Parental Divorce and Attitudes and Feelings toward Marriage and Divorce in Emerging Adulthood: New Insights from a Multiway-Frequency Analysis

Por Fanie Collardeau, Marion Ehrenberg
Publicado em 2016-04-01

The Childbirth Fear Questionnaire and the Wijma Delivery Expectancy Questionnaire as Screening Tools for Specific Phobia, Fear of Childbirth

Por Nichole Fairbrother, Arianne Albert, Fanie Collardeau, Cora Keeney
Publicado em 2022-04-01

A64 BURKITT LYMPHOMA AFTER PEDIATRIC LIVER TRANSPLANTATION

Por Laverdure, N, Collardeau, S, Patey, N, Lachaux, A, Alvarez, F
Publicado no J Can Assoc Gastroenterol (2018)

Maternal unwanted and intrusive thoughts of infant-related harm, obsessive-compulsive disorder and depression in the perinatal period: study protocol

Por Fanie Collardeau, Bryony Corbyn, John Abramowitz, Patricia A. Janssen, Sheila Woody, Nichole Fairbrother
Publicado em 2019-03-01

Maternal unwanted and intrusive thoughts of infant-related harm, obsessive-compulsive disorder and depression in the perinatal period: study protocol

Por Collardeau, Fanie, Corbyn, Bryony, Abramowitz, John, Janssen, Patricia A., Woody, Sheila, Fairbrother, Nichole
Publicado no BMC Psychiatry (2019)

The protein kinase PERK/EIF2AK3 regulates proinsulin processing not via protein synthesis but by controlling endoplasmic reticulum chaperones

Por Sowers, Carrie R., Wang, Rong, Bourne, Rebecca A., McGrath, Barbara C., Hu, Jingjie, Bevilacqua, Sarah C., Paton, James C., Paton, Adrienne W., Collardeau-Frachon, Sophie, Nicolino, Marc, Cavener, Douglas R.
Publicado no J Biol Chem (2018)

Clinical Heterogeneity of Immune Dysregulation, Polyendocrinopathy, Enteropathy, X-Linked Syndrome: A French Multicenter Retrospective Study

Por Duclaux-Loras, R., Charbit-Henrion, F., Neven, B., Nowak, J., Collardeau-Frachon, S., Malcus, C., Ray, P. F., Moshous, D., Beltrand, J., Goulet, O., Cerf-Bensussan, N., Lachaux, A., Rieux-Laucat, F., Ruemmele, F. M.
Publicado no Clin Transl Gastroenterol (2018)

Mutations in CECR1 associated with a neutrophil signature in peripheral blood

Por Belot, Alexandre, Wassmer, Evangeline, Twilt, Marinka, Lega, Jean-Christophe, Zeef, Leo AH, Oojageer, Anthony, Kasher, Paul R, Mathieu, Anne-Laure, Malcus, Christophe, Demaret, Julie, Fabien, Nicole, Collardeau-Frachon, Sophie, Mechtouff, Laura, Derex, Laurent, Walzer, Thierry, Rice, Gillian I, Durieu, Isabelle, Crow, Yanick J
Publicado em 2014

Loss of α1β1 Soluble Guanylate Cyclase, the Major Nitric Oxide Receptor, Leads to Moyamoya and Achalasia

Por Hervé, Dominique, Philippi, Anne, Belbouab, Reda, Zerah, Michel, Chabrier, Stéphane, Collardeau-Frachon, Sophie, Bergametti, Francoise, Essongue, Aurore, Berrou, Eliane, Krivosic, Valérie, Sainte-Rose, Christian, Houdart, Emmanuel, Adam, Frédéric, Billiemaz, Kareen, Lebret, Marilyne, Roman, Sabine, Passemard, Sandrine, Boulday, Gwenola, Delaforge, Audrey, Guey, Stéphanie, Dray, Xavier, Chabriat, Hugues, Brouckaert, Peter, Bryckaert, Maryjke, Tournier-Lasserve, Elisabeth
Publicado em 2014

Loss of α1β1 Soluble Guanylate Cyclase, the Major Nitric Oxide Receptor, Leads to Moyamoya and Achalasia

Por Hervé, Dominique, Philippi, Anne, Belbouab, Reda, Zerah, Michel, Chabrier, Stéphane, Collardeau-Frachon, Sophie, Bergametti, Francoise, Essongue, Aurore, Berrou, Eliane, Krivosic, Valérie, Sainte-Rose, Christian, Houdart, Emmanuel, Adam, Frédéric, Billiemaz, Kareen, Lebret, Marilyne, Roman, Sabine, Passemard, Sandrine, Boulday, Gwenola, Delaforge, Audrey, Guey, Stéphanie, Dray, Xavier, Chabriat, Hugues, Brouckaert, Peter, Bryckaert, Maryjke, Tournier-Lasserve, Elisabeth
Publicado em 2014

Novel NEK8 Mutations Cause Severe Syndromic Renal Cystic Dysplasia through YAP Dysregulation

Por Grampa, Valentina, Delous, Marion, Zaidan, Mohamad, Odye, Gweltas, Thomas, Sophie, Elkhartoufi, Nadia, Filhol, Emilie, Niel, Olivier, Silbermann, Flora, Lebreton, Corinne, Collardeau-Frachon, Sophie, Rouvet, Isabelle, Alessandri, Jean-Luc, Devisme, Louise, Dieux-Coeslier, Anne, Cordier, Marie-Pierre, Capri, Yline, Khung-Savatovsky, Suonavy, Sigaudy, Sabine, Salomon, Rémi, Antignac, Corinne, Gubler, Marie-Claire, Benmerah, Alexandre, Terzi, Fabiola, Attié-Bitach, Tania, Jeanpierre, Cécile, Saunier, Sophie
Publicado no PLoS Genet (2016)

Defects in t(6)A tRNA modification due to GON7 and YRDC mutations lead to Galloway-Mowat syndrome

Por Arrondel, Christelle, Missoury, Sophia, Snoek, Rozemarijn, Patat, Julie, Menara, Giulia, Collinet, Bruno, Liger, Dominique, Durand, Dominique, Gribouval, Olivier, Boyer, Olivia, Buscara, Laurine, Martin, Gaëlle, Machuca, Eduardo, Nevo, Fabien, Lescop, Ewen, Braun, Daniela A., Boschat, Anne-Claire, Sanquer, Sylvia, Guerrera, Ida Chiara, Revy, Patrick, Parisot, Mélanie, Masson, Cécile, Boddaert, Nathalie, Charbit, Marina, Decramer, Stéphane, Novo, Robert, Macher, Marie-Alice, Ranchin, Bruno, Bacchetta, Justine, Laurent, Audrey, Collardeau-Frachon, Sophie, van Eerde, Albertien M., Hildebrandt, Friedhelm, Magen, Daniella, Antignac, Corinne, van Tilbeurgh, Herman, Mollet, Géraldine
Publicado no Nat Commun (2019)