Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Ingo Germund"'
Autor:
Joszi Sweer, Ingo Germund, Markus Khalil, Christian Apitz, Kim ten Dam, Stefanie Wendt, Narayanswami Sreeram, Floris E.A. Udink ten Cate
Publikováno v:
International Journal of Cardiology Congenital Heart Disease, Vol 13, Iss , Pp 100475- (2023)
Background: Thyroid dysfunction may have adverse effects on Fontan hemodynamics. Data on thyroid function in pediatric Fontan patients with or without protein-losing enteropathy (PLE) are limited. Methods: This retrospective multicenter study include
Externí odkaz:
https://doaj.org/article/e36861b522a94f4cb435d730617c567e
Publikováno v:
Zeitschrift für Geburtshilfe und Neonatologie. 224:227-229
Autor:
Gerardus Bennink, Stijn S. Goossens, Narayanswami Sreeram, Ingo Germund, Floris E.A. Udink ten Cate
Publikováno v:
Echocardiography : a Journal of Cardiovascular Ultrasound and Allied Techniques, 36, 1211-1216
Echocardiography : a Journal of Cardiovascular Ultrasound and Allied Techniques, 36, 6, pp. 1211-1216
Echocardiography : a Journal of Cardiovascular Ultrasound and Allied Techniques, 36, 6, pp. 1211-1216
Contains fulltext : 208423.pdf (Publisher’s version ) (Closed access) We describe a Fontan patient with severe heart failure who was successfully treated with biventricular cardiac resynchronization therapy (CRT). Our case shows that strain imaging
Autor:
Narayanswami Sreeram, Ingo Germund, Lianne M. Geerdink, Floris E A Udink Ten Cate, Michael Huntgeburth
Publikováno v:
Cardiovascular Diagnosis and Therapy, 9, Suppl 2, pp. S326-s345
Cardiovascular Diagnosis and Therapy, 9, S326-S345. AME Publishing Company
Cardiovascular Diagnosis and Therapy, 9, S326-s345
Cardiovascular Diagnosis and Therapy, 9, S326-S345. AME Publishing Company
Cardiovascular Diagnosis and Therapy, 9, S326-s345
Contains fulltext : 215790.pdf (Publisher’s version ) (Open Access) Management of congenital heart disease (CHD) in adults (ACHD) remains an ongoing challenge due to the presence of residual hemodynamic lesions and development of ventricular dysfun
Autor:
Wolfgang Hohenfrost-Schmidt, Felix Berger, Hans-Heiner Kramer, Ingo Germund, Eva Brunnemer, Claus Neurohr, Kálmán Havasi, Bjoern Andrew Remppis, Michele D'Alto, Marius M. Hoeper, David Pittrow, Marion Delcroix, Michael Hofbeck, Christian Perings, Rhoia Neidenbach, Werner Scholtz, Tobias Lange, Oliver Distler, Gerhard-Paul Diller, Karsten Grossekreymborg, Christian Opitz, Heinrike Wilkens, Philipp Meyn, Rainer Kozlik-Feldmann, Sven Dittrich, Lina Gumbiene, Martin Claussen, Brigitte Stiller, Gabriele Riemekasten, Elena Jurevičienė, Helmut Baumgartner, Hubert Wirtz, Laura Scelsi, Cornelia Kropf-Sanchen, Attila Nemes, Leonhard Bruch, Ralf Ewert, Hans Klose, Iraklis Tsangaris, Dörte Huscher, Christian Grohé, Werner Budts, Katrin Milger-Kneidinger, Matthias Gorenflo, Dirk Skowasch, Gerd Stähler, Anton Vonk Noordegraaf, Michael Halank, Iveta Simkova, Oliver Miera, Andris Skride, Christian Apitz, Harald Kaemmerer, TC Köhler, Daniel Dumitrescu, Ingo Dähnert, Martin Koestenberger, Gerry Coghlan, Hossein Ardeschir Ghofrani, Stavros Konstantinides, Carmine Dario Vizza, Astrid E. Lammers, Stephan Rosenkranz, Martin Faehling, Ekkehard Grünig, Matthias Held, Dominik Harzheim, Georg Hansmann, Hans-Joachim Kabitz
Publikováno v:
Journal of Clinical Medicine
Volume 9
Issue 5
Journal of Clinical Medicine, Vol 9, Iss 1456, p 1456 (2020)
Journal of clinical medicine, Basel : MDPI, 2020, vol. 9, no. 5, art. no. 1456, p. [1-21]
Kaemmerer, H, Gorenflo, M, Huscher, D R, Pittrow, D, Apitz, C, Baumgartner, H, Berger, F, Bruch, L, Brunnemer, E, Budts, W, Claussen, M, Coghlan, G, Dähnert, I, D’alto, M, Delcroix, M, Distler, O, Dittrich, S, Dumitrescu, D, Ewert, R, Faehling, M, Germund, I, Ghofrani, H A, Grohé, C, Grossekreymborg, K, Halank, M, Hansmann, G, Harzheim, D, Nemes, A, Havasi, K, Held, M, Hoeper, M M, Hofbeck, M, Hohenfrost-Schmidt, W, Jurevičienė, E, Gumbienè, L, Kabitz, H-J, Klose, H, Köhler, T, Konstantinides, S, Köestenberger, M, Kozlik-Feldmann, R, Kramer, H-H, Kropf-Sanchen, C, Lammers, A, Lange, T, Meyn, P, Miera, O, Milger-Kneidinger, K, Neidenbach, R, Neurohr, C, Opitz, C, Perings, C, Remppis, B A, Riemekasten, G, Scelsi, L, Scholtz, W, Simkova, I, Skowasch, D, Skride, A, Stähler, G, Stiller, B, Tsangaris, I, Vizza, C D, Noordegraaf, A V, Wilkens, H, Wirtz, H, Diller, G-P, Grünig, E & Rosenkranz, S 2020, ' Pulmonary hypertension in adults with congenital heart disease: Real-world data from the international compera-chd registry ', Clinical Chemistry, vol. 9, no. 5, 1456 . https://doi.org/10.3390/jcm9051456
Clinical Chemistry, 9(5):1456
Volume 9
Issue 5
Journal of Clinical Medicine, Vol 9, Iss 1456, p 1456 (2020)
Journal of clinical medicine, Basel : MDPI, 2020, vol. 9, no. 5, art. no. 1456, p. [1-21]
Kaemmerer, H, Gorenflo, M, Huscher, D R, Pittrow, D, Apitz, C, Baumgartner, H, Berger, F, Bruch, L, Brunnemer, E, Budts, W, Claussen, M, Coghlan, G, Dähnert, I, D’alto, M, Delcroix, M, Distler, O, Dittrich, S, Dumitrescu, D, Ewert, R, Faehling, M, Germund, I, Ghofrani, H A, Grohé, C, Grossekreymborg, K, Halank, M, Hansmann, G, Harzheim, D, Nemes, A, Havasi, K, Held, M, Hoeper, M M, Hofbeck, M, Hohenfrost-Schmidt, W, Jurevičienė, E, Gumbienè, L, Kabitz, H-J, Klose, H, Köhler, T, Konstantinides, S, Köestenberger, M, Kozlik-Feldmann, R, Kramer, H-H, Kropf-Sanchen, C, Lammers, A, Lange, T, Meyn, P, Miera, O, Milger-Kneidinger, K, Neidenbach, R, Neurohr, C, Opitz, C, Perings, C, Remppis, B A, Riemekasten, G, Scelsi, L, Scholtz, W, Simkova, I, Skowasch, D, Skride, A, Stähler, G, Stiller, B, Tsangaris, I, Vizza, C D, Noordegraaf, A V, Wilkens, H, Wirtz, H, Diller, G-P, Grünig, E & Rosenkranz, S 2020, ' Pulmonary hypertension in adults with congenital heart disease: Real-world data from the international compera-chd registry ', Clinical Chemistry, vol. 9, no. 5, 1456 . https://doi.org/10.3390/jcm9051456
Clinical Chemistry, 9(5):1456
Introduction: Pulmonary hypertension (PH) is a common complication in patients with congenital heart disease (CHD), aggravating the natural, post-operative, or post-interventional course of the underlying anomaly. The various CHDs differ substantiall
Publikováno v:
Cardiology in the young. 30(2)
Background:Congenital heart disease is the most frequent malformation in newborns. The postoperative mortality of these patients can be assessed with the Risk Adjustment in Congenital Heart Surgery-1 (RACHS-1) score. This study evaluates whether the
Publikováno v:
Zeitschrift für Geburtshilfe und Neonatologie. 225:87-88
Die Erstvorstellung der 30-jährigen IG/0P erfolgte mit 26+1 Schwangerschaftswochen (SSW) zur weiteren Betreuung nach extern erfolgter Amniozentese und bereits molekulargenetisch gesicherter fetaler Tuberöser Sklerose (Mutation im TSC2-Gen).
Autor:
A. Udink, G. Kerst, Markus Khalil, Moritz Haustein, Michael Huntgeburth, K. Ten, B. Tanke, P. Koopman, L. Tjwa, Ingo Germund, L. Duijnhouwer, Christian Apitz, A. Helbing, U. Herberg, Konrad Brockmeier, Narayanswami Sreeram
Publikováno v:
51st Annual Meeting German Society for Pediatric Cardiology.
Autor:
B. Tanke, A. Udink, P. Koopman, Christian Apitz, Ingo Germund, Markus Khalil, A. Helbing, G. Kerst, Moritz Haustein, Michael Huntgeburth, Narayanswami Sreeram, Konrad Brockmeier, K. Ten, L. Duijnhouwer, U. Herberg
Publikováno v:
51st Annual Meeting German Society for Pediatric Cardiology.
Autor:
Christian Apitz, Tobias Hannes, Ingo Germund, Narayanswami Sreeram, Konrad Brockmeier, Floris E.A. Udink ten Cate, Markus Khalil, Michael Huntgeburth
Publikováno v:
Heart. 102:1115-1119
Objective A standardised diagnostic definition of protein-losing enteropathy (PLE) in Fontan patients serves both patient care and research. The present study determined whether a diagnostic definition of PLE was routinely used in published clinical