Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Bernard Debost"'
Autor:
Bernard Debost, Caroline Martin-Bonnet, Sylvie Di Filippo, Cecile Leconte, Claire Bertail-Galoin, Mohamed Bakloul, Thomas Perouse-de-Montclos, Anne Moulin-Zinsch
Publikováno v:
Archives of cardiovascular diseases
Archives of cardiovascular diseases, 2021, 114 (2), pp.115-121. ⟨10.1016/j.acvd.2020.06.005⟩
Archives of cardiovascular diseases, Elsevier/French Society of Cardiology, 2021, 114 (2), pp.115-121. ⟨10.1016/j.acvd.2020.06.005⟩
Archives of cardiovascular diseases, 2021, 114 (2), pp.115-121. ⟨10.1016/j.acvd.2020.06.005⟩
Archives of cardiovascular diseases, Elsevier/French Society of Cardiology, 2021, 114 (2), pp.115-121. ⟨10.1016/j.acvd.2020.06.005⟩
Summary Background Abnormal coronary pattern may complicate coronary transfer during arterial switch operation. Objective To evaluate the accuracy of echocardiography in assessing the anatomy of coronary arteries in neonates with transposition of the
Autor:
C Walton, Caroline Martin-Bonnet, Hervé Joly, Claire Bertail-Galoin, Nicolas Pangaud, Sylvie Di Filippo, Thomas Perouse de Montclos, Mohamed Bakloul, Bernard Debost
Publikováno v:
Pediatric Cardiology. 40:276-282
To assess the outcomes of neonates prenatally diagnosed with ventricular asymmetry and not operated on within the neonatal period and to determine the risk factors for left heart obstruction occurrence at follow-up. All neonates with prenatal asymmet
Autor:
Audrey Labalme, Jean-François Obadia, Patrick Edery, Sophie Dupuis-Girod, Marianne Till, Bernard Debost, Pauline Monin, Damien Sanlaville, Lucie Ravella, Nicolas Reynaud, Nadine Hanna, Audrey Putoux, Pauline Arnaud, Catherine Boileau, Coline Poizat-Amar, Jean-Christophe Zech, Eudeline Alix, Marie Faoucher, Caroline Schluth-Bolard
Publikováno v:
Cytogenetic and genome research
Cytogenetic and genome research, 2020, 160 (2), pp.72--79. ⟨10.1159/000506319⟩
Cytogenetic and genome research, 2020, 160 (2), pp.72--79. ⟨10.1159/000506319⟩
In this report, we present a new case of mosaic trisomy 13 with prolonged survival, firstly detected by array-CGH analysis which was carried out because of moderate intellectual disability with postaxial hexadactyly, dermatologic features, ventricula
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ed0021b89b58804ce14d8d6ce5cb6409
https://hal.science/hal-02901752
https://hal.science/hal-02901752
Autor:
Mohamed Bakloul, Nicolas Pangaud, Hervé Joly, Bernard Debost, Magali Veyrier, Corinne Ducreux, Claire Bertail-Galoin, Sylvie Di Filippo
Publikováno v:
Archives of Cardiovascular Diseases Supplements. 9:277-278