Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Päivi Pietilä‐Effati"'
Autor:
Pauli Pöyhönen, MD, MSc, Jukka Lehtonen, MD, Diana Velikanova, MD, Piia Simonen, MD, Valtteri Uusitalo, MD, Henriikka Mälkönen, MD, Hanna-Kaisa Nordenswan, MD, Tapani Vihinen, MD, Kari Kaikkonen, MD, Petri Haataja, MD, Tuomas Kerola, MD, Tuomas T. Rissanen, MD, Ville Vepsäläinen, MD, Aleksi Alatalo, MD, Päivi Pietilä-Effati, MD, Markku Kupari, MD
Publikováno v:
JACC: Advances, Vol 3, Iss 8, Pp 101102- (2024)
Background: Cardiac sarcoidosis (CS) is a rare but potentially fatal inflammatory cardiomyopathy. Objectives: The authors studied temporal changes in the incidence, characteristics, and outcome of CS. Methods: A retrospective analysis was made of a 3
Externí odkaz:
https://doaj.org/article/c7bb964c04b542a38e49cb21cbde217c
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 10, Iss 5, Pp n/a-n/a (2022)
Abstract Background Fabry disease (FD) is caused by a defect in α‐galactosidase A gene (GLA) which leads to a progressive accumulation of neutral shingolipids, mainly globotriaosylceramide and its metabolites in several organs. Pulmonary manifesta
Externí odkaz:
https://doaj.org/article/a76af33e41124870bcbce2226ec05a2e
Autor:
Hanna‐Kaisa Nordenswan, Jukka Lehtonen, Kaj Ekström, Anne Räisänen‐Sokolowski, Mikko I. Mäyränpää, Tapani Vihinen, Heikki Miettinen, Kari Kaikkonen, Petri Haataja, Tuomas Kerola, Tuomas T. Rissanen, Jorma Kokkonen, Aleksi Alatalo, Päivi Pietilä‐Effati, Seppo Utriainen, Markku Kupari
Publikováno v:
Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, Vol 10, Iss 6 (2021)
Background Cardiac sarcoidosis (CS) and giant cell myocarditis (GCM) share many histopathologic and clinical features. Whether they are parts of a one‐disease continuum has been discussed. Methods and Results We compared medical record data of 351
Externí odkaz:
https://doaj.org/article/e721c88217914129ba138dfcbf50dd48
Autor:
Päivi Pietilä‐Effati, Jukka T. Saarinen, Eliisa Löyttyniemi, Reijo Autio, Maria Saarenhovi, Maria K. Haanpää, Ilkka Kantola
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 7, Iss 10, Pp n/a-n/a (2019)
Abstract Background Fabry disease is caused by a deficient or an absent alfa‐galactosidase A activity and is an X‐linked disorder that results in organ damage and a shortened life span, especially in males. The severity of the disease depends on
Externí odkaz:
https://doaj.org/article/ebce6fa440654d8e89d6a8989064dcfe
Autor:
Hanna-Kaisa Nordenswan, Pauli Pöyhönen, Jukka Lehtonen, Kaj Ekström, Valtteri Uusitalo, Meri Niemelä, Tapani Vihinen, Kari Kaikkonen, Petri Haataja, Tuomas Kerola, Tuomas T. Rissanen, Aleksi Alatalo, Päivi Pietilä-Effati, Markku Kupari
Publikováno v:
Circulation. 146:964-975
Background: Cardiac sarcoidosis (CS) predisposes to sudden cardiac death (SCD). Guidelines for implantable cardioverter defibrillators (ICDs) in CS have been issued by the Heart Rhythm Society in 2014 and the American College of Cardiology/American H
Autor:
Päivi Pietilä‐Effati, Jukka T. Saarinen, Eliisa Löyttyniemi, Maria Saarenhovi, Reijo Autio, Ilkka Kantola
Publikováno v:
American Journal of Medical Genetics Part A.
Autor:
Mehdi Namdar, Albert Hagège, Eloisa Arbustini, Päivi Pietilä-Effati, Aleš Linhart, Roberto Barriales-Villa, Peter Nordbeck, Johanna Kuusisto, Iacopo Olivotto, Antonia Camporeale, Andreja Cokan Vujkovac, Perry M. Elliott, Maurizio Pieroni, James C. Moon
Publikováno v:
Journal of the American College of Cardiology. 77:922-936
Fabry disease (FD) is a rare X-linked inherited lysosomal storage disorder caused by deficient α-galactosidase A activity that leads to an accumulation of globotriasylceramide (Gb3) in affected tissues, including the heart. Cardiovascular involvemen
Autor:
Päivi Pietilä-Effati, Mathias Höglund, Aki Käräjämäki, Filip Höglund, Anne-Maria Nabb, Eija Matila, M. Juhani Koistinen
Publikováno v:
Scandinavian cardiovascular journal : SCJ. 56(1)
Cardiac resynchronization therapy (CRT) reduces the morbidity and mortality in advanced heart failure (HF) in about two-thirds of the patients. Approximately one-third of the patients do not respond to CRT. The overactivity of sympathetic nervous sys
Autor:
Tuomas Kerola, Piia Simonen, Kaj Ekström, Kari S. Kaikkonen, Tuomas T. Rissanen, Hanna-Kaisa Nordenswan, Heikki Miettinen, Mikko I. Mäyränpää, Markku Kupari, Aleksi Alatalo, Jorma O. Kokkonen, Riina Kandolin, Tapani Vihinen, Päivi Pietilä-Effati, Seppo Utriainen, Anne Räisänen-Sokolowski, Petri Haataja, Jukka Lehtonen
Publikováno v:
European Heart Journal. 40:3121-3128
Aims The present study was done to assess the role of sudden cardiac death (SCD) among the presenting manifestations of and fatalities from cardiac sarcoidosis (CS). Methods and results We analysed altogether 351 cases of CS presenting from year 1998
Autor:
Heikki Miettinen, Markku Kupari, Mikko I. Mäyränpää, Aleksi Alatalo, Jorma O. Kokkonen, Kaj Ekström, Anne Räisänen-Sokolowski, Päivi Pietilä-Effati, Tapani Vihinen, Hanna Kaisa Nordenswan, Tuomas T. Rissanen, Petri Haataja, Jukka Y. A. Lehtonen, Seppo Utriainen, Tuomas Kerola, Kari S. Kaikkonen
Background Cardiac sarcoidosis (CS) and giant cell myocarditis (GCM) share many histopathologic and clinical features. Whether they are parts of a one‐disease continuum has been discussed. Methods and Results We compared medical record data of 351
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4272a93af4f3b7302ddbd6f39fe28c0f
https://trepo.tuni.fi/handle/10024/131884
https://trepo.tuni.fi/handle/10024/131884