Rezultati - Verstraeten, Aline

Hide and seek: Somatic SMAD3 mutations in melorheostosis od Velchev, Joe Davis, Verstraeten, Aline, Loeys, Bart

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The fibrillinopathies: New insights with focus on the paradigm of opposing phenotypes for both FBN1 and FBN2 od Peeters, Silke, De Kinderen, Pauline, Meester, Josephina A. N., Verstraeten, Aline, Loeys, Bart L.

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Differences in manifestations of Marfan syndrome, Ehlers-Danlos syndrome, and Loeys-Dietz syndrome od Meester, Josephina A. N., Verstraeten, Aline, Schepers, Dorien, Alaerts, Maaike, Van Laer, Lut, Loeys, Bart L.

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FLNA mutations in surviving males presenting with connective tissue findings: two new case reports and review of the literature od Cannaerts, Elyssa, Shukla, Anju, Hasanhodzic, Mensuda, Alaerts, Maaike, Schepers, Dorien, Van Laer, Lut, Girisha, Katta M., Hojsak, Iva, Loeys, Bart, Verstraeten, Aline

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Two novel presentations of KCNMA1‐related pathology––Expanding the clinical phenotype of a rare channelopathy od Rodrigues Bento, Jotte, Feben, Candice, Kempers, Marlies, van Rij, Maartje, Woiski, Mallory, Devriendt, Koenraad, De Catte, Luc, Baldewijns, Marcella, Alaerts, Maaike, Meester, Josephina, Verstraeten, Aline, Hendson, Willy, Loeys, Bart

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Progress in aorta and peripheral cardiovascular disease research od Mazzolai, Lucia, Alatri, Adriano, Rivière, Alessandra Bura, De Carlo, Marco, Heiss, Christian, Espinola-Klein, Christine, Schlager, Oliver, Sillesen, Henrik, Staub, Daniel, Rodriguez-Palomares, José F, Verstraeten, Aline, Aboyans, Victor

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Corrigendum to: Progress in aorta and peripheral cardiovascular disease research od Mazzolai, Lucia, Alatri, Adriano, Rivière, Alessandra Bura, Carlo, Marco De, Heiss, Christian, Espinola-Klein, Christine, Schlager, Oliver, Sillesen, Henrik, Staub, Daniel, Rodriguez-Palomares, José F, Verstraeten, Aline, Aboyans, Victor

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Cardiogeneticsbank@UZA: A Collection of DNA, Tissues, and Cell Lines as a Translational Tool od Alaerts, Maaike, van de Beek, Gerarda, Luyckx, Ilse, Meester, Josephina, Schepers, Dorien, Verstraeten, Aline, Saenen, Johan, Van Craenenbroeck, Emeline, Goovaerts, Inge, Rodrigus, Inez, Laga, Steven, Hendriks, Jeroen, Goethals, Sofie, De Wilde, Annemieke, Smits, Elke, Jorens, Philippe, Huizing, Manon, Van Laer, Lut, Loeys, Bart

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Novel LOX Variants in Five Families with Aortic/Arterial Aneurysm and Dissection with Variable Connective Tissue Findings od Van Gucht, Ilse, Krebsova, Alice, Diness, Birgitte Rode, Laga, Steven, Adlam, Dave, Kempers, Marlies, Samani, Nilesh J., Webb, Tom R., Baranowska, Ania A., Van Den Heuvel, Lotte, Perik, Melanie, Luyckx, Ilse, Peeters, Nils, Votypka, Pavel, Macek, Milan, Meester, Josephina, Van Laer, Lut, Verstraeten, Aline, Loeys, Bart L.

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Confirmation of the role of pathogenic SMAD6 variants in bicuspid aortic valve-related aortopathy od Luyckx, Ilse, MacCarrick, Gretchen, Kempers, Marlies, Meester, Josephina, Geryl, Céline, Rombouts, Olivier, Peeters, Nils, Claes, Charlotte, Boeckx, Nele, Sakalihasan, Natzi, Jacquinet, Adeline, Hoischen, Alexander, Vandeweyer, Geert, Van Lent, Sarah, Saenen, Johan, Van Craenenbroeck, Emeline, Timmermans, Janneke, Duijnhouwer, Anthonie, Dietz, Harry, Van Laer, Lut, Loeys, Bart, Verstraeten, Aline

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Mutated ATP10B increases Parkinson’s disease risk by compromising lysosomal glucosylceramide export od Martin, Shaun, Smolders, Stefanie, Van den Haute, Chris, Heeman, Bavo, van Veen, Sarah, Crosiers, David, Beletchi, Igor, Verstraeten, Aline, Gossye, Helena, Gelders, Géraldine, Pals, Philippe, Hamouda, Norin Nabil, Engelborghs, Sebastiaan, Martin, Jean-Jacques, Eggermont, Jan, De Deyn, Peter Paul, Cras, Patrick, Baekelandt, Veerle, Vangheluwe, Peter, Van Broeckhoven, Christine

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A dynamic mucin mRNA signature associates with COVID-19 disease presentation and severity od Smet, Annemieke, Breugelmans, Tom, Michiels, Johan, Lamote, Kevin, Arras, Wout, De Man, Joris G., Heyndrickx, Leo, Hauner, Anne, Huizing, Manon, Malhotra-Kumar, Surbhi, Lammens, Martin, Hotterbeekx, An, Kumar-Singh, Samir, Verstraeten, Aline, Loeys, Bart, Verhoeven, Veronique, Jacobs, Rita, Dams, Karolien, Coenen, Samuel, Ariën, Kevin K., Jorens, Philippe G., De Winter, Benedicte Y.

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Bi-allelic Loss-of-Function Mutations in the NPR-C Receptor Result in Enhanced Growth and Connective Tissue Abnormalities od Boudin, Eveline, de Jong, Tjeerd R., Prickett, Tim C.R., Lapauw, Bruno, Toye, Kaatje, Van Hoof, Viviane, Luyckx, Ilse, Verstraeten, Aline, Heymans, Hugo S.A., Dulfer, Eelco, Van Laer, Lut, Berry, Ian R., Dobbie, Angus, Blair, Ed, Loeys, Bart, Espiner, Eric A., Wit, Jan M., Van Hul, Wim, Houpt, Peter, Mortier, Geert R.

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Copy number variation analysis in bicuspid aortic valve-related aortopathy identifies TBX20 as a contributing gene od Luyckx, Ilse, Kumar, Ajay A., Reyniers, Edwin, Dekeyser, Emily, Vanderstraeten, Kathleen, Vandeweyer, Geert, Wünnemann, Florian, Preuss, Christoph, Mazzella, Jean-Michaël, Goudot, Guillaume, Messas, Emmanuel, Albuisson, Juliette, Jeunemaitre, Xavier, Eriksson, Per, Mohamed, Salah A., Kempers, Marlies, Salemink, Simone, Duijnhouwer, Anthonie, Andelfinger, Gregor, Dietz, Harry C, Verstraeten, Aline, Van Laer, Lut, Loeys, Bart L.

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Loss-of-function mutations in the X-linked biglycan gene cause a severe syndromic form of thoracic aortic aneurysms and dissections od Meester, Josephina A.N., Vandeweyer, Geert, Pintelon, Isabel, Lammens, Martin, Van Hoorick, Lana, De Belder, Simon, Waitzman, Kathryn, Young, Luciana, Markham, Larry W., Vogt, Julie, Richer, Julie, Beauchesne, Luc M., Unger, Sheila, Superti-Furga, Andrea, Prsa, Milan, Dhillon, Rami, Reyniers, Edwin, Dietz, Harry C., Wuyts, Wim, Mortier, Geert, Verstraeten, Aline, Van Laer, Lut, Loeys, Bart L.

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Candidate Gene Resequencing in a Large Bicuspid Aortic Valve-Associated Thoracic Aortic Aneurysm Cohort: SMAD6 as an Important Contributor od Gillis, Elisabeth, Kumar, Ajay A., Luyckx, Ilse, Preuss, Christoph, Cannaerts, Elyssa, van de Beek, Gerarda, Wieschendorf, Björn, Alaerts, Maaike, Bolar, Nikhita, Vandeweyer, Geert, Meester, Josephina, Wünnemann, Florian, Gould, Russell A., Zhurayev, Rustam, Zerbino, Dmytro, Mohamed, Salah A., Mital, Seema, Mertens, Luc, Björck, Hanna M., Franco-Cereceda, Anders, McCallion, Andrew S., Van Laer, Lut, Verhagen, Judith M. A., van de Laar, Ingrid M. B. H., Wessels, Marja W., Messas, Emmanuel, Goudot, Guillaume, Nemcikova, Michaela, Krebsova, Alice, Kempers, Marlies, Salemink, Simone, Duijnhouwer, Toon, Jeunemaitre, Xavier, Albuisson, Juliette, Eriksson, Per, Andelfinger, Gregor, Dietz, Harry C., Verstraeten, Aline, Loeys, Bart L.

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Corrigendum: Candidate Gene Resequencing in a Large Bicuspid Aortic Valve-Associated Thoracic Aortic Aneurysm Cohort: SMAD6 as an Important Contributor od Gillis, Elisabeth, Kumar, Ajay A., Luyckx, Ilse, Preuss, Christoph, Cannaerts, Elyssa, van de Beek, Gerarda, Wieschendorf, Björn, Alaerts, Maaike, Bolar, Nikhita, Vandeweyer, Geert, Meester, Josephina, Wünnemann, Florian, Gould, Russell A., Zhurayev, Rustam, Zerbino, Dmytro, Mohamed, Salah A., Mital, Seema, Mertens, Luc, Björck, Hanna M., Franco-Cereceda, Anders, McCallion, Andrew S., Van Laer, Lut, Verhagen, Judith M. A., van de Laar, Ingrid M. B. H., Wessels, Marja W., Messas, Emmanuel, Goudot, Guillaume, Nemcikova, Michaela, Krebsova, Alice, Kempers, Marlies, Salemink, Simone, Duijnhouwer, Toon, Jeunemaitre, Xavier, Albuisson, Juliette, Eriksson, Per, Andelfinger, Gregor, Dietz, Harry C., Verstraeten, Aline, Loeys, Bart L.

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A mutation update on the LDS‐associated genes TGFB2/3 and SMAD2/3 od Schepers, Dorien, Tortora, Giada, Morisaki, Hiroko, MacCarrick, Gretchen, Lindsay, Mark, Liang, David, Mehta, Sarju G., Hague, Jennifer, Verhagen, Judith, van de Laar, Ingrid, Wessels, Marja, Detisch, Yvonne, van Haelst, Mieke, Baas, Annette, Lichtenbelt, Klaske, Braun, Kees, van der Linde, Denise, Roos‐Hesselink, Jolien, McGillivray, George, Meester, Josephina, Maystadt, Isabelle, Coucke, Paul, El‐Khoury, Elie, Parkash, Sandhya, Diness, Birgitte, Risom, Lotte, Scurr, Ingrid, Hilhorst‐Hofstee, Yvonne, Morisaki, Takayuki, Richer, Julie, Désir, Julie, Kempers, Marlies, Rideout, Andrea L., Horne, Gabrielle, Bennett, Chris, Rahikkala, Elisa, Vandeweyer, Geert, Alaerts, Maaike, Verstraeten, Aline, Dietz, Hal, Van Laer, Lut, Loeys, Bart

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ROBO4 Variants Predispose Individuals to Bicuspid Aortic Valve and Thoracic Aortic Aneurysm od Gould, Russell A, Aziz, Hamza, Woods, Courtney E, Seman-Senderos, Manuel Alejandro, Sparks, Elizabeth, Preuss, Christoph, Wünnemann, Florian, Bedja, Djahida, Moats, Cassandra R, McClymont, Sarah A, Rose, Rebecca, Sobeira, Nara, Ling, Hua, MacCarrick, Gretchen, Anand Kumar, Ajay, Luyckx, Ilse, Cannaerts, Elyssa, Verstraeten, Aline, Björk, Hanna M, Lehsau, Ann-Cathrin, Jaskula-Ranga, Vinod, Lauridsen, Henrik, Shah, Asad A, Bennett, Christopher L, Ellinor, Patrick T, Lin, Honghuang, Isselbacher, Eric M, Cardenas, Christian Lacks Lino, Butcher, Jonathan T, Hughes, G. Chad, Lindsay, Mark E., Mertens, Luc, Franco-Cereceda, Anders, Verhagen, Judith MA, Wessels, Marja, Mohamed, Salah A, Per, Eriksson, Mital, Seema, Laer, Lut Van, Loeys, Bart L, Andelfinger, Gregor, McCallion, Andrew S, Dietz, Harry C

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Global investigation and meta-analysis of the C9orf72 (G(4)C(2))(n) repeat in Parkinson disease od Theuns, Jessie, Verstraeten, Aline, Sleegers, Kristel, Wauters, Eline, Gijselinck, Ilse, Smolders, Stefanie, Crosiers, David, Corsmit, Ellen, Elinck, Ellen, Sharma, Manu, Krüger, Rejko, Lesage, Suzanne, Brice, Alexis, Chung, Sun Ju, Kim, Mi-Jung, Kim, Young Jin, Ross, Owen A., Wszolek, Zbigniew K., Rogaeva, Ekaterina, Xi, Zhengrui, Lang, Anthony E., Klein, Christine, Weissbach, Anne, Mellick, George D., Silburn, Peter A., Hadjigeorgiou, Georgios M., Dardiotis, Efthimios, Hattori, Nobutaka, Ogaki, Kotaro, Tan, Eng-King, Zhao, Yi, Aasly, Jan, Valente, Enza Maria, Petrucci, Simona, Annesi, Grazia, Quattrone, Aldo, Ferrarese, Carlo, Brighina, Laura, Deutschländer, Angela, Puschmann, Andreas, Nilsson, Christer, Garraux, Gaëtan, LeDoux, Mark S., Pfeiffer, Ronald F., Boczarska-Jedynak, Magdalena, Opala, Grzegorz, Maraganore, Demetrius M., Engelborghs, Sebastiaan, De Deyn, Peter Paul, Cras, Patrick, Cruts, Marc, Van Broeckhoven, Christine

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