Morel Y - Search Results

1

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.

2

Transient hyper-17-hydroxyprogesteronemia: a clinical subgroup of patients diagnosed at neonatal screening for congenital adrenal hyperplasia.

Cavarzere P, Samara-Boustani D, Flechtner I, Dechaux M, Elie C, Tardy V, Morel Y, Polak M. Cavarzere P, et al. Among authors: morel y. Eur J Endocrinol. 2009 Aug;161(2):285-92. doi: 10.1530/EJE-09-0145. Epub 2009 May 18. Eur J Endocrinol. 2009. PMID: 19451212

3

Gene symbol: CYP21A2.

Tardy VT, Morel Y. Tardy VT, et al. Among authors: morel y. Hum Genet. 2007 Apr;121(2):293. Hum Genet. 2007. PMID: 17598237 No abstract available.

4

Gene symbol: CYP21A2.

Tardy VT, Morel Y. Tardy VT, et al. Among authors: morel y. Hum Genet. 2007 Apr;121(2):293-4. Hum Genet. 2007. PMID: 17598238 No abstract available.

5

Gene symbol: CYP21A2.

Tardy VT, Morel Y. Tardy VT, et al. Among authors: morel y. Hum Genet. 2007 Apr;121(2):294. Hum Genet. 2007. PMID: 17598239 No abstract available.

6

Phenotype-genotype correlation in 56 women with nonclassical congenital adrenal hyperplasia due to 21-hydroxylase deficiency.

Deneux C, Tardy V, Dib A, Mornet E, Billaud L, Charron D, Morel Y, Kuttenn F. Deneux C, et al. Among authors: morel y. J Clin Endocrinol Metab. 2001 Jan;86(1):207-13. doi: 10.1210/jcem.86.1.7131. J Clin Endocrinol Metab. 2001. PMID: 11232002

7

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

8

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.

9

CYP21A2 gene mutation analysis in Moroccan patients with classic form of 21-hydroxylase deficiency: high regional prevalence of p.Q318X mutation and identification of a novel p.L353R mutation.

Abid F, Tardy V, Gaouzi A, El Hessni A, Morel Y, Chabraoui L. Abid F, et al. Among authors: morel y. Clin Chem Lab Med. 2008;46(12):1707-13. doi: 10.1515/CCLM.2008.339. Clin Chem Lab Med. 2008. PMID: 18973462

10

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

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