Resultats de la cerca - Marie Laure Raffin‐Sanson

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  1. 1
    Familial Gestational Hyperthyroidism Caused by a Mutant Thyrotropin Receptor Hypersensitive to Human Chorionic Gonadotropin

    Familial Gestational Hyperthyroidism Caused by a Mutant Thyrotropin Receptor Hypersensitive to Human Chorionic Gonadotropin per Patrice Rodien, C Brémont, Marie-Laure Raffin Sanson, Jasmine Parma, Jacqueline Van Sande, Sabine Costagliola, Jean-Pierre Luton, Gilbert Vassart, Laurence Duprez

    Publicat 1998
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  2. 2
    Expression of progesterone and estradiol receptors in normal adrenal cortex, adrenocortical tumors, and primary pigmented nodular adrenocortical disease

    Expression of progesterone and estradiol receptors in normal adrenal cortex, adrenocortical tumors, and primary pigmented nodular adrenocortical disease per 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

    Publicat 2008
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  3. 3
    <i>TAC3</i>and<i>TACR3</i>Defects Cause Hypothalamic Congenital Hypogonadotropic Hypogonadism in Humans

    <i>TAC3</i>and<i>TACR3</i>Defects Cause Hypothalamic Congenital Hypogonadotropic Hypogonadism in Humans per 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

    Publicat 2010
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  4. 4
    DUSP5 and DUSP6, two ERK specific phosphatases, are markers of a higher MAPK signaling activation in BRAF mutated thyroid cancers

    DUSP5 and DUSP6, two ERK specific phosphatases, are markers of a higher MAPK signaling activation in BRAF mutated thyroid cancers per 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

    Publicat 2017
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  5. 5
    Pituitary surgery as alternative to dopamine agonists treatment for microprolactinomas: a cohort study

    Pituitary surgery as alternative to dopamine agonists treatment for microprolactinomas: a cohort study per 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

    Publicat 2021
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  6. 6
    Phosphodiesterase 11A (PDE11A) and Genetic Predisposition to Adrenocortical Tumors

    Phosphodiesterase 11A (PDE11A) and Genetic Predisposition to Adrenocortical Tumors per 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

    Publicat 2008
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  7. 7
    Progestin-associated shift of meningioma mutational landscape

    Progestin-associated shift of meningioma mutational landscape per 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

    Publicat 2017
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  8. 8
    [The pituitary and hormonal calcium regulation system].

    [The pituitary and hormonal calcium regulation system]. per 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

    Publicat 1971
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  9. 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 patients with macroadenomas

    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... per 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

    Publicat 2007
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  10. 10
    SFE/SFEDP adrenal insufficiency French consensus: Introduction and handbook

    SFE/SFEDP adrenal insufficiency French consensus: Introduction and handbook per 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

    Publicat 2018
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  11. 11
    Phosphodiesterase 11A (<i>PDE11A</i>) Genetic Variants May Increase Susceptibility to Prostatic Cancer

    Phosphodiesterase 11A (<i>PDE11A</i>) Genetic Variants May Increase Susceptibility to Prostatic Cancer per 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

    Publicat 2010
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  12. 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 Testicular Tumors in CNC as a Modifier of the Phenotype

    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... per 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

    Publicat 2010
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  13. 13
    Functional Phosphodiesterase 11A Mutations May Modify the Risk of Familial and Bilateral Testicular Germ Cell Tumors

    Functional Phosphodiesterase 11A Mutations May Modify the Risk of Familial and Bilateral Testicular Germ Cell Tumors per 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

    Publicat 2009
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  14. 14
    Pangenomic Classification of Pituitary Neuroendocrine Tumors

    Pangenomic Classification of Pituitary Neuroendocrine Tumors per 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

    Publicat 2019
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  15. 15
    <i>ARMC5</i>Mutations in a Large Cohort of Primary Macronodular Adrenal Hyperplasia: Clinical and Functional Consequences

    <i>ARMC5</i>Mutations in a Large Cohort of Primary Macronodular Adrenal Hyperplasia: Clinical and Functional Consequences per 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

    Publicat 2015
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  16. 16
    Pregnancy in Women Previously Treated for an Adrenocortical Carcinoma

    Pregnancy in Women Previously Treated for an Adrenocortical Carcinoma per 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

    Publicat 2015
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  17. 17
    Small-intestinal dysfunction accompanies the complex endocrinopathy of human proprotein convertase 1 deficiency

    Small-intestinal dysfunction accompanies the complex endocrinopathy of human proprotein convertase 1 deficiency per 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

    Publicat 2003
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  18. 18
    Small-intestinal dysfunction accompanies the complex endocrinopathy of human proprotein convertase 1 deficiency

    Small-intestinal dysfunction accompanies the complex endocrinopathy of human proprotein convertase 1 deficiency per 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

    Publicat 2003
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  19. 19
    Clinical Outcome, Hormonal Status, Gonadotrope Axis, and Testicular Function in 219 Adult Men Born With Classic 21-Hydroxylase Deficiency. A French National Survey

    Clinical Outcome, Hormonal Status, Gonadotrope Axis, and Testicular Function in 219 Adult Men Born With Classic 21-Hydroxylase Deficiency. A French National Survey per 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

    Publicat 2015
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  20. 20
    Identification of predictive criteria for pathogenic variants of primary bilateral macronodular adrenal hyperplasia (PBMAH) gene <i>ARMC5</i> in 352 unselected patients

    Identification of predictive criteria for pathogenic variants of primary bilateral macronodular adrenal hyperplasia (PBMAH) gene <i>ARMC5</i> in 352 unselected patients per 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

    Publicat 2022
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