Phenotypic Homogeneity and Genotypic Variability in a Large Series of Congenital Isolated ACTH-Deficiency Patients with TPIT Gene Mutations
Couture, C, Saveanu, A, Barlier, A, Carel, J. C, Fassnacht, M, Flück, C. E, Houang, M, Maes, M, Phan-Hug, F, Enjalbert, A, Drouin, J, Brue, T, Vallette, S
Published in The journal of clinical endocrinology and metabolism (01.03.2012)
Published in The journal of clinical endocrinology and metabolism (01.03.2012)
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Journal Article
Pseudotumor of the Pituitary due to PROP-1 Deletion
Teinturier, C., Vallette, S., Adamsbaum, C., Bendaoud, M., Brue, T., Bougneres, P.F.
Published in Journal of Pediatric Endocrinology and Metabolism (2002)
Published in Journal of Pediatric Endocrinology and Metabolism (2002)
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Journal Article
Congenital Isolated Adrenocorticotropin Deficiency: An Underestimated Cause of Neonatal Death, Explained by TPIT Gene Mutations
Vallette-Kasic, Sophie, Brue, Thierry, Pulichino, Anne-Marie, Gueydan, Magali, Barlier, Anne, David, Michel, Nicolino, Marc, Malpuech, Georges, Déchelotte, Pierre, Deal, Cheri, Van Vliet, Guy, De Vroede, Monique, Riepe, Felix G., Partsch, Carl-Joachim, Sippell, Wolfgang G., Berberoglu, Merih, Atasay, Begüm, de Zegher, Francis, Beckers, Dominique, Kyllo, Jennifer, Donohoue, Patricia, Fassnacht, Martin, Hahner, Stefanie, Allolio, Bruno, Noordam, C., Dunkel, Leo, Hero, Matti, Pigeon, B., Weill, Jacques, Yigit, Sevket, Brauner, Raja, Heinrich, Juan Jorge, Cummings, Elizabeth, Riddell, Christie, Enjalbert, Alain, Drouin, Jacques
Published in The journal of clinical endocrinology and metabolism (01.03.2005)
Published in The journal of clinical endocrinology and metabolism (01.03.2005)
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Journal Article
Markers of tumor invasion are major predictive factors for the long-term outcome of corticotroph microadenomas treated by transsphenoidal adenomectomy
VALLETTE-KASIC, S, DUFOUR, H, BRUE, T, MUGNIER, M, TROUILLAS, J, VALDES-SOCIN, H, CARON, P, MORANGE, S, GIRARD, N, GRISOLI, F, JAQUET, P
Published in European journal of endocrinology (01.12.2000)
Published in European journal of endocrinology (01.12.2000)
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A Neonatal Form of Isolated ACTH Deficiency Frequently Associated with Tpit Gene Mutations
Vallette-Kasic, S., Pulichino, A.-M., Gueydan, M., Barlier, A., David, M., Malpuech, G., Deal, C., Van Vliet, G., de Vroede, M., Riepe, F., Partsch, C.-J., Sippell, W., Berberoglu, M., Atasay, B., de Zegher, F., Kyllo, J., Donohoue, P., Dechelotte, P., Fassnacht, M., Noordam, K., Dunkel, L., Pigeon, B., Weill, J., Yigit, S., Brauner, R., Leger, J., Heinrich, J.J., Enjalbert, A., Brue, T., Drouin, J.
Published in Endocrine research (01.01.2004)
Published in Endocrine research (01.01.2004)
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Journal Article
Role of Brg1 and HDAC2 in GR trans-repression of the pituitary POMC gene and misexpression in Cushing disease
Bilodeau, Steve, Vallette-Kasic, Sophie, Gauthier, Yves, Figarella-Branger, Dominique, Brue, Thierry, Berthelet, France, Lacroix, André, Batista, Dalia, Stratakis, Constantine, Hanson, Jeanette, Meij, Björn, Drouin, Jacques
Published in Genes & development (15.10.2006)
Published in Genes & development (15.10.2006)
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Journal Article
Tpit determines alternate fates during pituitary cell differentiation
Pulichino, Anne-Marie, Vallette-Kasic, Sophie, Tsai, Judy Peih-Ying, Couture, Catherine, Gauthier, Yves, Drouin, Jacques
Published in Genes & development (15.03.2003)
Published in Genes & development (15.03.2003)
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Journal Article
Human and mouse TPIT gene mutations cause early onset pituitary ACTH deficiency
Pulichino, Anne-Marie, Vallette-Kasic, Sophie, Couture, Catherine, Gauthier, Yves, Brue, Thierry, David, Michel, Malpuech, Georges, Deal, Cheri, Van Vliet, Guy, De Vroede, Monique, Riepe, Felix G, Partsch, Carl-Joachim, Sippell, Wolfgang G, Berberoglu, Merih, Atasay, Begüm, Drouin, Jacques
Published in Genes & development (15.03.2003)
Published in Genes & development (15.03.2003)
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Journal Article
PROP1 Gene Screening in Patients with Multiple Pituitary Hormone Deficiency Reveals Two Sites of Hypermutability and a High Incidence of Corticotroph Deficiency
Vallette-Kasic, S., Barlier, A., Teinturier, C., Diaz, A., Manavela, M., Berthezène, F., Bouchard, P., Chaussain, J. L., Brauner, R., Pellegrini-Bouiller, I., Jaquet, P., Enjalbert, A., Brue, T.
Published in The journal of clinical endocrinology and metabolism (01.09.2001)
Published in The journal of clinical endocrinology and metabolism (01.09.2001)
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Journal Article
PROP1 gene screening in patients with multiple pituitary hormone deficiency reveals two sites of hypermutability and a high incidence of corticotroph deficiency
VALLETTE-KASIC, S, BARLIER, A, JAQUET, P, ENJALBERT, A, BRUE, T, TEINTURIER, C, DIAZ, A, MANAVELA, M, BERTHEZENE, F, BOUCHARD, P, CHAUSSAIN, J. L, BRAUNER, R, PELLEGRINI-BOUILLER, I
Published in The journal of clinical endocrinology and metabolism (01.09.2001)
Published in The journal of clinical endocrinology and metabolism (01.09.2001)
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Journal Article
An Uncommon Phenotype with Familial Central Hypogonadism Caused by a Novel PROP1 Gene Mutant Truncated in the Transactivation Domain
Reynaud, Rachel, Barlier, Anne, Vallette-Kasic, Sophie, Saveanu, Alexandru, Guillet, Marie-Pierre, Simonin, Gilbert, Enjalbert, Alain, Valensi, Paul, Brue, Thierry
Published in The journal of clinical endocrinology and metabolism (01.08.2005)
Published in The journal of clinical endocrinology and metabolism (01.08.2005)
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Journal Article
A Familial Form of Congenital Hypopituitarism Due to a PROP1 Mutation in a Large Kindred: Phenotypic and in Vitro Functional Studies
Reynaud, Rachel, Chadli-Chaieb, Molka, Vallette-Kasic, Sophie, Barlier, Anne, Sarles, Jacques, Pellegrini-Bouiller, Isabelle, Enjalbert, Alain, Chaieb, Larbi, Brue, Thierry
Published in The journal of clinical endocrinology and metabolism (01.11.2004)
Published in The journal of clinical endocrinology and metabolism (01.11.2004)
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Journal Article
Low estriol levels in the maternal triple-marker screen as a predictor of isolated adrenocorticotropic hormone deficiency caused by a new mutation in the TPIT gene
Weintrob, Naomi, Drouin, Jacques, Vallette-Kasic, Sophie, Taub, Ellen, Marom, Daphna, Lebenthal, Yael, Klinger, Gil, Bron-Harlev, Efrat, Shohat, Mordechai
Published in Pediatrics (Evanston) (01.02.2006)
Published in Pediatrics (Evanston) (01.02.2006)
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Journal Article
Transcription factors of the anterior pituitary and combined hypopituitarism
Vallette, S, Pellegrini-Bouiller, I, Jaquet, P, Enjalbert, A, Brue, T
Published in Annales d'endocrinologie (01.09.1999)
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Published in Annales d'endocrinologie (01.09.1999)
Journal Article
Differential Regulation of Proopiomelanocortin and Pituitary-Restricted Transcription Factor (TPIT), a New Marker of Normal and Adenomatous Human Corticotrophs
Vallette-Kasic, Sophie, Figarella-Branger, Dominique, Grino, Michel, Pulichino, Anne-Marie, Dufour, Henry, Grisoli, François, Enjalbert, Alain, Drouin, Jacques, Brue, Thierry
Published in The journal of clinical endocrinology and metabolism (01.07.2003)
Published in The journal of clinical endocrinology and metabolism (01.07.2003)
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Journal Article
An uncommon phenotype with familial central hypogonadism caused by a novel PROP-1 gene mutant truncated in the transactivation domain
Reynaud, Rachel, Barlier, Anne A., Vallette-Kasic, S., Saveanu, Alexandru, Guillet, M.P., Simonin, Gilles, Enjalbert, A., Valensi, P., Brue, Thierry
Published in The journal of clinical endocrinology and metabolism (2005)
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Published in The journal of clinical endocrinology and metabolism (2005)
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