Publications by authors named "Thomas Mir"

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CDKL1 variants affecting ciliary formation predispose to thoracic aortic aneurysm and dissection.
Theresa Nauth, Melanie Philipp, Sina Renner, Martin D Burkhalter, Helke Schüler, Thomas S Mir

J Clin Invest· December 2025

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Intrinsic cardiomyopathy in pediatric Marfan syndrome: predictive factors and risk assessments.
Jonas Kneußel, Jakob Olfe, Veronika C Stark, Yskert von Kodolitsch, Rainer G Kozlik-Feldmann, Thomas S Mir

Pediatr Res· October 2025

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Thoracic Aortic Disease in Patients With Heterozygous Variants Outside the Central Region of .
Till Joscha Demal, Marco Sachse, Celia Metzlaff, Helke Schüler, Katalin Szöcs, Thomas S Mir

Circ Genom Precis Med· June 2025

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A Staged Biventricular Approach Combining the Starnes and Cone Procedures in Ebstein's Anomaly: A Case Report and Literature Review.
Paul Linnenbank, Daniel Biermann, Eike Philipp Schneider, Ida Hüners, Nora Lang, Thomas S Mir

Children (Basel)· June 2025

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Late diagnosis of Marfan syndrome is associated with unplanned aortic surgery and cardiovascular death.
Jason Claus, Lauritz Schoof, Thomas S Mir, Anna Lena Kammal, Gerhard Schön

J Thorac Cardiovasc Surg· April 2025

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Initial outcomes of novel guideline-directed pharmacotherapy for systemic right heart failure in adults with congenital heart disease.
Ann-Kristin Lassen, Yevheniia Artemenko, Michael Jerosch-Herold, Ines Kowalewski, Jakob Olfe, Thomas S Mir

Cardiovasc Diagn Ther· April 2025

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Management of aortic disease in children with FBN1-related Marfan syndrome.
Laura Muiño-Mosquera, Elena Cervi, Katya De Groote, Wendy Dewals, Zina Fejzic, Thomas S Mir

Eur Heart J· October 2024

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Patient experiences of interprofessional collaboration and intersectoral communication in rare disease healthcare in Germany - a mixed-methods study.
Laura Inhestern, Ramona Otto, Maja Brandt, David Zybarth, Ralf Oheim, Thomas S Mir

Orphanet J Rare Dis· May 2024

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TGFβ level in healthy and children with Marfan syndrome-effective reduction under sartan therapy.
Veronika C Stark, Jakob Olfe, Daniel Diaz-Gil, Yskert von Kodolitsch, Rainer Kozlik-Feldmann, Thomas S Mir

Front Pediatr· February 2024

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Long-Term Antibody Response to SARS-CoV-2 in Children.
Gabor A Dunay, Madalena Barroso, Mathias Woidy, Marta K Danecka, Geraldine Engels, Thomas S Mir

J Clin Immunol· January 2023

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Specific CD4+ T Cell Responses to Ancestral SARS-CoV-2 in Children Increase With Age and Show Cross-Reactivity to Beta Variant.
Kevin Paul, Freya Sibbertsen, Daniela Weiskopf, Marc Lütgehetmann, Madalena Barroso, Thomas S Mir

Front Immunol· August 2022

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Tricuspid valve prolapse as an early predictor for severe phenotype in children with Marfan syndrome.
Veronika C Stark, Jakob Olfe, Jannis Pesch, Enver Tahir, Julius M Weinrich, Thomas S Mir

Acta Paediatr· June 2022

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Phenotypic analysis of the pediatric immune response to SARS-CoV-2 by flow cytometry.
Freya Sibbertsen, Laura Glau, Kevin Paul, Thomas S Mir, Søren W Gersting

Cytometry A· March 2022

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Expanding the clinical spectrum of COL2A1 related disorders by a mass like phenotype.
Till Joscha Demal, Tasja Scholz, Helke Schüler, Jakob Olfe, Anja Fröhlich, Thomas S Mir

Sci Rep· March 2022

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Impact of chest wall deformity on cardiac function by CMR and feature-tracking strain analysis in paediatric patients with Marfan syndrome.
Hy Van Lam, Michael Groth, Thomas Mir, Peter Bannas, Gunnar K Lund

Eur Radiol· June 2021

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Genotype-Phenotype Correlation in Children: The Impact of Variants on Pediatric Marfan Care.
Veronika C Stark, Flemming Hensen, Kerstin Kutsche, Fanny Kortüm, Jakob Olfe, Thomas S Mir

Genes (Basel)· July 2020

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Marfan Syndrome Versus Bicuspid Aortic Valve Disease: Comparative Analysis of Obstetric Outcome and Pregnancy-Associated Immediate and Long-Term Aortic Complications.
Betül Toprak, Katalin Szöcs, Elvin Zengin-Sahm, Christoph Sinning, Amra Hot, Thomas S Mir

J Clin Med· April 2020

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Case-matched Comparison of Cardiovascular Outcome in Loeys-Dietz Syndrome versus Marfan Syndrome.
Kristina Mühlstädt, Julie De Backer, Yskert von Kodolitsch, Kerstin Kutsche, Laura Muiño Mosquera, Thomas S Mir

J Clin Med· November 2019

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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.
Sina Renner, Helke Schüler, Malik Alawi, Verena Kolbe, Meike Rybczynski, Thomas S Mir

Genet Med· August 2019

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Cardiovascular Biomarkers in Amniotic Fluid, Umbilical Arterial Blood, Umbilical Venous Blood, and Maternal Blood at Delivery, and Their Reference Values for Full-Term, Singleton, Cesarean Deliveries.
Martin E Blohm, Florian Arndt, Glenn M Fröschle, Nora Langenbach, Jan Sandig, Thomas S Mir

Front Pediatr· July 2019

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The transition of pediatric Marfan patients to adult care: a challenge and its risks.
Veronika C Stark, Katrin Doering, Yskert von Kodolitsch, Rainer Kozlik-Feldmann, Götz C Mueller, Thomas S Mir

Cardiovasc Diagn Ther· December 2018

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"Tailored" endovascular pulmonary valve and root replacement for rupture of a dilated homograft.
Götz Christoph Müller, Christoph Sinning, Elvin Zengin-Sahm, Veronika Stark, Thomas S Mir

Cardiovasc Diagn Ther· December 2018

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The Pulmonary Artery in Pediatric Patients with Marfan Syndrome: An Underestimated Aspect of the Disease.
Veronika C Stark, Michael Huemmer, Jakob Olfe, Goetz C Mueller, Rainer Kozlik-Feldmann, Thomas S Mir

Pediatr Cardiol· August 2018

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Towards a Tissue-Engineered Contractile Fontan-Conduit: The Fate of Cardiac Myocytes in the Subpulmonary Circulation.
Daniel Biermann, Alexandra Eder, Florian Arndt, Hatim Seoudy, Hermann Reichenspurner, Thomas Mir

PLoS One· June 2017

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The role of the multidisciplinary health care team in the management of patients with Marfan syndrome.
Yskert von Kodolitsch, Meike Rybczynski, Marina Vogler, Thomas S Mir, Helke Schüler

J Multidiscip Healthc· November 2016

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