About: Thierry Brue

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An Entity of Type : foaf:Person, within Data Space : data.idref.fr associated with source document(s)

Attributes	Values
type	Person
sameAs	Brue, Thierry (19..-....) Brue, Thierry (19..-....) Brue, Thierry (19..-....) Brue, Thierry (19..-....) Brue, Thierry (19..-....) Brue, Thierry (19..-....)
Life Event	http://www.idref.fr/058613439/birth
preferred label	Brue, Thierry (19..-....)
name	Thierry Brue
dbpedia-owl:citizenship	http://sws.geonames.org/3017382/
Language	http://lexvo.org/id/iso639-3/fra
isni:identifierValid	000000000691818X
Given name	Thierry
familyName	Brue
has biographical i...tion (Deprecated)	Directeur de thèse. Professeur des universités (endocrinologie, diabète, maladies métaboliques), praticien hospitalier (en 2001). Unité mixte de recherche 6544 \"Interactions cellulaires neuroendocriniennes\" (ICNE) ; Service d'endocrinologie et des maladies métaboliques
gender	male
ORCID iD	0000-0001-8482-6691
Scopus ID	7004413343
is sameAs of	Brue, Thierry (19..-....) Brue, Thierry (19..-....) Brue, Thierry (19..-....)
is Thesis advisor of	http://www.sudoc.fr/060064021/id http://www.sudoc.fr/175360960/id http://www.sudoc.fr/152108165/id http://www.sudoc.fr/14966060X/id Bases moléculaires des hypopituitarismes congénitaux http://www.sudoc.fr/129271993/id Facteurs de transcription à l'homéodomaine, du modèle murin à l'hypopituitarisme humain http://www.sudoc.fr/165184957/id http://www.sudoc.fr/058613463/id http://www.sudoc.fr/204584892/id http://www.sudoc.fr/113297149/id http://www.sudoc.fr/151576769/id http://www.sudoc.fr/053691350/id http://www.sudoc.fr/067207782/id http://www.sudoc.fr/114101728/id http://www.sudoc.fr/179348663/id http://www.sudoc.fr/246615761/id Mécanismes physiopathologiques des hypopituitarismes congénitaux multiples http://www.sudoc.fr/280828810/id http://www.sudoc.fr/246959371/id
is Praeses of	http://www.sudoc.fr/203213459/id New regulatory mechanisms in the growth of endocrine tumors, digestive neuroendocrine tumors, pitiutary adenomas http://www.sudoc.fr/203770056/id http://www.sudoc.fr/236162470/id
is Author of	http://www.sudoc.fr/135511003/id Le diabète http://www.sudoc.fr/041683498/id http://www.sudoc.fr/078177375/id http://www.sudoc.fr/04327515X/id Looking beyond the thyroid: advances in the understanding of pheochromocytoma and hyperparathyroidism phenotypes in MEN2 and of non-MEN2 familial forms Intérêt du diagnostic génétique des déficits hypophysaires combinés sur une série de 197 patients. Comparaison du (68)Ga-DOTATATE TEP/TDM et du (18)F-FDOPA TEP/TDM pour le diagnostic des tumeurs neuroendocrines pancréatiques chez une patiente atteinte de NEM1 The role of CBP/p300 interactions and Pit-1 dimerization in the pathophysiological mechanism of combined pituitary hormone deficiency. Identifying the Deleterious Effect of Rare LHX4 Allelic Variants, a Challenging Issue THe Cables1 Gene in Glucocorticoid Regulation of Pituitary Corticotrope Growth and Cushing Disease Discordant biological parameters of remission in acromegaly do not increase the risk of hypertension or diabetes: a study with the Liege Acromegaly Survey database Successful IVF pregnancy despite inadequate ovarian steroidogenesis due to congenital lipoid adrenal hyperplasia (CLAH): a case report Pituitary carcinomas and aggressive pituitary tumours: merits and pitfalls of temozolomide treatment. Signs and symptoms of acromegaly at diagnosis: the physician's and the patient's perspectives in the ACRO-POLIS study (vol 63, pg 120, 2019) Pegvisomant in combination or pegvisomant alone after failure of somatostatin analogs in acromegaly patients: an observational French ACROSTUDY cohort study (September, 10.1007/s12020-020-02501-3, 2020) Cushing Syndrome Is Associated With Subclinical LV Dysfunction and Increased Epicardial Adipose Tissue Deficit in Anterior Pituitary Function and Variable Immune Deficiency (DAVID) in Children Presenting with Adrenocorticotropin Deficiency and Severe Infections Genetic screening in 195 patients with combined pituitary hormone deficiency : experience of the GENHYPOPIT Network. Ghrelin receptor (GHS-R1a) and its constitutive activity in somatotroph adenomas: a new co-targeting therapy using GHS-R1a inverse agonists and somatostatin analogs. Molecular mechanisms of pituitary organogenesis: In search of novel regulatory genes. Pituitary Transcription Factors: From Congenital Deficiencies to Gene Therapy Les mutations Sox3 ne sont pas une cause fréquente d'insuffisance antéhypophysaire congénitale. Aryl hydrocarbon receptor interacting protein gene mutations in familial isolated pituitary adenomas : analysis in 73 families. Guidelines of the Pituitary Society for the diagnosis and management of prolactinomas Cancerous leptomeningitis and familial congenital hypopituitarism Ketoconazole revisited: a preoperative or postoperative treatment in Cushing's disease. Women's perceptions of femininity after craniopharyngioma: a qualitative study http://id.erudit.org/iderudit/009702ar#id https://orbi.uliege.be/handle/2268/65943#id https://orbi.uliege.be/handle/2268/156991#id Pre-term birth in women exposed to Cushing’s disease: the baby-cush study Prognostic factors in prolactin pituitary tumors: clinical, histological, and molecular data from a series of 94 patients with a long postoperative follow-up. [Genetic aspects of growth hormone deficiency]. Epilepsy related to hypothalamic hamartomas : surgical management with special reference to ga surgery Pasireotide for acromegaly: long-term outcomes from an extension to the Phase III PAOLA study Pegvisomant in combination or pegvisomant alone after failure of somatostatin analogs in acromegaly patients: an observational French ACROSTUDY cohort study https://orbi.uliege.be/handle/2268/75614#id https://orbi.uliege.be/handle/2268/12090#id https://orbi.uliege.be/handle/2268/179174#id https://orbi.uliege.be/handle/2268/184919#id https://orbi.uliege.be/handle/2268/191465#id https://orbi.uliege.be/handle/2268/213184#id X chromosome gene dosage as a determinant of congenital malformations and of age-related comorbidity risk in patients with Turner syndrome, from childhood to early adulthood Temozolomide treatment in aggressive pituitary tumors and pituitary carcinomas: a French multicenter experience. Natural history, treatment, and long-term follow up of patients with multiple endocrine neoplasia type 2B: an international, multicentre, retrospective study Inactivation of PITX2 transcription factor induced apoptosis of gonadotroph tumoral cells. Pituitary gland: Gamma Knife for Cushing disease — time for a reappraisal? Pituitary stalk interruption syndrome in 83 patients: novel HESX1 mutation and severe hormonal prognosis in malformative forms Role of Brg1 and HDAC2 in GR trans-repression of the pituitary POMC gene and misexpression in Cushing disease. Mutations in the Aryl Hydrocarbon Receptor Interacting Protein Gene Are Not Highly Prevalent among Subjects with Sporadic Pituitary Adenomas https://orbi.uliege.be/handle/2268/75617#id https://orbi.uliege.be/handle/2268/163173#id

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