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Page 1
Aberrant Splicing Is the Pathogenicity Mechanism of the p.Glu314Lys Variant in CYP11A1 Gene.
Goursaud C, Mallet D, Janin A, Menassa R, Tardy-Guidollet V, Russo G, Lienhardt-Roussie A, Lecointre C, Plotton I, Morel Y, Roucher-Boulez F. Goursaud C, et al. Among authors: mallet d. Front Endocrinol (Lausanne). 2018 Sep 5;9:491. doi: 10.3389/fendo.2018.00491. eCollection 2018. Front Endocrinol (Lausanne). 2018. PMID: 30233493 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.
Endocrine screening in 32 consecutive patients with hypospadias.
Feyaerts A, Forest MG, Morel Y, Mure PY, Morel-Journel N, Mallet D, Nicolino M, Chatelain P, David M, Mouriquand P. Feyaerts A, et al. Among authors: mallet d. J Urol. 2002 Aug;168(2):720-5; discussion 725. J Urol. 2002. PMID: 12131359
A novel mutation L260P of the steroidogenic acute regulatory protein gene in three unrelated patients of Swiss ancestry with congenital lipoid adrenal hyperplasia.
Flück CE, Maret A, Mallet D, Portrat-Doyen S, Achermann JC, Leheup B, Theintz GE, Mullis PE, Morel Y. Flück CE, et al. Among authors: mallet d. J Clin Endocrinol Metab. 2005 Sep;90(9):5304-8. doi: 10.1210/jc.2005-0874. Epub 2005 Jun 28. J Clin Endocrinol Metab. 2005. PMID: 15985476 Free article.
78 results