Morel Y - Search Results

1

Clinical and molecular characterization of a cohort of 161 unrelated women with nonclassical congenital adrenal hyperplasia due to 21-hydroxylase deficiency and 330 family members.

Bidet M, Bellanné-Chantelot C, Galand-Portier MB, Tardy V, Billaud L, Laborde K, Coussieu C, Morel Y, Vaury C, Golmard JL, Claustre A, Mornet E, Chakhtoura Z, Mowszowicz I, Bachelot A, Touraine P, Kuttenn F. Bidet M, et al. Among authors: morel y. J Clin Endocrinol Metab. 2009 May;94(5):1570-8. doi: 10.1210/jc.2008-1582. Epub 2009 Feb 10. J Clin Endocrinol Metab. 2009. PMID: 19208730

2

Fertility in women with nonclassical congenital adrenal hyperplasia due to 21-hydroxylase deficiency.

Bidet M, Bellanné-Chantelot C, Galand-Portier MB, Golmard JL, Tardy V, Morel Y, Clauin S, Coussieu C, Boudou P, Mowzowicz I, Bachelot A, Touraine P, Kuttenn F. Bidet M, et al. Among authors: morel y. J Clin Endocrinol Metab. 2010 Mar;95(3):1182-90. doi: 10.1210/jc.2009-1383. Epub 2010 Jan 15. J Clin Endocrinol Metab. 2010. PMID: 20080854

3

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

4

Follow-up of 68 children with congenital adrenal hyperplasia due to 21-hydroxylase deficiency: relevance of genotype for management.

Pinto G, Tardy V, Trivin C, Thalassinos C, Lortat-Jacob S, Nihoul-Fékété C, Morel Y, Brauner R. Pinto G, et al. Among authors: morel y. J Clin Endocrinol Metab. 2003 Jun;88(6):2624-33. doi: 10.1210/jc.2002-021433. J Clin Endocrinol Metab. 2003. PMID: 12788866

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

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

7

Clinical Outcome, Hormonal Status, Gonadotrope Axis, and Testicular Function in 219 Adult Men Born With Classic 21-Hydroxylase Deficiency. A French National Survey.

Bouvattier C, Esterle L, Renoult-Pierre P, de la Perrière AB, Illouz F, Kerlan V, Pascal-Vigneron V, Drui D, Christin-Maitre S, Galland F, Brue T, Reznik Y, Schillo F, Pinsard D, Piguel X, Chabrier G, Decoudier B, Emy P, Tauveron I, Raffin-Sanson ML, Bertherat J, Kuhn JM, Caron P, Cartigny M, Chabre O, Dewailly D, Morel Y, Touraine P, Tardy-Guidollet V, Young J. Bouvattier C, et al. Among authors: morel y. J Clin Endocrinol Metab. 2015 Jun;100(6):2303-13. doi: 10.1210/jc.2014-4124. Epub 2015 Mar 30. J Clin Endocrinol Metab. 2015. PMID: 25822101

8

Molecular genetic analysis of Tunisian patients with a classic form of 21-hydroxylase deficiency: identification of four novel mutations and high prevalence of Q318X mutation.

Kharrat M, Tardy V, M'Rad R, Maazoul F, Jemaa LB, Refaï M, Morel Y, Chaabouni H. Kharrat M, et al. Among authors: morel y. J Clin Endocrinol Metab. 2004 Jan;89(1):368-74. doi: 10.1210/jc.2003-031056. J Clin Endocrinol Metab. 2004. PMID: 14715874

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

How a patient homozygous for a 30-kb deletion of the C4-CYP 21 genomic region can have a nonclassic form of 21-hydroxylase deficiency.

L'Allemand D, Tardy V, Grüters A, Schnabel D, Krude H, Morel Y. L'Allemand D, et al. Among authors: morel y. J Clin Endocrinol Metab. 2000 Dec;85(12):4562-7. doi: 10.1210/jcem.85.12.7018. J Clin Endocrinol Metab. 2000. PMID: 11134109

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