Zobrazeno 1 - 10
of 46
pro vyhledávání: '"Rhoia, Neidenbach"'
Autor:
Alina Gansterer, Paula Moliterno, Rhoia Neidenbach, Caroline Ollerieth, Sarah Czernin, Juergen Scharhag, Kurt Widhalm
Publikováno v:
JMIR Pediatrics and Parenting, Vol 7, Pp e50289-e50289 (2024)
Abstract BackgroundCOVID-19 mitigation measures enhanced increases in children’s weight and BMI due to decreased physical activity and increased energy intake. Overweight and obesity were major worldwide problems before the pandemic, and COVID-19
Externí odkaz:
https://doaj.org/article/bf6aaa1617a74b06b1238c791ba4076b
Autor:
Sebastian Freilinger, Caroline Andonian, Jürgen Beckmann, Peter Ewert, Harald Kaemmerer, Nora Lang, Nicole Nagdyman, Renate Oberhoffer-Fritz, Lars Pieper, Jörg Schelling, Fabian von Scheidt, Rhoia Neidenbach
Publikováno v:
International Journal of Cardiology Congenital Heart Disease, Vol 4, Iss , Pp 100185- (2021)
Background: Although there is sufficient evidence that sex-/gender-based differences can influence treatment decisions and healthcare for adults with congenital heart disease (ACHD), there are major research shortfalls in this regard. The aim of this
Externí odkaz:
https://doaj.org/article/4d6d319ed6ee4751a20d52fe27c18f42
Autor:
Rhoia Neidenbach, Sebastian Freilinger, Fabian Stöcker, Peter Ewert, Nicole Nagdyman, Renate Oberhoffer-Fritz, Lars Pieper, Harald Kaemmerer, Alfred Hager
Publikováno v:
Cardiovascular Diagnosis and Therapy. 13:11-24
Autor:
Fabian Stöcker, Rhoia Neidenbach, Celina Fritz, Renate M. Oberhoffer, Peter Ewert, Alfred Hager, Nicole Nagdyman
Publikováno v:
Frontiers in Pediatrics, Vol 7 (2019)
Introduction: As survival of previously considered as lethal congenital heart disease forms is the case in our days, issues regarding quality of life including sport and daily activities emerge. In patients with Fontan circulation, there is no pump t
Externí odkaz:
https://doaj.org/article/be88d5db44ba4cf6ab0f17d736116b0f
Autor:
Gideon Marchie du Sarvaas, Rolf M. F. Berger, Alfred Hager, Graziella Eshuis, Julia Hock, Hiske van Duinen, Hans L. Hillege, Rhoia Neidenbach, Freek van den Heuvel
Publikováno v:
Heart, 108(3), 186-193. BMJ PUBLISHING GROUP
ObjectivesThis study aimed to provide a perspective for the interpretation of exercise capacity (peakVO2) in patients with repaired Tetralogy of Fallot (patients with rTOF) by describing the course of peakVO2from patients aged 6–63 years.MethodsA r
Autor:
Harald Kaemmerer, Sebastian Freilinger, Rhoia Neidenbach, Stephan Achenbach, Caroline Andonian, Peter Ewert, Fokko de Haan, Nicole Nagdyman, Jörg Schelling, Michael Hofbeck, Ulrike Bauer, Michael Huntgeburth, Thomas Meinertz
Publikováno v:
Der Internist. 63:95-102
Autor:
Michael Huntgeburth, Sebastian Freilinger, Peter Ewert, Christopher Hohmann, Nicole Nagdyman, Harald Kaemmerer, Lars Pieper, Felix Pieringer, Christof Kolb, Carsten Lennerz, Rhoia Neidenbach
Publikováno v:
Cardiovasc Diagn Ther
BACKGROUND: Patients with congenital heart defects (CHD) are prone to residua, sequels and complications from the underlying anomaly, where cardiac arrhythmias are one of the major causes for hospitalization, morbidity and mortality. The importance o
Autor:
Caroline Andonian, Jörg Schelling, Peter Ewert, Rhoia Neidenbach, Nicole Nagdyman, Michael Huntgeburth, Sebastian Freilinger, Harald Kaemmerer
Publikováno v:
DMW - Deutsche Medizinische Wochenschrift. 146:1192-1199
Currently, due to medical advances, more than 500 000 patients with congenital heart defects (CHD) are living in Germany, including more than 330 000 adults. In CHD, the aspect of transition from childhood and adolescence to adulthood is becoming inc
Autor:
Paul C. Helm, Harald Kaemmerer, Günter Breithardt, Elisabeth J. Sticker, Roland Keuchen, Rhoia Neidenbach, Gerhard-Paul Diller, Oktay Tutarel, Ulrike M. M. Bauer
Publikováno v:
Frontiers in Pediatrics, Vol 5 (2017)
BackgroundA growing number of adults with congenital heart disease (ACHD) pose a particular challenge for health care systems across the world. Upon turning into 18 years, under the German national health care system, ACHD patients are required to sw
Externí odkaz:
https://doaj.org/article/ee47cd1acf154feaaeecbe1692b1515f
Autor:
Attila Nemes, Lars Pieper, Ann-Sophie Kaemmerer, Nicole Nagdyman, Kathrin Nebel, Kálmán Havasi, Sebastian Freilinger, Rhoia Neidenbach, Peter Ewert, Lavinia Seidel, Caroline Andonian
Publikováno v:
Cardiovasc Diagn Ther
Background All patients with congenital heart disease (CHD) are chronically ill from their cardiac disease. Despite the increasing evidence that aortic alterations are becoming relevant, the importance of aortopathy in CHD has long been underestimate