Begeot M - Search Results

1

Nonclassic lipoid congenital adrenal hyperplasia masquerading as familial glucocorticoid deficiency.

Metherell LA, Naville D, Halaby G, Begeot M, Huebner A, Nürnberg G, Nürnberg P, Green J, Tomlinson JW, Krone NP, Lin L, Racine M, Berney DM, Achermann JC, Arlt W, Clark AJ. Metherell LA, et al. Among authors: begeot m. J Clin Endocrinol Metab. 2009 Oct;94(10):3865-71. doi: 10.1210/jc.2009-0467. Epub 2009 Sep 22. J Clin Endocrinol Metab. 2009. PMID: 19773404 Free PMC article.

2

Mutations in MRAP, encoding a new interacting partner of the ACTH receptor, cause familial glucocorticoid deficiency type 2.

Metherell LA, Chapple JP, Cooray S, David A, Becker C, Rüschendorf F, Naville D, Begeot M, Khoo B, Nürnberg P, Huebner A, Cheetham ME, Clark AJ. Metherell LA, et al. Among authors: begeot m. Nat Genet. 2005 Feb;37(2):166-70. doi: 10.1038/ng1501. Epub 2005 Jan 16. Nat Genet. 2005. PMID: 15654338

3

Mutations in a novel gene, encoding a single transmembrane domain protein are associated with familial glucocorticoid deficiency type 2.

Metherell LA, Cooray S, Huebner A, Ruschendorf F, Naville D, Begeot M, Clark AJ. Metherell LA, et al. Among authors: begeot m. Endocr Res. 2004 Nov;30(4):889-90. doi: 10.1081/erc-200044136. Endocr Res. 2004. PMID: 15666841 No abstract available.

4

Exclusion of the adrenocorticotropin (ACTH) receptor (MC2R) locus in some families with ACTH resistance but no mutations of the MC2R coding sequence (familial glucocorticoid deficiency type 2).

Naville D, Weber A, Genin E, Durand P, Clark AJ, Bégeot M. Naville D, et al. Among authors: begeot m. J Clin Endocrinol Metab. 1998 Oct;83(10):3592-6. doi: 10.1210/jcem.83.10.5166. J Clin Endocrinol Metab. 1998. PMID: 9768670

5

Genetics of ACTH insensitivity syndromes.

Clark JL, Metherell LA, Naville D, Begeot M, Huebner A. Clark JL, et al. Among authors: begeot m. Ann Endocrinol (Paris). 2005 Jun;66(3):247-9. doi: 10.1016/s0003-4266(05)81757-3. Ann Endocrinol (Paris). 2005. PMID: 15988386 Review.

6

Linkage of one gene for familial glucocorticoid deficiency type 2 (FGD2) to chromosome 8q and further evidence of heterogeneity.

Génin E, Huebner A, Jaillard C, Faure A, Halaby G, Saka N, Clark AJ, Durand P, Bégeot M, Naville D. Génin E, et al. Among authors: begeot m. Hum Genet. 2002 Oct;111(4-5):428-34. doi: 10.1007/s00439-002-0806-3. Epub 2002 Aug 24. Hum Genet. 2002. PMID: 12384787

7

Familial glucocorticoid deficiency type 2 in two neonates.

Ramachandran P, Penhoat A, Naville D, Begeot M, Osama Abdel-Wareth L, Reza Sedaghatian M. Ramachandran P, et al. Among authors: begeot m. J Perinatol. 2003 Jan;23(1):62-6. doi: 10.1038/sj.jp.7210813. J Perinatol. 2003. PMID: 12556930

8

Demonstration by transfection studies that mutations in the adrenocorticotropin receptor gene are one cause of the hereditary syndrome of glucocorticoid deficiency.

Naville D, Barjhoux L, Jaillard C, Faury D, Despert F, Esteva B, Durand P, Saez JM, Begeot M. Naville D, et al. Among authors: begeot m. J Clin Endocrinol Metab. 1996 Apr;81(4):1442-8. doi: 10.1210/jcem.81.4.8636348. J Clin Endocrinol Metab. 1996. PMID: 8636348

9

Syndrome of congenital adrenocortical unresponsiveness to ACTH. Report of six patients.

Berberoğlu M, Aycan Z, Ocal G, Begeot M, Naville D, Akar N, Adiyaman P, Evliyaoglu O, Penhoat A. Berberoğlu M, et al. Among authors: begeot m. J Pediatr Endocrinol Metab. 2001 Sep-Oct;14(8):1113-8. doi: 10.1515/jpem-2001-0807. J Pediatr Endocrinol Metab. 2001. PMID: 11592568

10

Doghman M, Delagrange P, Blondet A, Berthelon MC, Durand P, Naville D, Bégeot M. Doghman M, et al. Among authors: begeot m. Endocrinology. 2004 Feb;145(2):541-7. doi: 10.1210/en.2003-0605. Epub 2003 Oct 30. Endocrinology. 2004. PMID: 14592963

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

97 results

Search Page

Filters