Ludivine Drougat
Overview
Explore the profile of Ludivine Drougat including associated specialties, affiliations and a list of published articles.
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Articles
15
Citations
336
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0
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Recent Articles
1.
Maria A, Borges K, Lira R, Hassib Thome C, Berthon A, Drougat L, et al.
Mol Cell Endocrinol
. 2021 Mar;
528:111243.
PMID: 33716050
Adrenocortical cancer (ACC) is a rare and aggressive type of endocrine tumor with high risk of recurrence and metastasis. The overall survival of patients diagnosed with ACC is low and...
2.
Faillot S, Foulonneau T, Neou M, Espiard S, Garinet S, Vaczlavik A, et al.
Endocr Relat Cancer
. 2020 Nov;
28(1):79-95.
PMID: 33151900
Benign adrenal tumors cover a spectrum of lesions with distinct morphology and steroid secretion. Current classification is empirical. Beyond a few driver mutations, pathophysiology is not well understood. Here, a...
3.
Drougat L, Settas N, Ronchi C, Bathon K, Calebiro D, Maria A, et al.
Genet Med
. 2020 Oct;
23(1):239.
PMID: 33082560
No abstract available.
4.
Espiard S, Drougat L, Settas N, Haydar S, Bathon K, London E, et al.
Endocr Relat Cancer
. 2020 Oct;
27(11):647-656.
PMID: 33055300
Genetic variants in components of the protein kinase A (PKA) enzyme have been associated with various defects and neoplasms in the context of Carney complex (CNC) and in isolated cases,...
5.
Drougat L, Settas N, Ronchi C, Bathon K, Calebiro D, Maria A, et al.
Genet Med
. 2020 Sep;
23(1):174-182.
PMID: 32895490
Purpose: Protein kinase A (PKA) subunit defects (in PRKAR1A and PRKACA) are known to contribute to adrenal tumor pathogenesis. We studied the PRKAR1B gene for any genetic changes in bilateral...
6.
Maria A, Tatsi C, Berthon A, Drougat L, Settas N, Hannah-Shmouni F, et al.
Endocr Relat Cancer
. 2020 Jul;
27(9):509-517.
PMID: 32638579
Mutations in the protein kinase A (PKA) regulatory subunit type 1A (PRKAR1A) and armadillo repeat-containing 5 (ARMC5) genes cause Cushing's syndrome (CS) due to primary pigmented nodular adrenocortical disease (PPNAD)...
7.
Cavalcante I, Vaczlavik A, Drougat L, Lotfi C, Perlemoine K, Ribes C, et al.
Endocr Relat Cancer
. 2020 Feb;
27(4):221-230.
PMID: 32023208
ARMC5 (Armadillo repeat containing 5 gene) was identified as a new tumor suppressor gene responsible for hereditary adrenocortical tumors and meningiomas. ARMC5 is ubiquitously expressed and encodes a protein which...
8.
Drougat L, Espiard S, Bertherat J
Eur J Endocrinol
. 2015 Aug;
173(4):M121-31.
PMID: 26264719
Long-term consequences of cortisol excess are frequent despite appropriate treatment after cure of Cushing's syndrome. This might be due to diagnostic delay, often difficult to reduce in rare diseases. The...
9.
Drougat L, Omeiri H, Lefevre L, Ragazzon B
Front Endocrinol (Lausanne)
. 2015 Jun;
6:96.
PMID: 26106367
Adrenocortical tumors (ACTs) are typically unilateral and can be classified as benign adrenocortical adenomas (ACAs) or malignant adrenocortical cancers (ACCs). In rare cases, tumors may occur in both adrenal glands...
10.
Espiard S, Drougat L, Libe R, Assie G, Perlemoine K, Guignat L, et al.
J Clin Endocrinol Metab
. 2015 Apr;
100(6):E926-35.
PMID: 25853793
Context: Primary bilateral macronodular adrenal hyperplasia (PBMAH) is a rare cause of primary adrenal Cushing's syndrome (CS). ARMC5 germline mutations have been identified recently in PBMAH. Objective: To determine the...