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Cardiomyocyte maturation alters molecular stress response capacities and determines cell survival upon mitochondrial dysfunction

Free radical biology & medicine, 2024-03, Vol.213, p.248-265

2024

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A Specific IFIH1 Gain-of-Function Mutation Causes Singleton-Merten Syndrome

American journal of human genetics, 2015-02, Vol.96 (2), p.275-282

2015

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Single Ostium of the Right and Left Coronary Artery From the Right Pulmonary Artery

The Annals of thoracic surgery, 2018-02, Vol.105 (2), p.e67-e69

2018

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Inhibition of mitochondrial respiration has fundamentally different effects on proliferation, cell survival and stress response in immature versus differentiated cardiomyocyte cell lines

Frontiers in cell and developmental biology, 2022-09, Vol.10, p.1011639-1011639

2022

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Way of Planning a Complex Interventional Treatment with Support of a 3-Dimensional Printed Heart Model in a Patient with Interrupted Aortic Arch Type A

Pediatric cardiology, 2023-03, Vol.44 (3), p.732-735

2023

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Cardiac CT in the Preoperative Diagnostics of Neonates with Congenital Heart Disease: Radiation Dose Optimization by Omitting Test Bolus or Bolus Tracking

Academic radiology, 2020-05, Vol.27 (5), p.e102-e108

2020

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Valve-Sparing Aortic Root Replacement in an 8-Month-Old Infant With Loeys-Dietz Syndrome

The Annals of thoracic surgery, 2019-05, Vol.107 (5), p.e321-e323

2019

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Heart transplantation surgery in children and young adults with congenital heart disease

Journal of cardiothoracic surgery, 2023-11, Vol.18 (1), p.1-342, Article 342

2023

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Ventricular assist devices in paediatric cardiomyopathy and congenital heart disease: An analysis of the German National Register for Congenital Heart Defects

International journal of cardiology, 2021-11, Vol.343, p.37-44

2021

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Extubation in the Operating Room After Fontan Procedure: Does It Make a Difference?

Pediatric cardiology, 2019-03, Vol.40 (3), p.468-476

2019

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Against all odds—late repair of multiple shunt lesions in a patient with Down syndrome: a case report

European heart journal : case reports, 2021-07, Vol.5 (7)

2021

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Multiple giant cell lesions in patients with Noonan syndrome and cardio-facio-cutaneous syndrome

European journal of human genetics : EJHG, 2009-04, Vol.17 (4), p.420-425

2009

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Cardiomyopathy in congenital disorders of glycosylation

Cardiology in the young, 2003-08, Vol.13 (4), p.345-351

2003

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Images in cardiovascular medicine. Life-threatening neonatal arrhythmia: successful treatment and confirmation of clinically suspected extreme long QT-syndrome-3

Circulation (New York, N.Y.), 2004-05, Vol.109 (18), p.e205-e206

2004

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Should All Stage-One Norwood Patients Receive a Prolonged Period of Postoperative Mechanical Circulatory Support?

The Annals of thoracic surgery, 2005-03, Vol.79 (3), p.1098-1099

2005

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Prediction of prognosis in patients with tetralogy of Fallot based on deep learning imaging analysis

Heart (British Cardiac Society), 2020-07, Vol.106 (13), p.1007-1014

2020

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Long-term single-center experience of defibrillator therapy in children and adolescents

International journal of cardiology, 2018-11, Vol.271, p.105-108

2018

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Singleton–Merten syndrome: An autosomal dominant disorder with variable expression

American journal of medical genetics. Part A, 2013-02, Vol.161 (2), p.360-370

2013

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Impact of Right Ventricular Pressure Load After Repair of Tetralogy of Fallot

Journal of the American Heart Association, 2022-04, Vol.11 (7), p.e022694-e022694

2022

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German Registry for Cardiac Operations and Interventions in Patients with Congenital Heart Disease: Report 2020-Comprehensive Data from 6 Years of Experience

The Thoracic and cardiovascular surgeon, 2021-12, Vol.69 (S 03), p.e21-e31

2021

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A Defect in Dolichol Phosphate Biosynthesis Causes a New Inherited Disorder with Death in Early Infancy

American journal of human genetics, 2007-03, Vol.80 (3), p.433-440

2007

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Stenting of Native Right Ventricular Outflow Tract Obstructions in Symptomatic Infants

Journal of interventional cardiology, 2015-06, Vol.28 (3), p.279-287

2015

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Life-Threatening Neonatal Arrhythmia: Successful Treatment and Confirmation of Clinically Suspected Extreme Long QT-Syndrome-3

Circulation (New York, N.Y.), 2004-05, Vol.109 (18)

2004

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Severe transient myocardial ischaemia caused by hypertrophic cardiomyopathy in a patient with congenital disorder of glycosylation type Ia

European journal of pediatrics, 2002-10, Vol.161 (10), p.524-527

2002

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Cardiomyocyte maturation alters molecular stress response capacities and determines cell survival upon mitochondrial dysfunction

A Specific IFIH1 Gain-of-Function Mutation Causes Singleton-Merten Syndrome

Single Ostium of the Right and Left Coronary Artery From the Right Pulmonary Artery

Inhibition of mitochondrial respiration has fundamentally different effects on proliferation, cell survival and stress response in immature versus differentiated cardiomyocyte cell lines

Way of Planning a Complex Interventional Treatment with Support of a 3-Dimensional Printed Heart Model in a Patient with Interrupted Aortic Arch Type A

Cardiac CT in the Preoperative Diagnostics of Neonates with Congenital Heart Disease: Radiation Dose Optimization by Omitting Test Bolus or Bolus Tracking

Valve-Sparing Aortic Root Replacement in an 8-Month-Old Infant With Loeys-Dietz Syndrome

Heart transplantation surgery in children and young adults with congenital heart disease

Ventricular assist devices in paediatric cardiomyopathy and congenital heart disease: An analysis of the German National Register for Congenital Heart Defects

Extubation in the Operating Room After Fontan Procedure: Does It Make a Difference?

Against all odds—late repair of multiple shunt lesions in a patient with Down syndrome: a case report

Multiple giant cell lesions in patients with Noonan syndrome and cardio-facio-cutaneous syndrome

Cardiomyopathy in congenital disorders of glycosylation

Images in cardiovascular medicine. Life-threatening neonatal arrhythmia: successful treatment and confirmation of clinically suspected extreme long QT-syndrome-3

Should All Stage-One Norwood Patients Receive a Prolonged Period of Postoperative Mechanical Circulatory Support?

Prediction of prognosis in patients with tetralogy of Fallot based on deep learning imaging analysis

Long-term single-center experience of defibrillator therapy in children and adolescents

Singleton–Merten syndrome: An autosomal dominant disorder with variable expression

Impact of Right Ventricular Pressure Load After Repair of Tetralogy of Fallot

German Registry for Cardiac Operations and Interventions in Patients with Congenital Heart Disease: Report 2020-Comprehensive Data from 6 Years of Experience

A Defect in Dolichol Phosphate Biosynthesis Causes a New Inherited Disorder with Death in Early Infancy

Stenting of Native Right Ventricular Outflow Tract Obstructions in Symptomatic Infants

Fetoneonatale Lunge

Life-Threatening Neonatal Arrhythmia: Successful Treatment and Confirmation of Clinically Suspected Extreme Long QT-Syndrome-3

Severe transient myocardial ischaemia caused by hypertrophic cardiomyopathy in a patient with congenital disorder of glycosylation type Ia

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