B Delemer
Overview
Explore the profile of B Delemer including associated specialties, affiliations and a list of published articles.
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Articles
58
Citations
992
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Recent Articles
1.
E B, Bismuth E, Joubert M, M J, Renard E, E R, et al.
Diabetes Metab
. 2025 Mar;
:101637.
PMID: 40073966
The advent of automated insulin delivery (AID) systems in 2020 marked a disruptive event in managing type 1 diabetes, benefiting children and adults alike. By 2024, advances in real-world data...
2.
Vitellius G, Donadille B, Decoudier B, Leroux A, Deguelte S, Barraud S, et al.
Endocrine
. 2022 Aug;
78(1):201-204.
PMID: 35925470
The most frequent endocrine Carney complex manifestation is a bilateral primary pigmented nodular adrenocortical disease and bilateral adrenalectomy (BA) is therefore its main treatment. In this study, a 40 years...
3.
Mosbah H, Donadille B, Vatier C, Janmaat S, Atlan M, Badens C, et al.
Orphanet J Rare Dis
. 2022 Apr;
17(Suppl 1):170.
PMID: 35440056
Dunnigan syndrome, or Familial Partial Lipodystrophy type 2 (FPLD2; ORPHA 2348), is a rare autosomal dominant disorder due to pathogenic variants of the LMNA gene. The objective of the French...
4.
Tetu C, Gaubil-Kaladjian I, Barbe C, Diaz Cives A, Barrois M, Bertin E, et al.
Gynecol Obstet Fertil Senol
. 2021 Mar;
49(9):709-715.
PMID: 33766790
No abstract available.
5.
Truong L, Bazin C, Gomis P, Decoudier B, Delemer B, Litre C
Neurochirurgie
. 2021 Jan;
67(2):104-111.
PMID: 33450264
Background: Rathke's cleft cysts are benign cystic lesions of the sellar region, which may cause headache, pituitary deficiencies and visual disturbances from mass effect. Their management is not standardized yet....
6.
Tubiana-Rufi N, Schaepelynck P, Franc S, Chaillous L, Joubert M, Renard E, et al.
Diabetes Metab
. 2020 Nov;
47(3):101206.
PMID: 33152550
Automated closed-loop (CL) insulin therapy has come of age. This major technological advance is expected to significantly improve the quality of care for adults, adolescents and children with type 1...
7.
Amodru V, Petrossians P, Colao A, Delemer B, Maione L, Neggers S, et al.
Endocrine
. 2020 Jun;
70(1):134-142.
PMID: 32562181
Purpose: Acromegaly is a rare disease due to growth hormone (GH)-secreting pituitary adenoma. GH and IGF-1 levels are usually congruent, indicating either remission or active disease; however, a discrepancy between...
8.
Ly S, Naman A, Chaufour-Higel B, Patey M, Arndt C, Delemer B, et al.
Pituitary
. 2017 Aug;
20(6):709-710.
PMID: 28831662
Pituitary apoplexy (PA), defined by the occurrence of a massive hemorrhagic necrotic rearrangement within a pituitary adenoma, is rare. Its occurrence can be associated with certain risk factors, including anticoagulation....
9.
Lecomte P, Binquet C, Le Bras M, Tabarin A, Cardot-Bauters C, Borson-Chazot F, et al.
World J Surg
. 2017 Aug;
42(1):143-152.
PMID: 28785839
Objective: To evaluate the natural history of MEN1-related bronchial endocrine tumors (br-NETs) and to determine their histological characteristics, survival and causes of death. br-NETs frequency ranges from 3 to 13%...
10.
Franck S, Korevaar T, Petrossians P, Daly A, Chanson P, Jaffrain-Rea M, et al.
Eur J Endocrinol
. 2017 Jan;
176(4):421-431.
PMID: 28100630
Background: Effective treatment of acromegaly with pegvisomant (PEGV), a growth hormone receptor antagonist, requires an appropriate dose titration. PEGV doses vary widely among individual patients, and various covariates may affect...