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.
Epigenetic/circadian clocks and PCOS.
Hum Reprod
; 2024 Apr 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-38600622
3.
Stratification of the risk of ovarian dysfunction by studying the complexity of intermediate and premutation alleles of the FMR1 gene.
Am J Med Genet A
; 194(4): e63479, 2024 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-37987117
4.
NOBOX gene variants in premature ovarian insufficiency: ethnicity-dependent insights.
J Assist Reprod Genet
; 41(1): 135-146, 2024 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-37921973
5.
18F-fluorocholine PET/CT detects parathyroid gland hyperplasia as well as adenoma: 401 PET/CTs in one center.
Q J Nucl Med Mol Imaging
; 67(2): 96-113, 2023 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-36995286
6.
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
7.
Multiple endocrine neoplasia type 1 or 4: detection of hyperfunctioning parathyroid glands with 18F-fluorocholine PET/CT. Illustrative cases and pitfalls.
Q J Nucl Med Mol Imaging
; 66(2): 130-140, 2022 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-35005879
8.
Prevalence of lifetime eating disorders in infertile women seeking pregnancy with pulsatile gonadotropin-releasing hormone therapy.
Eat Weight Disord
; 26(2): 709-715, 2021 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-32239478
9.
Mutations involving the SRY-related gene SOX8 are associated with a spectrum of human reproductive anomalies.
Hum Mol Genet
; 27(7): 1228-1240, 2018 04 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29373757
10.
How can we make pregnancy safe for women with Turner syndrome?
Am J Med Genet C Semin Med Genet
; 181(1): 100-107, 2019 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-30767364
11.
An Application of NGS for Molecular Investigations in Perrault Syndrome: Study of 14 Families and Review of the Literature.
Hum Mutat
; 37(12): 1354-1362, 2016 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-27650058
12.
Intraadrenal corticotropin in bilateral macronodular adrenal hyperplasia.
N Engl J Med
; 369(22): 2115-25, 2013 Nov 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-24283225
13.
Spontaneous fertility and pregnancy outcomes amongst 480 women with Turner syndrome.
Hum Reprod
; 31(4): 782-8, 2016 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-26874361
14.
Toward a multi-country monitoring system of reproductive health in the context of endocrine disrupting chemical exposure.
Eur J Public Health
; 26(1): 76-83, 2016 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-26330492
15.
The CORALIE study: improving patient education to help new users better understand their oral contraceptive.
Eur J Contracept Reprod Health Care
; 21(5): 388-94, 2016 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-27530618
16.
Androgenic steroid excess in women.
Ann Endocrinol (Paris)
; 85(2): 142-149, 2024 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-38040089
17.
Fertility care among people with primary ciliary dyskinesia.
Pediatr Pulmonol
; 59(2): 281-290, 2024 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-37933800
18.
Diagnostic and referral pathways in patients with rare lipodystrophy and insulin-resistance syndromes: key milestones assessed from a national reference center.
Orphanet J Rare Dis
; 19(1): 177, 2024 Apr 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-38678257
19.
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
20.
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