Higher risk of death among MEN1 patients with mutations in the JunD interacting domain: a Groupe d'etude des Tumeurs Endocrines (GTE) cohort study.
Julien Thevenon
,
Abderrahmane Bourredjem
,
Laurence Faivre
,
Catherine Cardot-Bauters
,
Alain Calender
,
et al.
Article dans une revue
hal-00935869v1
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Pasireotide is more effective than octreotide, alone or combined with everolimus on human meningioma in vitro
Thomas Graillon
,
David Romano
,
Céline Defilles
,
Christophe Lisbonis
,
Alexandru Saveanu
,
et al.
Oncotarget , 2017, 8, pp.55361 - 55373
Article dans une revue
hal-01731578v1
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[Clinical and genetic aspects of combined pituitary hormone deficiencies]
Frederic Castinetti
,
Rachel Reynaud
,
Alexandru Saveanu
,
M.-H. Quentien
,
F. Albarel
,
et al.
Article dans une revue
hal-00396962v1
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Beyond MEN1, When to Think About MEN4? Retrospective Study on 5600 Patients in the French Population and Literature Review
Benjamin Chevalier
,
Lucie Coppin
,
Pauline Romanet
,
Thomas Cuny
,
Jean-Christophe Maïza
,
et al.
Article dans une revue
hal-04522637v1
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Reciprocal Interactions between Fibroblast and Pancreatic Neuroendocrine Tumor Cells: Putative Impact of the Tumor Microenvironment
Thomas Cuny
,
Peter M van Koetsveld
,
Grégoire Mondielli
,
Fadime Dogan
,
Wouter W de Herder
,
et al.
Article dans une revue
hal-03727414v1
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Co-Targeting MAP Kinase and Pi3K-Akt-mTOR Pathways in Meningioma: Preclinical Study of Alpelisib and Trametinib
Grégoire Mondielli
,
Gregory Mougel
,
Florent Darriet
,
Catherine Roche
,
Adeline Querdray
,
et al.
Article dans une revue
hal-03778338v1
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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
,
et al.
Pediatrics , 2015, 135 (4), pp.e1079-83
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hal-01188625v1
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Using Digital Droplet Polymerase Chain Reaction to Detect the Mosaic GNAS Mutations in Whole Blood DNA or Circulating Cell-Free DNA in Fibrous Dysplasia and McCune-Albright Syndrome
Pauline Romanet
,
Pascal Philibert
,
Frederic Fina
,
Thomas Cuny
,
Catherine Roche
,
et al.
The Journal of Pediatrics , 2018
Article dans une revue
hal-01975613v1
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A novel dysfunctional LHX4 mutation with high phenotypical variability in patients with hypopituitarism.
Frederic Castinetti
,
Alexandru Saveanu
,
Rachel Reynaud
,
M. H. Quentien
,
A. Buffin
,
et al.
Article dans une revue
hal-00396966v1
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Identifying the Deleterious Effect of Rare LHX4 Allelic Variants, a Challenging Issue
Claire Rochette
,
Nicolas Jullien
,
Alexandru Saveanu
,
Emmanuelle Caldagues
,
Ignacio Bergada
,
et al.
Article dans une revue
hal-01211758v1
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Génétique des hypopituitarismes antérieurs.
Rachel Reynaud
,
Anne A. Barlier
,
Alexandru Saveanu
,
M.H. Quentien
,
A. Enjalbert
,
et al.
Annales d'Endocrinologie , 2005, 66, pp.250-257
Article dans une revue
hal-00017717v1
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Radio-chemotherapy feasibility for biopsy-only unresectable IDH wild-type glioblastomas (BO-GBM)
Vincent Harlay
,
Romain Appay
,
Celine Bequet
,
Gregorio Petrirena
,
Chantal Campello
,
et al.
Article dans une revue
hal-04254204v1
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Multiple congenital malformations arise from somatic mosaicism for constitutively active Pik3ca signalling
Elise Marechal
,
Anne Poliard
,
Kilian Henry
,
Mathias Moreno
,
Mathilde Legrix
,
et al.
2023
Pré-publication, Document de travail
hal-03809038v1
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Pitx2 et son mutant dominant négatif : outil thérapeutique potentiel dans la perspective de thérapie génique des adénomes hypophysaires ?
J. Acunzo
,
C. Roche
,
G. Gunz
,
I. Pellegrini
,
S. Drouva
,
et al.
Pitx2 et son mutant dominant négatif : outil thérapeutique potentiel dans la perspective de thérapie génique des adénomes hypophysaires ? , Sep 2007, TOURS, France
Communication dans un congrès
hal-00142529v1
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Pituitary transcription factors : from congenital deficiencies to gene therapy.
M.H. Quentien
,
Anne A. Barlier
,
J.L Franc
,
I. Pellegrini
,
Thierry Brue
,
et al.
Neuroendocrinology , 2006, sous presse, sous presse
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hal-00088998v1
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Genetic testing in prolactinomas: a cohort study
Amina Boukerrouni
,
Thomas Cuny
,
Thibaut Anjou
,
Isabelle Raingeard
,
Amandine Ferrière
,
et al.
European Journal of Endocrinology , 2023
Article dans une revue
hal-04256264v1
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IGSF1 mutations are the most frequent genetic aetiology of thyrotropin deficiency
Rachel Fourneaux
,
Rachel Reynaud
,
Gregory Mougel
,
Sarah Castets
,
Patricia Bretones
,
et al.
Article dans une revue
hal-04035130v1
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Relevance of coexpression of somatostatin and dopamine D2 receptors in pituitary adenomas
Alexandru Saveanu
,
P. Jaquet
,
Thierry Brue
,
Anne A. Barlier
Article dans une revue
istex
hal-00531973v1
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Genetic causes of combined pituitary hormone deficiencies in humans.
Frederic Castinetti
,
Rachel Reynaud
,
Alexandru Saveanu
,
Anne A. Barlier
,
Thierry Brue
Article dans une revue
hal-00701542v1
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First report of bilateral pheochromocytoma in the clinical spectrum of HIF2A-related polycythemia-paraganglioma syndrome.
David Taïeb
,
Chunzhang Yang
,
Blandine Delenne
,
Zhengping Zhuang
,
Anne A. Barlier
,
et al.
Article dans une revue
hal-00966232v1
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Pathological and Genetic Characterization of Bilateral Adrenomedullary Hyperplasia in a Patient with Germline MAX Mutation
Pauline Romanet
,
Carole Guerin
,
Pascal Pedini
,
Wassim Essamet
,
Frederic Castinetti
,
et al.
Article dans une revue
hal-03983075v1
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Prospective comparison of Ga-68-DOTATATE and F-18-FDOPA PET/CT in patients with various pheochromocytomas and paragangliomas with emphasis on sporadic cases
Aurelien Archier
,
Arthur Varoquaux
,
Philippe Garrigue
,
Marion Montava
,
Carole Guérin
,
et al.
Article dans une revue
hal-01482530v1
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Kinome rewiring during acquired drug resistance in neuroendocrine neoplasms
Corinne Gerard
,
Marie Lagarde
,
Flora Poizat
,
Sandrine Oziel-Taieb
,
Vincent Garcia
,
et al.
Article dans une revue
hal-03164671v1
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Should the GCM2 gene be tested when screening for familial primary hyperparathyroidism?
Lucie Coppin
,
Margaux Dufosse
,
Pauline Romanet
,
Sophie Giraud
,
Marie-Odile North
,
et al.
Article dans une revue
hal-03216133v1
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From pseudohypoparathyroidism to inactivating PTH/PTHrP signalling disorder (iPPSD), a novel classification proposed by the EuroPHP network
Susanne Thiele
,
Giovanna Mantovani
,
Anne A. Barlier
,
Valentina Boldrin
,
Paolo Bordogna
,
et al.
Article dans une revue
hal-01473947v1
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Germline mutations in the new E1' cryptic exon of the VHL gene in patients with tumours of von Hippel- Lindau disease spectrum or with paraganglioma
Alexandre Buffet
,
Bruna Calsina
,
Shahida Flores
,
Sophie Giraud
,
Marion Lenglet
,
et al.
Article dans une revue
hal-02484923v1
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Looking beyond the thyroid: advances in the understanding of pheochromocytoma and hyperparathyroidism phenotypes in MEN2 and of non-MEN2 familial forms
Carole Guerin
,
Pauline Romanet
,
David Taieb
,
Thierry Brue
,
André Lacroix
,
et al.
Article dans une revue
hal-01731588v1
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Lessons from monogenic causes of growth hormone deficiency
Thierry Brue
,
Alexandru Saveanu
,
Nicolas Jullien
,
Teddy Fauquier
,
Frederic Castinetti
,
et al.
Article dans une revue
hal-01731589v1
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Paraganglioma of the organ of Zuckerkandl associated with a somatic HIF2α mutation: A case report
Ahmad Esmaeel Abdullah
,
Carole Guerin
,
Alessio Imperiale
,
Anne A. Barlier
,
Stephanie Battini
,
et al.
Article dans une revue
hal-01731575v1
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Expression of somatostatin receptors, dopamine D₂ receptors, noradrenaline transporters, and vesicular monoamine transporters in 52 pheochromocytomas and paragangliomas.
Alexandru Saveanu
,
Mihaela Muresan
,
Catherine de Micco
,
David Taieb
,
Anne-Laure Germanetti
,
et al.
Article dans une revue
hal-00625459v1
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