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(36) Anandakumar, Harithaa (1) Annibale, Paolo Dr. (4) Arnau Soler, Aleix Dr. (2) Bader, Michael Prof. Dr. (21) Bahr, Lina Samira Dr. (2) Bähring, Sylvia Dr. (1) Bahry, Ella Dr. (2) Barke, Niclas (1) Bartels-Klein, Eireen (2) Bartolomaeus, Hendrik (3) Bartolomaeus, Theda (4) Baumann, Elisabeth (1) Bayram, Safak (1) Begay-Müller, Valerie Dr. (2) Bernert, Carola (1) Beule, Dieter Dr. (21) Birchmeier, Walter Prof. Dr. (3) Birchmeier-Kohler, Carmen Prof. Dr. (2) Birkner, Till (3) Birol, Melissa Dr. (1) Blachut, Susanne (1) Blankenstein, Thomas Prof. Dr. (6) Blume, Alexander Dr. (2) Blüthgen, Nils (3) Bock-Bierbaum, Tobias Dr. (1) Borodina, Tatiana Dr. (4) Bouman, Brigitte Joanne (1) Braeuning, Caroline (2) Brüning, Ulrike Dr. (2) Bunse, Mario Dr. (4) Cakmak-Görür, Nese Dr. (1) Chekulaeva, Marina Dr. (1) Chen, Chia-Yu (1) Chen, Wei Prof. Dr. (1) Chu, Van Trung Dr. (2) Cibin, Penelope (1) Clauß, Julian (1) Collins, Russell Thomas Dr. (2) Conrad, Thomas Dr. (4) Coscia, Fabian Dr. (6) Crocini, Claudia Dr. (1) Dahlmann, Mathias Dr. (7) Dartsch, Josephine (1) Daumke, Oliver Prof. Dr. (6) Dechend, Ralf Priv. 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(11) (-) Spuler, Simone Prof. (12) (-) Wurmus, Ricardo (1) Bioinformatics and Omics Data Science (1) Genetik von Angeborenen Herzerkrankungen (11) Genomdiversifikation & Integrität (1) Genomics (2) Myologie (12) Pluripotent Stem Cells (1) Proteom Dynamik (1) Proteomics (1) Proteomics and Metabolomics (1) RNA Biologie und Posttranscriptionale Regulation (1) Systembiologie von Gen-regulatorischen Elementen (1) Translational Bioinformatics (1) 1992 (1) 1993 (2) 1994 (2) 1995 (1) 1996 (4) 1997 (3) 1998 (2) 1999 (2) 2002 (1) 2003 (1) 2004 (4) 2005 (4) 2006 (6) 2007 (4) 2008 (6) 2009 (6) 2010 (9) 2011 (7) 2012 (8) 2013 (7) 2014 (10) 2015 (9) 2016 (9) 2017 (7) 2018 (6) 2019 (15) 2020 (10) 2021 (14) (-) 2022 (24) 2023 (13) 2024 (1) 24 Ergebnisse: Active Filter: Klaassen, Sabine Prof. Dr. med.Spuler, Simone Prof.Wurmus, Ricardo2022 Sortieren: Treffgenauigkeit Neueste nach älteste Älteste nach neueste 10. März 2022 / Front Neurol Assessing the relationship of patient reported outcome measures with functional status in dysferlinopathy: a Rasch analysis approach A.G. Mayhew M.K. James U. Moore H. Sutherland M. Jacobs J. Feng L.P. Lowes L.N. Alfano R. Muni Lofra L.E. Rufibach K. Rose T. Duong L. Bello I. Pedrosa-Hernández S. Holsten C. Sakamoto A. Canal N. Sánchez-Aguilera Práxedes S. Thiele C. Siener B. Vandevelde B. DeWolf E. Maron H. Gordish-Dressman H. Hilsden M. Guglieri J.Y. Hogrel A.M. Blamire P.G. Carlier S. Spuler J.W. Day K.J. Jones D.X. Bharucha-Goebel E. Salort-Campana A. Pestronk M.C. Walter C. Paradas T. Stojkovic M. Mori-Yoshimura E. Bravver J. Díaz-Manera E. Pegoraro J.R. Mendell V. Straub 01. Oktober 2022 / Monatsschr Kinderheilkd Kardiomyopathie im Neugeborenenalter: Forschungsfortschritte eröffnen neue diagnostische Möglichkeiten [Cardiomyopathy in neonatal age: advances in research open up new diagnostic possibilities] M. Frenzel S. Klaassen K. Klingel W. Knirsch O. Kretschmar J. Kühnisch A. Oxenius 01. Mai 2022 / Muscle Nerve Cardiac and pulmonary findings in dysferlinopathy: a 3-year, longitudinal study U. Moore R. Fernandez-Torron M. Jacobs H. Gordish J. Diaz-Manera M.K. James A.G. Mayhew E. Harris M. Guglieri L.E. Rufibach J. Feng A.M. Blamire P.G. Carlier S. Spuler J.W. Day K.J. Jones D.X. Bharucha-Goebel E. Salort-Campana A. Pestronk M.C. Walter C. Paradas T. Stojkovic M. Mori-Yoshimura E. Bravver E. Pegoraro L.P. Lowes J.R. Mendell K. Bushby J. Bourke V. Straub 09. Mai 2022 / Sci Rep Myofibrillar protein synthesis rates are increased in chronically exercised skeletal muscle despite decreased anabolic signaling H.T. Langer D. West J. Senden S. Spuler L.J.C. van Loon K. Baar 30. März 2022 / Eur J Prev Cardiol External validation of the HCM Risk-Kids model for predicting sudden cardiac death in childhood hypertrophic cardiomyopathy G. Norrish C. Qu E. Field E. Cervi D. Khraiche S. Klaassen T.H. Ojala G. Sinagra H. Yamazawa C. Marrone A. Popoiu F. Centeno S. Schouvey I. Olivotto S.M. Day S. Colan J. Rossano S.G. Wittekind S. Saberi M. Russell A. Helms J. Ingles C. Semsarian P.M. Elliott C.Y. Ho R.Z. Omar J.P. Kaski 21. Januar 2022 / iScience 4-phenylbutyrate restores localization and membrane repair to human dysferlin mutations K. Tominaga N. Tominaga E.O. Williams L. Rufibach V. Schöwel S. Spuler M. Viswanathan L.P. Guarente 21. Dezember 2022 / Front Mol Biosci Exercise blood-drop metabolic profiling links metabolism with perceived exertion T. Opialla B. Gollasch P.H.J.L. Kuich L. Klug G. Rahn A. Busjahn S. Spuler M. Boschmann J.A. Kirwan F.C. Luft S. Kempa 02. Dezember 2022 / Int J Mol Sci LMNA co-regulated gene expression as a suitable readout after precise gene correction H. Wang A. Krause H. Escobar S. Müthel E. Metzler S. Spuler 30. Juni 2022 / J Cardiovasc Dev Dis Left ventricular noncompaction in children: the role of genetics, morphology, and function for outcome S. Klaassen J. Kühnisch A. Schultze-Berndt F. Seidel 05. Juli 2022 / J Cardiovasc Dev Dis Pathogenic variants in cardiomyopathy disorder genes underlie pediatric myocarditis - Further impact of heterozygous immune disorder gene variants? F. Seidel K.T. Laser K. Klingel J. Dartsch S. Theisen T. Pickardt M. Holtgrewe A. Gärtner F. Berger D. Beule H. Milting S. Schubert S. Klaassen J. Kühnisch Seitennummerierung Erste Seite « First Vorherige Seite ‹ Previous Seite 1 Aktuelle Seite 2 Seite 3 Nächste Seite Next › Letzte Seite Last »
10. März 2022 / Front Neurol Assessing the relationship of patient reported outcome measures with functional status in dysferlinopathy: a Rasch analysis approach A.G. Mayhew M.K. James U. Moore H. Sutherland M. Jacobs J. Feng L.P. Lowes L.N. Alfano R. Muni Lofra L.E. Rufibach K. Rose T. Duong L. Bello I. Pedrosa-Hernández S. Holsten C. Sakamoto A. Canal N. Sánchez-Aguilera Práxedes S. Thiele C. Siener B. Vandevelde B. DeWolf E. Maron H. Gordish-Dressman H. Hilsden M. Guglieri J.Y. Hogrel A.M. Blamire P.G. Carlier S. Spuler J.W. Day K.J. Jones D.X. Bharucha-Goebel E. Salort-Campana A. Pestronk M.C. Walter C. Paradas T. Stojkovic M. Mori-Yoshimura E. Bravver J. Díaz-Manera E. Pegoraro J.R. Mendell V. Straub
01. Oktober 2022 / Monatsschr Kinderheilkd Kardiomyopathie im Neugeborenenalter: Forschungsfortschritte eröffnen neue diagnostische Möglichkeiten [Cardiomyopathy in neonatal age: advances in research open up new diagnostic possibilities] M. Frenzel S. Klaassen K. Klingel W. Knirsch O. Kretschmar J. Kühnisch A. Oxenius
01. Mai 2022 / Muscle Nerve Cardiac and pulmonary findings in dysferlinopathy: a 3-year, longitudinal study U. Moore R. Fernandez-Torron M. Jacobs H. Gordish J. Diaz-Manera M.K. James A.G. Mayhew E. Harris M. Guglieri L.E. Rufibach J. Feng A.M. Blamire P.G. Carlier S. Spuler J.W. Day K.J. Jones D.X. Bharucha-Goebel E. Salort-Campana A. Pestronk M.C. Walter C. Paradas T. Stojkovic M. Mori-Yoshimura E. Bravver E. Pegoraro L.P. Lowes J.R. Mendell K. Bushby J. Bourke V. Straub
09. Mai 2022 / Sci Rep Myofibrillar protein synthesis rates are increased in chronically exercised skeletal muscle despite decreased anabolic signaling H.T. Langer D. West J. Senden S. Spuler L.J.C. van Loon K. Baar
30. März 2022 / Eur J Prev Cardiol External validation of the HCM Risk-Kids model for predicting sudden cardiac death in childhood hypertrophic cardiomyopathy G. Norrish C. Qu E. Field E. Cervi D. Khraiche S. Klaassen T.H. Ojala G. Sinagra H. Yamazawa C. Marrone A. Popoiu F. Centeno S. Schouvey I. Olivotto S.M. Day S. Colan J. Rossano S.G. Wittekind S. Saberi M. Russell A. Helms J. Ingles C. Semsarian P.M. Elliott C.Y. Ho R.Z. Omar J.P. Kaski
21. Januar 2022 / iScience 4-phenylbutyrate restores localization and membrane repair to human dysferlin mutations K. Tominaga N. Tominaga E.O. Williams L. Rufibach V. Schöwel S. Spuler M. Viswanathan L.P. Guarente
21. Dezember 2022 / Front Mol Biosci Exercise blood-drop metabolic profiling links metabolism with perceived exertion T. Opialla B. Gollasch P.H.J.L. Kuich L. Klug G. Rahn A. Busjahn S. Spuler M. Boschmann J.A. Kirwan F.C. Luft S. Kempa
02. Dezember 2022 / Int J Mol Sci LMNA co-regulated gene expression as a suitable readout after precise gene correction H. Wang A. Krause H. Escobar S. Müthel E. Metzler S. Spuler
30. Juni 2022 / J Cardiovasc Dev Dis Left ventricular noncompaction in children: the role of genetics, morphology, and function for outcome S. Klaassen J. Kühnisch A. Schultze-Berndt F. Seidel
05. Juli 2022 / J Cardiovasc Dev Dis Pathogenic variants in cardiomyopathy disorder genes underlie pediatric myocarditis - Further impact of heterozygous immune disorder gene variants? F. Seidel K.T. Laser K. Klingel J. Dartsch S. Theisen T. Pickardt M. Holtgrewe A. Gärtner F. Berger D. Beule H. Milting S. Schubert S. Klaassen J. Kühnisch