Kalfa N - Search Results

1

The forkhead factor FOXL2: a novel tumor suppressor?

Benayoun BA, Kalfa N, Sultan C, Veitia RA. Benayoun BA, et al. Among authors: kalfa n. Biochim Biophys Acta. 2010 Jan;1805(1):1-5. doi: 10.1016/j.bbcan.2009.09.002. Epub 2009 Sep 10. Biochim Biophys Acta. 2010. PMID: 19747961 Review.

2

A nationwide study of granulosa cell tumors in pre- and postpubertal girls: missed diagnosis of endocrine manifestations worsens prognosis.

Kalfa N, Patte C, Orbach D, Lecointre C, Pienkowski C, Philippe F, Thibault E, Plantaz D, Brauner R, Rubie H, Guedj AM, Ecochard A, Paris F, Jeandel C, Baldet P, Sultan C. Kalfa N, et al. J Pediatr Endocrinol Metab. 2005 Jan;18(1):25-31. doi: 10.1515/jpem.2005.18.1.25. J Pediatr Endocrinol Metab. 2005. PMID: 15679066

3

Activating mutations of the stimulatory g protein in juvenile ovarian granulosa cell tumors: a new prognostic factor?

Kalfa N, Ecochard A, Patte C, Duvillard P, Audran F, Pienkowski C, Thibaud E, Brauner R, Lecointre C, Plantaz D, Guedj AM, Paris F, Baldet P, Lumbroso S, Sultan C. Kalfa N, et al. J Clin Endocrinol Metab. 2006 May;91(5):1842-7. doi: 10.1210/jc.2005-2710. Epub 2006 Feb 28. J Clin Endocrinol Metab. 2006. PMID: 16507630

4

Activating mutations of Gsalpha in kidney cancer.

Kalfa N, Lumbroso S, Boulle N, Guiter J, Soustelle L, Costa P, Chapuis H, Baldet P, Sultan C. Kalfa N, et al. J Urol. 2006 Sep;176(3):891-5. doi: 10.1016/j.juro.2006.04.023. J Urol. 2006. PMID: 16890646

5

Searching for somatic mutations in McCune-Albright syndrome: a comparative study of the peptidic nucleic acid versus the nested PCR method based on 148 DNA samples.

Kalfa N, Philibert P, Audran F, Ecochard A, Hannon T, Lumbroso S, Sultan C. Kalfa N, et al. Eur J Endocrinol. 2006 Dec;155(6):839-43. doi: 10.1530/eje.1.02301. Eur J Endocrinol. 2006. PMID: 17132753

6

Extinction of FOXL2 expression in aggressive ovarian granulosa cell tumors in children.

Kalfa N, Philibert P, Patte C, Ecochard A, Duvillard P, Baldet P, Jaubert F, Fellous M, Sultan C. Kalfa N, et al. Fertil Steril. 2007 Apr;87(4):896-901. doi: 10.1016/j.fertnstert.2006.11.016. Fertil Steril. 2007. PMID: 17430735 Free article.

7

FOXL2 and SOX9 as parameters of female and male gonadal differentiation in patients with various forms of disorders of sex development (DSD).

Hersmus R, Kalfa N, de Leeuw B, Stoop H, Oosterhuis JW, de Krijger R, Wolffenbuttel KP, Drop SL, Veitia RA, Fellous M, Jaubert F, Looijenga LH. Hersmus R, et al. Among authors: kalfa n. J Pathol. 2008 May;215(1):31-8. doi: 10.1002/path.2335. J Pathol. 2008. PMID: 18348162

8

Mutations of CXorf6 are associated with a range of severities of hypospadias.

Kalfa N, Liu B, Klein O, Audran F, Wang MH, Mei C, Sultan C, Baskin LS. Kalfa N, et al. Eur J Endocrinol. 2008 Oct;159(4):453-8. doi: 10.1530/EJE-08-0085. Epub 2008 Jul 17. Eur J Endocrinol. 2008. PMID: 18635673

9

Is hypospadias a genetic, endocrine or environmental disease, or still an unexplained malformation?

Kalfa N, Philibert P, Sultan C. Kalfa N, et al. Int J Androl. 2009 Jun;32(3):187-97. doi: 10.1111/j.1365-2605.2008.00899.x. Epub 2008 Jul 11. Int J Androl. 2009. PMID: 18637150 Review.

10

Aberrant expression of ovary determining gene FOXL2 in the testis and juvenile granulosa cell tumor in children.

Kalfa N, Fellous M, Boizet-Bonhoure B, Patte C, Duvillard P, Pienkowski C, Jaubert F, Ecochard A, Sultan C. Kalfa N, et al. J Urol. 2008 Oct;180(4 Suppl):1810-3. doi: 10.1016/j.juro.2008.03.097. Epub 2008 Aug 21. J Urol. 2008. PMID: 18721930

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