Y. von Kodolitsch

发表

Expanding the clinical spectrum of COL2A1 related disorders by a mass like phenotype

G. Rosenberger, C. Kubisch, M. Hempel, 2022, Scientific Reports.

Systemic Endothelial Dysfunction as an Early Predictor of Adverse Outcome in Heart Failure

T. Meinertz, V. Rudolph, S. Baldus, 2005, Arteriosclerosis, thrombosis, and vascular biology.

Comparison of aortic root replacement in patients with Marfan syndrome.

H. Reichenspurner, T. Meinertz, A. Bernhardt, 2011, European journal of cardio-thoracic surgery : official journal of the European Association for Cardio-thoracic Surgery.

Diagnosis and management of Marfan syndrome.

P. Robinson, C. Detter, Y. von Kodolitsch, 2008, Future cardiology.

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.

Pregnancy in adults with congenital heart disease.

S. Blankenberg, C. Sinning, C. Rickers, 2019, Cardiovascular diagnosis and therapy.

Improving medical care and prevention in adults with congenital heart disease-reflections on a global problem-part II: infective endocarditis, pulmonary hypertension, pulmonary arterial hypertension and aortopathy.

S. Achenbach, T. Meinertz, M. Weyand, 2018, Cardiovascular diagnosis and therapy.

Induction of Macrophage Chemotaxis by Aortic Extracts from Patients with Marfan Syndrome Is Related to Elastin Binding Protein

P. Robinson, R. Hetzer, S. Doelken, 2011, PloS one.

Case-matched Comparison of Cardiovascular Outcome in Loeys-Dietz Syndrome versus Marfan Syndrome

S. Blankenberg, C. Detter, K. Kutsche, 2019, Journal of clinical medicine.

Pediatric Patients with Marfan Syndrome: Frequency of Dural Ectasia and its Correlation with Common Cardiovascular Manifestations

T. Derlin, T. Bley, T. Mir, 2013, Fortschritte auf dem Gebiet der Röntgenstrahlen und der bildgebenden Verfahren.

Results of Modern Mitral Valve Repair in Patients with Marfan Syndrome

C. Detter, H. Reichenspurner, A. Bernhardt, 2013, Thoracic and Cardiovascular Surgeon.

The spectrum of syndromes and manifestations in individuals screened for suspected Marfan syndrome

P. Robinson, C. Detter, T. Meinertz, 2008, American journal of medical genetics. Part A.

Warfarin anticoagulation in acute type A aortic dissection survivors (WATAS).

S. Blankenberg, C. Detter, H. Reichenspurner, 2017, Cardiovascular diagnosis and therapy.

European reference network for rare vascular diseases (VASCERN) consensus statement for the screening and management of patients with pathogenic ACTA2 variants

E. Arbustini, J. Timmermans, B. Mulder, 2019, Orphanet Journal of Rare Diseases.

Non-contrast MR angiography at 1.5 Tesla for aortic monitoring in Marfan patients after aortic root surgery

G. Adam, T. Bley, P. Bannas, 2017, Journal of Cardiovascular Magnetic Resonance.

Comparison of Cine-MRI and Transthoracic Echocardiography for the Assessment of Aortic Root Diameters in Patients with Suspected Marfan Syndrome

T. Derlin, G. Adam, J. Yamamura, 2015, Fortschritte auf dem Gebiet der Röntgenstrahlen und der bildgebenden Verfahren.

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.

A standardized education protocol significantly reduces traumatic injuries and syncope recurrence: an observational study in 316 patients with vasovagal syncope.

S. Willems, B. Hoffmann, D. Steven, 2012, Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology.

Complete Antegrade Transapical Deployment of a Branched Aortic Arch Endograft

C. Detter, T. Kölbel, E. Debus, 2016, Journal of endovascular therapy : an official journal of the International Society of Endovascular Specialists.

Marfan Syndrome Versus Bicuspid Aortic Valve Disease: Comparative Analysis of Obstetric Outcome and Pregnancy-Associated Immediate and Long-Term Aortic Complications

S. Blankenberg, K. Hecher, C. Sinning, 2020, Journal of clinical medicine.

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.

Heart failure in adults with congenital heart disease: a narrative review.

P. Kirchhof, S. Blankenberg, C. Sinning, 2020, Cardiovascular diagnosis and therapy.

Anticoagulation management in adult patients with congenital heart disease: a narrative review.

P. Kirchhof, S. Blankenberg, G. Diller, 2020, Cardiovascular diagnosis and therapy.

Outcome of pregnancy in a contemporary cohort of adults with congenital heart disease-a 10-year, single-center experience.

P. Kirchhof, S. Blankenberg, K. Hecher, 2021, Cardiovascular diagnosis and therapy.

Improving medical care and prevention in adults with congenital heart disease-reflections on a global problem-part I: development of congenital cardiology, epidemiology, clinical aspects, heart failure, cardiac arrhythmia.

S. Achenbach, T. Meinertz, M. Weyand, 2018, Cardiovascular diagnosis and therapy.

Management of Ascending Aorta and Aortic Arch: Similarities and Differences Among Cardiovascular Guidelines

C. Detter, T. Athanasiou, T. Kölbel, 2021, Journal of endovascular therapy : an official journal of the International Society of Endovascular Specialists.

Therapeutic management of patients with Marfan syndrome: focus on cardiovascular involvement.

C. Nienaber, Y. Kodolitsch, Y. von Kodolitsch, 1999, Cardiology in review.

Endovascular Repair of Ascending Aortic Pathologies With Tubular Endografts: A Single-Center Experience

C. Detter, F. Rohlffs, N. Tsilimparis, 2019, Journal of endovascular therapy : an official journal of the International Society of Endovascular Specialists.

Emergency Use of Branched Thoracic Endovascular Repair in the Treatment of Aortic Arch Pathologies.

C. Detter, F. Rohlffs, Y. Law, 2019, The Annals of thoracic surgery.

Branched Endografts in the Aortic Arch Following Open Repair for Debakey Type I Aortic Dissection

C. Detter, S. Debus, F. Rohlffs, 2018, The Thoracic and Cardiovascular Surgeon.

High-density oligonucleotide-based resequencing assay for mutations causing syndromic and non-syndromic forms of thoracic aortic aneurysms and dissections.

M. Bonin, B. Keyser, M. Stuhrmann, 2013, Molecular and cellular probes.

Magnetic resonance angiography derived predictors of progressive dilatation and surgery of the aortic root in Marfan syndrome

G. Schön, B. Schoennagel, P. Bannas, 2022, PloS one.

Genetic diagnostics of inherited aortic diseases

K. Kutsche, Y. von Kodolitsch, Prof. Dr. med. Y. von Kodolitsch, 2017, Herz.

Marfan syndrome and the evolving spectrum of heritable thoracic aortic disease: do we need genetics for clinical decisions?

P. Robinson, H. Reichenspurner, T. Meinertz, 2010, VASA. Zeitschrift fur Gefasskrankheiten.

Retrospective analysis of the effect of angiotensin II receptor blocker versus β-blocker on aortic root growth in paediatric patients with Marfan syndrome

T. Mir, Y. von Kodolitsch, J. Weil, 2013, Heart.

Unravelling the Pathogenetic Mechanisms in Congenital Aortopathies: Need for an Integrative Translational Approach

H. Kaemmerer, E. Girdauskas, Y. von Kodolitsch, 2020, Journal of clinical medicine.

Chest radiography for the diagnosis of acute aortic syndrome.

C. Nienaber, V. Nicolas, T. Meinertz, 2004, The American journal of medicine.

[Intramural hemorrhage of the thoracic aorta].

C. Nienaber, V. Nicolas, A. Haverich, 1998, RoFo : Fortschritte auf dem Gebiete der Rontgenstrahlen und der Nuklearmedizin.

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.

I-SWOT as instrument to individually optimize therapy of thoracoabdominal aortic aneurysms

C. Detter, C. R. Blankart, E. Girdauskas, 2017, Gefässchirurgie.

International Registry of Patients Carrying TGFBR1 or TGFBR2 Mutations: Results of the MAC (Montalcino Aortic Consortium).

S. Lemaire, R. Jeremy, D. Milewicz, 2016, Circulation. Cardiovascular genetics.

The importance of genetic testing in the clinical management of patients with Marfan syndrome and related disorders.

J. Schmidtke, Y. von Kodolitsch, M. Arslan‐Kirchner, 2008, Deutsches Arzteblatt international.

Economic and care considerations of Marfan syndrome

C. R. Blankart, H. Schüler, Y. von Kodolitsch, 2016, Expert review of pharmacoeconomics & outcomes research.

Indomethacin Prevents the Progression of Thoracic Aortic Aneurysm in Marfan Syndrome Mice

P. Robinson, C. Ott, B. Muñóz-García, 2013, AORTA.

Antagonism of GxxPG fragments ameliorates manifestations of aortic disease in Marfan syndrome mice.

P. Robinson, C. Ott, P. Knaus, 2013, Human molecular genetics.

Bicuspid aortic valve and aortic coarctation in congenital heart disease-important aspects for treatment with focus on aortic vasculopathy.

S. Blankenberg, C. Sinning, C. Rickers, 2018, Cardiovascular diagnosis and therapy.

Comprehensive analysis of dural ectasia in 150 patients with a causative FBN1 mutation

S. Blankenberg, K. Kutsche, B. Keyser, 2014, Clinical genetics.

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

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

The transition of pediatric Marfan patients to adult care: a challenge and its risks.

T. Mir, R. Kozlik-Feldmann, J. Olfe, 2018, Cardiovascular diagnosis and therapy.

Clinical prediction of acute aortic dissection.

C. Nienaber, Y. Kodolitsch, Y. von Kodolitsch, 2000, Archives of internal medicine.

Single‐center experience with an inner branched arch endograft

C. Detter, S. Debus, F. Rohlffs, 2019, Journal of vascular surgery.

Branched versus fenestrated endografts for endovascular repair of aortic arch lesions.

C. Detter, F. Rohlffs, N. Tsilimparis, 2016, Journal of vascular surgery.

Intramural Hematoma of the Aorta: Predictors of Progression to Dissection and Rupture

C. Nienaber, R. Fattori, T. Meinertz, 2003, Circulation.

[Meta-analysis of the prognosis of thoracic aortic dissection: changing mortality in the last four decades].

C. Nienaber, Y. von Kodolitsch, 1992, Herz.

Proximal aortic dissection late after aortic valve surgery: 119 cases of a distinct clinical entity.

C. Nienaber, A. Haverich, Y. von Kodolitsch, 2000, The Thoracic and cardiovascular surgeon.

[Increased serum concentration of myosin heavy chain in aortic dissection: discussion of 2 cases].

Y. Yazaki, C. Nienaber, T. Meinertz, 1997, Zeitschrift fur Kardiologie.

Predictors of aneurysmal formation after surgical correction of aortic coarctation.

C. Nienaber, M. A. Aydin, T. Meinertz, 2002, Journal of the American College of Cardiology.

Diagnostic imaging of aortic diseases

C. Nienaber, Y. Kodolitsch, Y. von Kodolitsch, 1997, Der Radiologe.

Arrhythmia and impaired myocardial function in heritable thoracic aortic disease: An international retrospective cohort study.

A. Evangelista, A. Pini, G. Jondeau, 2022, European journal of medical genetics.

Late post-AVR progression of bicuspid aortopathy: link to hemodynamics

H. Reichenspurner, E. Girdauskas, Y. von Kodolitsch, 2017, General Thoracic and Cardiovascular Surgery.

Prognosis of early pre-discharge and late left ventricular dilatation by cardiac magnetic resonance imaging after acute myocardial infarction

G. Adam, S. Blankenberg, M. Saeed, 2021, The International Journal of Cardiovascular Imaging.

Lessons from the short- and mid-term outcome of medical rehabilitation in adults with congenital heart disease.

J. Beckmann, R. Oberhoffer, P. Ewert, 2021, Cardiovascular diagnosis and therapy.

A multi-institutional experience in vascular Ehlers-Danlos syndrome diagnosis.

P. Byers, D. Milewicz, D. Coleman, 2019, Journal of vascular surgery.

A multi-institutional experience in the aortic and arterial pathology in individuals with genetically confirmed vascular Ehlers-Danlos syndrome.

P. Byers, D. Milewicz, D. Coleman, 2019, Journal of vascular surgery.

Vascular type Ehlers-Danlos syndrome is associated with platelet dysfunction and low vitamin D serum concentration

C. Germer, B. Hartung, S. Hoffjan, 2016, Orphanet Journal of Rare Diseases.

Concomitant cardiovascular malformations in isolated bicuspid aortic valve disease: a retrospective cross-sectional study and meta-analysis

S. Blankenberg, G. Schön, K. Szöcs, 2022, Cardiovascular diagnosis and therapy.

Aortic aneurysms after correction of aortic coarctation: a systematic review.

H. Reichenspurner, T. Meinertz, Y. Kodolitsch, 2010, VASA. Zeitschrift fur Gefasskrankheiten.

Congenital heart disease in the ESC EORP Registry of Pregnancy and Cardiac disease (ROPAC)

Prague, K. Sliwa, A. Dirir, 2021 .

Pregnancy Outcomes in Women After Arterial Switch Operation for Transposition of the Great Arteries: Results From ROPAC (Registry of Pregnancy and Cardiac Disease) of the European Society of Cardiology EURObservational Research Programme

K. Sliwa, A. Dirir, S. Blankenberg, 2020, Journal of the American Heart Association.

Tricuspid valve prolapse as an early predictor for severe phenotype in children with Marfan syndrome

T. Mir, J. Olfe, Y. von Kodolitsch, 2022, Acta paediatrica.

Diagnosis of Thoracic Aortic Dissection: Magnetic Resonance Imaging Versus Transesophageal Echocardiography

W Bleifeld, C. Nienaber, V. Nicolas, 1992, Circulation.

Endovascular Treatment of Aortic Pathologies in Patients With Marfan Syndrome: Single-Center Experience

C. Detter, S. Debus, F. Rohlffs, 2021, Journal of endovascular therapy : an official journal of the International Society of Endovascular Specialists.

Safety and Effectiveness of TEVAR in Native Proximal Landing Zone 2 for Chronic Type B Aortic Dissection in Patients With Genetic Aortic Syndrome

F. Rohlffs, T. Kölbel, Y. von Kodolitsch, 2021, Journal of endovascular therapy : an official journal of the International Society of Endovascular Specialists.

Sleep apnea predicts cardiovascular death in patients with Marfan syndrome: a cohort study

S. Willems, C. Eickholt, E. Debus, 2022, EPMA Journal.

[Intramural hemorrhage of the thoracic aorta: diagnosis, therapy and prognosis of 209 in vivo diagnosed cases].

C. Nienaber, Y. von Kodolitsch, 1998, Zeitschrift fur Kardiologie.

[Ulcer of the thoracic aorta: diagnosis, therapy and prognosis].

C. Nienaber, Y. von Kodolitsch, 1998, Zeitschrift fur Kardiologie.

Assessment of aortic diameter in Marfan patients: intraindividual comparison of 3D-Dixon and 2D-SSFP magnetic resonance imaging

B. Schoennagel, P. Bannas, S. Sehner, 2022, European Radiology.

Simplified frozen elephant trunk technique for combined open and endovascular treatment of extensive aortic diseases.

C. Detter, H. Reichenspurner, E. Vettorazzi, 2019, European journal of cardio-thoracic surgery : official journal of the European Association for Cardio-thoracic Surgery.

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

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

HTAD patient pathway: Strategy for diagnostic work-up of patients and families with (suspected) heritable thoracic aortic diseases (HTAD) a statement from the HTAD working group of VASCERN.

J. Timmermans, M. Groenink, A. Evangelista, 2022, European journal of medical genetics.

Maximizing therapeutic success: The key concepts of individualized medical strategy (IMS)

C. Detter, H. Reichenspurner, A. Bernhardt, 2015 .

Augmentation index and the evolution of aortic disease in marfan-like syndromes.

P. Robinson, M. A. Aydin, T. Meinertz, 2010, American Journal of Hypertension.

Splice-site mutations in atherosclerosis candidate genes: relating individual information to phenotype.

R. Pyeritz, P. Rogan, Y. Kodolitsch, 1999, Circulation.

Features of Marfan syndrome not listed in the Ghent nosology – the dark side of the disease

R. Pyeritz, S. Morris, E. Neptune, 2019, Expert review of cardiovascular therapy.

The first systematic definition of Marfan syndrome (MFS) was the so-called Berlin criteria1 of 1986. After the discovery of FBN1 as the disease-causing gene for MFS in 1991,2 the criteria

K. Thorsen, M. Gaustadnes, C. Gravholt, 2019 .

Evaluating the quality of Marfan genotype–phenotype correlations in existing FBN1 databases

K. Thorsen, M. Gaustadnes, C. Gravholt, 2016, Genetics in Medicine.

Periodontal conditions in patients with Marfan syndrome – a multicenter case control study

B. Kahl-Nieke, W. Geurtsen, O. Bauss, 2013, BMC oral health.

Dural ectasia in individuals with Marfan‐like features but exclusion of mutations in the genes FBN1, TGFBR1 and TGFBR2

T. Meinertz, B. Keyser, J. Berger, 2011, Clinical genetics.

Dural ectasia in Loeys–Dietz syndrome: comprehensive study of 30 patients with a TGFBR1 or TGFBR2 mutation

S. Blankenberg, K. Kutsche, B. Keyser, 2014, Clinical genetics.

[Vascular surgery in the elderly : What is possible? What is reasonable?]

C. Behrendt, E. Debus, N. Tsilimparis, 2017, Der Chirurg; Zeitschrift fur alle Gebiete der operativen Medizen.

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.

Genotype–Phenotype Correlation in Children: The Impact of FBN1 Variants on Pediatric Marfan Care

F. Kortüm, K. Kutsche, T. Mir, 2020, Genes.

Clustering of mutations associated with mild Marfan-like phenotypes in the 3' region of FBN1 suggests a potential genotype-phenotype correlation.

P. Robinson, T. Rosenberg, C. Nienaber, 2000, American journal of medical genetics.

Diseases of the aorta.

C. Nienaber, Y. Kodolitsch, Y. von Kodolitsch, 1998, Cardiology clinics.

Severe eczema and Hyper-IgE in Loeys-Dietz-syndrome - contribution to new findings of immune dysregulation in connective tissue disorders.

L. Notarangelo, J. Walter, S. Ehl, 2014, Clinical immunology.

Identification of 29 novel and nine recurrent fibrillin‐1 (FBN1) mutations and genotype–phenotype correlations in 76 patients with Marfan syndrome

K. Rommel, M. Karck, J. Schmidtke, 2005, Human mutation.

Ten-year follow up after autologous rectus abdominis fascia sheath patch repair of aortic root abscess.

T. Meinertz, T. Münzel, Y. von Kodolitsch, 2004, The Journal of heart valve disease.

The spectrum of syndromes and manifestations in individuals screened for suspected Marfan syndrome

P. Robinson, C. Detter, T. Meinertz, 2008, American journal of medical genetics. Part A.

Predictors of proximal aortic dissection at the time of aortic valve replacement.

C. Nienaber, A. Haverich, Y. Kodolitsch, 1999, Circulation.

Kid-Short Marfan Score (Kid-SMS) Is a Useful Diagnostic Tool for Stratifying the Pre-Test Probability of Marfan Syndrome in Childhood

F. Arndt, T. Mir, R. Kozlik-Feldmann, 2015, Diseases.

The diagnosis of thoracic aortic dissection by noninvasive imaging procedures.

C. Nienaber, V. Nicolas, R. Spielmann, 1993, The New England journal of medicine.

Prospective risk stratification of sudden cardiac death in Marfan's syndrome.

S. Willems, B. Hoffmann, D. Steven, 2013, International journal of cardiology.

Frequency of sleep apnea in adults with the Marfan syndrome.

P. Robinson, T. Meinertz, A. Bernhardt, 2010, The American journal of cardiology.

Aortic valve repair in adult congenital heart disease.

C. Sinning, C. Rickers, J. Sachweh, 2018, Cardiovascular diagnosis and therapy.

Supportive care needs of patients with rare chronic diseases: multi-method, cross-sectional study

B. Löwe, V. Mautner, H. Klose, 2021, Orphanet Journal of Rare Diseases.

The role of the multidisciplinary health care team in the management of patients with Marfan syndrome

S. Blankenberg, C. Detter, R. Pyeritz, 2016, Journal of multidisciplinary healthcare.

Nonsurgical reconstruction of thoracic aortic dissection by stent-graft placement.

C. Nienaber, R. Fattori, V. Nicolas, 1999, The New England journal of medicine.

Expression Patterns of Circulating MicroRNAs in the Risk Stratification of Bicuspid Aortopathy

T. Zeller, E. Girdauskas, Y. von Kodolitsch, 2020, Journal of clinical medicine.

Inpatient rehabilitation for adult patients with Marfan syndrome: an observational pilot study

J. Lechinger, E. Hoberg, Y. von Kodolitsch, 2017, Orphanet Journal of Rare Diseases.

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

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

Observational Cohort Study of Ventricular Arrhythmia in Adults with Marfan Syndrome Caused by FBN1 Mutations

P. Robinson, S. Blankenberg, C. Detter, 2013, PloS one.

Intramural hemorrhage of the thoracic aorta. Diagnostic and therapeutic implications.

C. Nienaber, R. Spielmann, A. Haverich, 1995, Circulation.

Marfan syndrome: an update of genetics, medical and surgical management

P. Robinson, Peter N Robinson, Y. von Kodolitsch, 2007, Heart.

Chronic type B aortic dissection: indications and strategies for treatment.

F. Rohlffs, N. Tsilimparis, T. Kölbel, 2015, The Journal of cardiovascular surgery.

Acute Type A Aortic Dissection Treated Using a Tubular Stent-Graft in the Ascending Aorta and a Multibranched Stent-Graft in the Aortic Arch

C. Detter, F. Rohlffs, N. Tsilimparis, 2017, Journal of endovascular therapy : an official journal of the International Society of Endovascular Specialists.

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 .

4D flow cardiovascular magnetic resonance for monitoring of aortic valve repair in bicuspid aortic valve disease

H. Kooijman, G. Adam, B. Schoennagel, 2020, Journal of Cardiovascular Magnetic Resonance.

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.

The economic impact of Marfan syndrome: a non-experimental, retrospective, population-based matched cohort study

T. Stargardt, Y. von Kodolitsch, R. Linder, 2014, Orphanet Journal of Rare Diseases.

Morphologic and Functional Markers of Aortopathy in Patients With Bicuspid Aortic Valve Insufficiency Versus Stenosis.

T. Kuntze, M. Borger, E. Girdauskas, 2017, The Annals of thoracic surgery.

Guideline for the Treatment of Thoracic Aortic Dissection Type A: Summary of the S2k Guideline

H. von Tengg-Kobligk, H. Eggebrecht, M. Czerny, 2022, The Thoracic and Cardiovascular Surgeon.

Myocardial Function, Heart Failure and Arrhythmia in Marfan Syndrome: A Systematic Literature Review

J. De Backer, Y. von Kodolitsch, A. Demolder, 2020, Diagnostics.

Frequency and age-related course of mitral valve dysfunction in the Marfan syndrome.

P. Robinson, T. Meinertz, A. Bernhardt, 2010, American Journal of Cardiology.

Current and Emerging Imaging Techniques in Patients with Genetic Aortic Syndromes Aktuelle Bildgebungs-Strategien bei genetisch bedingten Erkrankungen der Aorta

G. Adam, P. Bannas, E. Girdauskas, 2019, RöFo - Fortschritte auf dem Gebiet der Röntgenstrahlen und der bildgebenden Verfahren.

Analysis of Strengths, Weaknesses, Opportunities, and Threats as a Tool for Translating Evidence into Individualized Medical Strategies (I-SWOT)

P. Robinson, C. Detter, S. Debus, 2015, AORTA.

Risk factors for impaired neurological outcome after thoracic aortic surgery

C. Detter, E. Vettorazzi, T. Kölbel, 2021, Journal of thoracic disease.

Ambulatory (24 h) blood pressure and arterial stiffness measurement in Marfan syndrome patients: a case control feasibility and pilot study

Y. von Kodolitsch, S. Wassertheurer, B. Hametner, 2016, BMC Cardiovascular Disorders.

Does statin therapy impact the proximal aortopathy in aortic valve disease?

T. Kuntze, E. Girdauskas, Y. von Kodolitsch, 2018, QJM : monthly journal of the Association of Physicians.

New Advances in Endovascular Therapy

C. Detter, S. Debus, F. Rohlffs, 2016, Journal of endovascular therapy : an official journal of the International Society of Endovascular Specialists.

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.

Tissue Doppler imaging identifies myocardial dysfunction in adults with marfan syndrome

Olaf Franzen, Jürgen Berger, M. A. Aydin, 2007, Clinical cardiology.

Augmentation index relates to progression of aortic disease in adults with Marfan syndrome.

Stephan Willems, Rodolfo Ventura, Olaf Franzen, 2009, American journal of hypertension.

Current diagnosis and management of late complications in adult congenital heart disease.

K. Niwa, H. Kaemmerer, Y. von Kodolitsch, 2021, Cardiovascular diagnosis and therapy.

Assessment of aortic root dimensions in patients with suspected Marfan syndrome: intraindividual comparison of contrast-enhanced and non-contrast magnetic resonance angiography with echocardiography.

G. Adam, P. Bannas, Y. von Kodolitsch, 2013, International journal of cardiology.

Body Image in Patients with Marfan Syndrome

L. B. Hansen, Y. von Kodolitsch, D. Benninghoven, 2020, Journal of clinical medicine.

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.

Coronary artery anomalies Part II: recent insights from clinical investigations.

T. Meinertz, O. Franzen, Y. von Kodolitsch, 2005, Zeitschrift fur Kardiologie.

Open repair of an aortic aneurysm in a patient with Loeys-Dietz syndrome using Gore hybrid vascular branch grafts

G. Daum, N. Tsilimparis, T. Kölbel, 2015, Journal of vascular surgery cases.

Three-dimensional color Doppler echocardiography for assessing shunt volume in atrial septal defects.

T. Meinertz, O. Franzen, Y. von Kodolitsch, 2004, Journal of the American Society of Echocardiography : official publication of the American Society of Echocardiography.

Markers of Lipid Metabolism Do Not Correlate with the Expression of Aortopathy in Patients with Bicuspid Aortic Valve Disease.

T. Kuntze, A. Bernhardt, E. Girdauskas, 2016, The Journal of heart valve disease.

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.

The CatLet score: a new coronary angiographic scoring tool accommodating the variable coronary anatomy for the first time.

M. Desai, P. Schoenhagen, T. Ruddy, 2019, Journal of thoracic disease.

Aortopathy in Bicuspid Aortic Valve Stenosis with Fusion of Right-Left versus Right-Non-Coronary Cusps: Are These Different Diseases?

T. Kuntze, I. Petersen, M. Borger, 2016, The Journal of heart valve disease.

[Marfan syndrome: prevalence and natural course of cardiovascular manifestations].

M. Raghunath, C. Nienaber, Y. von Kodolitsch, 1998, Zeitschrift für Kardiologie.

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

P. Robinson, S. Blankenberg, A. Bernhardt, 2015, The application of clinical genetics.

[Aortic valve replacement as an independent predictive factor for later development of aortic dissection].

C. Nienaber, T. Bregenzer, A. Haverich, 1998, Zeitschrift fur Kardiologie.

Intraindividual comparison of 1.5 T and 3 T non-contrast MR angiography for monitoring of aortic root diameters in Marfan patients.

G. Adam, J. Salamon, P. Bannas, 2021, International journal of cardiology.

Reliability of non-contrast magnetic resonance angiography-derived aortic diameters in Marfan patients: comparison of inner vs. outer vessel wall measurements

G. Adam, B. Schoennagel, P. Bannas, 2020, The International Journal of Cardiovascular Imaging.

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.

Diagnosis of Thoracic Aortic Dissection: Magnetic Resonance Imaging Versus Transesophageal Echocardiography

C. Nienaber, V. Nicolas, R. Spielmann, 1992, Circulation.

Augmentation index and the evolution of aortic disease in marfan-like syndromes.

P. Robinson, M. A. Aydin, T. Meinertz, 2010, American journal of hypertension.

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.

Tissue Doppler imaging identifies myocardial dysfunction in adults with marfan syndrome

P. Robinson, M. A. Aydin, T. Meinertz, 2007, Clinical Cardiology.

The CatLet score and outcome prediction in acute myocardial infarction for patients undergoing primary percutaneous intervention: A proof‐of‐concept study

P. Schoenhagen, T. Ruddy, J. Escaned, 2020, Catheterization and cardiovascular interventions : official journal of the Society for Cardiac Angiography & Interventions.

HTAD patient pathway: Strategy for diagnostic work-up of patients and families with (suspected) heritable thoracic aortic diseases (HTAD) a statement from the HTAD working group of VASCERN.

J. Timmermans, M. Groenink, A. Evangelista, 2022, European journal of medical genetics.