Y. Kodolitsch

H. Klemm, T. Meinertz, S. Baldus, 2008, Catheterization and cardiovascular interventions : official journal of the Society for Cardiac Angiography & Interventions.

Surgical revision of an uncommonly dislocated self-expanding Amplatzer septal occluder device.

T. Meinertz, T. Münzel, Y. Kodolitsch, 2004, The Annals of thoracic surgery.

Marfan Syndrome and Related Heritable Thoracic Aortic Aneurysms and Dissections.

A. De Paepe, B. Callewaert, P. Coucke, 2015, Current pharmaceutical design.

Physician-Modified Thoracic Stent-Graft With Low Distal Radial Force to Prevent Distal Stent-Graft–Induced New Entry Tears in Patients With Genetic Aortic Syndromes and Aortic Dissection

A. Wanhainen, F. Rohlffs, N. Tsilimparis, 2018, Journal of endovascular therapy : an official journal of the International Society of Endovascular Specialists.

Interpretation of sequence variants of the FBN1 gene: analog or digital? A commentary on decreased frequency of FBN1 missense variants in Ghent criteria-positive Marfan syndrome and characterization of novel FBN1 variants

K. Kutsche, Y. Kodolitsch, 2015, Journal of Human Genetics.

Endovascular Repair of Postdissection Thoracoabdominal Aortic Aneurysm in Patients With Vascular Ehlers-Danlos Syndrome

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

[Intramural hemorrhage of the thoracic aorta as a precursor of dissection].

C. Nienaber, R. Spielmann, A. Haverich, 1995, Zeitschrift fur Kardiologie.

Elevated serum levels of smooth muscle myosin heavy chain in aortic dissection: Discussion of two cases

Y. Yazaki, C. Nienaber, T. Meinertz, 1997 .

CHLAMYDIA INFECTION

A. L. Wong, J. Belmont, F. Lammert, 2001 .

Predicting severity of haemophilia A and B splicing mutations by information analysis

P. Rogan, Y. Kodolitsch, J. Berger, 2006, Haemophilia : the official journal of the World Federation of Hemophilia.

Doubly heterozygous LMNA and TTN mutations revealed by exome sequencing in a severe form of dilated cardiomyopathy

P. Robinson, G. Condorelli, G. Faggian, 2013, European Journal of Human Genetics.

Bicuspid Aortic Valve

H. Kaemmerer, Y. Kodolitsch, 2017 .

When Should Surgery Be Performed in Marfan Syndrome and Other Connective Tissue Disorders to Protect Against Type A Dissection

P. Robinson, J. Berger, Y. Kodolitsch, 2014 .

Results of Modern Mitral Valve Repair in Patients with Marfan Syndrome

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

Aortopathies: Clinical Manifestation

H. Kaemmerer, Y. Kodolitsch, 2017 .

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

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

Acute aortic dissection

T. Sundt, M. Czerny, T. Carrel, 2023, The Lancet.

How to Guide Stent-Graft Implantation in Type B Aortic Dissection?: Comparison of Angiography, Transesophageal Echocardiography, and Intravascular Ultrasound

Olaf Franzen, Christoph Dieckmann, Gunnar Lund, 2005, Circulation.

Value of Intravascular Ultrasound for Endovascular Stent‐Graft Placement in Aortic Dissection and Aneurysm

C. Nienaber, T. Rehders, T. Meinertz, 2003, Journal of cardiac surgery.

Diagnostic potential of combined transthoracic echocardiography and x‐ray computed tomography in suspected aortic dissection

C. Nienaber, R. Spielmann, Y. Kodolitsch, 1999, Clinical cardiology.

Self-assessment and Screening for Palliative Care Need in Patients with ChronicHeart Failure

C. Bokemeyer, K. Oechsle, Y. Kodolitsch, 2017 .

Self-assessment and Screening for Palliative Care Need in Patients with Chronic Heart Failure

C. Bokemeyer, K. Oechsle, Y. Kodolitsch, 2017 .

Impact of Age and Gender on Cardiac Pathology in Children and Adolescents With Marfan Syndrome

T. Mir, Y. Kodolitsch, M. Rybczynski, 2013, Pediatric Cardiology.

Heart rate turbulence and deceleration capacity for risk prediction of serious arrhythmic events in Marfan syndrome

Mario Jularic, Stephan Willems, Julia Moser, 2015, Clinical Research in Cardiology.

Comparison of conventional and transesophageal echocardiography with magnetic resonance imaging for anatomical mapping of thoracic aortic dissection

C. Nienaber, R. Spielmann, Y. Kodolitsch, 1994, The International Journal of Cardiac Imaging.

Arterial mechanical properties after replacement or reconstruction of the aortic root

P. Robinson, M. A. Aydin, A. Bernhardt, 2012 .

The Kid‐Short Marfan Score (Kid‐SMS) – an easy executable risk score for suspected paediatric patients with Marfan syndrome

T. Mir, Y. Kodolitsch, J. Weil, 2013, Acta paediatrica.

Clinical prediction of acute aortic dissection.

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

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

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

Chronic Idiopathic Intestinal Pseudo-obstruction

A. L. Wong, J. Belmont, M. Dichgans, 2011 .

[Cutaneous amyloidoses].

A. L. Wong, J. Belmont, D. Roden, 1990, Der Hautarzt; Zeitschrift fur Dermatologie, Venerologie, und verwandte Gebiete.

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

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

The diagnosis of thoracic aortic dissection by noninvasive imaging procedures.

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

Endovascular treatment of aortic aneurysms and dissections in patients with genetically triggered aortic diseases

F. Rohlffs, T. Kölbel, Y. Kodolitsch, 2022, Seminars in Vascular Surgery.

[Chronic venous insufficiency].

V Wienert, G Hauer, A Lentner, 1996, Der Chirurg; Zeitschrift fur alle Gebiete der operativen Medizen.

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

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

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.

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

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

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

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

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.

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.

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

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

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.

Diseases of the aorta.

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

Diagnostic imaging of aortic diseases

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

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.

Das akute Aortensyndrom

H. Eggebrecht, T. Meinertz, D. Baumgart, 2003 .

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

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

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

B. Keyser, J. Berger, Y. Kodolitsch, 2011, Clinical genetics.

Medizinische Versorgung von Erwachsenen mit angeborenen Herzfehlern

S. Dittrich, P. Ewert, M. Huntgeburth, 2019, Herz.

Diseases of the aorta.

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

Ocular manifestation in Marfan syndrome: corneal biomechanical properties relate to increased systemic score points

A. Frings, S. Linke, V. Druchkiv, 2018, Graefe's Archive for Clinical and Experimental Ophthalmology.

Congenital dysfibrinogenemia.

S. Lalani, K. Chayama, A. Cleare, 1984, Current problems in clinical biochemistry.

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

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