Morel Y - Search Results

1

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: morel y. 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

2

Genetic of gonadal determination.

Morel Y, Roucher F, Mallet D, Plotton I. Morel Y, et al. 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.

3

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. 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.

4

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: morel y. 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.

5

P450 Oxidoreductase Deficiency: Loss of Activity Caused by Protein Instability From a Novel L374H Mutation.

Parween S, Roucher-Boulez F, Flück CE, Lienhardt-Roussie A, Mallet D, Morel Y, Pandey AV. Parween S, et al. Among authors: morel y. J Clin Endocrinol Metab. 2016 Dec;101(12):4789-4798. doi: 10.1210/jc.2016-1928. Epub 2016 Sep 7. J Clin Endocrinol Metab. 2016. PMID: 27603900

6

[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. 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.

7

Letter to the Editor: "Characterization of the CYP11A1 Nonsynonymous Variant p.E314K in Children Presenting With Adrenal Insufficiency".

Roucher-Boulez F, Goursaud C, Mallet D, Morel Y. Roucher-Boulez F, et al. Among authors: morel y. J Clin Endocrinol Metab. 2019 May 1;104(5):1413-1414. doi: 10.1210/jc.2018-02415. J Clin Endocrinol Metab. 2019. PMID: 30500894 No abstract available.

8

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: morel y. 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.

9

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: morel y. 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.

10

Delayed diagnosis of congenital adrenal hyperplasia with salt wasting due to type II 3beta-hydroxysteroid dehydrogenase deficiency.

Johannsen TH, Mallet D, Dige-Petersen H, Müller J, Main KM, Morel Y, Forest MG. Johannsen TH, et al. Among authors: morel y. J Clin Endocrinol Metab. 2005 Apr;90(4):2076-80. doi: 10.1210/jc.2004-1374. Epub 2005 Jan 25. J Clin Endocrinol Metab. 2005. PMID: 15671104

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