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Anne Barlier

Showing results (81-90 of 166) with videos related to

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Endocrine Pathology|November 14, 2016
Pathological and Genetic Characterization of Bilateral Adrenomedullary Hyperplasia in a Patient with Germline MAX MutationPauline Romanet, Carole Guerin, Pascal Pedini, et al.
Endocrine-Related Cancer|February 22, 2011
Expression of somatostatin receptors, dopamine D₂ receptors, noradrenaline transporters, and vesicular monoamine transporters in 52 pheochromocytomas and paragangliomasAlexandru Saveanu, Mihaela Muresan, Catherine De Micco, et al.
Oncology Letters|April 30, 2017
Paraganglioma of the organ of Zuckerkandl associated with a somatic <i>HIF2</i>α mutation: A case reportAhmad Esmaeel Abdullah, Carole Guerin, Alessio Imperiale, et al.
Journal of Psychosocial Oncology|May 17, 2018
Psychological impact of von Hippel-Lindau genetic screening in patients with a previous history of hemangioblastoma of the central nervous systemClaire Rochette, Karine Baumstarck, Hélène Canoni-Zattara, et al.
European Journal of Human Genetics : EJHG|September 29, 2018
Heterozygous LHX3 mutations may lead to a mild phenotype of combined pituitary hormone deficiencyNicolas Jullien, Pauline Romanet, Mélanie Philippon, et al.
Endocrinology|August 4, 2011
Inactivation of PITX2 transcription factor induced apoptosis of gonadotroph tumoral cellsJulie Acunzo, Catherine Roche, Celine Defilles, et al.
European Journal of Clinical Investigation|January 16, 2014
18F-FDG PET/CT as a predictor of hereditary head and neck paragangliomasElise M Blanchet, Sophie Gabriel, Victoria Martucci, et al.
European Journal of Endocrinology|July 5, 2020
Germinal defects of SDHx genes in patients with isolated pituitary adenomaGrégory Mougel, Arnaud Lagarde, Frédérique Albarel, et al.
Head & Neck|December 26, 2018
Tumor multifocality with vagus nerve involvement as a phenotypic marker of SDHD mutation in patients with head and neck paragangliomas: A <sup>18</sup> F-FDOPA PET/CT studyVincent Amodru, Pauline Romanet, Ugo Scemama, et al.
Journal of Neuroendocrinology|June 16, 2023
Deficient anterior pituitary with common variable immune deficiency (DAVID syndrome): a new case and literature reportsThi Thom Mac, Frederic Castinetti, Céline Bar, et al.
Pageof 17

Showing results (81-90 of 166) with videos related to

Sort By:
Pageof 17
Endocrine Pathology|November 14, 2016
Pathological and Genetic Characterization of Bilateral Adrenomedullary Hyperplasia in a Patient with Germline MAX MutationPauline Romanet, Carole Guerin, Pascal Pedini, et al.
Endocrine-Related Cancer|February 22, 2011
Expression of somatostatin receptors, dopamine D₂ receptors, noradrenaline transporters, and vesicular monoamine transporters in 52 pheochromocytomas and paragangliomasAlexandru Saveanu, Mihaela Muresan, Catherine De Micco, et al.
Oncology Letters|April 30, 2017
Paraganglioma of the organ of Zuckerkandl associated with a somatic <i>HIF2</i>α mutation: A case reportAhmad Esmaeel Abdullah, Carole Guerin, Alessio Imperiale, et al.
Journal of Psychosocial Oncology|May 17, 2018
Psychological impact of von Hippel-Lindau genetic screening in patients with a previous history of hemangioblastoma of the central nervous systemClaire Rochette, Karine Baumstarck, Hélène Canoni-Zattara, et al.
European Journal of Human Genetics : EJHG|September 29, 2018
Heterozygous LHX3 mutations may lead to a mild phenotype of combined pituitary hormone deficiencyNicolas Jullien, Pauline Romanet, Mélanie Philippon, et al.
Endocrinology|August 4, 2011
Inactivation of PITX2 transcription factor induced apoptosis of gonadotroph tumoral cellsJulie Acunzo, Catherine Roche, Celine Defilles, et al.
European Journal of Clinical Investigation|January 16, 2014
18F-FDG PET/CT as a predictor of hereditary head and neck paragangliomasElise M Blanchet, Sophie Gabriel, Victoria Martucci, et al.
European Journal of Endocrinology|July 5, 2020
Germinal defects of SDHx genes in patients with isolated pituitary adenomaGrégory Mougel, Arnaud Lagarde, Frédérique Albarel, et al.
Head & Neck|December 26, 2018
Tumor multifocality with vagus nerve involvement as a phenotypic marker of SDHD mutation in patients with head and neck paragangliomas: A <sup>18</sup> F-FDOPA PET/CT studyVincent Amodru, Pauline Romanet, Ugo Scemama, et al.
Journal of Neuroendocrinology|June 16, 2023
Deficient anterior pituitary with common variable immune deficiency (DAVID syndrome): a new case and literature reportsThi Thom Mac, Frederic Castinetti, Céline Bar, et al.
Pageof 17