Cancer-associated Mutations in Congenital Pulmonary Malformations: A Prospective Cohort

Autor: Simon Garinet, Makan Rahshenas, Louise Galmiche-Rolland, Olivier Abbo, Arnaud Bonnard, Frédéric Hameury, Naziha Khen-Dunlop, Babak Khoshnood, Hélène Blons, Christophe Delacourt, Sabah Boudjemaa, Laure Choupeaux, Sophie Collardeau-Frachon, Virginie Fouquet, Edouard Habonimana, Erik Hervieux, Nathalie Lelong, Guillaume Levard, Thierry Jo Molina, Cecile Picard, Christophe Piolat, Rony Sfeir, Florence Biquard, Jean-Paul Bory, François Goffinet, Valat-Rigot As, Norbert Winer, Eve Mousty, Charles Muszynski, Alexandra Benachi, Laurent J. Salomon, Valérie Goua, Jean-Marie Jouannic, Gwenaelle Le Bouar, Jérôme Massardier, Jonathan Rosenblatt, Agnès Sartor, Catherine Thong-Vanh, Fabienne Prieur, Thibaud Quibel, Claudine Touboul, Jean Gondry, Loic Sentilhes, Valérie Bonfiglioli, Lionel Carbillon, Anne-Helene Saliou, Julien Saada, Alexandra Letourneau, Helene Laurichesse, Carole Egron, Loren Deslandes, Vanina Castaigne, Claire Dazel-Salonne, Julien Stirnemann, Philippe Roth, Thierry Bultez, Yves Ville, Vassilis Tsatsaris, Lucie Guilbaud, Anne-Marie Darras, Jean-Francois Oury, Cecile Fanget, Romain Favre, Anne Paris, Franck Perrotin, Nathalie Banaszkiewicz, Thameur Rakza, Mathieu Morin, Cynthia Trastour, Nicolas Mottet, Frederic Coatleven, Elisabeth Alanio, Olivier Morel, Estelle Perdriolle, Marie-Laure Eszto-Cambon, Insaf Berrazaga, Guillaume Podevin, Hala Feghali, Caroline Thumerelle, Rafaelle Mangione, Marie-Noelle Lebras, Héloise Ducoin, Bernard Romeo, Philippe Buisson, Pierrick Cros, Léa Roditis, Hiline Devries, Jacques Brouard, Thierry Petit, Isabelle Petit, Adam Kandem Simo, Maguelonne Pons, Olivier Jaby, Catherine Llerena, Edith Sabatier, Guillaune Thouvenin, Michele Larroquet, Sabine Irtan, Christine Grapin, Caroline Parico, François Varlet, Jacqueline Matis, François Becmeur, Isabelle Gibertini, Hubert Lardy, Stephan Denapolicocci, Antoine Deschildre, Jean Breaud, Jean-François Lecompte, Arnaud Fotso Kamdem, Frédéric Elbaz, Frédéric Lavrand, Mickael Pomedio, Francis Lefebvre, Jean Louis Lemelle, Vladimir Gomola, Clementine Vigier, Isabelle Monier

Publikováno v: American journal of respiratory and critical care medicine.

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::de1bf4e3db50e252c151f428724b9ce2
https://pubmed.ncbi.nlm.nih.gov/36288557

Cervical dilators concurrently with misoprostol to shorten labor in termination of pregnancy: a randomized trial

Autor: Olivia Anselem, Jean-Marie Jouannic, Norbert Winer, Hanane Bouchghoul, Alexandre Vivanti, Patrick Rozenberg, Vanina Castaigne, Estelle Perdriolle-Galet, Jerôme Massardier, Catherine Thong Vanh, Pierre-Yves Ancel, François Goffinet, Vassilis Tsatsaris

Publikováno v: American Journal of Obstetrics and Gynecology. 226:S193-S194

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::e98f698c0f38941d0d889a059a0c3115
https://doi.org/10.1016/j.ajog.2021.11.334

Prenatal Ultrasound Suspicion of Cystic Fibrosis in a Multiethnic Population: Is Extensive

Autor: Chadia, Mekki, Abdel, Aissat, Véronique, Mirlesse, Sophie, Mayer Lacrosniere, Elsa, Eche, Annick, Le Floch, Sandra, Whalen, Cecile, Prud'Homme, Christelle, Remus, Benoit, Funalot, Vanina, Castaigne, Pascale, Fanen, Alix, de Becdelièvre

Publikováno v: Genes

In families without a Cystic Fibrosis (CF) history, fetal ultrasound bowel abnormalities can unexpectedly reveal the disease. Isolated or in association, the signs can be fetal bowel hyperechogenicity, intestinal loop dilatation and non-visualization

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::d5629a4475d8f6d4f268e9eb9cfead21
https://pubmed.ncbi.nlm.nih.gov/33946859

Managing the Unusual Causes of Fetal Anemia

Autor: Vanina Castaigne, Stéphanie Friszer, Anne Cortey, Jean-Marie Jouannic, Thierry Leblanc, F. Pernot, Imane Ben M'Barek, A. Mailloux, Pauline Thomas, Lydie Da Costa, Cécile Toly Ndour, Emeline Maisonneuve

Publikováno v: Fetal diagnosis and therapy. 47(2)

Background: Rare causes of fetal anemia requiring intrauterine transfusion (IUT) are challenging for fetal medicine specialists. Objectives: The aim of this study was to describe the perinatal patterns and prognosis in a consecutive series of fetuses

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e03c8238b88af0fa11ca26943153a011
https://pubmed.ncbi.nlm.nih.gov/31505487

In utero ultrasound diagnosis of corpus callosum agenesis leading to the identification of orofaciodigital type 1 syndrome in female fetuses

Autor: Bernard Aral, Ange-Line Bruel, Maryse Bonnière, Lucile Boutaud, Maurizio Clementi, Tania Attié-Bitach, Vanina Castaigne, N. Joye, Antoinette Gelot, Bruno Carbonne, Christel Thauvin-Robinet, Marie-Pierre Cordier, Laurence Faivre, Laurent Guibaud, Michel Vekemans, Philippe Roth, Isabella Mammi, Claude Vibert-Guigue, Caroline Alby, Marie Gonzales, Estelle Lopez, Pascale Sonigo, Ferechté Razavi, Sophie Collardeau-Frachon

Publikováno v: Birth Defects Research Part A: Clinical and Molecular Teratology
Birth Defects Research Part A: Clinical and Molecular Teratology, Wiley, 2017, 〈10.1002/bdr2.1154〉
Birth Defects Research Part A: Clinical and Molecular Teratology, Wiley, 2018, 110 (4), pp.382-389. ⟨10.1002/bdr2.1154⟩

International audience; BACKGROUND:OFD1 syndrome is a rare ciliopathy inherited on a dominant X-linked mode, typically lethal in males in the first or second trimester of pregnancy. It is characterized by oral cavity and digital anomalies possibly as

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2cbcad84ec30abc1766b8385d31ebba2
https://hal-univ-bourgogne.archives-ouvertes.fr/hal-01662369