Morel Y - Search Results

1

Endocrine and molecular investigations in a cohort of 25 adolescent males with prominent/persistent pubertal gynecomastia.

Paris F, Gaspari L, Mbou F, Philibert P, Audran F, Morel Y, Biason-Lauber A, Sultan C. Paris F, et al. Among authors: morel y. Andrology. 2016 Mar;4(2):263-9. doi: 10.1111/andr.12145. Epub 2016 Feb 4. Andrology. 2016. PMID: 26845730 Free article.

2

Premature pubarche in Mediterranean girls: high prevalence of heterozygous CYP21 mutation carriers.

Paris F, Tardy V, Chalançon A, Picot MC, Morel Y, Sultan C. Paris F, et al. Among authors: morel y. Gynecol Endocrinol. 2010 May;26(5):319-24. doi: 10.3109/09513590903511505. Gynecol Endocrinol. 2010. PMID: 20059433 Free article.

3

In cases of familial primary ovarian insufficiency and disorders of gonadal development, consider NR5A1/SF-1 sequence variants.

Bertrand-Delepine J, Manouvrier-Hanu S, Cartigny M, Paris F, Mallet D, Philibert P, Morel Y, Lefevre C, Dewailly D, Catteau-Jonard S. Bertrand-Delepine J, et al. Among authors: morel y. Reprod Biomed Online. 2020 Jan;40(1):151-159. doi: 10.1016/j.rbmo.2019.10.002. Epub 2019 Oct 10. Reprod Biomed Online. 2020. PMID: 31831369

4

Postnatal changes of T, LH, and FSH in 46,XY infants with mutations in the AR gene.

Bouvattier C, Carel JC, Lecointre C, David A, Sultan C, Bertrand AM, Morel Y, Chaussain JL. Bouvattier C, et al. Among authors: morel y. J Clin Endocrinol Metab. 2002 Jan;87(1):29-32. doi: 10.1210/jcem.87.1.7923. J Clin Endocrinol Metab. 2002. PMID: 11788616

5

p.H62L, a rare mutation of the CYP21 gene identified in two forms of 21-hydroxylase deficiency.

Menassa R, Tardy V, Despert F, Bouvattier-Morel C, Brossier JP, Cartigny M, Morel Y. Menassa R, et al. Among authors: morel y. J Clin Endocrinol Metab. 2008 May;93(5):1901-8. doi: 10.1210/jc.2007-2701. Epub 2008 Mar 4. J Clin Endocrinol Metab. 2008. PMID: 18319307

6

Phenotype-genotype correlations of 13 rare CYP21A2 mutations detected in 46 patients affected with 21-hydroxylase deficiency and in one carrier.

Tardy V, Menassa R, Sulmont V, Lienhardt-Roussie A, Lecointre C, Brauner R, David M, Morel Y. Tardy V, et al. Among authors: morel y. J Clin Endocrinol Metab. 2010 Mar;95(3):1288-300. doi: 10.1210/jc.2009-1202. Epub 2010 Jan 15. J Clin Endocrinol Metab. 2010. PMID: 20080860

7

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

8

[Incomplete androgen insensitivity syndrome. Difficulties of diagnosis and management].

Forest MG, Mollard P, David M, Morel Y, Bertrand J. Forest MG, et al. Among authors: morel y. Arch Fr Pediatr. 1990 Feb;47(2):107-13. Arch Fr Pediatr. 1990. PMID: 2327864 French.

9

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. 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.

10

Long-term followup and comparison between genotype and phenotype in 29 cases of complete androgen insensitivity syndrome.

Cheikhelard A, Morel Y, Thibaud E, Lortat-Jacob S, Jaubert F, Polak M, Nihoul-Fekete C. Cheikhelard A, et al. Among authors: morel y. J Urol. 2008 Oct;180(4):1496-501. doi: 10.1016/j.juro.2008.06.045. Epub 2008 Aug 16. J Urol. 2008. PMID: 18710728

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