Zobrazeno 1 - 10
of 37
pro vyhledávání: '"Romy Franken"'
Autor:
Romy Franken, Stijntje Hibender, Alexander W den Hartog, Teodora Radonic, Carlie J M de Vries, Aeilko H Zwinderman, Maarten Groenink, Barbara J M Mulder, Vivian de Waard
Publikováno v:
PLoS ONE, Vol 9, Iss 9, p e107221 (2014)
AIMS:Patients with Marfan syndrome have an increased risk of life-threatening aortic complications, mostly preceded by aortic dilatation. In the FBN1(C1039G/+) Marfan mouse model, losartan decreases aortic root dilatation. We recently confirmed this
Externí odkaz:
https://doaj.org/article/291beb41452c49dbb62569b3b81539e6
Autor:
Ruifang Lu, Sanjay Sinha, Dieter P. Reinhardt, Shaynah Wanga, Adam Lee Fellows, Marjan Jahangiri, Vivian de Waard, Maarten Groenink, Javier Barallobre-Barreiro, Carlie J.M. de Vries, Barbara J.M. Mulder, Romy Franken, David R. Koolbergen, Rosa Viner, Manuel Mayr, Xiaoke Yin, Qiuru Xing, Aeilko H. Zwinderman, Ron Balm, Ferheen Baig, Philipp Skroblin, Hongorzul Davaapil, Marika Fava
Publikováno v:
Yin, X, Wanga, S, Fellows, A L, Barallobre-Barreiro, J, Lu, R, Davaapil, H, Franken, R, Fava, M, Baig, F, Skroblin, P, Xing, Q, Koolbergen, D R, Groenink, M, Zwinderman, A H, Balm, R, de Vries, C J M, Mulder, B J M, Viner, R, Jahangiri, M, Reinhardt, D P, Sinha, S, de Waard, V & Mayr, M 2019, ' Glycoproteomic Analysis of the Aortic Extracellular Matrix in Marfan Patients. ', Arteriosclerosis, Thrombosis, and Vascular Biology, vol. 39, no. 9, pp. 1859–1873 . https://doi.org/10.1161/ATVBAHA.118.312175
Arteriosclerosis, Thrombosis, and Vascular Biology
Arteriosclerosis, thrombosis, and vascular biology, 39(9), 1859-1873. Lippincott Williams and Wilkins
Arteriosclerosis, Thrombosis, and Vascular Biology
Arteriosclerosis, thrombosis, and vascular biology, 39(9), 1859-1873. Lippincott Williams and Wilkins
Supplemental Digital Content is available in the text.
Objective: Marfan syndrome (MFS) is caused by mutations in FBN1 (fibrillin-1), an extracellular matrix (ECM) component, which is modified post-translationally by glycosylation. This study ai
Objective: Marfan syndrome (MFS) is caused by mutations in FBN1 (fibrillin-1), an extracellular matrix (ECM) component, which is modified post-translationally by glycosylation. This study ai
Autor:
Cindy P. A. A. van Roomen, Luigi Amjg van Riel, Barbara J.M. Mulder, Shaynah Wanga, Ingeborg van der Made, Nicole van Vliet, Aeilko H. Zwinderman, Carlie J.M. de Vries, Romy Franken, Vivian de Waard, Maarten Groenink, Stijntje Hibender, Mariska Vos, Jeroen Essers, Yanto Ridwan
Publikováno v:
The Journal of Pathology. 243:294-306
Marfan syndrome (MFS) is a connective tissue disorder in which aortic rupture is the major cause of death. MFS patients with an aortic diameter below the advised limit for prophylactic surgery (
Autor:
Gerard Pals, Janneke Timmermans, Arthur J.H.A. Scholte, Maarten P. van den Berg, Romy Franken, Barbara J.M. Mulder, Maarten Groenink, Helena M. A. Feenstra, Vivian de Waard, Aeilko H. Zwinderman
Publikováno v:
European heart journal, 37(43), 3285-3290. Oxford University Press
European Heart Journal, 37, 43, pp. 3285-3290
Franken, R, Groenink, M, de Waard, V, Feenstra, H M A, Scholte, A J, van den Berg, M P, Pals, G, Zwinderman, A H, Timmermans, J & Mulder, B J M 2016, ' Genotype impacts survival in Marfan syndrome ', European Heart Journal, vol. 37, no. 43, pp. 3285-3290 . https://doi.org/10.1093/eurheartj/ehv739
European Heart Journal, 37(43), 3285-3290. Oxford University Press
European Heart Journal, 37(43). Oxford University Press
European Heart Journal, 37, 3285-3290
European Heart Journal, 36, 523-523
European Heart Journal, 37, 43, pp. 3285-3290
Franken, R, Groenink, M, de Waard, V, Feenstra, H M A, Scholte, A J, van den Berg, M P, Pals, G, Zwinderman, A H, Timmermans, J & Mulder, B J M 2016, ' Genotype impacts survival in Marfan syndrome ', European Heart Journal, vol. 37, no. 43, pp. 3285-3290 . https://doi.org/10.1093/eurheartj/ehv739
European Heart Journal, 37(43), 3285-3290. Oxford University Press
European Heart Journal, 37(43). Oxford University Press
European Heart Journal, 37, 3285-3290
European Heart Journal, 36, 523-523
Item does not contain fulltext AIMS: The aorta in Marfan syndrome (MFS) patients is variably affected. We investigated the assumed genotype-effect on protein production as a risk factor for a severe aortic phenotype in adult MFS patients. METHODS AND
Publikováno v:
Expert opinion on orphan drugs. 4(6):605-612
Introduction: Marfan syndrome (MFS) is an autosomal dominant disorder of the connective tissue with manifestations in skeletal, cardiovascular and ocular systems. Areas covered: This paper reviews the effect of FBN1 mutation on phenotype, novel surgi
Autor:
Aeilko H. Zwinderman, V. de Waard, Anje M. Spijkerboer, Janneke Timmermans, M. P. Van Den Berg, M. Groenink, Arthur J.H.A. Scholte, A.W. den Hartog, Gerard Pals, Romy Franken, B.J.M. Mulder
Publikováno v:
Netherlands heart journal, 24(11), 675-681. Bohn Stafleu van Loghum
Netherlands Heart Journal, 24(11), 675-681
Netherlands Heart Journal, 24(11), 675-681. Bohn, Stafleu, Van Loghum
Netherlands Heart Journal, 24(11), 675-681. Bohn Stafleu van Loghum
Netherlands Heart Journal
Netherlands Heart Journal, 24, 11, pp. 675-681
Netherlands Heart Journal, 24, 675-681
Netherlands Heart Journal, 24(11), 675-681
Netherlands Heart Journal, 24(11), 675-681. Bohn, Stafleu, Van Loghum
Netherlands Heart Journal, 24(11), 675-681. Bohn Stafleu van Loghum
Netherlands Heart Journal
Netherlands Heart Journal, 24, 11, pp. 675-681
Netherlands Heart Journal, 24, 675-681
Contains fulltext : 171721.pdf (Publisher’s version ) (Open Access) BACKGROUND: Mild biventricular dysfunction is often present in patients with Marfan syndrome. Losartan has been shown to reduce aortic dilatation in patients with Marfan syndrome.
Autor:
Romy Franken, Laura Gutiérrez García-Moreno, David Garcia-Dorado, Artur Evangelista, Valentina Galuppo, Barbara J.M. Mulder, Gisela Teixido-Tura, Mar Borregan
Publikováno v:
Heart (British Cardiac Society), 102(8), 626-632. BMJ Publishing Group
This study aimed to determine aortic disease severity in patients with Loeys-Dietz syndrome (LDS). Thirty-three patients with LDS diagnosed and followed up at our unit were included. After reviewing all family trees, 25 deceased family members with c
Autor:
Stijntje Hibender, Barbara J.M. Mulder, Carlie J.M. de Vries, Anique ter Braake, Aeilko H. Zwinderman, Maurice J. van den Hoff, Esther Lutgens, M. Groenink, Edith E. Schermer, Romy Franken, Y. M. Pinto, Cindy van Roomen, Vivian de Waard, Quinn Gunst, Ingeborg van der Made
Publikováno v:
Arteriosclerosis, thrombosis, and vascular biology, 36(8), 1618-1626. Lippincott Williams and Wilkins
Arteriosclerosis, Thrombosis, and Vascular Biology, 36, 1618-26
Arteriosclerosis, Thrombosis, and Vascular Biology, 36, 8, pp. 1618-26
Arteriosclerosis, Thrombosis, and Vascular Biology, 36, 1618-26
Arteriosclerosis, Thrombosis, and Vascular Biology, 36, 8, pp. 1618-26
Objective— Marfan syndrome (MFS) is a connective tissue disorder caused by mutations in the fibrillin-1 gene. Patients with MFS are at risk of aortic aneurysm formation and dissection. Usually, blood pressure–lowering drugs are used to reduce aor
Autor:
Abdelali el Morabit, Arthur J. Scholte, Nils Planken, Maarten Groenink, Aeilko H. Zwinderman, Henk A. Marquering, Vivian de Waard, Barbara J.M. Mulder, Maarten P. van den Berg, Romy Franken, Janneke Timmermans
Publikováno v:
International Journal of Cardiology, 194, 7-12
International Journal of Cardiology, 194, pp. 7-12
International Journal of Cardiology, 194, 7-12. ELSEVIER IRELAND LTD
International journal of cardiology, 194, 7-12. Elsevier Ireland Ltd
International Journal of Cardiology, 194, pp. 7-12
International Journal of Cardiology, 194, 7-12. ELSEVIER IRELAND LTD
International journal of cardiology, 194, 7-12. Elsevier Ireland Ltd
Background: Patients with Marfan syndrome (MFS) have a highly variable occurrence of aortic complications. Aortic tortuosity is often present in MFS and may help to identify patients at risk for aortic complications.Methods: 3D-visualization of the t
Autor:
David Alexander, Abdullah A. Alghamdi, Rafael Alonso-Gonzalez, Naser M. Ammash, Annalisa Angelini, Iain Armstrong, Sonya V. Babu-Narayan, Vivan J.M. Baggen, Cristina Basso, Elisabeth Bédard, Lee N. Benson, Maria Boutsikou, Craig S. Broberg, Albert V.G. Bruschke, Werner Budts, Alida L.P. Caforio, Marie Chaix, Anisa Chaudhry, Stavros Chryssanthopoulos, Preeti Choudhary, Dennis V. Cokkinos, Jack M. Colman, Michael S. Connelly, Domenico Corrado, Mark Cox, Gordon Cumming, Marianne Cumming, Michele D’Alto, Piers E.F. Daubeney, Mark J. Dayer, Barbara J. Deal, Joseph A. Dearani, Gerhard-Paul Diller, Konstantinos Dimopoulos, Annie Dore, Jacqueline Durbridge, Alexander R. Ellis, Sabine Ernst, Peter Ewert, Marny Fedrigo, Simon J. Finney, Romy Franken, Michael A. Gatzoulis, Marc Gewillig, George Giannakoulas, Matthias Greutmann, Hong Gu, Ankur Gulati B.A. Hons (Cantab), Carl Harries, Jane Heggie, Paul Herijgers, Siew Yen Ho, Kimberly Holst, Eric Horlick, Tim Hornung, Jan Janousek, Harald Kaemmerer, Juan Pablo Kaski, W. Aaron Kay, Paul Khairy, Abigail Khan, Philip J. Kilner, Adrienne H. Kovacs, Michael J. Landzberg, Olga Lazoura, Wei Li, Eric Lim, Emmanouil Liodakis, Carmen J. Lopez-Guarch, Koen Luyckx, Ariane Marelli, Elisabeth Martin, Constantine Mavroudis, Bryan Maxwell, Brian W. McCrindle, Doff B. McElhinney, Folkert J. Meijboom, François-Pierre Mongeon, Claudia Montanaro, Roisin Monteiro, Philip Moons, Barbara J.M. Mulder, Edward Nicol, Koichiro Niwa, Gabrielle Norrish, Clare O’Donnell, Erwin Notker Oechslin, Alexander R. Opotowsky, Mark Osten, Mehul B. Patel, Joseph K. Perloff, Frank A. Pigula, Kalliopi Pilichou, Nancy Poirier, Sanjay Kumar Prasad, Michael A. Quail, Jelena Radojevic Liegeois, Andrew N. Redington, Michael L. Rigby, Josep Rodés-Cabau, Anitra W. Romfh, Jolien W. Roos-Hesselink, Suzanne Rowsell, Michael B. Rubens, Fadi Sawaya, Markus Schwerzmann, Mary N. Sheppard, Darryl F. Shore, Harsimran S. Singh, Jane Somerville, Lars Søndergaard, Mark S. Spence, Philip J. Steer, Lorna Swan, András Szatmári, Shigeru Tateno, Upasana Tayal, Basil D. Thanopoulos, Judith Therrien, Gaetano Thiene, Sara A. Thorne, Daniel Tobler, John K. Triedman, Pedro T. Trindade, Oktay Tutarel, Judith J Tweedie, Anselm Uebing, Hideki Uemura, Lindsay Urbinelli, Glen S. Van Arsdell, Gruschen R. Veldtman, Hubert W. Vliegen, Inga Voges, Fiona Walker, Edward P. Walsh, Stephanie M. Ware, Gary D. Webb, Steven A. Webber, Tom Wong, Steve Yentis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::76526c094c33f53343f35169e2549283
https://doi.org/10.1016/b978-0-7020-6929-1.01002-9
https://doi.org/10.1016/b978-0-7020-6929-1.01002-9