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Year Number of Results
2002 1
2004 1
2005 2
2007 1
2008 2
2009 2
2011 4
2012 2
2014 2
2015 1
2016 2
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2019 4
2020 1
2022 3
2023 4
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31 results

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Page 1
Genetic of gonadal determination.
Morel Y, Roucher F, Mallet D, Plotton I. Morel Y, et al. Among authors: mallet d. Ann Endocrinol (Paris). 2014 May;75(2):32-9. doi: 10.1016/j.ando.2014.04.005. Epub 2014 Apr 29. Ann Endocrinol (Paris). 2014. PMID: 24793987 Review.
Case Report: Longitudinal follow-up and testicular sperm extraction in a patient with a pathogenic NR5A1 (SF-1) frameshift variant: p.(Phe70Serfs*5).
Teoli J, Mallet D, Renault L, Gay CL, Labrune E, Bretones P, Giscard D'Estaing S, Cuzin B, Dijoud F, Roucher-Boulez F, Plotton I. Teoli J, et al. Among authors: mallet d. Front Endocrinol (Lausanne). 2023 Jun 20;14:1171822. doi: 10.3389/fendo.2023.1171822. eCollection 2023. Front Endocrinol (Lausanne). 2023. PMID: 37409232 Free PMC article.
Genotype, Mortality, Morbidity, and Outcomes of 3β-Hydroxysteroid Dehydrogenase Deficiency in Algeria.
Ladjouze A, Donaldson M, Plotton I, Djenane N, Mohammedi K, Tardy-Guidollet V, Mallet D, Boulesnane K, Bouzerar Z, Morel Y, Roucher-Boulez F. Ladjouze A, et al. Among authors: mallet d. Front Endocrinol (Lausanne). 2022 Jun 10;13:867073. doi: 10.3389/fendo.2022.867073. eCollection 2022. Front Endocrinol (Lausanne). 2022. PMID: 35757411 Free PMC article.
Changes in the clinical management of 5α-reductase type 2 and 17β-hydroxysteroid dehydrogenase type 3 deficiencies in France.
Bonnet E, Winter M, Mallet D, Plotton I, Bouvattier C, Cartigny M, Martinerie L, Polak M, Bachelot A, Huet F, Baron S, Houang M, Soskin S, Lienhardt A, Bertherat J, Amouroux C, Bouty A, Duranteau L, Besson R, El Ghoneimi A, Samara-Boustani D, Becmeur F, Kalfa N, Paris F, Medjkane F, Brac de la Perrière A, Bretones P, Lejeune H, Nicolino M, Mouriquand P, Gorduza DB, Gay CL. Bonnet E, et al. Among authors: mallet d. Endocr Connect. 2023 Feb 14;12(3):e220227. doi: 10.1530/EC-22-0227. Print 2023 Mar 1. Endocr Connect. 2023. PMID: 36606580 Free PMC article.
Effect of Recombinant Gonadotropin on Testicular Function and Testicular Sperm Extraction in Five Cases of NR0B1 (DAX1) Pathogenic Variants.
Teoli J, Mezzarobba V, Renault L, Mallet D, Lejeune H, Chatelain P, Tixier F, Nicolino M, Peretti N, Giscard D'estaing S, Cuzin B, Dijoud F, Roucher-Boulez F, Plotton I. Teoli J, et al. Among authors: mallet d. Front Endocrinol (Lausanne). 2022 Mar 30;13:855082. doi: 10.3389/fendo.2022.855082. eCollection 2022. Front Endocrinol (Lausanne). 2022. PMID: 35432221 Free PMC article.
Epileptic encephalopathy as a new feature of the sudden infant death with dysgenesis of the testes syndrome caused by TSPYL1 variants.
Mazel B, Mallet D, Roucher-Boulez F, Signor CB, Bournez M, Darmency V, Bourgeois V, Poe C, El Khabbaz F, Vitobello A, Philippe C, Duffourd Y, Thauvin-Robinet C, Faivre L, Nambot S. Mazel B, et al. Among authors: mallet d. Am J Med Genet A. 2022 Dec;188(12):3540-3545. doi: 10.1002/ajmg.a.62966. Epub 2022 Sep 9. Am J Med Genet A. 2022. PMID: 36082874
31 results