M. Hillebrand

发表

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

D. Mitter, D. Wieczorek, R. Abou Jamra, 2019, Genetics in Medicine.

A simple clinical model to estimate the probability of Marfan syndrome.

S. Blankenberg, J. Schmidtke, B. Keyser, 2012, QJM : monthly journal of the Association of Physicians.

Total Serum Transforming Growth Factor‐β1 Is Elevated in the Entire Spectrum of Genetic Aortic Syndromes

P. Robinson, S. Blankenberg, T. Zeller, 2014, Clinical cardiology.

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

C. Bokemeyer, S. Balabanov, W. Fiedler, 2014, PloS one.

Analysis of phenotype and genotype information for the diagnosis of Marfan syndrome

S. Blankenberg, C. Detter, J. Schmidtke, 2012, Clinical genetics.

Evaluation of microribonucleic acids as potential biomarkers in the bicuspid aortic valve-associated aortopathy.

S. Blankenberg, H. Reichenspurner, T. Zeller, 2018, Interactive cardiovascular and thoracic surgery.

The Freestyle Valve in Severe Necrotizing Aortic Root Endocarditis: Comorbidity Upon Outcome.

A. Ozga, L. Hansen, F. Riess, 2021, The Thoracic and cardiovascular surgeon.

Central pulse pressure and augmentation index in asymptomatic bicuspid aortic valve disease.

P. Robinson, H. Hense, H. Schunkert, 2011, International journal of cardiology.

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

P. Robinson, S. Blankenberg, J. Schmidtke, 2014, Orphanet Journal of Rare Diseases.

The Value of Circulating Biomarkers in Bicuspid Aortic Valve-Associated Aortopathy

C. Detter, L. Conradi, A. Bernhardt, 2016, The Thoracic and Cardiovascular Surgeon.

Ascending aortic aneurysm and aortic valve dysfunction in bicuspid aortic valve disease.

P. Robinson, C. Detter, S. Willems, 2013, International Journal of Cardiology.

The Application of Clinical Genetics Dovepress Perspectives on the Revised Ghent Criteria for the Diagnosis of Marfan Syndrome

P. Robinson, S. Blankenberg, A. Bernhardt, 2022 .

FBN1 gene mutation characteristics and clinical features for the prediction of mitral valve disease progression.

P. Robinson, C. Detter, B. Hoffmann, 2013, International Journal of Cardiology.

Diagnostic accuracy study of routine echocardiography for bicuspid aortic valve: a retrospective study and meta-analysis.

S. Blankenberg, C. Detter, A. Bernhardt, 2017, Cardiovascular diagnosis and therapy.

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

D. Mitter, D. Wieczorek, R. Abou Jamra, 2019, Genetics in Medicine.

Percutaneous left atrial unloading to prevent pulmonary oedema and to facilitate ventricular recovery under extracorporeal membrane oxygenation therapy.

S. Blankenberg, E. Lubos, A. Bernhardt, 2018, Interactive cardiovascular and thoracic surgery.

Predictors of outcome of mitral valve prolapse in patients with the Marfan syndrome.

P. Robinson, T. Meinertz, A. Bernhardt, 2011, The American journal of cardiology.

Perspectives on the revised Ghent criteria for the diagnosis of Marfan syndrome

S. Blankenberg, A. Bernhardt, K. Püschel, 2015 .

The Application of Clinical Genetics Dovepress Perspectives on the Revised Ghent Criteria for the Diagnosis of Marfan Syndrome

P. Robinson, S. Blankenberg, A. Bernhardt, 2022 .

Mitral valve prolapse syndrome and MASS phenotype: Stability of aortic dilatation but progression of mitral valve prolapse☆

S. Blankenberg, K. Kutsche, B. Keyser, 2016, International journal of cardiology. Heart & vasculature.

FBN1 gene mutation characteristics and clinical features for the prediction of mitral valve disease progression.

P. Robinson, C. Detter, B. Hoffmann, 2013, International journal of cardiology.