Rezultati pretrage - Marie-Laure Raffin-Sanson
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1
Familial Gestational Hyperthyroidism Caused by a Mutant Thyrotropin Receptor Hypersensitive to Human Chorionic Gonadotropin od Patrice Rodien, C Brémont, Marie-Laure Raffin Sanson, Jasmine Parma, Jacqueline Van Sande, Sabine Costagliola, Jean-Pierre Luton, Gilbert Vassart, Laurence Duprez
Izdano 1998Artigo -
2
Expression of progesterone and estradiol receptors in normal adrenal cortex, adrenocortical tumors, and primary pigmented nodular adrenocortical disease od Patricia de Crémoux, Dan Rosenberg, J Goussard, Catherine Brémont-Weil, Frédérique Tissier, Carine Tran‐Perennou, Lionel Groussin, Xavier Bertagna, Jérôme Bertherat, Marie Laure Raffin‐Sanson
Izdano 2008Artigo -
3
<i>TAC3</i>and<i>TACR3</i>Defects Cause Hypothalamic Congenital Hypogonadotropic Hypogonadism in Humans od Jacques Young, Jérôme Bouligand, Bruno Francou, Marie-Laure Raffin-Sanson, Stéphanie Gaillez, Marc Jeanpierre, Michaël Grynberg, Peter Kamenický, Philippe Chanson, Sylvie Brailly‐Tabard, Anne Guiochon‐Mantel
Izdano 2010Artigo -
4
DUSP5 and DUSP6, two ERK specific phosphatases, are markers of a higher MAPK signaling activation in BRAF mutated thyroid cancers od Camille Buffet, Hecale-Perlemoine Karine, Léopoldine Bricaire, Florent Dumont, Camille Baudry, Frédérique Tissier, Jérôme Bertherat, Béatrix Cochand‐Priollet, Marie‐Laure Raffin‐Sanson, Françoise Cormier, Lionel Groussin
Izdano 2017Artigo -
5
Pituitary surgery as alternative to dopamine agonists treatment for microprolactinomas: a cohort study od Bertrand Baussart, Chiara Villa, Anne Jouinot, Marie‐Laure Raffin‐Sanson, L. Foubert, Laure Cazabat, Michèle Bernier, Fidéline Bonnet-Serrano, Anthony Dohan, Jérôme Bertherat, Guillaume Assié, S. Gaillard
Izdano 2021Artigo -
6
Phosphodiesterase 11A (PDE11A) and Genetic Predisposition to Adrenocortical Tumors od Rossella Libé, Amato Fratticci, Joël Coste, Frédérique Tissier, Anélia Horvath, Bruno Ragazzon, Fernande René-Corail, Lionel Groussin, Xavier Bertagna, Marie Laure Raffin‐Sanson, Constantine A. Stratakis, Jérôme Bertherat
Izdano 2008Artigo -
7
Progestin-associated shift of meningioma mutational landscape od Matthieu Peyre, S. Gaillard, C. De Marcellus, Marine Giry, Franck Bielle, Chiara Villa, Anne‐Laure Boch, Hugues Loiseau, Bertrand Baussart, Laure Cazabat, Marie Laure Raffin‐Sanson, Marc Sanson, Michel Kalamarides
Izdano 2017Artigo -
8
[The pituitary and hormonal calcium regulation system]. od Laure Cazabat, Rossella Libé, Karine Perlemoine, Fernande René-Corail, Nelly Burnichon, Anne‐Paule Gimenez‐Roqueplo, Laurence Dupasquier-Fediaevsky, Xavier Bertagna, Éric Clauser, Philippe Chanson, Jérôme Bertherat, Marie‐Laure Raffin‐Sanson
Izdano 1971Artigo -
9
Germline inactivating mutations of the aryl hydrocarbon receptor-interacting protein gene in a large cohort of sporadic acromegaly: mutations are found in a subset of young patient... od Laure Cazabat, Rossella Libé, Karine Perlemoine, Fernande René-Corail, Nelly Burnichon, Anne‐Paule Gimenez‐Roqueplo, Laurence Dupasquier-Fediaevsky, Xavier Bertagna, Éric Clauser, Philippe Chanson, Jérôme Bertherat, Marie‐Laure Raffin‐Sanson
Izdano 2007Artigo -
10
SFE/SFEDP adrenal insufficiency French consensus: Introduction and handbook od Yves Reznik, Pascal Barat, Jérôme Bertherat, Claire Bouvattier, Frédéric Castinetti, Olivier Chabre, Philippe Chanson, Christine Cortet, Brigitte Delemer, B. Goichot, Damien Gruson, Laurence Guignat, Emmanuelle Proust-Lemoine, Marie-Laure Raffin Sanson, Rachel Reynaud, Dinane Samara Boustani, Dominique Simon, Antoine Tabarin, Delphine Zénaty
Izdano 2018Artigo -
11
Phosphodiesterase 11A (<i>PDE11A</i>) Genetic Variants May Increase Susceptibility to Prostatic Cancer od Fábio R. Faucz, Anélia Horvath, Anya Rothenbühler, Madson Q. Almeida, Rossella Libé, Marie-Laure Raffin-Sanson, Jérôme Bertherat, Dirce Maria Carraro, Fernando Augusto Soares, Gustavo de Campos Molina, Antônio Hugo José Fróes Marques Campos, Rodrigo Bertollo de Alexandre, Marcelo L. Bendhack, Maria Nesterova, Constantine A. Stratakis
Izdano 2010Artigo -
12
Frequent Phosphodiesterase 11A Gene (<i>PDE11A</i>) Defects in Patients with Carney Complex (CNC) Caused by<i>PRKAR1A</i>Mutations:<i>PDE11A</i>May Contribute to Adrenal and Testic... od Rossella Libé, Anélia Horvath, Delphine Vezzosi, Amato Fratticci, Joël Coste, Karine Perlemoine, Bruno Ragazzon, Marine Guillaud-Bataille, Lionel Groussin, Éric Clauser, Marie‐Laure Raffin‐Sanson, J E Siegel, Jason Moran, Limor Drori-Herishanu, Fábio R. Faucz, Maya Lodish, Maria Nesterova, Xavier Bertagna, Jérôme Bertherat, Constantine A. Stratakis
Izdano 2010Artigo -
13
Functional Phosphodiesterase 11A Mutations May Modify the Risk of Familial and Bilateral Testicular Germ Cell Tumors od Anélia Horvath, Larissa A. Korde, Mark H. Greene, Rossella Libé, Paulo de Sá Osório, Fábio R. Faucz, Marie Laure Raffin‐Sanson, Kit Man Tsang, Limor Drori-Herishanu, Yianna Patronas, Elaine F. Remmers, Maria Nikita, Jason Moran, J Greene, Maria Nesterova, Maria J. Merino, Jérôme Bertherat, Constantine A. Stratakis
Izdano 2009Artigo -
14
Pangenomic Classification of Pituitary Neuroendocrine Tumors od Mario Néou, Chiara Villa, Roberta Armignacco, Anne Jouinot, Marie‐Laure Raffin‐Sanson, Amandine Septier, Franck Letourneur, Ségolène Diry, Marc Diedisheim, Brigitte Izac, Cassandra Gaspar, Karine Perlemoine, Victoria Verjus, Michèle Bernier, A. Boulin, Jean‐François Emile, Xavier Bertagna, Florence Jaffrézic, Dénis Laloë, Bertrand Baussart, Jérôme Bertherat, S. Gaillard, Guillaume Assié
Izdano 2019Artigo -
15
<i>ARMC5</i>Mutations in a Large Cohort of Primary Macronodular Adrenal Hyperplasia: Clinical and Functional Consequences od Stéphanie Espiard, Ludivine Drougat, Rossella Libé, Guillaume Assié, Karine Perlemoine, Laurence Guignat, Gaëlle Barrande, Françoise Brücker-Davis, Françoise Doullay, Stéphanie Lopez, E. Sonnet, Florence Torremocha, D Pinsard, Nathalie Chabbert‐Buffet, Marie‐Laure Raffin‐Sanson, Lionel Groussin, Françoise Borson‐Chazot, Joël Coste, Xavier Bertagna, Constantine A. Stratakis, Felix Beuschlein, Bruno Ragazzon, Jérôme Bertherat
Izdano 2015Artigo -
16
Pregnancy in Women Previously Treated for an Adrenocortical Carcinoma od Pauline de Corbière, Katrin Ritzel, Laure Cazabat, Jacques Ropers, M. Schott, Rossella Libé, Ann‐Cathrin Koschker, Sophie Leboulleux, Timo Deutschbein, Christine Do Cao, Stefanie Hahner, Delphine Drui, Konstanze Miehle, Philippe Caron, Jens Waldmann, Olivier Chabre, Marcus Quinkler, Philippe Touraine, Maria Candida Barisson Villares Fragoso, Jérôme Bertherat, Xavier Bertagna, Martin Faßnacht, Marie‐Laure Raffin‐Sanson
Izdano 2015Artigo -
17
Small-intestinal dysfunction accompanies the complex endocrinopathy of human proprotein convertase 1 deficiency od Robert S. Jackson, John W.M. Creemers, I. Sadaf Farooqi, Marie‐Laure Raffin‐Sanson, Andrea Varró, Graham J. Dockray, Jens J. Holst, Patricia L. Brubaker, Pierre Corvol, Kenneth S. Polonsky, Diane Ostrega, Kenneth L. Becker, Xavier Bertagna, John C. Hutton, Anne White, Mehul Dattani, Khalid Hussain, Stephen Middleton, Thomasina M. Nicole, Peter J. Milla, Keith Lindley, Stephen O’Rahilly
Izdano 2003Artigo -
18
Small-intestinal dysfunction accompanies the complex endocrinopathy of human proprotein convertase 1 deficiency od Robert S. Jackson, John W.M. Creemers, I. Sadaf Farooqi, Marie‐Laure Raffin‐Sanson, Andrea Varró, Graham J. Dockray, Jens J. Holst, Patricia L. Brubaker, Pierre Corvol, Kenneth S. Polonsky, Diane Ostrega, Kenneth L. Becker, Xavier Bertagna, John C. Hutton, Anne White, Mehul Dattani, Khalid Hussain, Stephen Middleton, Thomasina M. Nicole, Peter J. Milla, Keith Lindley, Stephen O’Rahilly
Izdano 2003Artigo -
19
Clinical Outcome, Hormonal Status, Gonadotrope Axis, and Testicular Function in 219 Adult Men Born With Classic 21-Hydroxylase Deficiency. A French National Survey od Claire Bouvattier, Laure Esterle, Peggy Renoult-Pierre, Aude Brac de la Perrière, F. Illouz, V. Kerlan, V. Pascal-Vigneron, Delphine Drui, Sophie Christin-Maître, F. Galland, Thierry Brue, Yves Reznik, F. Schillo, D Pinsard, Xavier Piguel, G. Chabrier, Bénédicte Decoudier, Philippe Émy, Igor Tauveron, Marie-Laure Raffin-Sanson, Jérôme Bertherat, Jean‐Marc Kuhn, Philippe Caron, Maryse Cartigny, Olivier Chabre, Didier Dewailly, Yves Morel, Philippe Touraine, Véronique Tardy-Guidollet, Jacques Young
Izdano 2015Artigo -
20
Identification of predictive criteria for pathogenic variants of primary bilateral macronodular adrenal hyperplasia (PBMAH) gene <i>ARMC5</i> in 352 unselected patients od Lucas Bouys, Anna Vaczlavik, Anne Jouinot, Patricia Vaduva, Stéphanie Espiard, Guillaume Assié, Rossella Libé, Karine Perlemoine, Bruno Ragazzon, Laurence Guignat, Lionel Groussin, Léopoldine Bricaire, Isadora Pontes Cavalcante, Fidéline Bonnet-Serrano, Hervé Lefèbvre, Marie‐Laure Raffin‐Sanson, Nicolas Chevalier, Philippe Touraine, Christel Jublanc, Camille Vatier, Gérald Raverot, Magalie Haissaguerre, Luigi Maione, Matthias Kroiß, Martin Faßnacht, Sophie Christin-Maître, Éric Pasmant, Françoise Borson‐Chazot, Antoine Tabarin, Marie‐Christine Vantyghem, Martín Reincke, Peter Kamenický, Marie-Odile North, Jérôme Bertherat
Izdano 2022Artigo
Alati za pretragu:
Povezani predmeti
Internal medicine
Medicine
Biology
Endocrinology
Genetics
Gene
Cancer research
Hormone
Missense mutation
Mutation
Germline
Nonsense mutation
Cancer
Cohort
Environmental health
Paleontology
Phenotype
Population
Pregnancy
Allele
Bioinformatics
Congenital adrenal hyperplasia
Context (archaeology)
Exon
Germline mutation
Gigantism
Immunohistochemistry
Molecular biology
Pediatric endocrinology
Pediatrics