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Phenotypical, biological, and molecular heterogeneity of 5α-reductase deficiency: an extensive international experience of 55 patients.
Maimoun L, Philibert P, Cammas B, Audran F, Bouchard P, Fenichel P, Cartigny M, Pienkowski C, Polak M, Skordis N, Mazen I, Ocal G, Berberoglu M, Reynaud R, Baumann C, Cabrol S, Simon D, Kayemba-Kay's K, De Kerdanet M, Kurtz F, Leheup B, Heinrichs C, Tenoutasse S, Van Vliet G, Grüters A, Eunice M, Ammini AC, Hafez M, Hochberg Z, Einaudi S, Al Mawlawi H, Nuñez CJ, Servant N, Lumbroso S, Paris F, Sultan C. Maimoun L, et al. Among authors: paris f. J Clin Endocrinol Metab. 2011 Feb;96(2):296-307. doi: 10.1210/jc.2010-1024. Epub 2010 Dec 8. J Clin Endocrinol Metab. 2011. PMID: 21147889
Identification and functional analysis of a new WNT4 gene mutation among 28 adolescent girls with primary amenorrhea and müllerian duct abnormalities: a French collaborative study.
Philibert P, Biason-Lauber A, Rouzier R, Pienkowski C, Paris F, Konrad D, Schoenle E, Sultan C. Philibert P, et al. Among authors: paris f. J Clin Endocrinol Metab. 2008 Mar;93(3):895-900. doi: 10.1210/jc.2007-2023. Epub 2008 Jan 8. J Clin Endocrinol Metab. 2008. PMID: 18182450
McCune-Albright syndrome: molecular genetics.
Lumbroso S, Paris F, Sultan C. Lumbroso S, et al. Among authors: paris f. J Pediatr Endocrinol Metab. 2002;15 Suppl 3:875-82. J Pediatr Endocrinol Metab. 2002. PMID: 12199345 Review.
Ambiguous genitalia in the newborn.
Sultan C, Paris F, Jeandel C, Lumbroso S, Galifer RB. Sultan C, et al. Among authors: paris f. Semin Reprod Med. 2002 Aug;20(3):181-8. doi: 10.1055/s-2002-35382. Semin Reprod Med. 2002. PMID: 12428198 Review.
Disorders of androgen action.
Sultan C, Lumbroso S, Paris F, Jeandel C, Terouanne B, Belon C, Audran F, Poujol N, Georget V, Gobinet J, Jalaguier S, Auzou G, Nicolas JC. Sultan C, et al. Among authors: paris f. Semin Reprod Med. 2002 Aug;20(3):217-28. doi: 10.1055/s-2002-35386. Semin Reprod Med. 2002. PMID: 12428202 Review.
451 results