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Refinado por: Nome da Publicação: Archives Of Cardiovascular Diseases Supplements remover
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Mitral Valve Dystrophy: What role do leukocytes play?
Mitral Valve Dystrophy: What role do leukocytes play?
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Mitral Valve Dystrophy: What role do leukocytes play?

Delwarde, Constance ; Le Vély, Benjamin ; Kayvanjoo, Amir H. ; Aumond, Pascal ; Remy, Séverine ; Monassier, Laurent ; Toquet, Claire ; Schott, Jean-Jacques ; Le Tourneau, Thierry ; Mass, Elvira ; Mérot, Jean ; Capoulade, Romain

Archives of cardiovascular diseases supplements, 2022-06, Vol.14 (2), p.204 [Periódico revisado por pares]

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2
Non-coding deletion induces 3D chromatin remodelling and PITX2 expression dysregulation associated with a new syndromic cardiac disorder
Non-coding deletion induces 3D chromatin remodelling and PITX2 expression dysregulation associated with a new syndromic cardiac disorder
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Non-coding deletion induces 3D chromatin remodelling and PITX2 expression dysregulation associated with a new syndromic cardiac disorder

Baudic, Manon ; Murata, Hiroshigue ; Bosada, Fernanda ; Melo, Uirá Souto ; Ishikawa, Taisuke ; Aizawa, Takanori ; Guedon, Amaury ; Baron, Estelle ; Foucal, Adrien ; Lindenbaum, Pierre ; Le Scouarnec, Solena ; Makita, Naomasa ; Le Marec, Hervé ; Vieyres, Claude ; Mundlos, Stephan ; Christoffels, Vincent M. ; Makiyama, Takeru ; Probst, Vincent ; Schott, Jean-Jacques ; Barc, Julien

Archives of cardiovascular diseases supplements, 2022-06, Vol.14 (2), p.209 [Periódico revisado por pares]

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3
Familial recurrence patterns in congenitally corrected transposition of the great arteries: An international study
Familial recurrence patterns in congenitally corrected transposition of the great arteries: An international study
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Familial recurrence patterns in congenitally corrected transposition of the great arteries: An international study

Tortigue, Marine ; Nield, Lynne E. ; McLeod, Christopher J. ; Belli, Emre ; Babu-Narayan, Sonya ; Prigent, Solène ; Boet, Angèle ; Conway, Miriam ; Elder, Robert W. ; Ladouceur, Magalie ; Khairy, Paul ; Kowalik, Eva ; Kalfa, David M. ; Barron, David J. ; Mussa, Shafi ; Hiippala, Anita ; Temple, Joel ; Abadir, Sylvia ; Le Gloan, Laurianne ; Lachaud, Mathias ; Sanatani, Shubhayan ; Thambo, Jean-Benoît ; Grunenwald Gronier, Céline ; Amedro, Pascal ; Vaksmann, Guy ; Charbonneau, Anne ; Koutbi, Linda ; Ovaert, Caroline ; Houeijeh, Ali ; Combes, Nicolas ; Maury, Philippe ; Duthoit, Guillaume ; Hiel, Bérengère ; Erickson, Christopher C. ; Bonnet, Caroline ; Van Hare, George F. ; Dina, Christian ; Karakachoff, Matilde ; Karsenty, Clément ; Fournier, Emmanuelle ; Le Bloa, Mathieu ; Pass, Robert H. ; Liberman, Leonardo ; Happonen, Juha-Matti ; Perry, James C. ; Fraisse, Alain ; Gatzoulis, Michael A. ; Abrams, Dominic J. ; Dubin, Anne M. ; Yen Ho, Siew ; Redon, Richard ; Bacha, Emile A. ; Schott, Jean-Jacques ; Baruteau, Alban-Elouen

Archives of cardiovascular diseases supplements, 2021-09, Vol.13 (4), p.284-285 [Periódico revisado por pares]

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4
SCN5A mutations in 442 neonates and children: Genotype-phenotype correlation and identification of higher-risk subgroups
SCN5A mutations in 442 neonates and children: Genotype-phenotype correlation and identification of higher-risk subgroups
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SCN5A mutations in 442 neonates and children: Genotype-phenotype correlation and identification of higher-risk subgroups

Baruteau, Alban-Elouen ; Kyndt, Florence ; Behr, Elijah ; Vink, Arja ; Lachaud, Matthias ; Joong, Anna ; Schott, Jean-Jacques ; Horie, Minoru ; Denjoy, Isabelle ; Crotti, Lia ; Shimizu, Wataru ; Bos, Johan ; Stephenson, Elizabeth ; Wong, Leonie ; Abrams, Dominic ; Davis, Andrew ; Winbo, Annika ; Dubin, Anne ; Sanatani, Shubhayan ; Liberman, Leonardo ; Kaski, Juan-Pablo ; Rudic, Boris ; Kwok, Sit Yee ; Rieubland, Claudine ; Tfelt-Hansen, Jacob ; Van Hare, George ; Guyomarc’h-Delasalle, Béatrice ; Blom, Nico ; Wijeyeratne, Yanushi ; Gourraud, Jean-Baptiste ; Le Marec, Hervé ; Ozawa, Junichi ; Fressart, Véronique ; Lupoglazoff, Jean-Marc ; Dagradi, Federica ; Spazzolini, Carla ; Aiba, Takeshi ; Tester, David ; Zahavich, Laura ; Beauséjour-Ladouceur, Virginie ; Jadhav, Mangesh ; Skinner, Jonathan ; Franciosi, Sonia ; Krahn, Andrew ; Abdelsayed, Mena ; Ruben, Peter ; Yung, Tak-Cheung ; Ackerman, Michael ; Wilde, Arthur ; Schwartz, Peter ; Probst, Vincent

Archives of cardiovascular diseases supplements, 2019-09, Vol.11 (4), p.e381-e382 [Periódico revisado por pares]

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5
0216 : Involvement of the receptor-type tyrosine-protein phosphatase F gene PTPRF, a cell adhesion-like molecule, in Mitral Valve Prolapse (MVP)
0216 : Involvement of the receptor-type tyrosine-protein phosphatase F gene PTPRF, a cell adhesion-like molecule, in Mitral Valve Prolapse (MVP)
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0216 : Involvement of the receptor-type tyrosine-protein phosphatase F gene PTPRF, a cell adhesion-like molecule, in Mitral Valve Prolapse (MVP)

Labbé, Pauline ; Rimbert, Antoine ; Jobbe-Duval, Antoine ; Lecointe, Simon ; Le Scouarnec, Solena ; Kyndt, Florence ; Le Tourneau, Thierry ; Schott, Jean-Jacques ; Merot, Jean

Archives of cardiovascular diseases supplements, 2016-04, Vol.8 (3), p.262 [Periódico revisado por pares]

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6
0030: ARHGAP 24/ (FilGAP); a new gene responsible for mitral valve prolapse
0030: ARHGAP 24/ (FilGAP); a new gene responsible for mitral valve prolapse
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0030: ARHGAP 24/ (FilGAP); a new gene responsible for mitral valve prolapse

Duval, Damien ; Rimbert, Antoine ; Kyndt, Florence ; Tourneau, Thierry Le ; Probst, Vincent ; Schott, Jean-Jacques ; Mérot, Jean

Archives of cardiovascular diseases supplements, 2014-04, Vol.6, p.72-73 [Periódico revisado por pares]

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7
0233: Mental stress test for the diagnosis of congenital long QT syndrom: a pilot study
0233: Mental stress test for the diagnosis of congenital long QT syndrom: a pilot study
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0233: Mental stress test for the diagnosis of congenital long QT syndrom: a pilot study

Huchet, François ; Gourraud, Jean-Baptiste ; Kyndt, Florence ; Thollet, Aurelie ; Schott, Jean-Jacques ; Redon, Richard ; Barc, Julien ; Marec, Hervé Le ; Probst, Vincent

Archives of cardiovascular diseases supplements, 2016-01, Vol.8 (1), p.66 [Periódico revisado por pares]

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8
0493: Mutations in the gene encoding FilGAP as a cause for mitral valve prolapse
0493: Mutations in the gene encoding FilGAP as a cause for mitral valve prolapse
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0493: Mutations in the gene encoding FilGAP as a cause for mitral valve prolapse

Rimbert, Antoine ; Duval, Damien ; Kyndt, Florence ; Lecointe, Simon ; Probst, Vincent ; Le Tourneau, Thierry ; Mérot, Jean ; Schott, Jean-Jacques

Archives of cardiovascular diseases supplements, 2015-01, Vol.7 (1), p.51 [Periódico revisado por pares]

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9
0207 : Functional explorations of genes near genetic risk loci for mitral valve prolapse involve TNS1 and LMCD1 in valve development and integrity
0207 : Functional explorations of genes near genetic risk loci for mitral valve prolapse involve TNS1 and LMCD1 in valve development and integrity
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0207 : Functional explorations of genes near genetic risk loci for mitral valve prolapse involve TNS1 and LMCD1 in valve development and integrity

Bouatia-Naji, Nabila ; Dina, Christian ; Tucker, Nathan ; Toomer, Katelyn ; Slaugenhaupt, Susan ; Levine, Robert ; Schott, Jean-Jacques ; Hagège, Albert ; Norris, Russell ; Milan, David ; Jenuemaitre, Xavier

Archives of cardiovascular diseases supplements, 2015-04, Vol.7 (2), p.204 [Periódico revisado por pares]

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10
0211 : Implications of baselines 2010 task force criterias on ventricular arrhythmias in ARVC
0211 : Implications of baselines 2010 task force criterias on ventricular arrhythmias in ARVC
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0211 : Implications of baselines 2010 task force criterias on ventricular arrhythmias in ARVC

Amara, Nelly ; Gourraud, Jean-Baptiste ; Denis, Arnaud ; Mabo, Philippe ; Thollet, Aurélie ; Kyndt, Florence ; Barc, Julien ; Schott, Jean-Jacques ; Le Marec, Hervé ; Redon, Richard ; Probst, Vincent

Archives of cardiovascular diseases supplements, 2015-04, Vol.7 (2), p.169 [Periódico revisado por pares]

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