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Anne Barlier

Showing results (11-20 of 166) with videos related to

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Clinical Nuclear Medicine|February 26, 2014
In vivo and in vitro evidence of somatostatin receptors expression in a dedifferentiated retroperitoneal liposarcomaAlessio Imperiale, Marie-Pierre Chenard, Serge Rohr, et al.
Neuroendocrinology|June 4, 2020
Parasellar MeningiomasThomas Graillon, Jean Regis, Anne Barlier, et al.
Frontiers in Endocrinology|October 14, 2024
Challenges in molecular diagnosis of multiple endocrine neoplasiaPauline Romanet, Théo Charnay, Nicolas Sahakian, et al.
Thyroid : Official Journal of the American Thyroid Association|July 19, 2023
<i>Letter to the Editor:</i> The Somatic <i>RET</i> M918T Variant May Modify the Natural History of Germline <i>RET</i> L790F MEN2-Related Medullary Thyroid CarcinomaNicolas Sahakian, Pauline Romanet, Delphine Mirebeau-Prunier, et al.
Annales D'Endocrinologie|June 6, 2026
Pituitary Developmental Gene Defects and Their Contribution to Growth Hormone DeficiencyKarine Aouchiche, Rachel Reynaud, Theo Charnay, et al.
European Archives of Oto-Rhino-Laryngology : Official Journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : Affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery|November 8, 2007
Cervical paragangliomas: is SDH genetic analysis systematically required?Nicolas Fakhry, Patricia Niccoli-Sire, Anne Barlier-Seti, et al.
Pediatrics|March 25, 2015
Case report of GNAS epigenetic defect revealed by a congenital hypothyroidismPauline Romanet, Lindsay Osei, Irène Netchine, et al.
Journal of Clinical Medicine|May 24, 2018
Functioning Mediastinal Paraganglioma Associated with a Germline Mutation of von Hippel-Lindau GeneThibault Bahougne, Pauline Romanet, Amira Mohamed, et al.
Endocrine|May 17, 2019
Genetic analysis of adult Slovenian patients with combined pituitary hormone deficiencyKatica Bajuk Studen, Magdalena Avbelj Stefanija, Alexandru Saveanu, et al.
Clinical Endocrinology|December 16, 2024
CSNK2B Mutation: A Rare Cause of IGHDKarine Aouchiche, Pauline Romanet, Anne Barlier, et al.
Pageof 17

Showing results (11-20 of 166) with videos related to

Sort By:
Pageof 17
Clinical Nuclear Medicine|February 26, 2014
In vivo and in vitro evidence of somatostatin receptors expression in a dedifferentiated retroperitoneal liposarcomaAlessio Imperiale, Marie-Pierre Chenard, Serge Rohr, et al.
Neuroendocrinology|June 4, 2020
Parasellar MeningiomasThomas Graillon, Jean Regis, Anne Barlier, et al.
Frontiers in Endocrinology|October 14, 2024
Challenges in molecular diagnosis of multiple endocrine neoplasiaPauline Romanet, Théo Charnay, Nicolas Sahakian, et al.
Thyroid : Official Journal of the American Thyroid Association|July 19, 2023
<i>Letter to the Editor:</i> The Somatic <i>RET</i> M918T Variant May Modify the Natural History of Germline <i>RET</i> L790F MEN2-Related Medullary Thyroid CarcinomaNicolas Sahakian, Pauline Romanet, Delphine Mirebeau-Prunier, et al.
Annales D'Endocrinologie|June 6, 2026
Pituitary Developmental Gene Defects and Their Contribution to Growth Hormone DeficiencyKarine Aouchiche, Rachel Reynaud, Theo Charnay, et al.
European Archives of Oto-Rhino-Laryngology : Official Journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : Affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery|November 8, 2007
Cervical paragangliomas: is SDH genetic analysis systematically required?Nicolas Fakhry, Patricia Niccoli-Sire, Anne Barlier-Seti, et al.
Pediatrics|March 25, 2015
Case report of GNAS epigenetic defect revealed by a congenital hypothyroidismPauline Romanet, Lindsay Osei, Irène Netchine, et al.
Journal of Clinical Medicine|May 24, 2018
Functioning Mediastinal Paraganglioma Associated with a Germline Mutation of von Hippel-Lindau GeneThibault Bahougne, Pauline Romanet, Amira Mohamed, et al.
Endocrine|May 17, 2019
Genetic analysis of adult Slovenian patients with combined pituitary hormone deficiencyKatica Bajuk Studen, Magdalena Avbelj Stefanija, Alexandru Saveanu, et al.
Clinical Endocrinology|December 16, 2024
CSNK2B Mutation: A Rare Cause of IGHDKarine Aouchiche, Pauline Romanet, Anne Barlier, et al.
Pageof 17