Anne Barlier
Anne Barlier
Zweryfikowany adres z univ-amu.fr
Tytuł
Cytowane przez
Cytowane przez
Rok
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
3282001
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
3222007
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 Heliövaara, ML Jaffrain-Rea, ...
The Journal of Clinical Endocrinology & Metabolism 95 (11), E373-E383, 2010
3122010
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 (6), 719-729, 2010
2802010
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
2552014
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
1942002
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
1592006
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
1522009
High prevalence of AIP gene mutations following focused screening in young patients with sporadic pituitary macroadenomas.
MA Tichomirowa, A Barlier, A Daly, M Jaffrain-Rea, C Ronchi, M Yaneva, ...
European Journal of Endocrinology 165 (4), 509-15, 2011
1502011
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
1472007
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
1402015
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
1342015
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
1341998
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
1332001
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
1292009
Genetic analysis in young patients with sporadic pituitary macroadenomas: Beside AIP don't forget MEN1 genetic analysis.
T Cuny, M Pertuit, M Sahnoun-Fathallah, A Daly, G Occhi, MF Odou, ...
European Journal of Endocrinology, 2013
1212013
A new mutation of the gene encoding the transcription factor Pit-1 is responsible for combined pituitary hormone deficiency
I Pellegrini-Bouiller, P Belicar, A Barlier, G Gunz, JP Charvet, P Jaquet, ...
The Journal of Clinical Endocrinology & Metabolism 81 (8), 2790-2796, 1996
1191996
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, 2011
1102011
The analysis of quantitative expression of somatostatin and dopamine receptors in gastro-entero-pancreatic tumours opens new therapeutic strategies
D O’Toole, A Saveanu, A Couvelard, G Gunz, A Enjalbert, P Jaquet, ...
European Journal of Endocrinology 155 (6), 849-857, 2006
1102006
Quinagolide–a valuable treatment option for hyperprolactinaemia
A Barlier, P Jaquet
European journal of endocrinology 154 (2), 187-195, 2006
1092006
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Prace 1–20