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Results 1 to 25 of 65

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Radiothérapie et radiochirurgie des adénomes hypophysaires : Adénomes hypophysaires = Radiotherapy and radiosurgery of pituitary adenomasCASTINETTI, Frédéric; BRUE, Thierry.La Presse médicale (1983). 2009, Vol 38, Num 1, pp 133-139, issn 0755-4982, 7 p.Article

La génétique moléculaire au service de l'endocrinologueBERTHERAT, Jérôme; BRUE, Thierry; CHANSON, Philippe et al.Annales d'endocrinologie. 2005, Vol 66, Num 3, issn 0003-4266, 150 p.Conference Proceedings

Les laminopathies : lipodystrophies, insulino-résistance, syndromes de vieillissement accéléré... et les autres = Laminopathies: lipodystrophies, insulin resistance, syndromes of accelerated ageing... and othersVIGOUROUX, C.Annales d'endocrinologie. 2005, Vol 66, Num 3, pp 270-278, issn 0003-4266, 9 p.Conference Paper

Apport de la génomique dans les pathologies hypophysaires : Apport de la génomique en pathologie endocrinienne = Contribution of genomics to pituitary pathologySAVEANU, Alexandru; BORLIER, Anne; BRUE, Thierry et al.Métabolismes, hormones, diabètes et nutrition. 2008, Vol 12, Num 2, issn 1762-3065, 84-92 [8 p.]Article

Acromégalie : actualité physiopathologique et diagnostique = Acromegaly: pathophysiological and diagnostic topicalitiesBRUE, Thierry; SAVEANU, Alexandru; VALLETTE-KASIC, Sophie et al.MTE. Médecine thérapeutique endocrinologie. 2000, Vol OCT, pp 19-24, issn 1295-9359, NSArticle

Tests génétiques, le cadre législatif en France et en Europe = Genetic testing, the legal setting in France and EuropeDELPECH, M.Annales d'endocrinologie. 2005, Vol 66, Num 3, pp 292-293, issn 0003-4266, 2 p.Conference Paper

Pituitary Stem Cell Update and Potential Implications for Treating HypopituitarismCASTINETTI, Frederic; DAVIS, Shannon W; BRUE, Thierry et al.Endocrine reviews. 2011, Vol 32, Num 4, pp 453-471, issn 0163-769X, 19 p.Article

The role of SF1/DAX1 in adrenal and reproductive functionACHERMANN, J. C.Annales d'endocrinologie. 2005, Vol 66, Num 3, pp 233-239, issn 0003-4266, 7 p.Conference Paper

Intérêt de la génétique au décours d'un diagnostic d'hypocalcémie = Contribution of genetic testing after diagnostis of hypocalcemiaLIENHARDT-ROUSSIE, A.Annales d'endocrinologie. 2005, Vol 66, Num 3, pp 207-215, issn 0003-4266, 9 p.Conference Paper

La génétique moléculaire au service de l'endocrinologie. Aspects éthiques et réglementaires. Informations aux mineurs = Molecular genetics in endocrinologyCONTE-DEVOLX, B.Annales d'endocrinologie. 2005, Vol 66, Num 3, pp 289-291, issn 0003-4266, 3 p.Conference Paper

Medical Treatment of Cushing's Syndrome: Glucocorticoid Receptor Antagonists and MifepristoneCASTINETTI, Frederic; CONTE-DEVOLX, Bernard; BRUE, Thierry et al.Neuroendocrinology (Basel). 2010, Vol 92, pp 125-130, issn 0028-3835, 6 p., SUP1Conference Paper

Delayed diagnosis of Sheehan's syndrome in a developed country: a retrospective cohort studyRAMIANDRASOA, Cynthia; CASTINETTI, Frédéric; RAINGEARD, Isabelle et al.European journal of endocrinology. 2013, Vol 169, Num 4, pp 431-438, issn 0804-4643, 8 p.Article

The desmopressin test as a predictive factor of outcome after pituitary surgery for Cushing's diseaseVALERO, René; VALLETTE-KASIC, Sophie; CONTE-DEVOLX, Bernard et al.European journal of endocrinology. 2004, Vol 151, Num 6, pp 727-733, issn 0804-4643, 7 p.Article

Anomalies génétiques du récepteur aux androgènes et ambiguïté sexuelle avec fonction testiculaire normale à la naissance = Genetic anomalies of the androgen receptor and sexual ambiguity with normal testicular function at birthMOREL, Y; MICHEL-CALEMARD, L; MALLET, D et al.Annales d'endocrinologie. 2005, Vol 66, Num 3, pp 217-224, issn 0003-4266, 8 p.Conference Paper

Syndromes of thyroid hormone resistanceBECK-PECCOZ, P; MANNAVOLA, D; PERSAN, L et al.Annales d'endocrinologie. 2005, Vol 66, Num 3, pp 264-269, issn 0003-4266, 6 p.Conference Paper

Genetic causes of combined pituitary hormone deficiencies in humansCASTINETTI, Frédéric; REYNAUD, Rachel; SAVEANU, Alexandru et al.Annales d'endocrinologie. 2012, Vol 73, Num 2, pp 53-55, issn 0003-4266, 3 p.Conference Paper

Pharmacokinetic Evidence for Suboptimal Treatment of Adrenal Insufficiency with Currently Available Hydrocortisone TabletsSIMON, Nicolas; CASTINETTI, Frederic; OULIAC, Floriane et al.Clinical pharmacokinetics. 2010, Vol 49, Num 7, pp 455-463, issn 0312-5963, 9 p.Article

Inactivating and activating mutations of the Gs alpha geneSPADA, A; MANTOVANI, G; LANIA, A et al.Annales d'endocrinologie. 2005, Vol 66, Num 3, pp 258-263, issn 0003-4266, 6 p.Conference Paper

Aspects psychologiques du diagnostic génétique des tumeurs endocrines = Psychological aspects of genetic diagnosis of endocrine tumorsGIMENEZ-ROQUEPLO, Anne-Paule; LAHLOU-LAFORET, Khadija.Annales d'endocrinologie. 2005, Vol 66, Num 3, pp 284-288, issn 0003-4266, 5 p.Conference Paper

Bilateral neck exploration in patients with primary hyperparathyroidism and discordant imaging results: a single-centre studyPHILIPPON, Melanie; GUERIN, Carole; CASTINETTI, Frederic et al.European journal of endocrinology. 2014, Vol 170, Num 5, pp 719-725, issn 0804-4643, 7 p.Article

Temozolomide Treatment in Aggressive Pituitary Tumors and Pituitary Carcinomas: A French Multicenter ExperienceRAVEROT, Gérald; STURM, Nathalie; DUFOUR, Henry et al.The Journal of clinical endocrinology and metabolism. 2010, Vol 95, Num 10, pp 4592-4599, issn 0021-972X, 8 p.Article

Aryl hydrocarbon receptor-interacting protein gene mutations in familial isolated pituitary adenomas : Analysis in 73 familiesDALY, Adrian F; VANBELLINGHEN, Jean-Francois; RAVEROT, Gérald et al.The Journal of clinical endocrinology and metabolism. 2007, Vol 92, Num 5, pp 1891-1896, issn 0021-972X, 6 p.Article

Congenital isolated adrenocorticotropin deficiency : An underestimated cause of neonatal death, explained by TPIT gene mutationsVALLETTE-KASIC, Sophie; BRUE, Thierry; VAN VLIET, Guy et al.The Journal of clinical endocrinology and metabolism. 2005, Vol 90, Num 3, pp 1323-1331, issn 0021-972X, 9 p.Article

Tpit, un nouveau membre de la famille des gènes à boîte T, est impliqué dans la déficience isolée en ACTH = Tpit, a pituitary cell-restricted T-box factor, involved in ACTH deficiencyPULICHINO, Anne-Marie; LAMOLET, Bruno; BRUE, Thierry et al.MS. Médecine sciences. 2001, Vol 17, Num 11, pp 1203-1207, issn 0767-0974Article

High prevalence of AIP gene mutations following focused screening in young patients with sporadic pituitary macroadenomasTICHOMIROWA, Maria A; BARLIER, Anne; DESAILLOUD, Rachel et al.European journal of endocrinology. 2011, Vol 165, Num 4, pp 509-515, issn 0804-4643, 7 p.Article

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