Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Krista Heliö"'
Publikováno v:
BMC Cardiovascular Disorders, Vol 23, Iss 1, Pp 1-5 (2023)
Abstract Background Primary tumors of the heart are a rare phenomenon. Lymphatic malformations are congenital anomalies of the lymphatic system that tend to grow progressively. Lymphatic malformations are typically found in the cervical and axillary
Externí odkaz:
https://doaj.org/article/c2fbee5bfb42480abbc6ade4f760b9f7
Autor:
Krista Heliö, Marcos Cicerchia, Julie Hathaway, Johanna Tommiska, Johanna Huusko, Inka Saarinen, Lotta Koskinen, Mikko Muona, Ville Kytölä, Janica Djupsjöbacka, Massimiliano Gentile, Pertteli Salmenperä, Tero-Pekka Alastalo, Christian Steinberg, Tiina Heliö, Jussi Paananen, Samuel Myllykangas, Juha Koskenvuo
Publikováno v:
Frontiers in Cardiovascular Medicine, Vol 10 (2023)
BackgroundFamilial dilated cardiomyopathy (DCM) causes heart failure and may lead to heart transplantation. DCM is typically a monogenic disorder with autosomal dominant inheritance. Currently disease-causing variants have been reported in over 60 ge
Externí odkaz:
https://doaj.org/article/ff822a1fa0e341c99b73042e74defdfd
Autor:
Krista Heliö, Eveliina Brandt, Satu Vaara, Sini Weckström, Liisa Harjama, Riina Kandolin, Johanna Järviö, Katariina Hannula-Jouppi, Tiina Heliö, Miia Holmström, Juha W. Koskenvuo
Publikováno v:
Frontiers in Cardiovascular Medicine, Vol 10 (2023)
BackgroundPathogenic variants in DSP associate with cardiac and cutaneous manifestations including arrhythmogenic right ventricular cardiomyopathy, dilated cardiomyopathy, curly or wavy hair, and palmoplantar keratoderma (PPK). Episodes of myocardial
Externí odkaz:
https://doaj.org/article/acb68496b6f44932b464562c1ecf086a
Autor:
Julie Hathaway, Krista Heliö, Inka Saarinen, Jonna Tallila, Eija H. Seppälä, Sari Tuupanen, Hannu Turpeinen, Tiia Kangas-Kontio, Jennifer Schleit, Johanna Tommiska, Ville Kytölä, Miko Valori, Mikko Muona, Johanna Sistonen, Massimiliano Gentile, Pertteli Salmenperä, Samuel Myllykangas, Jussi Paananen, Tero-Pekka Alastalo, Tiina Heliö, Juha Koskenvuo
Publikováno v:
BMC Cardiovascular Disorders, Vol 21, Iss 1, Pp 1-11 (2021)
Abstract Background Genetic testing in hypertrophic cardiomyopathy (HCM) is a published guideline-based recommendation. The diagnostic yield of genetic testing and corresponding HCM-associated genes have been largely documented by single center studi
Externí odkaz:
https://doaj.org/article/1a8328a56c1a4010ae5eb9b873a650f5
Autor:
Krista Heliö, Tiia Kangas-Kontio, Sini Weckström, Sari U. M. Vanninen, Katriina Aalto-Setälä, Tero-Pekka Alastalo, Samuel Myllykangas, Tiina M. Heliö, Juha W. Koskenvuo
Publikováno v:
BMC Medical Genetics, Vol 21, Iss 1, Pp 1-10 (2020)
Abstract Background Dilated cardiomyopathy (DCM) is a condition characterized by dilatation and systolic dysfunction of the left ventricle in the absence of severe coronary artery disease or abnormal loading conditions. Mutations in the titin (TTN) a
Externí odkaz:
https://doaj.org/article/3b5599019431428285de3a23f7339742
Autor:
Krista Heliö, Mikko I. Mäyränpää, Inka Saarinen, Saija Ahonen, Heidi Junnila, Johanna Tommiska, Sini Weckström, Miia Holmström, Mia Toivonen, Kjell Nikus, Julie Hathaway, Pauli Siivonen, Mikko Muona, Johanna Sistonen, Pertteli Salmenperä, Massimiliano Gentile, Jussi Paananen, Samuel Myllykangas, Tero-Pekka Alastalo, Tiina Heliö, Juha Koskenvuo
Publikováno v:
Frontiers in Genetics, Vol 12 (2021)
Background: Familial dilated cardiomyopathy (DCM) is a monogenic disorder typically inherited in an autosomal dominant pattern. We have identified two Finnish families with familial cardiomyopathy that is not explained by a variant in any previously
Externí odkaz:
https://doaj.org/article/1aa59acef3044845853059e28698c9e3
Autor:
Juha W Koskenvuo, Inka Saarinen, Saija Ahonen, Johanna Tommiska, Sini Weckström, Eija H Seppälä, Sari Tuupanen, Tiia Kangas-Kontio, Jennifer Schleit, Krista Heliö, Julie Hathaway, Anders Gummesson, Pia Dahlberg, Tiina H Ojala, Ville Vepsäläinen, Ville Kytölä, Mikko Muona, Johanna Sistonen, Pertteli Salmenperä, Massimiliano Gentile, Jussi Paananen, Samuel Myllykangas, Tero-Pekka Alastalo, Tiina Heliö
Publikováno v:
PLoS ONE, Vol 16, Iss 2, p e0245681 (2021)
BackgroundFamilial dilated cardiomyopathy (DCM) is typically a monogenic disorder with dominant inheritance. Although over 40 genes have been linked to DCM, more than half of the patients undergoing comprehensive genetic testing are left without mole
Externí odkaz:
https://doaj.org/article/81628bdf5aaa4625b9953c9f6ecf95db
Autor:
Krista Heliö, Julie Hathaway, Marcos Cicerchia, Johanna Tommiska, Johanna Huusko, Inka Saarinen, Lotta Koskinen, Mikko Muona, Ville Kytölä, Janica Djupsjobacka, Massimiliano Gentile, Pertteli Salmenperä, Tero-Pekka Alastalo, Tiina Heliö, Jussi Paananen, Samuel Myllykangas, Juha Koskenvuo
Publikováno v:
Heart Rhythm. 20:S246-S247
Autor:
Jonna Tallila, Johanna Tommiska, Samuel Myllykangas, Inka Saarinen, Krista Heliö, Pertteli Salmenperä, Eija H. Seppälä, Johanna Sistonen, Tero-Pekka Alastalo, Massimiliano Gentile, Tiina Heliö, Tiia Kangas-Kontio, Jennifer Schleit, Sari Tuupanen, Jussi Paananen, Juha W. Koskenvuo, Miko Valori, Ville Kytola, Hannu Turpeinen, Mikko Muona, Julie Hathaway
Publikováno v:
BMC Cardiovascular Disorders, Vol 21, Iss 1, Pp 1-11 (2021)
BMC Cardiovascular Disorders
BMC Cardiovascular Disorders
BackgroundGenetic testing in hypertrophic cardiomyopathy (HCM) is a published guideline-based recommendation. The diagnostic yield of genetic testing and corresponding HCM-associated genes have been largely documented by single center studies and car
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6d184e5436f5dd41a871cbeaa2fbb7fd
http://hdl.handle.net/10138/329626
http://hdl.handle.net/10138/329626
Autor:
Samuel Myllykangas, Julie Hathaway, Pia Dahlberg, Tero-Pekka Alastalo, Sini Weckström, Krista Heliö, Saija Ahonen, Tiia Kangas-Kontio, Mikko Muona, Massimiliano Gentile, Pertteli Salmenperä, Eija H. Seppälä, Sari Tuupanen, Tiina Heliö, Johanna Sistonen, Johanna Tommiska, Juha W. Koskenvuo, Inka Saarinen, Jennifer Schleit, Tiina Ojala, Ville Kytola, Ville Vepsäläinen, Anders Gummesson, Jussi Paananen
Publikováno v:
PLoS ONE
PLoS ONE, Vol 16, Iss 2, p e0245681 (2021)
PLoS ONE, Vol 16, Iss 2, p e0245681 (2021)
Background Familial dilated cardiomyopathy (DCM) is typically a monogenic disorder with dominant inheritance. Although over 40 genes have been linked to DCM, more than half of the patients undergoing comprehensive genetic testing are left without mol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ba81c9e7cc43c22f62715634c74af463
http://hdl.handle.net/10138/329668
http://hdl.handle.net/10138/329668