de la Perriere AB - Search Results

Year	Number of Results
1999	1
2007	1
2010	1
2011	1
2012	2
2013	1
2015	2
2016	1
2017	1
2018	4
2019	1
2020	1
2021	3
2022	1
2023	1
2024	2

1

MANAGEMENT OF ENDOCRINE DISEASE Hyperandrogenic states in women: pitfalls in laboratory diagnosis.

Pugeat M, Plotton I, de la Perrière AB, Raverot G, Déchaud H, Raverot V. Pugeat M, et al. Among authors: de la perriere ab. Eur J Endocrinol. 2018 Apr;178(4):R141-R154. doi: 10.1530/EJE-17-0776. Epub 2018 Feb 16. Eur J Endocrinol. 2018. PMID: 29453202 Review.

2

Detection and management of late-onset 21-hydroxylase deficiency in women with hyperandrogenism.

Young J, Tardy V, de la Perrière AB, Bachelot A, Morel Y; French Society of Endocrinology. Young J, et al. Among authors: de la perriere ab. Ann Endocrinol (Paris). 2010 Feb;71(1):14-8. doi: 10.1016/j.ando.2009.12.009. Epub 2010 Jan 12. Ann Endocrinol (Paris). 2010. PMID: 20070950 Review.

3

Masculinizing surgery in disorders/differences of sex development: clinician- and participant-evaluated appearance and function.

van de Grift TC, Rapp M, Holmdahl G, Duranteau L, Nordenskjold A; dsd-LIFE group. van de Grift TC, et al. BJU Int. 2022 Mar;129(3):394-405. doi: 10.1111/bju.15369. Epub 2021 Mar 31. BJU Int. 2022. PMID: 33587786 Free PMC article.

4

Quality of Life in Men With Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency.

Verhees MJM, Engels M, Span PN, Sweep FCGJ, van Herwaarden AE, Falhammar H, Nordenström A, Webb EA, Richter-Unruh A, Bouvattier C, de la Perrière AB, Arlt W, Reisch N, Köhler B, Rapp M, Stikkelbroeck NMML, Roeleveld N, Claahsen-van der Grinten HL. Verhees MJM, et al. Among authors: de la perriere ab. Front Endocrinol (Lausanne). 2021 Mar 19;12:626646. doi: 10.3389/fendo.2021.626646. eCollection 2021. Front Endocrinol (Lausanne). 2021. PMID: 33815285 Free PMC article.

5

Voice dissatisfaction in individuals with a disorder of sex development.

Nygren U, Södersten M, Thyen U, Köhler B, Nordenskjöld A; dsd-LIFE Group. Nygren U, et al. Clin Endocrinol (Oxf). 2019 Jul;91(1):219-227. doi: 10.1111/cen.14000. Epub 2019 May 15. Clin Endocrinol (Oxf). 2019. PMID: 31026085

6

NOBOX gene variants in premature ovarian insufficiency: ethnicity-dependent insights.

Jordan P, Verebi C, Perol S, Grotto S, Fouveaut C, Christin-Maitre S, de la Perrière AB, Grouthier V, Jonard-Catteau S, Touraine P, Plu-Bureau G, Dupont JM, El Khattabi L, Bienvenu T. Jordan P, et al. Among authors: de la perriere ab. J Assist Reprod Genet. 2024 Jan;41(1):135-146. doi: 10.1007/s10815-023-02981-y. Epub 2023 Nov 3. J Assist Reprod Genet. 2024. PMID: 37921973

7

Fatty liver index, gamma-glutamyltransferase, and early carotid plaques.

Kozakova M, Palombo C, Eng MP, Dekker J, Flyvbjerg A, Mitrakou A, Gastaldelli A, Ferrannini E; RISC Investigators. Kozakova M, et al. Hepatology. 2012 May;55(5):1406-15. doi: 10.1002/hep.25555. Hepatology. 2012. PMID: 22334565

8

Xenoestrogen interaction with human sex hormone-binding globulin (hSHBG).

Déchaud H, Ravard C, Claustrat F, de la Perrière AB, Pugeat M. Déchaud H, et al. Among authors: de la perriere ab. Steroids. 1999 May;64(5):328-34. doi: 10.1016/s0039-128x(98)00114-7. Steroids. 1999. PMID: 10406482

9

Self- and proxy-reported outcomes after surgery in people with disorders/differences of sex development (DSD) in Europe (dsd-LIFE).

Rapp M, Duranteau L, van de Grift TC, Schober J, Hirschberg AL, Krege S, Nordenstrom A, Roehle R, Thyen U, Bouvattier C, Kreukels BPC, Nordenskjold A; dsd-LIFE group. Rapp M, et al. J Pediatr Urol. 2021 Jun;17(3):353-365. doi: 10.1016/j.jpurol.2020.12.007. Epub 2020 Dec 13. J Pediatr Urol. 2021. PMID: 33358555

10

Shifting the landscape: Dominant C-terminal rare missense FOXL2 variants in non-syndromic primary ovarian failure etiology.

Jordan P, Verebi C, Hervé B, Perol S, Chakhtoura Z, Courtillot C, Bachelot A, Karila D, Renard C, Grouthier V, de la Croix SM, Bernard V, Fouveaut C, de la Perrière AB, Jonard-Catteau S, Touraine P, Plu-Bureau G, Dupont JM, Christin-Maitre S, Bienvenu T. Jordan P, et al. Among authors: de la perriere ab. Clin Genet. 2024 Apr 1. doi: 10.1111/cge.14526. Online ahead of print. Clin Genet. 2024. PMID: 38558253

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