigree, 3. Good health, Survival Rate, INSIGHTS, Targeted sequencing, cardiovascular system, Female, Cardiology and Cardiovascular Medicine, Sarcomeres, Heterozygote, medicine.medical_specialty, Population, 03 medical and health sciences, ALPHA-TROPOMYOSIN, Internal medicine, Genetics, medicine, Humans, cardiovascular diseases, education, business.industry, MORTALITY, Cardiomyopathy, Hypertrophic, medicine.disease, Confidence interval, HEAVY-CHAIN GENE, 3121 General medicine, internal medicine and other clinical medicine, Heart failure, Mutation, MYH7, business, Cardiac Myosins, Follow-Up Studies, Forecasting

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f890b9088a120a8e9c7462ee06ea1f6bTest
https://doi.org/10.1002/ehf2.12420Test