Mallet D - Search Results

1

Evolution of steroids during pregnancy: Maternal, placental and fetal synthesis.

Morel Y, Roucher F, Plotton I, Goursaud C, Tardy V, Mallet D. Morel Y, et al. Among authors: mallet d. Ann Endocrinol (Paris). 2016 Jun;77(2):82-9. doi: 10.1016/j.ando.2016.04.023. Epub 2016 May 4. Ann Endocrinol (Paris). 2016. PMID: 27155772 Review.

2

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

3

Gonadal dysgenesis without adrenal insufficiency in a 46, XY patient heterozygous for the nonsense C16X mutation: a case of SF1 haploinsufficiency.

Mallet D, Bretones P, Michel-Calemard L, Dijoud F, David M, Morel Y. Mallet D, et al. J Clin Endocrinol Metab. 2004 Oct;89(10):4829-32. doi: 10.1210/jc.2004-0670. J Clin Endocrinol Metab. 2004. PMID: 15472171

4

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.

5

[Genetic anomalies of the androgen receptor and sexual ambiguity with normal testicular function at birth].

Morel Y, Michel-Calemard L, Mallet D. Morel Y, et al. Among authors: mallet d. Ann Endocrinol (Paris). 2005 Jun;66(3):217-24. doi: 10.1016/s0003-4266(05)81753-6. Ann Endocrinol (Paris). 2005. PMID: 15988382 Review. French. No abstract available.

6

Heterozygous mutation of steroidogenic factor-1 in 46,XY subjects may mimic partial androgen insensitivity syndrome.

Coutant R, Mallet D, Lahlou N, Bouhours-Nouet N, Guichet A, Coupris L, Croué A, Morel Y. Coutant R, et al. Among authors: mallet d. J Clin Endocrinol Metab. 2007 Aug;92(8):2868-73. doi: 10.1210/jc.2007-0024. Epub 2007 May 8. J Clin Endocrinol Metab. 2007. PMID: 17488792

7

Studies of a cohort of 46,XY with DSD including steroid biosynthesis deficiencies.

Morel Y, Plotton I, Mallet D, Nicolino M, Bertrand AM, David M, Nihoul-Fekete C, Chatelain P. Morel Y, et al. Among authors: mallet d. Adv Exp Med Biol. 2011;707:15-7. doi: 10.1007/978-1-4419-8002-1_4. Adv Exp Med Biol. 2011. PMID: 21691946 No abstract available.

8

REMOVAL: Pelvic MRI in a 17-year-old XY girl with 5-alpha reductase deficiency and a homozygous Gly115Asp mutation in SRD5A2.

Sarfati J, Trabado S, Rocher L, Mallet D, Betari-Tabet B, Morel Y, Young J. Sarfati J, et al. Among authors: mallet d. Ann Endocrinol (Paris). 2011 Sep;72(4):310-313. doi: 10.1016/j.ando.2011.07.001. Epub 2011 Aug 10. Ann Endocrinol (Paris). 2011. PMID: 21835392 Retracted.

9

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.

10

A late 17α-hydroxylase deficiency diagnosis that leads to the discovery of a new CYP17 gene mutation.

Guenego A, Morel Y, Ionesco O, Mallet D, Priou-Guesdon M. Guenego A, et al. Among authors: mallet d. Ann Endocrinol (Paris). 2015 Feb;76(1):71-4. doi: 10.1016/j.ando.2014.11.003. Epub 2015 Jan 19. Ann Endocrinol (Paris). 2015. PMID: 25613935

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