Works by DE BACKER, Julie


Results: 71
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    Case-matched Comparison of Cardiovascular Outcome in Loeys-Dietz Syndrome versus Marfan Syndrome.

    Published in:
    Journal of Clinical Medicine, 2019, v. 8, n. 12, p. 2079, doi. 10.3390/jcm8122079
    By:
    • Mühlstädt, Kristina;
    • De Backer, Julie;
    • von Kodolitsch, Yskert;
    • Kutsche, Kerstin;
    • Muiño Mosquera, Laura;
    • Brickwedel, Jens;
    • Girdauskas, Evaldas;
    • Mir, Thomas S.;
    • Mahlmann, Adrian;
    • Tsilimparis, Nikolaos;
    • Staebler, Axel;
    • Schoof, Lauritz;
    • Seidel, Heide;
    • Berger, Jürgen;
    • Bernhardt, Alexander M.;
    • Blankenberg, Stefan;
    • Kölbel, Tilo;
    • Detter, Christian;
    • Szöcs, Katalin;
    • Kaemmerer, Harald
    Publication type:
    Article
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    Genetic counselling and testing in adults with congenital heart disease: A consensus document of the ESC Working Group of Grown-Up Congenital Heart Disease, the ESC Working Group on Aorta and Peripheral Vascular Disease and the European Society of Human Genetics

    Published in:
    European Journal of Preventive Cardiology, 2020, v. 27, n. 13, p. 1423, doi. 10.1177/2047487319854552
    By:
    • De Backer, Julie;
    • Bondue, Antoine;
    • Budts, Werner;
    • Evangelista, Arturo;
    • Gallego, Pastora;
    • Jondeau, Guillaume;
    • Loeys, Bart;
    • Peña, Maria L;
    • Teixido-Tura, Gisela;
    • van de Laar, Ingrid;
    • Verstraeten, Aline;
    • Roos Hesselink, Jolien
    Publication type:
    Article
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    Cardiovascular manifestations in men and women carrying a FBN1 mutation.

    Published in:
    European Heart Journal, 2010, v. 31, n. 18, p. 2223
    By:
    • Détaint, Delphine;
    • Faivre, Laurence;
    • Collod-Beroud, Gwenaelle;
    • Child, Anne H.;
    • Loeys, Bart L.;
    • Binquet, Christine;
    • Gautier, Elodie;
    • Arbustini, Eloisa;
    • Mayer, Karin;
    • Arslan-Kirchner, Mine;
    • Stheneur, Chantal;
    • Halliday, Dorothy;
    • Beroud, Christophe;
    • Bonithon-Kopp, Claire;
    • Claustres, Mireille;
    • Plauchu, Henri;
    • Robinson, Peter N.;
    • Kiotsekoglou, Anatoli;
    • De Backer, Julie;
    • Adès, Lesley
    Publication type:
    Article
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    New insights into the structural role of EMILINs within the human skin microenvironment.

    Published in:
    Scientific Reports, 2024, v. 14, n. 1, p. 1, doi. 10.1038/s41598-024-81509-5
    By:
    • Schiavinato, Alvise;
    • Marcous, Fady;
    • Zuk, Alexandra V.;
    • Keene, Douglas R.;
    • Tufa, Sara F.;
    • Mosquera, Laura M.;
    • Zigrino, Paola;
    • Mauch, Cornelia;
    • Eckes, Beate;
    • Francois, Katrien;
    • De Backer, Julie;
    • Hunzelmann, Nicolas;
    • Moinzadeh, Pia;
    • Krieg, Thomas;
    • Callewaert, Bert;
    • Sengle, Gerhard
    Publication type:
    Article
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    Aortic disease in Marfan syndrome is caused by overactivation of sGC-PRKG signaling by NO.

    Published in:
    Nature Communications, 2021, v. 12, n. 1, p. 1, doi. 10.1038/s41467-021-22933-3
    By:
    • de la Fuente-Alonso, Andrea;
    • Toral, Marta;
    • Alfayate, Alvaro;
    • Ruiz-Rodríguez, María Jesús;
    • Bonzón-Kulichenko, Elena;
    • Teixido-Tura, Gisela;
    • Martínez-Martínez, Sara;
    • Méndez-Olivares, María José;
    • López-Maderuelo, Dolores;
    • González-Valdés, Ileana;
    • Garcia-Izquierdo, Eusebio;
    • Mingo, Susana;
    • Martín, Carlos E.;
    • Muiño-Mosquera, Laura;
    • De Backer, Julie;
    • Nistal, J. Francisco;
    • Forteza, Alberto;
    • Evangelista, Arturo;
    • Vázquez, Jesús;
    • Campanero, Miguel R.
    Publication type:
    Article
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    2024 ESC Guidelines for the management of peripheral arterial and aortic diseases: Developed by the task force on the management of peripheral arterial and aortic diseases of the European Society of Cardiology (ESC) Endorsed by the European Association for Cardio-Thoracic Surgery (EACTS), the European Reference Network on Rare Multisystemic Vascular Diseases (VASCERN), and the European Society of Vascular Medicine (ESVM)

    Published in:
    European Heart Journal, 2024, v. 45, n. 36, p. 3538, doi. 10.1093/eurheartj/ehae179
    By:
    • Mazzolai, Lucia;
    • Teixido-Tura, Gisela;
    • Lanzi, Stefano;
    • Boc, Vinko;
    • Bossone, Eduardo;
    • Brodmann, Marianne;
    • Bura-Rivière, Alessandra;
    • Backer, Julie De;
    • Deglise, Sebastien;
    • Corte, Alessandro Della;
    • Heiss, Christian;
    • Kałużna-Oleksy, Marta;
    • Kurpas, Donata;
    • McEniery, Carmel M;
    • Mirault, Tristan;
    • Pasquet, Agnes A;
    • Pitcher, Alex;
    • Schaubroeck, Hannah A I;
    • Schlager, Oliver;
    • Sirnes, Per Anton
    Publication type:
    Article
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    Mutations in the facilitative glucose transporter GLUT10 alter angiogenesis and cause arterial tortuosity syndrome.

    Published in:
    Nature Genetics, 2006, v. 38, n. 4, p. 452, doi. 10.1038/ng1764
    By:
    • Coucke, Paul J.;
    • Willaert, Andy;
    • Wessels, Marja W.;
    • Callewaert, Bert;
    • Zoppi, Nicoletta;
    • De Backer, Julie;
    • Fox, Joyce E.;
    • Mancini, Grazia M. S.;
    • Kambouris, Marios;
    • Gardella, Rita;
    • Facchetti, Fabio;
    • Willems, Patrick J.;
    • Forsyth, Ramses;
    • Dietz, Harry C.;
    • Barlati, Sergio;
    • Colombi, Marina;
    • Loeys, Bart;
    • De Paepe, Anne
    Publication type:
    Article
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    A syndrome of altered cardiovascular, craniofacial, neurocognitive and skeletal development caused by mutations in TGFBR1 or TGFBR2.

    Published in:
    Nature Genetics, 2005, v. 37, n. 3, p. 275, doi. 10.1038/ng1511
    By:
    • Loeys, Bart L;
    • Chen, Junji;
    • Neptune, Enid R;
    • Judge, Daniel P;
    • Podowski, Megan;
    • Holm, Tammy;
    • Meyers, Jennifer;
    • Leitch, Carmen C;
    • Katsanis, Nicholas;
    • Sharifi, Neda;
    • Xu, F Lauren;
    • Myers, Loretha A;
    • Spevak, Philip J;
    • Cameron, Duke E;
    • Backer, Julie De;
    • Hellemans, Jan;
    • Chen, Yan;
    • Davis, Elaine C;
    • Webb, Catherine L;
    • Kress, Wolfram
    Publication type:
    Article
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    Bicuspid Aortic Valve Disease with Early-Onset Complications: Characteristics and Aortic Outcomes.

    Published in:
    Hearts, 2024, v. 5, n. 3, p. 253, doi. 10.3390/hearts5030018
    By:
    • Selbst, Maximilian A.;
    • Ward, Colin R.;
    • Svetgoff, Megan L.;
    • Michelena, Hector I.;
    • Sabate-Rotes, Anna;
    • De Backer, Julie;
    • Mosquera, Laura Muiño;
    • Yetman, Anji T.;
    • Bissell, Malenka M.;
    • Andreassi, Maria Grazia;
    • Foffa, Ilenia;
    • Hui, Dawn S.;
    • Caffarelli, Anthony;
    • Kim, Yuli Y.;
    • Guo, Dongchuan;
    • Citro, Rodolfo;
    • De Marco, Margot;
    • Tretter, Justin T.;
    • Morris, Shaine A.;
    • McBride, Kim L.
    Publication type:
    Article
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    Perspectives on the revised Ghent criteria for the diagnosis of Marfan syndrome.

    Published in:
    Application of Clinical Genetics, 2015, v. 8, p. 137, doi. 10.2147/TACG.S60472
    By:
    • von Kodolitsch, Yskert;
    • De Backer, Julie;
    • Schüler, Helke;
    • Bannas, Peter;
    • Behzadi, Cyrus;
    • Bernhardt, Alexander M.;
    • Hillebrand, Mathias;
    • Fuisting, Bettina;
    • Sheikhzadeh, Sara;
    • Rybczynski, Meike;
    • Kölbel, Tilo;
    • Püschel, Klaus;
    • Blankenberg, Stefan;
    • Robinson, Peter N.
    Publication type:
    Article
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    Sex, pregnancy and aortic disease in Marfan syndrome.

    Published in:
    PLoS ONE, 2017, v. 12, n. 7, p. 1, doi. 10.1371/journal.pone.0181166
    By:
    • Renard, Marjolijn;
    • Muiño-Mosquera, Laura;
    • Manalo, Elise C.;
    • Tufa, Sara;
    • Carlson, Eric J.;
    • Keene, Douglas R.;
    • De Backer, Julie;
    • Sakai, Lynn Y.
    Publication type:
    Article
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    Body mass index in adults with congenital heart disease.

    Published in:
    Congenital Heart Disease, 2019, v. 14, n. 3, p. 479, doi. 10.1111/chd.12751
    By:
    • Vandekerckhove, Kristof;
    • De Wolf, Daniel;
    • Zaqout, Mahmoud;
    • Michels, Nathalie;
    • De Henauw, Stefaan;
    • Demulier, Laurent;
    • De Backer, Julie;
    • Bove, Thierry;
    • François, Katrien
    Publication type:
    Article
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    Mitral Annular Disjunction in Heritable Thoracic Aortic Disease: Insights From the Montalcino Aortic Consortium.

    Published in:
    Journal of the American Heart Association, 2024, v. 13, n. 21, p. 1, doi. 10.1161/JAHA.124.036274
    By:
    • Asokan, Kishan L.;
    • Landes, Jennifer R.;
    • Renders, Wannes;
    • Muiño Mosquera, Laura;
    • De Backer, Julie;
    • Jantzen, David W.;
    • Yetman, Anji T.;
    • Teixido-Tura, Gisela;
    • Evangelista, Arturo;
    • Jeremy, Richmond;
    • Jones, Edward G.;
    • Morris, Shaine;
    • Doan, Tam;
    • Ouzonian, Maral;
    • Braverman, Alan;
    • Jondeau, Guillaume;
    • Milleron, Olivier;
    • Milewicz, Dianna M.;
    • Prakash, Siddharth K.
    Publication type:
    Article
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    Rare genomic copy number variants implicate new candidate genes for bicuspid aortic valve.

    Published in:
    PLoS ONE, 2024, v. 19, n. 9, p. 1, doi. 10.1371/journal.pone.0304514
    By:
    • Carlisle, Steven G.;
    • Albasha, Hasan;
    • Michelena, Hector I.;
    • Sabate-Rotes, Anna;
    • Bianco, Lisa;
    • De Backer, Julie;
    • Mosquera, Laura Muiño;
    • Yetman, Anji T.;
    • Bissell, Malenka M.;
    • Andreassi, Maria Grazia;
    • Foffa, Ilenia;
    • Hui, Dawn S.;
    • Caffarelli, Anthony;
    • Kim, Yuli Y.;
    • Guo, Dongchuan;
    • Citro, Rodolfo;
    • De Marco, Margot;
    • Tretter, Justin T.;
    • McBride, Kim L.;
    • Milewicz, Dianna M.
    Publication type:
    Article
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    The main pulmonary artery in adults: a controlled multicenter study with assessment of echocardiographic reference values, and the frequency of dilatation and aneurysm in Marfan syndrome.

    Published in:
    Orphanet Journal of Rare Diseases, 2014, v. 9, n. 1, p. 330, doi. 10.1186/s13023-014-0203-8
    By:
    • Sheikhzadeh, Sara;
    • De Backer, Julie;
    • Rahimian Gorgan, Neda;
    • Rybczynski, Meike;
    • Hillebrand, Mathias;
    • Schüler, Helke;
    • Bernhardt, Alexander M.;
    • Koschyk, Dietmar;
    • Bannas, Peter;
    • Keyser, Britta;
    • Mortensen, Kai;
    • Radke, Robert M.;
    • Mir, Thomas S.;
    • Kölbel, Tilo;
    • Robinson, Peter N.;
    • Schmidtke, Jörg;
    • Berger, Jürgen;
    • Blankenberg, Stefan;
    • von Kodolitsch, Yskert
    Publication type:
    Article
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    Different levels of care for follow-up of adults with congenital heart disease: a cost analysis scrutinizing the impact on medical costs, hospitalizations, and emergency department visits.

    Published in:
    European Journal of Health Economics, 2021, v. 22, n. 6, p. 951, doi. 10.1007/s10198-021-01300-5
    By:
    • Willems, Ruben;
    • Ombelet, Fouke;
    • Goossens, Eva;
    • De Groote, Katya;
    • Budts, Werner;
    • Moniotte, Stéphane;
    • de Hosson, Michèle;
    • Van Bulck, Liesbet;
    • Marelli, Ariane;
    • Moons, Philip;
    • De Backer, Julie;
    • Annemans, Lieven
    Publication type:
    Article
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    Comprehensive clinical and molecular assessment of 32 probands with congenital contractural arachnodactyly: Report of 14 novel mutations and review of the literature.

    Published in:
    Human Mutation, 2009, v. 30, n. 3, p. 334, doi. 10.1002/humu.20854
    By:
    • Callewaert, Bert L.;
    • Loeys, Bart L.;
    • Ficcadenti, Anna;
    • Vermeer, Sascha;
    • Landgren, Magnus;
    • Kroes, Hester Y.;
    • Yaron, Yuval;
    • Pope, Michael;
    • Foulds, Nicola;
    • Boute, Odile;
    • Galán, Francisco;
    • Kingston, Helen;
    • Van der Aa, Nathalie;
    • Salcedo, Iratxe;
    • Swinkels, Marielle E.;
    • Wallgren-Pettersson, Carina;
    • Gabrielli, Orazio;
    • De Backer, Julie;
    • Coucke, Paul J.;
    • De Paepe, Anne M.
    Publication type:
    Article
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    Features of Marfan syndrome not listed in the Ghent nosology - the dark side of the disease.

    Published in:
    2019
    By:
    • von Kodolitsch, Yskert;
    • Demolder, Anthony;
    • Girdauskas, Evaldas;
    • Kaemmerer, Harald;
    • Kornhuber, Katharina;
    • Muino Mosquera, Laura;
    • Morris, Shaine;
    • Neptune, Enid;
    • Pyeritz, Reed;
    • Rand-Hendriksen, Svend;
    • Rahman, Alexander;
    • Riise, Nina;
    • Robert, Leema;
    • Staufenbiel, Ingmar;
    • Szöcs, Katalin;
    • Vanem, Thy Thy;
    • Linke, Stephan J.;
    • Vogler, Marina;
    • Yetman, Anji;
    • De Backer, Julie
    Publication type:
    journal article
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    Predictors of Rapid Aortic Root Dilation and Referral for Aortic Surgery in Marfan Syndrome.

    Published in:
    Pediatric Cardiology, 2018, v. 39, n. 7, p. 1453, doi. 10.1007/s00246-018-1916-6
    By:
    • Hoskoppal, Arvind;
    • Menon, Shaji;
    • Trachtenberg, Felicia;
    • Burns, Kristin M.;
    • De Backer, Julie;
    • Gelb, Bruce D.;
    • Gleason, Marie;
    • James, Jeanne;
    • Lai, Wyman W.;
    • Liou, Aimee;
    • Mahony, Lynn;
    • Olson, Aaron K.;
    • Pyeritz, Reed E.;
    • Sharkey, Angela M.;
    • Stylianou, Mario;
    • Wechsler, Stephanie Burns;
    • Young, Luciana;
    • Levine, Jami C.;
    • Tierney, Elif Seda Selamet;
    • Lacro, Ronald V.
    Publication type:
    Article
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    A new dimension in patent foramen ovale size estimation.

    Published in:
    Echocardiography, 2020, v. 37, n. 7, p. 1049, doi. 10.1111/echo.14696
    By:
    • Demulier, Laurent;
    • Paelinck, Bernard Pierre;
    • Coomans, Ilse;
    • Hemelsoet, Dimitri;
    • De Backer, Julie;
    • Campens, Laurence;
    • De Wolf, Daniel
    Publication type:
    Article