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Anne Barlier
Anne Barlier
在 univ-amu.fr 的电子邮件经过验证
标题
引用次数
引用次数
年份
Clinical Characteristics and Therapeutic Responses in Patients with Germ-Line AIP Mutations and Pituitary Adenomas: An International Collaborative Study
AF Daly, MA Tichomirowa, P Petrossians, E Heliovaara, ML Jaffrain-Rea, ...
The Journal of Clinical Endocrinology & Metabolism 95 (11), E373-E383, 2010
3982010
Aryl hydrocarbon receptor-interacting protein gene mutations in familial isolated pituitary adenomas: analysis in 73 families
AF Daly, JF Vanbellinghen, SK Khoo, ML Jaffrain-Rea, LA Naves, ...
The Journal of Clinical Endocrinology & Metabolism 92 (5), 1891-1896, 2007
3642007
Imprinting of the Gsα gene GNAS1 in the pathogenesis of acromegaly
BE Hayward, A Barlier, M Korbonits, AB Grossman, P Jacquet, A Enjalbert, ...
The Journal of clinical investigation 107 (6), R31-R36, 2001
3492001
Gigantism and Acromegaly Due to Xq26 Microduplications and GPR101 Mutation
G Trivellin, AF Daly, FR Faucz, B Yuan, L Rostomyan, DO Larco, ...
New England Journal of Medicine 371 (25), 2363-2374, 2014
3332014
Absence of IDH mutation identifies a novel radiologic and molecular subtype of WHO grade II gliomas with dismal prognosis
P Metellus, B Coulibaly, C Colin, AM de Paula, A Vasiljevic, D Taieb, ...
Acta neuropathologica 120, 719-729, 2010
3212010
Demonstration of enhanced potency of a chimeric somatostatin-dopamine molecule, BIM-23A387, in suppressing growth hormone and prolactin secretion from human pituitary …
A Saveanu, E Lavaque, G Gunz, A Barlier, S Kim, JE Taylor, MD Culler, ...
The Journal of Clinical Endocrinology & Metabolism 87 (12), 5545-5552, 2002
1982002
Clinical and genetic characterization of pituitary gigantism: an international collaborative study in 208 patients
L Rostomyan, AF Daly, P Petrossians, E Nachev, AR Lila, AL Lecoq, ...
Endocrine-related cancer 22 (5), 745-757, 2015
1902015
Genetic screening of combined pituitary hormone deficiency: experience in 195 patients
R Reynaud, M Gueydan, A Saveanu, S Vallette-Kasic, A Enjalbert, T Brue, ...
The Journal of Clinical Endocrinology & Metabolism 91 (9), 3329-3336, 2006
1842006
High prevalence of AIP gene mutations following focused screening in young patients with sporadic pituitary macroadenomas
MA Tichomirowa, A Barlier, AF Daly, ML Jaffrain-Rea, C Ronchi, ...
European Journal of Endocrinology 165 (4), 509-515, 2011
1772011
Heterogeneous genetic background of the association of pheochromocytoma/paraganglioma and pituitary adenoma: results from a large patient cohort
J Dénes, F Swords, E Rattenberry, K Stals, M Owens, T Cranston, ...
The Journal of Clinical Endocrinology & Metabolism 100 (3), E531-E541, 2015
1762015
Expression of aryl hydrocarbon receptor (AHR) and AHR-interacting protein in pituitary adenomas: pathological and clinical implications
ML Jaffrain-Rea, M Angelini, D Gargano, MA Tichomirowa, AF Daly, ...
Endocrine-related cancer 16 (3), 1029-1043, 2009
1682009
Genetic analysis in young patients with sporadic pituitary macroadenomas: besides AIP don't forget MEN1 genetic analysis
T Cuny, M Pertuit, M Sahnoun-Fathallah, A Daly, G Occhi, MF Odou, ...
European Journal of Endocrinology 168 (4), 533-541, 2013
1602013
Mutations in the Aryl Hydrocarbon Receptor Interacting Protein Gene Are Not Highly Prevalent among Subjects with Sporadic Pituitary Adenomas
A Barlier, JF Vanbellinghen, AF Daly, M Silvy, ML Jaffrain-Rea, J Trouillas, ...
The Journal of Clinical Endocrinology & Metabolism 92 (5), 1952-1955, 2007
1602007
From pseudohypoparathyroidism to inactivating PTH/PTHrP signalling disorder (iPPSD), a novel classification proposed by the EuroPHP network
S Thiele, G Mantovani, A Barlier, V Boldrin, P Bordogna, L De Sanctis, ...
European Journal of Endocrinology 175 (6), P1-P17, 2016
1472016
PROP1 Gene Screening in Patients with Multiple Pituitary Hormone Deficiency Reveals Two Sites of Hypermutability and a High Incidence of Corticotroph Deficiency
S Vallette-Kasic, A Barlier, C Teinturier, A Diaz, M Manavela, ...
The Journal of Clinical Endocrinology & Metabolism 86 (9), 4529-4535, 2001
1462001
18F-FDG avidity of pheochromocytomas and paragangliomas: a new molecular imaging signature?
D Taïeb, F Sebag, A Barlier, L Tessonnier, FF Palazzo, I Morange, ...
Journal of Nuclear Medicine 50 (5), 711-717, 2009
1432009
Pronostic and Therapeutic Consequences of Gsα Mutations in Somatotroph Adenomas
A Barlier, G Gunz, AJ Zamora, I Morange-Ramos, D Figarella-Branger, ...
The Journal of Clinical Endocrinology & Metabolism 83 (5), 1604-1610, 1998
1431998
Congenital Isolated Adrenocorticotropin Deficiency: An Underestimated Cause of Neonatal Death, Explained by TPIT Gene Mutations
S Vallette-Kasic, T Brue, AM Pulichino, M Gueydan, A Barlier, M David, ...
The Journal of Clinical Endocrinology & Metabolism 90 (3), 1323-1331, 2005
1372005
Quinagolide–a valuable treatment option for hyperprolactinaemia
A Barlier, P Jaquet
European journal of endocrinology 154 (2), 187-195, 2006
1342006
Pituitary stalk interruption syndrome in 83 patients: novel HESX1 mutation and severe hormonal prognosis in malformative forms
R Reynaud, F Albarel, A Saveanu, N Kaffel, F Castinetti, P Lecomte, ...
European journal of endocrinology 164 (4), 457-465, 2011
1332011
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