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European Journal of Ophthalmology
|
March 29, 2018
Ocular manifestations of Marfan syndrome in children and adolescents
Daniel J Salchow, Petra Gehle
Interdisciplinary Cardiovascular and Thoracic Surgery
|
February 21, 2023
Aorto-aortic bypass in an infant with middle aortic syndrome and Marfan syndrome: a 15-year follow-up
Roland Heck, Björn Fischer-Zirnsak, Joachim Photiadis, et al.
Interactive Cardiovascular and Thoracic Surgery
|
June 11, 2022
Different ascending aortic phenotypes with similar mutations in 2 patients with Loeys-Dietz syndrome type 2
Roland Heck, Björn Fischer-Zirnsak, Joachim Photiadis, et al.
The British Journal of Ophthalmology
|
November 18, 2017
Ocular findings in Loeys-Dietz syndrome
Catharina Busch, Robert Voitl, Barbara Goergen, et al.
The Annals of Thoracic Surgery
|
January 23, 2013
Reverse graft placement in the Florida sleeve procedure for aortic root aneurysm
Takeshi Komoda, Satsuki Komoda, Petra Gehle, et al.
Plos One
|
September 21, 2017
Biometric and structural ocular manifestations of Marfan syndrome
Petra Gehle, Barbara Goergen, Daniel Pilger, et al.
Global Heart
|
May 13, 2024
Updated 2022 ACC/AHA Guideline Improves Concordance Between TTE and CT in Monitoring Marfan Snydrome and Related Disorders, but Relevant Measurement Differences Remain Frequent
Johannes Kolck, Tobias Daniel Trippel, Karla Philipp, et al.
Journal of Cachexia, Sarcopenia and Muscle
|
June 17, 2021
Artificial intelligence-based analysis of body composition in Marfan: skeletal muscle density and psoas muscle index predict aortic enlargement
Nick Lasse Beetz, Christoph Maier, Seyd Shnayien, et al.
Scientific Reports
|
September 13, 2022
Discrepancy of echocardiography and computed tomography in initial assessment and 2-year follow-up for monitoring Marfan syndrome and related disorders
Nick Lasse Beetz, Tobias Daniel Trippel, Karla Philipp, et al.
European Journal of Human Genetics : EJHG
|
January 21, 2011
Three novel mutations in the ACTA2 gene in German patients with thoracic aortic aneurysms and dissections
Sabine Hoffjan, Stephan Waldmüller, Wulf Blankenfeldt, et al.
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of 3
Search research articles
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Showing results (1-10 of 21) with videos related to
Sort By:
Page
of 3
European Journal of Ophthalmology
|
March 29, 2018
Ocular manifestations of Marfan syndrome in children and adolescents
Daniel J Salchow, Petra Gehle
Interdisciplinary Cardiovascular and Thoracic Surgery
|
February 21, 2023
Aorto-aortic bypass in an infant with middle aortic syndrome and Marfan syndrome: a 15-year follow-up
Roland Heck, Björn Fischer-Zirnsak, Joachim Photiadis, et al.
Interactive Cardiovascular and Thoracic Surgery
|
June 11, 2022
Different ascending aortic phenotypes with similar mutations in 2 patients with Loeys-Dietz syndrome type 2
Roland Heck, Björn Fischer-Zirnsak, Joachim Photiadis, et al.
The British Journal of Ophthalmology
|
November 18, 2017
Ocular findings in Loeys-Dietz syndrome
Catharina Busch, Robert Voitl, Barbara Goergen, et al.
The Annals of Thoracic Surgery
|
January 23, 2013
Reverse graft placement in the Florida sleeve procedure for aortic root aneurysm
Takeshi Komoda, Satsuki Komoda, Petra Gehle, et al.
Plos One
|
September 21, 2017
Biometric and structural ocular manifestations of Marfan syndrome
Petra Gehle, Barbara Goergen, Daniel Pilger, et al.
Global Heart
|
May 13, 2024
Updated 2022 ACC/AHA Guideline Improves Concordance Between TTE and CT in Monitoring Marfan Snydrome and Related Disorders, but Relevant Measurement Differences Remain Frequent
Johannes Kolck, Tobias Daniel Trippel, Karla Philipp, et al.
Journal of Cachexia, Sarcopenia and Muscle
|
June 17, 2021
Artificial intelligence-based analysis of body composition in Marfan: skeletal muscle density and psoas muscle index predict aortic enlargement
Nick Lasse Beetz, Christoph Maier, Seyd Shnayien, et al.
Scientific Reports
|
September 13, 2022
Discrepancy of echocardiography and computed tomography in initial assessment and 2-year follow-up for monitoring Marfan syndrome and related disorders
Nick Lasse Beetz, Tobias Daniel Trippel, Karla Philipp, et al.
European Journal of Human Genetics : EJHG
|
January 21, 2011
Three novel mutations in the ACTA2 gene in German patients with thoracic aortic aneurysms and dissections
Sabine Hoffjan, Stephan Waldmüller, Wulf Blankenfeldt, et al.
Page
of 3