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Page 1
Progressive Atrial Conduction Defects Associated With Bone Malformation Caused by a Connexin-45 Mutation.
Seki A, Ishikawa T, Daumy X, Mishima H, Barc J, Sasaki R, Nishii K, Saito K, Urano M, Ohno S, Otsuki S, Kimoto H, Baruteau AE, Thollet A, Fouchard S, Bonnaud S, Parent P, Shibata Y, Perrin JP, Le Marec H, Hagiwara N, Mercier S, Horie M, Probst V, Yoshiura KI, Redon R, Schott JJ, Makita N. Seki A, et al. Among authors: baruteau ae. J Am Coll Cardiol. 2017 Jul 18;70(3):358-370. doi: 10.1016/j.jacc.2017.05.039. J Am Coll Cardiol. 2017. PMID: 28705318 Free article.
Characteristics and long-term outcome of non-immune isolated atrioventricular block diagnosed in utero or early childhood: a multicentre study.
Baruteau AE, Fouchard S, Behaghel A, Mabo P, Villain E, Thambo JB, Marçon F, Gournay V, Rouault F, Chantepie A, Guillaumont S, Godart F, Bonnet C, Fraisse A, Schleich JM, Lusson JR, Dulac Y, Leclercq C, Daubert JC, Schott JJ, Le Marec H, Probst V. Baruteau AE, et al. Eur Heart J. 2012 Mar;33(5):622-9. doi: 10.1093/eurheartj/ehr347. Epub 2011 Sep 14. Eur Heart J. 2012. PMID: 21920962
Parental electrocardiographic screening identifies a high degree of inheritance for congenital and childhood nonimmune isolated atrioventricular block.
Baruteau AE, Behaghel A, Fouchard S, Mabo P, Schott JJ, Dina C, Chatel S, Villain E, Thambo JB, Marçon F, Gournay V, Rouault F, Chantepie A, Guillaumont S, Godart F, Martins RP, Delasalle B, Bonnet C, Fraisse A, Schleich JM, Lusson JR, Dulac Y, Daubert JC, Le Marec H, Probst V. Baruteau AE, et al. Circulation. 2012 Sep 18;126(12):1469-77. doi: 10.1161/CIRCULATIONAHA.111.069161. Epub 2012 Aug 16. Circulation. 2012. PMID: 22899775 Free article.
Inherited progressive cardiac conduction disorders.
Baruteau AE, Probst V, Abriel H. Baruteau AE, et al. Curr Opin Cardiol. 2015 Jan;30(1):33-9. doi: 10.1097/HCO.0000000000000134. Curr Opin Cardiol. 2015. PMID: 25426816 Free article. Review.
Cardiac Phenotype and Long-Term Follow-Up of Patients With Mutations in NKX2-5 Gene.
Maury P, Gandjbakhch E, Baruteau AE, Bessière F, Kyndt F, Bouvagnet P, Rollin A, Bonnet D, Probst V, Maltret A. Maury P, et al. Among authors: baruteau ae. J Am Coll Cardiol. 2016 Nov 29;68(21):2389-2390. doi: 10.1016/j.jacc.2016.08.064. J Am Coll Cardiol. 2016. PMID: 27884258 Free article. No abstract available.
Differential calcium sensitivity in NaV 1.5 mixed syndrome mutants.
Abdelsayed M, Baruteau AE, Gibbs K, Sanatani S, Krahn AD, Probst V, Ruben PC. Abdelsayed M, et al. Among authors: baruteau ae. J Physiol. 2017 Sep 15;595(18):6165-6186. doi: 10.1113/JP274536. Epub 2017 Aug 20. J Physiol. 2017. PMID: 28734073 Free PMC article.
SCN5A mutations in 442 neonates and children: genotype-phenotype correlation and identification of higher-risk subgroups.
Baruteau AE, Kyndt F, Behr ER, Vink AS, Lachaud M, Joong A, Schott JJ, Horie M, Denjoy I, Crotti L, Shimizu W, Bos JM, Stephenson EA, Wong L, Abrams DJ, Davis AM, Winbo A, Dubin AM, Sanatani S, Liberman L, Kaski JP, Rudic B, Kwok SY, Rieubland C, Tfelt-Hansen J, Van Hare GF, Guyomarc'h-Delasalle B, Blom NA, Wijeyeratne YD, Gourraud JB, Le Marec H, Ozawa J, Fressart V, Lupoglazoff JM, Dagradi F, Spazzolini C, Aiba T, Tester DJ, Zahavich LA, Beauséjour-Ladouceur V, Jadhav M, Skinner JR, Franciosi S, Krahn AD, Abdelsayed M, Ruben PC, Yung TC, Ackerman MJ, Wilde AA, Schwartz PJ, Probst V. Baruteau AE, et al. Eur Heart J. 2018 Aug 14;39(31):2879-2887. doi: 10.1093/eurheartj/ehy412. Eur Heart J. 2018. PMID: 30059973 Free article.
114 results