Publications by authors named "Pertuit Morgane"

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Deconvoluted Methylation Profiles Discriminate between Closely Related Melanocytic Nevi.
Daniel Aldea, Nicolas Macagno, Elise Marechal, Mathias Moreno, Pauline Romanet, Morgane Pertuit

J Invest Dermatol· May 2025

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CSNK2B Mutation: A Rare Cause of IGHD.
Karine Aouchiche, Pauline Romanet, Anne Barlier, Thierry Brue, Morgane Pertuit

Clin Endocrinol (Oxf)· April 2025

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Phenotype and genotype of 23 patients with hypopituitarism and pathogenic GLI2 variants.
Karine Aouchiche, Camille Charmensat, Pertuit Morgane, Cécile Teinturier, Patricia Bretones

Eur J Endocrinol· February 2025

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A novel gene mutation in patients with isolated ACTH deficiency from distinct families with a common geographical origin.
Théo Charnay, Gregory Mougel, Cyril Amouroux, Iva Gueorguieva, Florence Joubert, Morgane Pertuit

Front Endocrinol (Lausanne)· March 2023

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Psychological impact of von Hippel-Lindau genetic screening in patients with a previous history of hemangioblastoma of the central nervous system.
Claire Rochette, Karine Baumstarck, Hélène Canoni-Zattara, Ahmad Esmaeel Abdullah, Dominique Figarella-Branger, Morgane Pertuit

J Psychosoc Oncol· August 2019

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UMD-MEN1 Database: An Overview of the 370 MEN1 Variants Present in 1676 Patients From the French Population.
Pauline Romanet, Amira Mohamed, Sophie Giraud, Marie-Françoise Odou, Marie-Odile North, Morgane Pertuit

J Clin Endocrinol Metab· March 2019

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ALK-TPM3 rearrangement in adult renal cell carcinoma: Report of a new case showing loss of chromosome 3 and literature review.
Yohan Bodokh, Damien Ambrosetti, Valérie Kubiniek, Branwel Tibi, Matthieu Durand, Morgane Pertuit

Cancer Genet· February 2018

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Paraganglioma of the organ of Zuckerkandl associated with a somatic α mutation: A case report.
Ahmad Esmaeel Abdullah, Carole Guerin, Alessio Imperiale, Anne Barlier, Stéphanie Battini, Morgane Pertuit

Oncol Lett· March 2017

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In vitro impact of pegvisomant on growth hormone-secreting pituitary adenoma cells.
Thomas Cuny, Caroline Zeiller, Martin Bidlingmaier, Céline Défilles, Catherine Roche, Morgane Pertuit

Endocr Relat Cancer· July 2016

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Somatic gain-of-function HIF2A mutations in sporadic central nervous system hemangioblastomas.
David Taïeb, Anne Barlier, Chunzhang Yang, Morgane Pertuit, Aurélie Tchoghandjian

J Neurooncol· February 2016

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Case report of GNAS epigenetic defect revealed by a congenital hypothyroidism.
Pauline Romanet, Lindsay Osei, Irène Netchine, Morgane Pertuit, Alain Enjalbert

Pediatrics· April 2015

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18F-FDG PET/CT as a predictor of hereditary head and neck paragangliomas.
Elise M Blanchet, Sophie Gabriel, Victoria Martucci, Nicolas Fakhry, Clara C Chen, Morgane Pertuit

Eur J Clin Invest· October 2014

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A MEN1 syndrome with a paraganglioma.
Yvan Jamilloux, Judith Favier, Morgane Pertuit, Manuela Delage-Corre, Stéphanie Lopez

Eur J Hum Genet· February 2014

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Genetic analysis in young patients with sporadic pituitary macroadenomas: besides AIP don't forget MEN1 genetic analysis.
Thomas Cuny, Morgane Pertuit, Mona Sahnoun-Fathallah, Adrian Daly, Gianluca Occhi

Eur J Endocrinol· April 2013

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Ras and Rap1 govern spatiotemporal dynamic of activated ERK in pituitary living cells.
Caroline Zeiller, Marie-Pierre Blanchard, Morgane Pertuit, Sylvie Thirion, Alain Enjalbert

Cell Signal· December 2012

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Regulation of the RAP1/RAF-1/extracellularly regulated kinase-1/2 cascade and prolactin release by the phosphoinositide 3-kinase/AKT pathway in pituitary cells.
David Romano, Morgane Pertuit, Ramahefarizo Rasolonjanahary, Jean-Vianney Barnier, Karine Magalon

Endocrinology· December 2006

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