Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Julia Schwemmlein"'
Publikováno v:
Current Heart Failure Reports. 19:27-37
Purpose of Review We review therapeutic approaches aimed at restoring function of the failing heart by targeting mitochondrial reactive oxygen species (ROS), ion handling, and substrate utilization for adenosine triphosphate (ATP) production. Recent
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::11261e38d62bb6d1038b063baed5ddce
https://doi.org/10.1007/s11897-022-00539-0
https://doi.org/10.1007/s11897-022-00539-0
Autor:
Leticia Prates Roma, Anna-Florentine Schiuma, Kai Schuh, Martin van der Laan, Jan Dudek, Julia Schwemmlein, Sarah Atighetchi, Michael Böhm, Edoardo Bertero, Christopher Carlein, Andreas Müller, Carolin Brune, Peter Rehling, Markus Hoth, Andrey Kazakov, Michaela Kuhn, Mathias Hohl, Christoph Maack, Ulrich Laufs, Michael Kohlhaas, Vasco Sequeira, Ilona Kutschka, Marco Abeßer, Kai Münker, Alexander Nickel, Reinhard Kappl, Karina von der Malsburg, Alexander von der Malsburg
Publikováno v:
Circulation. 144:1694-1713
Background: Barth syndrome (BTHS) is caused by mutations of the gene encoding tafazzin, which catalyzes maturation of mitochondrial cardiolipin and often manifests with systolic dysfunction during early infancy. Beyond the first months of life, BTHS
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3dc7d7ca51902412ab37f2eea26fcb04
https://doi.org/10.1161/circulationaha.121.053755
https://doi.org/10.1161/circulationaha.121.053755
Autor:
Edoardo, Bertero, Alexander, Nickel, Michael, Kohlhaas, Mathias, Hohl, Vasco, Sequeira, Carolin, Brune, Julia, Schwemmlein, Marco, Abeßer, Kai, Schuh, Ilona, Kutschka, Christopher, Carlein, Kai, Münker, Sarah, Atighetchi, Andreas, Müller, Andrey, Kazakov, Reinhard, Kappl, Karina, von der Malsburg, Martin, van der Laan, Anna-Florentine, Schiuma, Michael, Böhm, Ulrich, Laufs, Markus, Hoth, Peter, Rehling, Michaela, Kuhn, Jan, Dudek, Alexander, von der Malsburg, Leticia, Prates Roma, Christoph, Maack
Publikováno v:
Circulation. 144(21)
Barth syndrome (BTHS) is caused by mutations of the gene encoding tafazzin, which catalyzes maturation of mitochondrial cardiolipin and often manifests with systolic dysfunction during early infancy. Beyond the first months of life, BTHS cardiomyopat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::bcf43f159d12506e4114c3628bb70e29
https://pubmed.ncbi.nlm.nih.gov/34648376
https://pubmed.ncbi.nlm.nih.gov/34648376