Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Judith M A Verhagen"'
Autor:
Jolien W Roos-Hesselink, Michelle Michels, Tamas Szili-torok, Judith M A Verhagen, Rohit E Bhagwandien, Sing-Chien Yap, DOMINIC THEUNS, Amira Assaf, Rafi Sakhi
Publikováno v:
Open Heart, Vol 8, Iss 2 (2021)
Objective Patients with heart disease are at increased risk for sudden cardiac death. Guidelines recommend an implantable loop recorder (ILR) for symptomatic patients when symptoms are sporadic and possibly arrhythmia-related. In clinical practice, a
Externí odkaz:
https://doaj.org/article/fd2c37e41fd4467eb9ef5494a3b0b12e
Autor:
Roy Huurman, Daniel J. Bowen, Ferit O. Mutluer, Bernardo Loff Barreto, Marjon A. van Slegtenhorst, Judith M. A. Verhagen, Alexander Hirsch, Annemien E. van den Bosch, Michelle Michels, Arend F. L. Schinkel
Publikováno v:
Echocardiography, 39(9), 1209-1218. Wiley-Blackwell Publishing Ltd
BACKGROUND: Genetic testing of relatives of hypertrophic cardiomyopathy (HCM) patients has led to a large group of genotype-positive, phenotype-negative (G+/Ph-) subjects. Prediction of progression to overt HCM in these subjects is challenging. While
Autor:
Stephan A. C. Schoonvelde, Claudine W. B. Ruijmbeek, Judith M. A. Verhagen, Debby M. E. I. Hellebrekers, Marcel J. M. Kofflard, Michelle Michels, Alexander Hirsch
Publikováno v:
Radiology: Cardiothoracic Imaging, 5(2):e230014. Radiological Society of North America Inc.
Radiol Cardiothorac Imaging
Radiol Cardiothorac Imaging
Left ventricular hypertrophy (LVH) has a broad differential diagnosis. Pathogenic variants of mitochondrial DNA are a rare cause of LVH, and cardiac MRI is a powerful technique that may aid in differentiating such rare causes. This case report presen
Autor:
Elisabeth Gillis, Ajay A. Kumar, Ilse Luyckx, Christoph Preuss, Elyssa Cannaerts, Gerarda van de Beek, Björn Wieschendorf, Maaike Alaerts, Nikhita Bolar, Geert Vandeweyer, Josephina Meester, Florian Wünnemann, Russell A. Gould, Rustam Zhurayev, Dmytro Zerbino, Salah A. Mohamed, Seema Mital, Luc Mertens, Hanna M. Björck, Anders Franco-Cereceda, Andrew S. McCallion, Lut Van Laer, Judith M. A. Verhagen, Ingrid M. B. H. van de Laar, Marja W. Wessels, Emmanuel Messas, Guillaume Goudot, Michaela Nemcikova, Alice Krebsova, Marlies Kempers, Simone Salemink, Toon Duijnhouwer, Xavier Jeunemaitre, Juliette Albuisson, Per Eriksson, Gregor Andelfinger, Harry C. Dietz, Aline Verstraeten, Bart L. Loeys, Mibava Leducq Consortium
Publikováno v:
Frontiers in Physiology, Vol 8 (2017)
Externí odkaz:
https://doaj.org/article/00bba679614b4010927e1186b126fa61
Autor:
Judith M. A. Verhagen, Joyce Burger, Jos A. Bekkers, Alexander T. den Dekker, Jan H. von der Thüsen, Marina Zajec, Hennie T. Brüggenwirth, Marianne L. T. van der Sterre, Myrthe van den Born, Theo M. Luider, Wilfred F. J. van IJcken, Marja W. Wessels, Jeroen Essers, Jolien W. Roos-Hesselink, Ingrid van der Pluijm, Ingrid M. B. H. van de Laar, Erwin Brosens
Publikováno v:
International Journal of Molecular Sciences
International Journal of Molecular Sciences; Volume 23; Issue 1; Pages: 438
International Journal of Molecular Sciences, 23(1):438. Multidisciplinary Digital Publishing Institute (MDPI)
International Journal of Molecular Sciences, Vol 23, Iss 438, p 438 (2022)
International Journal of Molecular Sciences; Volume 23; Issue 1; Pages: 438
International Journal of Molecular Sciences, 23(1):438. Multidisciplinary Digital Publishing Institute (MDPI)
International Journal of Molecular Sciences, Vol 23, Iss 438, p 438 (2022)
Thoracic aortic aneurysm is a potentially life-threatening disease with a strong genetic contribution. Despite identification of multiple genes involved in aneurysm formation, little is known about the specific underlying mechanisms that drive the pa
Autor:
Nikki van der Velde, Roy Huurman, H. Carlijne Hassing, Ricardo P. J. Budde, Marjon A. van Slegtenhorst, Judith M. A. Verhagen, Arend F. L. Schinkel, Michelle Michels, Alexander Hirsch
Publikováno v:
Frontiers in Cardiovascular Medicine, 8:727405. Frontiers Media S.A.
Frontiers in Cardiovascular Medicine, Vol 8 (2021)
Frontiers in Cardiovascular Medicine
Frontiers in Cardiovascular Medicine, Vol 8 (2021)
Frontiers in Cardiovascular Medicine
Background: Carriers of pathogenic DNA variants (G+) causing hypertrophic cardiomyopathy (HCM) can be identified by genetic testing. Several abnormalities have been brought forth as pre-clinical expressions of HCM, some of which can be identified by
Autor:
Roy Huurman, Nikki van der Velde, Arend F L Schinkel, H Carlijne Hassing, Ricardo P J Budde, Marjon A van Slegtenhorst, Judith M A Verhagen, Alexander Hirsch, Michelle Michels
Publikováno v:
European Heart Journal Cardiovascular Imaging, 23(9), 1144-1154. Oxford University Press
Aims Genetic testing in relatives of hypertrophic cardiomyopathy (HCM) patients leads to early identification of pathogenic DNA variant carriers (G+), before the onset of left ventricular hypertrophy. Routine phenotyping consists of electrocardiograp
Autor:
Elisabeth Gillis, Ajay A. Kumar, Ilse Luyckx, Christoph Preuss, Elyssa Cannaerts, Gerarda van de Beek, Björn Wieschendorf, Maaike Alaerts, Nikhita Bolar, Geert Vandeweyer, Josephina Meester, Florian Wünnemann, Russell A. Gould, Rustam Zhurayev, Dmytro Zerbino, Salah A. Mohamed, Seema Mital, Luc Mertens, Hanna M. Björck, Anders Franco-Cereceda, Andrew S. McCallion, Lut Van Laer, Judith M. A. Verhagen, Ingrid M. B. H. van de Laar, Marja W. Wessels, Emmanuel Messas, Guillaume Goudot, Michaela Nemcikova, Alice Krebsova, Marlies Kempers, Simone Salemink, Toon Duijnhouwer, Xavier Jeunemaitre, Juliette Albuisson, Per Eriksson, Gregor Andelfinger, Harry C. Dietz, Aline Verstraeten, Bart L. Loeys, Mibava Leducq Consortium
Publikováno v:
Frontiers in Physiology, Vol 8 (2017)
Frontiers in Physiology
Frontiers in Physiology
textabstractIn the original article, we noted two mutation annotation errors. The correction of these two mistakes does not change the scientific conclusions in any way. The authors apologize for these nomenclature errors. Please find below the corre
Autor:
Russell A, Gould, Hamza, Aziz, Courtney E, Woods, Manuel Alejandro, Seman-Senderos, Elizabeth, Sparks, Christoph, Preuss, Florian, Wünnemann, Djahida, Bedja, Cassandra R, Moats, Sarah A, McClymont, Rebecca, Rose, Nara, Sobreira, Hua, Ling, Gretchen, MacCarrick, Ajay Anand, Kumar, Ilse, Luyckx, Elyssa, Cannaerts, Aline, Verstraeten, Hanna M, Björk, Ann-Cathrin, Lehsau, Vinod, Jaskula-Ranga, Henrik, Lauridsen, Asad A, Shah, Christopher L, Bennett, Patrick T, Ellinor, Honghuang, Lin, Eric M, Isselbacher, Christian Lacks, Lino Cardenas, Jonathan T, Butcher, G Chad, Hughes, Mark E, Lindsay, Luc, Mertens, Anders, Franco-Cereceda, Judith M A, Verhagen, Marja, Wessels, Salah A, Mohamed, Per, Eriksson, Seema, Mital, Lut, Van Laer, Bart L, Loeys, Gregor, Andelfinger, Andrew S, McCallion
Publikováno v:
Nature genetics. 51(1)
Bicuspid aortic valve (BAV) is a common congenital heart defect (population incidence, 1-2%)
Publikováno v:
Nederlands tijdschrift voor geneeskunde. 155(40)
22q11.2 deletion syndrome is an autosomal dominant syndrome mostly diagnosed in childhood.We present a case of a male with a ventricular septum defect, hypoparathyroidism and mild facial abnormalities, in which the diagnosis of 22q11.2 deletion syndr