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The ‘Survivorship Passport’ for childhood cancer survivors

European journal of cancer (1990), 2018-10, Vol.102, p.69-81

2018

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Creating a unique, multi-stakeholder Paediatric Oncology Platform to improve drug development for children and adolescents with cancer

European journal of cancer (1990), 2015-01, Vol.51 (2), p.218-224

2015

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The SIOPE strategic plan: A European cancer plan for children and adolescents

Journal of cancer policy, 2016-06, Vol.8, p.17-32

2016

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Abstract 2219: The European Paediatric Oncology off-patent medicines Consortium (EPOC) pharmacokinetic/pharmacodynamic study of doxorubicin

Cancer research (Chicago, Ill.), 2013-04, Vol.73 (8_Supplement), p.2219-2219

2013

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Psychosoziale Unterstützung von Patienten und ihren Angehörigen

Pädiatrische Hämatologie und Onkologie, p.1070-1076

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WO SIND SHAKESPEARES SCHWESTERN HEUTE? EIN VERGLEICH AMERIKANISCHER UND DEUTSCHER DRAMATIKERINNEN DER GEGENWART. (GERMAN TEXT) (WOMEN)

BODE, GERLIND EMMA

1984

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ProQuest

Postpartum hormones oxytocin and prolactin cause pro-arrhythmic prolongation of cardiac repolarization in long QT syndrome type 2

Europace (London, England), 2019-07, Vol.21 (7), p.1126-1138

2019

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Transgenic LQT2, LQT5, and LQT2‐5 rabbit models with decreased repolarisation reserve for prediction of drug‐induced ventricular arrhythmias

British journal of pharmacology, 2020-08, Vol.177 (16), p.3744-3759

2020

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Pronounced effects of HERG-blockers E-4031 and erythromycin on APD, spatial APD dispersion and triangulation in transgenic long-QT type 1 rabbits

PloS one, 2014-09, Vol.9 (9), p.e107210-e107210

2014

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Oxytocin exerts harmful cardiac repolarization prolonging effects in drug-induced LQTS

International journal of cardiology. Heart & vasculature, 2022-06, Vol.40, p.101001-101001, Article 101001

2022

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Spatial correlation of action potential duration and diastolic dysfunction in transgenic and drug-induced LQT2 rabbits

Heart rhythm, 2013-10, Vol.10 (10), p.1533-1541

2013

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A novel LMNA nonsense mutation causes two distinct phenotypes of cardiomyopathy with high risk of sudden cardiac death in a large five-generation family

Europace (London, England), 2018-12, Vol.20 (12), p.2003-2013

2018

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Electro-mechanical (dys-)function in long QT syndrome type 1

International journal of cardiology, 2019-01, Vol.274, p.144-151

2019

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Abstract 15529: Transgenic Short QT Syndrome Type 1 Rabbits (HERG-N588K) Mimic the Human Phenotype with Shortened Cardiac Repolarization, Ventricular Fibrillation, and Sudden Death

Circulation (New York, N.Y.), 2014-11, Vol.130 (suppl_2)

2014

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Differential Effects of the [beta]-Adrenoceptor Blockers Carvedilol and Metoprolol on SQT1- and SQT2-Mutant Channels

Journal of cardiovascular electrophysiology, 2013-10, Vol.24 (10), p.1163

2013

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Differential Effects of the β-Adrenoceptor Blockers Carvedilol and Metoprolol on SQT1- and SQT2-Mutant Channels

Journal of cardiovascular electrophysiology, 2013-10, Vol.24 (10), p.1163-1171

2013

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Pharmacological Activation of Kv11.1 in Transgenic Long QT-1 Rabbits

Journal of cardiovascular pharmacology, 2011-02, Vol.57 (2), p.223-230

2011

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Pronounced Effects of HERG-Blockers E-4031 and Erythromycin on APD, Spatial APD Dispersion and Triangulation in Transgenic Long-QT Type 1 Rabbits: e107210

PloS one, 2014-09, Vol.9 (9)

2014

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The ‘Survivorship Passport’ for childhood cancer survivors

Creating a unique, multi-stakeholder Paediatric Oncology Platform to improve drug development for children and adolescents with cancer

The SIOPE strategic plan: A European cancer plan for children and adolescents

Abstract 2219: The European Paediatric Oncology off-patent medicines Consortium (EPOC) pharmacokinetic/pharmacodynamic study of doxorubicin

Psychosoziale Unterstützung von Patienten und ihren Angehörigen

WO SIND SHAKESPEARES SCHWESTERN HEUTE? EIN VERGLEICH AMERIKANISCHER UND DEUTSCHER DRAMATIKERINNEN DER GEGENWART. (GERMAN TEXT) (WOMEN)

Transgenic short-QT syndrome 1 rabbits mimic the human disease phenotype with QT/action potential duration shortening in the atria and ventricles and increased ventricular tachycardia/ventricular fibrillation inducibility

Postpartum hormones oxytocin and prolactin cause pro-arrhythmic prolongation of cardiac repolarization in long QT syndrome type 2

Transgenic LQT2, LQT5, and LQT2‐5 rabbit models with decreased repolarisation reserve for prediction of drug‐induced ventricular arrhythmias

Pronounced effects of HERG-blockers E-4031 and erythromycin on APD, spatial APD dispersion and triangulation in transgenic long-QT type 1 rabbits

Oxytocin exerts harmful cardiac repolarization prolonging effects in drug-induced LQTS

Spatial correlation of action potential duration and diastolic dysfunction in transgenic and drug-induced LQT2 rabbits

A novel LMNA nonsense mutation causes two distinct phenotypes of cardiomyopathy with high risk of sudden cardiac death in a large five-generation family

Electro-mechanical (dys-)function in long QT syndrome type 1

Abstract 15529: Transgenic Short QT Syndrome Type 1 Rabbits (HERG-N588K) Mimic the Human Phenotype with Shortened Cardiac Repolarization, Ventricular Fibrillation, and Sudden Death

Differential Effects of the [beta]-Adrenoceptor Blockers Carvedilol and Metoprolol on SQT1- and SQT2-Mutant Channels

Differential Effects of the β-Adrenoceptor Blockers Carvedilol and Metoprolol on SQT1- and SQT2-Mutant Channels

Pharmacological Activation of Kv11.1 in Transgenic Long QT-1 Rabbits

Pronounced Effects of HERG-Blockers E-4031 and Erythromycin on APD, Spatial APD Dispersion and Triangulation in Transgenic Long-QT Type 1 Rabbits: e107210

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