Detalhe da pesquisa
1.
Shifting the landscape: Dominant C-terminal rare missense FOXL2 variants in non-syndromic primary ovarian failure etiology.
Clin Genet
; 2024 Apr 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-38558253
2.
Fertility and pregnancy outcomes in women with nonclassic 21-hydroxylase deficiency.
Clin Endocrinol (Oxf)
; 98(3): 315-322, 2023 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-36325983
3.
Combining metabolomics and machine learning models as a tool to distinguish non-classic 21-hydroxylase deficiency from polycystic ovary syndrome without adrenocorticotropic hormone testing.
Hum Reprod
; 38(2): 266-276, 2023 02 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36427016
4.
Pituitary surgery outcome in patients 75 years and older: a retrospective study.
Acta Neurochir (Wien)
; 165(11): 3409-3420, 2023 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-37736839
5.
Sexual Dimorphisms, Anti-Hormonal Therapy and Cardiac Arrhythmias.
Int J Mol Sci
; 22(3)2021 Feb 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-33540539
6.
Androgenic Effects on Ventricular Repolarization: A Translational Study From the International Pharmacovigilance Database to iPSC-Cardiomyocytes.
Circulation
; 140(13): 1070-1080, 2019 09 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-31378084
7.
Immune Checkpoint Inhibitor-Associated Primary Adrenal Insufficiency: WHO VigiBase Report Analysis.
Oncologist
; 25(8): 696-701, 2020 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-32390168
8.
Dlx5 and Dlx6 control uterine adenogenesis during post-natal maturation: possible consequences for endometriosis.
Hum Mol Genet
; 25(1): 97-108, 2016 Jan 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-26512061
9.
Role of Foxl2 in uterine maturation and function.
Hum Mol Genet
; 24(11): 3092-103, 2015 Jun 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-25687138
10.
Long-term outcome of ovarian function in women with intermittent premature ovarian insufficiency.
Clin Endocrinol (Oxf)
; 86(2): 223-228, 2017 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-27177971
11.
Sperm cryopreservation in young males with congenital adrenal hyperplasia (CAH).
Clin Endocrinol (Oxf)
; 97(6): 860-862, 2022 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-35746828
12.
Hypogonadism as a Reversible Cause of Torsades de Pointes in Men.
Circulation
; 138(1): 110-113, 2018 07 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-29967236
13.
Long-term outcomes in non-CAH 46,XX DSD.
Front Endocrinol (Lausanne)
; 15: 1372887, 2024.
Artigo
em Inglês
| MEDLINE | ID: mdl-38752171
14.
Ovarian reserve in patients with FMR1 gene premutation and the role of fertility preservation.
Ann Endocrinol (Paris)
; 2024 May 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-38702011
15.
Prognostic impact of hypothalamic perforation in adult patients with craniopharyngioma: a cohort study.
J Clin Endocrinol Metab
; 2024 Jan 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-38287910
16.
Position statement on the diagnosis and management of congenital pituitary deficiency in adults: The French National Diagnosis and Treatment Protocol (NDTP).
Ann Endocrinol (Paris)
; 2024 Mar 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-38452869
17.
The permissive role of prolactin as a regulator of luteinizing hormone action in the female mouse ovary and extragonadal tumorigenesis.
Am J Physiol Endocrinol Metab
; 305(7): E845-52, 2013 Oct 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-23921141
18.
Associations between visceral adipose tissue, inflammation and sex steroid concentrations in men.
Clin Endocrinol (Oxf)
; 78(3): 373-8, 2013 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-22469460
19.
Changes in the clinical management of 5α-reductase type 2 and 17ß-hydroxysteroid dehydrogenase type 3 deficiencies in France.
Endocr Connect
; 12(3)2023 Mar 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36606580
20.
The Severity of Congenital Hypothyroidism With Gland-In-Situ Predicts Molecular Yield by Targeted Next-Generation Sequencing.
J Clin Endocrinol Metab
; 108(9): e779-e788, 2023 08 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-36884306