Zobrazeno 1 - 10
of 31
pro vyhledávání: '"Satu Kärkkäinen"'
Autor:
Laura Ollila, Johanna Kuusisto, Keijo Peuhkurinen, Satu Kärkkäinen, Petri Tuomainen, Maija Kaartinen, Olayinka Raheem, Bjarne Udd, Jarkko Magga, Janne Rapola, Annukka M. Lahtinen, Eero Lehtonen, Miia Holmström, Sari Kivistö, Elisabeth Widén, Markku Saksa, Tiina Heliö
Publikováno v:
Cardiogenetics, Vol 3, Iss 1, Pp e1-e1 (2013)
LMNA mutations are amongst the most important causes of familial dilated cardiomyopathy. The most important cause of arrhythmogenic right ventricular cardiomyopathy (ARVC) is desmosomal pathology. The aim of the study was to elucidate the role of LMN
Externí odkaz:
https://doaj.org/article/1ac03474f93c4cf9817d65b3387c2ae0
Autor:
Mikko Taina, Ritva Vanninen, Marja Hedman, Pekka Jäkälä, Satu Kärkkäinen, Tero Tapiola, Petri Sipola
Publikováno v:
PLoS ONE, Vol 8, Iss 11, p e79519 (2013)
BACKGROUND: Ischemic strokes without a well-defined etiology are labeled as cryptogenic, and account for 30-40% of strokes in stroke registries. The left atrial appendage (LAA) is the most typical origin for intracardiac thrombus formation when assoc
Externí odkaz:
https://doaj.org/article/2a89c1b59beb498499ef7f450befde0e
Autor:
Marko Sysi-Aho, Juha Koikkalainen, Tuulikki Seppänen-Laakso, Maija Kaartinen, Johanna Kuusisto, Keijo Peuhkurinen, Satu Kärkkäinen, Margareta Antila, Kirsi Lauerma, Eeva Reissell, Raija Jurkko, Jyrki Lötjönen, Tiina Heliö, Matej Orešič
Publikováno v:
PLoS ONE, Vol 6, Iss 1, p e15744 (2011)
Dilated cardiomyopathy (DCM), characterized by left ventricular dilatation and systolic dysfunction, constitutes a significant cause for heart failure, sudden cardiac death or need for heart transplantation. Lamin A/C gene (LMNA) on chromosome 1p12 i
Externí odkaz:
https://doaj.org/article/268eb6061f0948ca9461ace159bd6b9f
Autor:
Mikko Hakulinen, Tuomas Koivumäki, Juanita Niño Quintero, Marja Hedman, Marko Vauhkonen, Satu Kärkkäinen, Matti J. Kortelainen
Publikováno v:
Journal of Nuclear Cardiology. 25:1633-1641
Respiratory motion (RM) complicates the analysis of myocardial perfusion (MP) single-photon emission computed tomography (SPECT) images. The effects of RM on left ventricular (LV) functional variables have not been thoroughly investigated. Thoracic e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::32bc21b1b05d78cbbaf6647986f702e0
https://doi.org/10.1007/s12350-017-0844-9
https://doi.org/10.1007/s12350-017-0844-9
Autor:
Jan Fedacko, Esko Vanninen, Johanna Kuusisto, Jarkko Magga, Petri Tuomainen, Keijo Peuhkurinen, Ari Puhakka, Kati Miettinen, Satu Kärkkäinen
Publikováno v:
World Journal of Cardiovascular Diseases. :107-119
Objectives: We set out to study cardiac autonomic tone in patients with idiopathic dilated cardio-myopathy (IDC), and whether it correlates with other established markers of disease progression and patient ultimate outcome. Design: Fifty-one IDC pati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6cd4d62626e80e04046c7757c1732307
https://doi.org/10.4236/wjcd.2015.55014
https://doi.org/10.4236/wjcd.2015.55014
Autor:
Keijo Peuhkurinen, Esko Vanninen, Petri Tuomainen, Johanna Kuusisto, Kati Miettinen, Jarkko Magga, Jan Fedacko, Satu Kärkkäinen
Publikováno v:
Clinical Physiology and Functional Imaging. 34:133-137
Summary Background Atrial fibrillation (AF) is common in idiopathic dilated cardiomyopathy (IDC). We explored the clinical characteristics of IDC patients with chronic AF compared with those with sinus rhythm (SR). Methods A group of patients with ID
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::767dcd4d33f7f49ee809940c0679a05d
https://doi.org/10.1111/cpf.12075
https://doi.org/10.1111/cpf.12075
Autor:
Laura, Ollila, Kjell, Nikus, Miia, Holmström, Mikko, Jalanko, Raija, Jurkko, Maija, Kaartinen, Juha, Koskenvuo, Johanna, Kuusisto, Satu, Kärkkäinen, Eeva, Palojoki, Eeva, Reissell, Päivi, Piirilä, Tiina, Heliö
Publikováno v:
Open Heart
Objective Mutations in the LMNA gene encoding lamins A and C of the nuclear lamina are a frequent cause of cardiomyopathy accounting for 5–8% of familial dilated cardiomyopathy (DCM). Our aim was to study disease onset, presentation and progression
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c9ef7223436e2565252f6285cf7b4468
https://pubmed.ncbi.nlm.nih.gov/28123761
https://pubmed.ncbi.nlm.nih.gov/28123761
Autor:
Maija Kaartinen, Risto Kaaja, Eeva Reissell, Johanna Kuusisto, Tiina Heliö, Eeva Palojoki, Satu Kärkkäinen
Publikováno v:
European Journal of Heart Failure. 12:630-633
This retrospective case report describes 11 pregnancies in five women. All of the women were carriers of the lamin A/C gene mutation known to cause dilated cardiomyopathy, often together with atrioventricular conduction disturbances. The penetrance o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::91dd7c3358e572b1e16b373223caed27
https://doi.org/10.1093/eurjhf/hfq059
https://doi.org/10.1093/eurjhf/hfq059
Autor:
Kazuya Machida, Bernard A. Liu, Christopher M. Thompson, Haimin Zhang, Bruce J. Mayer, Kevin Dierck, G. Herma Renkema, Piers Nash, Karl Jablonowski, Kalle Saksela, Martin R. Schiller, Peter Nollau, Dong-Guk Shin, Tony Pawson, Debra K. Newman, Satu Kärkkäinen
Publikováno v:
Molecular Cell. 26:899-915
Protein tyrosine phosphorylation controls many aspects of signaling in multicellular organisms. One of the major consequences of tyrosine phosphorylation is the creation of binding sites for proteins containing Src homology 2 (SH2) domains. To profil
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e3bf9f83621cc670c68521adc9fe4a80
https://doi.org/10.1016/j.molcel.2007.05.031
https://doi.org/10.1016/j.molcel.2007.05.031
Autor:
Eija Saastamoinen, Tiina Heliö, Keijo Peuhkurinen, Seppo Parkkila, Mari Leppilampi, Markku S. Nieminen, Maija Kaartinen, Jokke Hannuksela, Satu Kärkkäinen, Pentti Nieminen
Publikováno v:
European Journal of Heart Failure. 7:103-108
Background: Hereditary hemochromatosis (HH), a common autosomal recessive disease, leads to excessive iron accumulation in some organs, including the heart. It is therefore not surprising that cardiomyopathy is one of the most severe complications of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::778d5a6d29603b719516fb0cbfce634f
https://doi.org/10.1016/j.ejheart.2004.03.007
https://doi.org/10.1016/j.ejheart.2004.03.007