Hakutulokset - Dietz, Hal

Utility of Genetic Testing in Elite Volleyball Players with Aortic Root Dilation Tekijä Herrick, Nicole, Davis, Christopher, Vargas, Lisa, Dietz, Hal, Grossfeld, Paul

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Novel MYH11 and ACTA2 mutations reveal a role for enhanced TGFβ signaling in FTAAD Tekijä Renard, Marjolijn, Callewaert, Bert, Baetens, Machteld, Campens, Laurence, MacDermot, Kay, Fryns, Jean-Pierre, Bonduelle, Maryse, Dietz, Hal, Gaspar, Isabel Mendes, Cavaco, Diogo, Stattin, Eva-Lena, Schrander-Stumpel, Constance, Coucke, Paul, Loeys, Bart, De Paepe, Anne, De Backer, Julie

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Surgical Treatment of Patients Enrolled in the National Registry of Genetically Triggered Thoracic Aortic Conditions (GenTAC) Tekijä Song, Howard K., Bavaria, Joseph E., Kindem, Mark W., Holmes, Kathryn W., Milewicz, Dianna M., Maslen, Cheryl L., Pyeritz, Reed E., Basson, Craig T., Eagle, Kim, Tolunay, H. Eser, Kroner, Barbara L., Dietz, Hal, Menashe, Victor, Devereux, Richard B., Desvigne-Nickens, Patrice, Ravekes, William, Weinsaft, Jonathan W., Brambilla, Donald, Stylianou, Mario P., Hendershot, Tabitha, Mitchell, Megan S., LeMaire, Scott A.

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Angiotensin receptor blockers and β blockers in Marfan syndrome: an individual patient data meta-analysis of randomised trials Tekijä Pitcher, Alex, Spata, Enti, Emberson, Jonathan, Davies, Kelly, Halls, Heather, Holland, Lisa, Wilson, Kate, Reith, Christina, Child, Anne H, Clayton, Tim, Dodd, Matthew, Flather, Marcus, Jin, Xu Yu, Sandor, George, Groenink, Maarten, Mulder, Barbara, De Backer, Julie, Evangelista, Arturo, Forteza, Alberto, Teixido-Turà, Gisela, Boileau, Catherine, Jondeau, Guillaume, Milleron, Olivier, Lacro, Ronald V, Sleeper, Lynn A, Chiu, Hsin-Hui, Wu, Mei-Hwan, Neubauer, Stefan, Watkins, Hugh, Dietz, Hal, Baigent, Colin

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Aortic Complications Associated With Pregnancy in Marfan Syndrome: The NHLBI National Registry of Genetically Triggered Thoracic Aortic Aneurysms and Cardiovascular Conditions (Gen... Tekijä Roman, Mary J., Pugh, Norma L., Hendershot, Tabitha P., Devereux, Richard B., Dietz, Hal, Holmes, Kathryn, Eagle, Kim A., LeMaire, Scott A., Milewicz, Dianna M., Morris, Shaine A., Pyeritz, Reed E., Ravekes, William J., Shohet, Ralph V., Silberbach, Michael, Dietz, Harry C., Habashi, Jennifer, Prakash, Siddharth K., Maslen, Cheryl L., Song, Howard K., Bavaria, Joseph E., Milewski, Karianna, Weinsaft, Jonathan W., McDonnell, Nazli, Asch, Federico M., Tolunay, H. Eser, Desvigne‐Nickens, Patrice, Tseng, Hung, Kroner, Barbara L.

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A mutation update on the LDS‐associated genes TGFB2/3 and SMAD2/3 Tekijä 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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