Zobrazeno 1 - 10
of 39
pro vyhledávání: '"Maïté, Tauber"'
Autor:
Amar Abderrhamani, Najate Achamrah, Benjamin Allès, Maud Alligier, Chloé Amouyal, Sébastien André, Fabrizio Andreelli, Barbara Antuna-Puente, Gérard Apfeldorfer, Roberto Arienzo, Isabelle Arnulf, Judith Aron-Wisnewski, Estelle Aubry, Antoine Avignon, Anne Bachelot, Pascal Barat, Robert Barouki, Jean-Philippe Bastard, Marie Bastin, Thibaut Batisse, Bernard Bauduceau, Catherine Bauters, Pierre Bel Lassen, Alice Bellicha, Audrey Bergouignan, Rebecca Bienvenot, Philip Böhme, Amélie Bonnefond, Lyse Bordier, Yves Boirie, Anne-Laure Borel, Philippe Bouchard, Jean-Luc Bouillot, Marie-Christine Boutron-Ruault, Édith Brot-Laroche, Robert Caiazzo, Claire Carette, Caroline Carriere, Audrey Carriere-Pazat, Louis Casteilla, Dominique-Adèle Cassuto, Marie-Aline Charles, Didier Chapelot, Hélène Charreire, Nicolas Chevalier, Jean-Marc Chevallier, Cécile Ciangura, Karine Clément, Moïse Coëffier, Philippe Cornet, Christine Cortet, Muriel Coupaye, Sébastien Czernichow, Jérôme Dargent, Nathalie Delzenne, Philippe Deruelle, Jean-Claude Desport, Magalie Desseigne, Bruno Detournay, Sébastien Dharancy, Emmanuel Disse, Bruno Donadille, Claire Douillard, Béatrice Dubern, Sophie Dubreuil, Martine Duclos, Hélène Duez, Sophie Dunoyer, Charlotte Dupont, Vincent Durlach, Dominique Durrer-Schutz, Sophie Duverne, Harold Eburdery, Stéphanie Espiard, Nathalie Esser, Amandine Everard, Pauline Faucher, Philippe Fayemendy, Soraya Fellahi, Bruno Fève, Alicia Fillon, Vanessa Folope, Isabelle Fontanille, Marie-Laure Frelut, Philippe Froguel, Bénédicte Gaborit, Blandine Gatta-Cherifi, Christelle Guillet, Laurent Grange, Catherine Grangeard, Iva Gueorguieva, Serge Halimi, Hélène Hanaire, Solveig Heide, Barbara Heude, Sylvain Iceta, Sonja Janmaat, Isabelle Jéru, Pierre Jésus, Anne-Sophie Joly, Béatrice Jouret, Chantal Julia, Sabrina Julien-Sweerts, Min Ji Kim, Miriam Ladsous, Jean-Daniel Lalau, Dominique Langin, Olivier Lascols, Guillaume Lassailly, Claire de La Serre, Martine Laville, Sophie Laye, Jean-Michel Lecerf, Armelle Leturque, Rachel Lévy, Yasmine Lienard, Guillaume Losserand, Aïcha Maghroudi, Christophe Magnan, Geneviève Marcelin, Camille Marciniak, Philippe Marre, Lucile Marty, Philippe Mathurin, Joane Matta, Matthieu Mencia-Huerta, Andréanne Michaud, Vincent Miramont, Caroline Mocquot, Sandrine Monnery-Patris, Émilie Montastier, Pauline Morigny, Héléna Mosbah, Nathalie Negro, Audrey Neyrinck, Jean-Michel Oppert, Naïma Oukhouya Daoud, Filippo Pacini, Julien Paccou, Nicolas Paquot, François Pattou, Soazig Péron-Le Lay, Pierre Peuteuil, Tigran Poghosyan, Christine Poitou, Jean-Pierre Poulain, Guillaume Pourcher, Didier Quilliot, Jocelyne Raison, Marc Raucoules-Aimé, Gérard Ribes, Nathalie Rigal, Patrick Ritz, Claire Rives-Lange, Pauline Riviere, Maud Robert, Julie Rodriguez, Monique Romon, Cindy Rose, Romain Rozier, Thibault de Saint Pol, Frédéric Sanguignol, André Scheen, Jean-Louis Schlienger, Nathalie Sermondade, Yasmine Sebti, Chantal Simon, Luc Tappy, Maïté Tauber, Hélène Thibault, David Thivel, Philippe Valet, Marie-Christine Vantyghem, Camille Vatier, Bruno Verges, Hélène Verkindt, Bernard Vialettes, Corinne Vigouroux, Stéphane Walrand, Bernard Waysfeld, Jamila Zammouri, Jean-Philippe Zermati, Olivier Ziegler, Jean-Daniel Zucker
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::221d665124ba91637fec50ba42b41eed
https://doi.org/10.1016/b978-2-294-76753-1.09993-8
https://doi.org/10.1016/b978-2-294-76753-1.09993-8
Autor:
Agnès Linglart, Rachel Reynaud, Patrice Rodien, Frederic Castinetti, Alexandru Saveanu, N. Galon-Faure, E. Marquant, Nora Soumeya Fedala, Christine Cortet-Rudelli, Chantal Stuckens, Ignacio Bergadá, Maïté Tauber, Julia Vergier, Michel Polak, Mohamed El Kholy, Zinet Turki, Marc Nicolino, Raja Brauner, Marie Helene Quentien, Thierry Brue, Anne Barlier, Nicolas Jullien
Publikováno v:
Clinical Endocrinology
Clinical Endocrinology, 2021, 94 (2), pp.277-289. ⟨10.1111/cen.14355⟩
Clinical Endocrinology, Wiley, 2021, 94 (2), pp.277-289. ⟨10.1111/cen.14355⟩
Clinical Endocrinology, 2021, 94 (2), pp.277-289. ⟨10.1111/cen.14355⟩
Clinical Endocrinology, Wiley, 2021, 94 (2), pp.277-289. ⟨10.1111/cen.14355⟩
Context The international GENHYPOPIT network collects phenotypical data and screens genetic causes of non‐acquired hypopituitarism. Aims To describe main phenotype patterns and their evolution through life. Design Patients were screened according t
Autor:
Florence Menesguen, Jean-Michel Oppert, A.-C. Paepegaey, Graziella Pinto, Muriel Coupaye, Maïté Tauber, A. Jaziri, B. Dubern, Michel Polak, Christine Poitou
Publikováno v:
Endocrine Connections, Vol 7, Iss 5, Pp 663-672 (2018)
Endocrine Connections
Endocrine Connections
Context The transition of patients with Prader–Willi syndrome (PWS) to adult life for medical care is challenging because of multiple comorbidities, including hormone deficiencies, obesity and cognitive and behavioral disabilities. Objective To ass
Autor:
Claude Cances, Maïté Tauber, Hélène Cavé, Marie-Bernadette Delisle, Aurore Siegfried, Marie Denuelle, Najat Loukh
Publikováno v:
American Journal of Medical Genetics Part A. 173:1061-1065
Noonan syndrome (NS), an autosomal dominant disorder, is characterized by short stature, congenital heart defects, developmental delay, and facial dysmorphism. PTPN11 mutations are the most common cause of NS. PTPN11 encodes a non-receptor protein ty
Autor:
Natacha Lehman, Didier Lacombe, Delphine Héron, Frédérique Debomy, Sylvie Manouvrier, Frédéric Huet, Patrick Edery, Laurence Faivre, Sylvie Odent, Myriam Mikaty, Jennifer Gallard, Sophie Chancenotte, Sandrine Vinault, Maïté Tauber, David Geneviève, Coralie Rastel, Nicole Philip, Christine Binquet, Mathieu Bordes, Alain Verloes, Jamal Ghoumid, Elodie Gautier, Christel Thauvin-Robinet, Emilie Schmitt, Jenny Cornaton, Marie Bournez, Nolwenn Jean, Catherine Lejeune, Delphine Minot, Alice Masurel, Pierre-Henri Roux-Levy
Publikováno v:
European Journal of Medical Genetics
European Journal of Medical Genetics, Elsevier, 2020, 63 (12), pp.104064. ⟨10.1016/j.ejmg.2020.104064⟩
European Journal of Medical Genetics, 2020, 63 (12), pp.104064. ⟨10.1016/j.ejmg.2020.104064⟩
European Journal of Medical Genetics, Elsevier, 2020, 63 (12), pp.104064. ⟨10.1016/j.ejmg.2020.104064⟩
European Journal of Medical Genetics, 2020, 63 (12), pp.104064. ⟨10.1016/j.ejmg.2020.104064⟩
International audience; Prader-Willi syndrome (PWS) is a rare genetic neurodevelopmental disorder with a characteristic behavioural phenotype. A multidisciplinary approach to care is required to prevent multiple medical complications in individuals a
Autor:
Anne Pavy-Le Traon, Maïté Tauber, Julie Cortadellas, Catherine Molinas, Rachel Debs, Gwenaelle Diene
Publikováno v:
Revue Neurologique. 176:S42
Introduction Les patients atteints de PWS ont un risque cardiovasculaire plus eleve dont le mecanisme precis n’est pas connu, possiblement en lien avec un dysfonctionnement du systeme nerveux autonome (SNA). Objectifs Dans cette etude, nous avons e
Autor:
Michel Polak, Enzo Cohen, Sophie Rose, Frédéric Brioude, Nathalie Collot, Daniela Larizza, Marie Legendre, Florence Dastot, Juliane Léger, Anne Marie Bertrand, Philippe Duquesnoy, Marie Laure Sobrier, Philippe Touraine, Mohamad Maghnie, Bruno Copin, Maïté Tauber, Irène Netchine, Serge Amselem, Isabelle Oliver-Petit, Laura González Briceño, Thomas Edouard
Publikováno v:
Journal of Clinical Endocrinology and Metabolism
Journal of Clinical Endocrinology and Metabolism, 2017, 102 (1), pp.290-301. ⟨10.1210/jc.2016-3158⟩
Journal of Clinical Endocrinology and Metabolism, 2017, 102 (1), pp.290-301. ⟨10.1210/jc.2016-3158⟩
Context:LHX4 encodes a LIM-homeodomain transcription factor that is implicated in early pituitary development. In humans, only 13 heterozygous LHX4 mutations have been associated with congenital hypopituitarism.Objective:The aims of this study were t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6bc5b5c9a76b91c88f01890a72f3dac8
https://www.hal.inserm.fr/inserm-03837720
https://www.hal.inserm.fr/inserm-03837720
Autor:
Grégoire, Benoist, Antoine, Bourrillon, Christophe, Delacourt, Christèle, Gras-Le Guen, Benoit, Billy (de), Agnès, Liard-Zmuda, Patrick, Tounian, François, Angoulvant, Jean-Baptiste, Arnoux, Frédéric, Auber, Guillaume, Aubertin, Georges, Audry, Stéphane, Auvin, Justine, Bacchetta, Martine, Balençon, Pascal, Barat, Marc, Bellaïche, Jacques, Beltrand, Etienne, Bidat, Arnaud, Bonnard, Claire, Bouvattier, Dominique, Bremond-Gignac, Frédéric, Brioude, Olivier, Brissaud, Jean-Claude, Carel, Ania, Carsin, Mireille, Castanet, Brigitte, Chabrol, Gérard, Chéron, Bertrand, Chevallier, Jacques, Cheymol, Pierre, Corre, Régis, Coutant, Laurianne, Coutier, Pierrick, Cros, Jean-Christophe, Cuvellier, Jean-Hugues, Dalle, Stéphane, Dauger, Céline, Delestrain, Amandine, Divaret-Chauveau, François, Doz, David, Drummond, Béatrice, Dubern, Sophie, Dugue, Thomas, Édouard, Brigitte, Fauroux, Albert, Faye, Pierre, Fayoux, Cyril, Flamant, Elisabeth, Fournier-Charrière, Virginie, Gandemer, Alexandra, Gauthier, Olivia, Gillion-Boyer, Lisa, Giovannini-Chami, Emmanuel, Grimprel, Alice, Hadchouel-Duvergé, Sébastien, Héritier, Christina, Ioan Iulia, Pierre-Henri, Jarreau, Etienne, Javouhey, Eric, Jeziorski, Elsa, Kermorvant, Béatrice, Kugener, François, Labarthe, André, Labbé, Géraldine, Labouret, Elise, Launay, Rémi, Laporte, Nicolas, Leboulanger, Joël, Lechevallier, Juliane, Léger, Stéphanie, Lejeune, Stéphanie, Leroux, Guillaume, Lezmi, Anne, Lienhardt-Roussie, Agnès, Linglart, Mathie, Lorrot, Natalie, Loundon, Jehanne, Malek, Christophe, Marguet, Aude, Marie Cardine, Laetitia, Martinerie, Emmanuel, Mas, Thierry, Merrot, Matthieu, Milh, Despina, Moshous, Pierre-Yves, Mure, Javotte, Nancy, Nadia, Nathan, Irene, Netchine, Marc, Nicolino, Richard, Nicollas, Sylvie, Odent, Caroline, Ovaert, Françoise, Paris, Laurent, Pasquier, Aurélie, Phulpin, Capucine, Picard, Georges, Picherot, Guillaume, Podevin, Michel, Polak, Philippe, Ravasse, Rachel, Reynaud, Sylvie, Rossignol, Sébastien, Rouget, Jean-Christophe, Rozé, Philippe, Sachs, Frédérique, Sauvat, Cyril, Schweitzer, Isabelle, Sermet-Gaudelus, Chantal, Stheneur, Isabelle, Talon, Aline, Tamalet, Maïté, Tauber, Jessica, Taytard, Jean-Benoît, Thambo, Caroline, Thumerelle, Renaud, Tournemire (de), Barbara, Tourniaire, Michel, Tsimaratos, François, Varlet, Alain, Verloes, Ariane, Zaloszyc, Catherine, Cyteval, Philippe, Petit, Damien, Bonnard, Emmanuel, Lescanne
Publikováno v:
In Pédiatrie Edition: Eighth Edition. 2020:xxix-xxxii
Autor:
Jean-Michel Oppert, Graziella Pinto, Florence Menesguen, Muriel Coupaye, Maïté Tauber, A.-C. Paepegaey, A. Jaziri, Michel Polak, B. Dubern, Christine Poitou
Publikováno v:
Annales d'Endocrinologie. 79:232
Introduction Le syndrome de Prader–Willi (SPW) est le plus frequent des obesites syndromiques. Le passage a l’âge adulte est souvent difficile du fait des deficits hormonaux, de l’obesite et des troubles du comportement. Nous avons evalue la p
Publikováno v:
Respiratory Physiology & Neurobiology
Respiratory Physiology & Neurobiology, 2009, 168 (1-2), pp.119-124. ⟨10.1016/j.resp.2009.03.010⟩
Respiratory Physiology & Neurobiology, 2009, 168 (1-2), pp.119-124. ⟨10.1016/j.resp.2009.03.010⟩
Prader-Willi syndrome (PWS) is a multigenic disorder caused by the loss of paternal expression of genes in the 15q11-q13 region. It is a complex and progressive disease. From birth, patients present breathing disorders (apnea, rhythm instability, hyp