User profiles for Anne Barlier
 | Anne BarlierAix Marseille University Verified email at univ-amu.fr Cited by 9334 |
Clinical Characteristics and Therapeutic Responses in Patients with Germ-Line AIP Mutations and Pituitary Adenomas: An International Collaborative Study
…, E Heliovaara, ML Jaffrain-Rea, A Barlier… - The Journal of …, 2010 - academic.oup.com
Context: AIP mutations (AIPmut) give rise to a pituitary adenoma predisposition that occurs
in familial isolated pituitary adenomas and less often in sporadic cases. The clinical and …
in familial isolated pituitary adenomas and less often in sporadic cases. The clinical and …
Aryl hydrocarbon receptor-interacting protein gene mutations in familial isolated pituitary adenomas: analysis in 73 families
Context: An association between germline aryl hydrocarbon receptor-interacting protein (AIP)
gene mutations and pituitary adenomas was recently shown. Objective: The objective of …
gene mutations and pituitary adenomas was recently shown. Objective: The objective of …
[HTML][HTML] Imprinting of the Gsα gene GNAS1 in the pathogenesis of acromegaly
BE Hayward, A Barlier, M Korbonits… - The Journal of …, 2001 - Am Soc Clin Investig
Approximately 40% of growth hormone–secreting pituitary adenomas have somatic mutations
in the GNAS1 gene (the so-called gsp oncogene). These mutations at codon 201 or codon …
in the GNAS1 gene (the so-called gsp oncogene). These mutations at codon 201 or codon …
[HTML][HTML] Gigantism and Acromegaly Due to Xq26 Microduplications and GPR101 Mutation
…, P Kamenický, WE Farrell, A Barlier… - … England Journal of …, 2014 - Mass Medical Soc
Background Increased secretion of growth hormone leads to gigantism in children and
acromegaly in adults; the genetic causes of gigantism and acromegaly are poorly understood. …
acromegaly in adults; the genetic causes of gigantism and acromegaly are poorly understood. …
Absence of IDH mutation identifies a novel radiologic and molecular subtype of WHO grade II gliomas with dismal prognosis
…, AM de Paula, A Vasiljevic, D Taieb, A Barlier… - Acta …, 2010 - Springer
The phenotypic heterogeneity of low-grade gliomas (LGGs) is still inconsistently explained
by known molecular abnormalities in patients treated according to the present standards of …
by known molecular abnormalities in patients treated according to the present standards of …
[HTML][HTML] Clinical and genetic characterization of pituitary gigantism: an international collaborative study in 208 patients
Cyclooxygenase-2 (COX-2) is associated with breast tumour progression. Clinical and molecular
studies implicate human epidermal growth factor receptor 2 (HER2) in the regulation of …
studies implicate human epidermal growth factor receptor 2 (HER2) in the regulation of …
Genetic analysis in young patients with sporadic pituitary macroadenomas: besides AIP don't forget MEN1 genetic analysis
…, G Weryha, A Enjalbert, A Barlier - European Journal of …, 2013 - academic.oup.com
Context Germline mutations in the aryl hydrocarbon receptor interacting protein gene (AIP)
have been identified in young patients (age ≤30 years old) with sporadic pituitary …
have been identified in young patients (age ≤30 years old) with sporadic pituitary …
Heterogeneous genetic background of the association of pheochromocytoma/paraganglioma and pituitary adenoma: results from a large patient cohort
…, K Skordilis, P Gabrovska, A Barlier… - The Journal of …, 2015 - academic.oup.com
Context: Pituitary adenomas and pheochromocytomas/paragangliomas (pheo/PGL) can occur
in the same patient or in the same family. Coexistence of the two diseases could be due to …
in the same patient or in the same family. Coexistence of the two diseases could be due to …
From pseudohypoparathyroidism to inactivating PTH/PTHrP signalling disorder (iPPSD), a novel classification proposed by the EuroPHP network
S Thiele, G Mantovani, A Barlier… - European Journal of …, 2016 - academic.oup.com
Objective Disorders caused by impairments in the parathyroid hormone (PTH) signalling
pathway are historically classified under the term pseudohypoparathyroidism (PHP), which …
pathway are historically classified under the term pseudohypoparathyroidism (PHP), which …
High prevalence of AIP gene mutations following focused screening in young patients with sporadic pituitary macroadenomas
Background Aryl hydrocarbon receptor interacting protein (AIP) mutations (AIPmut) cause
aggressive pituitary adenomas in young patients, usually in the setting of familial isolated …
aggressive pituitary adenomas in young patients, usually in the setting of familial isolated …