Recherche - Archive ouverte HAL

137 résultats

	Pour les 137 documents Envoyer sur ORCID RSS ATOM Exporter BibTeX XML-TEI CSV RTF EndNote PDF HTML Export avancé	Page : Page précédente 1 2 3 4 5 Page suivante	triés par Pertinence Auteur A→Z Auteur Z→A Titre A→Z Titre Z→A Date de publication croissante Date de publication décroissante Date de dépôt croissante Date de dépôt décroissante

		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	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		[Clinical and genetic aspects of combined pituitary hormone deficiencies] Frederic Castinetti , Rachel Reynaud , Alexandru Saveanu , M.-H. Quentien , F. Albarel , et al. Annales d'Endocrinologie, 2008, 69 (1), pp.7-17. ⟨10.1016/j.ando.2008.01.001⟩ Article dans une revue hal-00396962v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		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. Cancers, 2022, 14 (14), pp.3481. ⟨10.3390/cancers14143481⟩ Article dans une revue hal-03727414v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		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. Cancers, 2022, 14 (18), pp.4448. ⟨10.3390/cancers14184448⟩ Article dans une revue hal-03778338v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		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 Article dans une revue hal-01188625v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		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	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		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. Journal of Clinical Endocrinology and Metabolism, 2008, 93 (7), pp.2790-9. ⟨10.1210/jc.2007-2389⟩ Article dans une revue hal-00396966v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		Identifying the Deleterious Effect of Rare LHX4 Allelic Variants, a Challenging Issue Claire Rochette , Nicolas Jullien , Alexandru Saveanu , Emmanuelle Caldagues , Ignacio Bergada , et al. PLoS ONE, 2015, 10 (e0126648), ⟨10.1371/journal.pone.0126648⟩ Article dans une revue hal-01211758v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		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. Human Molecular Genetics, 2013, 22 (10), pp.1940-8. ⟨10.1093/hmg/ddt039⟩ Article dans une revue hal-00935869v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		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. Journal of Clinical Endocrinology and Metabolism, 2024, ⟨10.1210/clinem/dgae055⟩ Article dans une revue hal-04522637v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		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	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		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. Neuro-Oncology Practice, 2023, 10 (6), pp.536-543. ⟨10.1093/nop/npad028⟩ Article dans une revue hal-04254204v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		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	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		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	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		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 Article dans une revue hal-00088998v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		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	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		IGSF1 mutations are the most frequent genetic aetiology of thyrotropin deficiency Rachel Fourneaux , Rachel Reynaud , Gregory Mougel , Sarah Castets , Patricia Bretones , et al. European Journal of Endocrinology, 2022, 187 (6), pp.787-795. ⟨10.1530/EJE-22-0520⟩ Article dans une revue hal-04035130v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		Relevance of coexpression of somatostatin and dopamine D2 receptors in pituitary adenomas Alexandru Saveanu , P. Jaquet , Thierry Brue , Anne A. Barlier Molecular and Cellular Endocrinology, 2008, 286 (1-2), pp.206. ⟨10.1016/j.mce.2007.12.008⟩ Article dans une revue istex hal-00531973v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		Genetic causes of combined pituitary hormone deficiencies in humans. Frederic Castinetti , Rachel Reynaud , Alexandru Saveanu , Anne A. Barlier , Thierry Brue Annales d'Endocrinologie, 2012, 73 (2), pp.53-5. ⟨10.1016/j.ando.2012.03.025⟩ Article dans une revue hal-00701542v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		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. Journal of Clinical Endocrinology and Metabolism, 2013, 98 (5), pp.E908-13. ⟨10.1210/jc.2013-1217⟩ Article dans une revue hal-00966232v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		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. Endocrine Pathology, 2017, 28 (4), pp.302 - 307. ⟨10.1007/s12022-016-9460-5⟩ Article dans une revue hal-03983075v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		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. European Journal of Nuclear Medicine and Molecular Imaging, 2016, 43 (7), pp.1248-1257. ⟨10.1007/s00259-015-3268-2⟩ Article dans une revue hal-01482530v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		Kinome rewiring during acquired drug resistance in neuroendocrine neoplasms Corinne Gerard , Marie Lagarde , Flora Poizat , Sandrine Oziel-Taieb , Vincent Garcia , et al. Endocrine-Related Cancer, 2021, 28 (1), pp.39-51. ⟨10.1530/ERC-19-0142⟩ Article dans une revue hal-03164671v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		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. European Journal of Endocrinology, 2016, 175 (6), pp.P1--P17. ⟨10.1530/EJE-16-0107⟩ Article dans une revue hal-01473947v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		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. European Journal of Endocrinology, 2020, 182, pp.57 - 65. ⟨10.1530/eje-19-0641⟩ Article dans une revue hal-03216133v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		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. Journal of Medical Genetics, 2020, pp.1 - 8. ⟨10.1136/jmedgenet-2019-106519⟩ Article dans une revue hal-02484923v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		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. Endocrine-Related Cancer, 2018, 25 (2), pp.T15 - T28. ⟨10.1530/ERC-17-0266⟩ Article dans une revue hal-01731588v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		Lessons from monogenic causes of growth hormone deficiency Thierry Brue , Alexandru Saveanu , Nicolas Jullien , Teddy Fauquier , Frederic Castinetti , et al. Annales d'Endocrinologie, 2017, 78 (2), pp.77 - 79. ⟨10.1016/j.ando.2017.04.001⟩ Article dans une revue hal-01731589v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		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. Oncology Letters, 2017, 13 (3), pp.1083 - 1086. ⟨10.3892/ol.2017.5599⟩ Article dans une revue hal-01731575v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More
		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. Endocrine-Related Cancer, 2011, 18 (2), pp.287-300. ⟨10.1530/ERC-10-0175⟩ Article dans une revue hal-00625459v1	Envoyer sur ORCID Exporter BibTeX XML-TEI Dublin Core DC Terms EndNote DataCite Export avancé Partager Gmail Facebook X LinkedIn More

Filtrer vos résultats

Pasireotide is more effective than octreotide, alone or combined with everolimus on human meningioma in vitro

[Clinical and genetic aspects of combined pituitary hormone deficiencies]

Reciprocal Interactions between Fibroblast and Pancreatic Neuroendocrine Tumor Cells: Putative Impact of the Tumor Microenvironment

Co-Targeting MAP Kinase and Pi3K-Akt-mTOR Pathways in Meningioma: Preclinical Study of Alpelisib and Trametinib

Case report of GNAS epigenetic defect revealed by a congenital hypothyroidism.

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

A novel dysfunctional LHX4 mutation with high phenotypical variability in patients with hypopituitarism.

Identifying the Deleterious Effect of Rare LHX4 Allelic Variants, a Challenging Issue

Higher risk of death among MEN1 patients with mutations in the JunD interacting domain: a Groupe d'etude des Tumeurs Endocrines (GTE) cohort study.

Beyond MEN1, When to Think About MEN4? Retrospective Study on 5600 Patients in the French Population and Literature Review

Génétique des hypopituitarismes antérieurs.

Radio-chemotherapy feasibility for biopsy-only unresectable IDH wild-type glioblastomas (BO-GBM)

Multiple congenital malformations arise from somatic mosaicism for constitutively active Pik3ca signalling

Pitx2 et son mutant dominant négatif : outil thérapeutique potentiel dans la perspective de thérapie génique des adénomes hypophysaires ?

Pituitary transcription factors : from congenital deficiencies to gene therapy.

Genetic testing in prolactinomas: a cohort study

IGSF1 mutations are the most frequent genetic aetiology of thyrotropin deficiency

Relevance of coexpression of somatostatin and dopamine D2 receptors in pituitary adenomas

Genetic causes of combined pituitary hormone deficiencies in humans.

First report of bilateral pheochromocytoma in the clinical spectrum of HIF2A-related polycythemia-paraganglioma syndrome.

Pathological and Genetic Characterization of Bilateral Adrenomedullary Hyperplasia in a Patient with Germline MAX Mutation

Prospective comparison of Ga-68-DOTATATE and F-18-FDOPA PET/CT in patients with various pheochromocytomas and paragangliomas with emphasis on sporadic cases

Kinome rewiring during acquired drug resistance in neuroendocrine neoplasms

From pseudohypoparathyroidism to inactivating PTH/PTHrP signalling disorder (iPPSD), a novel classification proposed by the EuroPHP network

Should the GCM2 gene be tested when screening for familial primary hyperparathyroidism?

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

Looking beyond the thyroid: advances in the understanding of pheochromocytoma and hyperparathyroidism phenotypes in MEN2 and of non-MEN2 familial forms

Lessons from monogenic causes of growth hormone deficiency

Paraganglioma of the organ of Zuckerkandl associated with a somatic HIF2α mutation: A case report

Expression of somatostatin receptors, dopamine D₂ receptors, noradrenaline transporters, and vesicular monoamine transporters in 52 pheochromocytomas and paragangliomas.