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Mathias Hillebrand

University of Hamburg

19

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290

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Next-generation sequencing of 32 genes associated with hereditary aortopathies and related disorders of connective tissue in a cohort of 199 patients

2019 Genetics in Medicine
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Percutaneous left atrial unloading to prevent pulmonary oedema and to facilitate ventricular recovery under extracorporeal membrane oxygenation therapy

2018 Interactive Cardiovascular and Thoracic Surgery
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Evaluation of microribonucleic acids as potential biomarkers in the bicuspid aortic valve-associated aortopathy

2018 Interactive Cardiovascular and Thoracic Surgery
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Therapie der bikuspiden Aortenklappenerkrankung

2016
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Mitral valve prolapse syndrome and MASS phenotype: stability of aortic dilatation but progression of mitral valve prolapse

2016 IJC Heart & Vasculature
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Perspectives on the revised Ghent criteria for the diagnosis of Marfan syndrome

2015 The application of clinical genetics
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The main pulmonary artery in adults: a controlled multicenter study with assessment of echocardiographic reference values, and the frequency of dilatation and aneurysm in Marfan syndrome

2014 Orphanet Journal of Rare Diseases
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Total serum transforming growth factor-β1 is elevated in the entire spectrum of genetic aortic syndromes.

2014 Clinical Cardiology
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Overexpression of Gremlin-1 in Patients with Loeys-Dietz Syndrome: Implications on Pathophysiology and Early Disease Detection

2014 PLOS ONE
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Ascending aortic aneurysm and aortic valve dysfunction in bicuspid aortic valve disease

2013 International Journal of Cardiology
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