检索结果 - Anne Barlier

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  1. 1
    First Report of Bilateral Pheochromocytoma in the Clinical Spectrum of<i>HIF2A</i>-Related Polycythemia-Paraganglioma Syndrome

    First Report of Bilateral Pheochromocytoma in the Clinical Spectrum of<i>HIF2A</i>-Related Polycythemia-Paraganglioma Syndrome 由 David Taïeb, Chunzhang Yang, B. Delenne, Zhengping Zhuang, Anne Barlier, F. Sébag, Karel Pacák

    出版 2013
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  2. 2
    Genetic Screening of Combined Pituitary Hormone Deficiency: Experience in 195 Patients

    Genetic Screening of Combined Pituitary Hormone Deficiency: Experience in 195 Patients 由 Rachel Reynaud, Magali Gueydan, Alexandru Saveanu, Sophie Vallette-Kasic, A Enjalbert, Thierry Brue, Anne Barlier

    出版 2006
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  3. 3
    Imprinting of the Gsα gene GNAS1 in the pathogenesis of acromegaly

    Imprinting of the Gsα gene GNAS1 in the pathogenesis of acromegaly 由 Bruce E. Hayward, Anne Barlier, Márta Korbonits, Ashley Grossman, Philippe Jacquet, A Enjalbert, David T. Bonthron

    出版 2001
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  4. 4
    The analysis of quantitative expression of somatostatin and dopamine receptors in gastro-entero-pancreatic tumours opens new therapeutic strategies

    The analysis of quantitative expression of somatostatin and dopamine receptors in gastro-entero-pancreatic tumours opens new therapeutic strategies 由 Dermot O’Toole, Alexandru Saveanu, Anne Couvelard, Ginette Gunz, A Enjalbert, P Jaquet, Philippe Ruszniewski, Anne Barlier

    出版 2006
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  5. 5
    Somatostatinergic ligands in dopamine-sensitive and -resistant prolactinomas

    Somatostatinergic ligands in dopamine-sensitive and -resistant prolactinomas 由 Alessandra Fusco, Ginette Gunz, P Jaquet, Henry Dufour, Anne Laure Germanetti, Michael D. Culler, Anne Barlier, Alexandru Saveanu

    出版 2008
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  6. 6
    Pronostic and Therapeutic Consequences of G<sub>s</sub>α Mutations in Somatotroph Adenomas<sup>1</sup>

    Pronostic and Therapeutic Consequences of G<sub>s</sub>α Mutations in Somatotroph Adenomas<sup>1</sup> 由 Anne Barlier, Ginette Gunz, A.J. Zamora, I. Morange‐Ramos, Dominique Figarella‐Branger, H. Dufour, A Enjalbert, P Jaquet

    出版 1998
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  7. 7
    Demonstration of Enhanced Potency of a Chimeric Somatostatin-Dopamine Molecule, BIM-23A387, in Suppressing Growth Hormone and Prolactin Secretion from Human Pituitary Somatotroph Adenoma Cells

    Demonstration of Enhanced Potency of a Chimeric Somatostatin-Dopamine Molecule, BIM-23A387, in Suppressing Growth Hormone and Prolactin Secretion from Human Pituitary Somatotroph A... 由 Alexandru Saveanu, Esteban Lavaque, Ginette Gunz, Anne Barlier, S. Kim, John E. Taylor, Michael D. Culler, A Enjalbert, P Jaquet

    出版 2002
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  8. 8
    MECHANISMS IN ENDOCRINOLOGY: An update in the genetic aetiologies of combined pituitary hormone deficiency

    MECHANISMS IN ENDOCRINOLOGY: An update in the genetic aetiologies of combined pituitary hormone deficiency 由 Frédéric Castinetti, Rachel Reynaud, Alexandru Saveanu, Nicolas Jullien, M.-H. Quentien, C. Rochette, Anne Barlier, A Enjalbert, Thierry Brue

    出版 2016
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  9. 9
    A new mutation of the gene encoding the transcription factor Pit-1 is responsible for combined pituitary hormone deficiency.

    A new mutation of the gene encoding the transcription factor Pit-1 is responsible for combined pituitary hormone deficiency. 由 I. Pellegrini-Bouiller, P. Bélicar, Anne Barlier, Ginette Gunz, J P Charvet, P Jaquet, Thierry Brue, B. Vialettes, A Enjalbert

    出版 1996
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  10. 10
    Functional characterization of nonmetastatic paraganglioma and pheochromocytoma by <sup>18</sup>F‐<scp>FDOPA PET</scp>: focus on missed lesions

    Functional characterization of nonmetastatic paraganglioma and pheochromocytoma by <sup>18</sup>F‐<scp>FDOPA PET</scp>: focus on missed lesions 由 S. Gabriel, Elise M. Blanchet, F. Sébag, Clara C. Chen, Nicolas Fakhry, Arnaud Devèze, Anne Barlier, Isabelle Morange, Karel Pacák, David Taïeb

    出版 2012
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  11. 11
    McCune-Albright Syndrome: A Detailed Pathological and Genetic Analysis of Disease Effects in an Adult Patient

    McCune-Albright Syndrome: A Detailed Pathological and Genetic Analysis of Disease Effects in an Adult Patient 由 В. Н. Васильев, Adrian Daly, Albert Thiry, Patrick Pétrossians, Frédéric Fina, Liliya Rostomyan, Monique Silvy, A Enjalbert, Anne Barlier, Albert Beckers

    出版 2014
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  12. 12
    Octreotide therapy in meningiomas: in vitro study, clinical correlation, and literature review

    Octreotide therapy in meningiomas: in vitro study, clinical correlation, and literature review 由 Thomas Graillon, David Romano, Céline Defilles, Alexandru Saveanu, Amira Mohamed, Dominique Figarella‐Branger, Pierre‐Hugues Roche, S. Fuentès, Olivier Chinot, Henry Dufour, Anne Barlier

    出版 2016
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  13. 13
    Mutations in the<i>Aryl Hydrocarbon Receptor Interacting Protein</i>Gene Are Not Highly Prevalent among Subjects with Sporadic Pituitary Adenomas

    Mutations in the<i>Aryl Hydrocarbon Receptor Interacting Protein</i>Gene Are Not Highly Prevalent among Subjects with Sporadic Pituitary Adenomas 由 Anne Barlier, Jean-François Vanbellinghen, Adrian Daly, Monique Silvy, Marie‐Lise Jaffrain‐Rea, Jacqueline Trouillas, Gianluca Tamagno, Laure Cazabat, Vincent Bours, Thierry Brue, A Enjalbert, Albert Beckers

    出版 2007
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  14. 14
    Pituitary stalk interruption syndrome in 83 patients: novel HESX1 mutation and severe hormonal prognosis in malformative forms

    Pituitary stalk interruption syndrome in 83 patients: novel HESX1 mutation and severe hormonal prognosis in malformative forms 由 Rachel Reynaud, F. Albarel, Alexandru Saveanu, N. Kaffel, Frédéric Castinetti, Philippe Lecomte, Raja Brauner, G. Simonin, Jean Gaudart, Eva M. Carmona, A Enjalbert, Anne Barlier, Thierry Brue

    出版 2011
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  15. 15
    Simultaneous Hyper- and Hypomethylation at Imprinted Loci in a Subset of Patients with<i>GNAS</i>Epimutations Underlies a Complex and Different Mechanism of Multilocus Methylation Defect in Pseudohypoparathyroidism Type 1b

    Simultaneous Hyper- and Hypomethylation at Imprinted Loci in a Subset of Patients with<i>GNAS</i>Epimutations Underlies a Complex and Different Mechanism of Multilocus Methylation... 由 Stéphanie Maupetit‐Mehouas, Salah Azzi, Virginie Steunou, Nathalie Sakakini, Caroline Silve, Christelle Reynès, Guiomar Pérez de Nanclares, Boris Keren, Sandra Chantot‐Bastaraud, Anne Barlier, Agnès Linglart, Irène Netchine

    出版 2013
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  16. 16
    Gene fusions in poroma, porocarcinoma and related adnexal skin tumours: An update

    Gene fusions in poroma, porocarcinoma and related adnexal skin tumours: An update 由 Thibault Kervarrec, Daniel Pissaloux, Franck Tirode, Arnaud de la Fouchardière, Pierre Sohier, É. Frouin, Aymeric Hamard, Roland Houben, David Schrama, Anne Barlier, B. Cribier, Maxime Battistella, Nicolas Macagno

    出版 2023
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  17. 17
    A Potential Inhibitory Role for the New Truncated Variant of Somatostatin Receptor 5, sst5TMD4, in Pituitary Adenomas Poorly Responsive to Somatostatin Analogs

    A Potential Inhibitory Role for the New Truncated Variant of Somatostatin Receptor 5, sst5TMD4, in Pituitary Adenomas Poorly Responsive to Somatostatin Analogs 由 Mario Durán‐Prado, Alexandru Saveanu, Raúl M. Luque, Manuel D. Gahete, Francisco Gracia‐Navarro, P Jaquet, Henry Dufour, Marı́a M. Malagón, Michael D. Culler, Anne Barlier, Justo P. Castaño

    出版 2010
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  18. 18
    <sup>18</sup>F-FDG Avidity of Pheochromocytomas and Paragangliomas: A New Molecular Imaging Signature?

    <sup>18</sup>F-FDG Avidity of Pheochromocytomas and Paragangliomas: A New Molecular Imaging Signature? 由 David Taïeb, F. Sébag, Anne Barlier, Laurent Tessonnier, Fausto Palazzo, Isabelle Morange, Patricia Niccoli‐Sire, Nicolas Fakhry, Cathérine De Micco, Serge Cammilleri, A Enjalbert, Jean‐François Henry, O. Mundler

    出版 2009
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  19. 19
    Deficit in Anterior Pituitary Function and Variable Immune Deficiency (DAVID) in Children Presenting with Adrenocorticotropin Deficiency and Severe Infections

    Deficit in Anterior Pituitary Function and Variable Immune Deficiency (DAVID) in Children Presenting with Adrenocorticotropin Deficiency and Severe Infections 由 Marie-Hélène Quentien, Brigitte Delemer, Dimitrios T. Papadimitriou, Pierre‐François Souchon, R. Jaussaud, Anne Pagnier, Martine Münzer, Nicolas Jullien, Rachel Reynaud, N. Galon-Faure, A Enjalbert, Anne Barlier, Thierry Brue

    出版 2011
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  20. 20
    Phenotypic Homogeneity and Genotypic Variability in a Large Series of Congenital Isolated ACTH-Deficiency Patients with <i>TPIT</i> Gene Mutations

    Phenotypic Homogeneity and Genotypic Variability in a Large Series of Congenital Isolated ACTH-Deficiency Patients with <i>TPIT</i> Gene Mutations 由 Catherine Couture, Alexandru Saveanu, Anne Barlier, Jean‐Claude Carel, Martin Faßnacht, C.E. Flück, Muriel Houang, Michaël Maes, Franziska Phan-Hug, A Enjalbert, Jacques Drouin, Thierry Brue, Sophie Vallette

    出版 2011
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