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Acromicric dysplasia: long term outcome and evidence of autosomal dominant inheritance.
Faivre L, Le Merrer M, Baumann C, Polak M, Chatelain P, Sulmont V, Cousin J, Bost M, Cordier MP, Zackai E, Russell K, Finidori G, Pouliquen JC, Munnich A, Maroteaux P, Cormier-Daire V. Faivre L, et al. Among authors: polak m. J Med Genet. 2001 Nov;38(11):745-9. doi: 10.1136/jmg.38.11.745. J Med Genet. 2001. PMID: 11694546 Free PMC article.
[The Prader-Willi syndrome].
Diene G, Postel-Vinay A, Pinto G, Polak M, Tauber M. Diene G, et al. Among authors: polak m. Ann Endocrinol (Paris). 2007 Jun;68(2-3):129-37. doi: 10.1016/j.ando.2007.03.002. Epub 2007 May 17. Ann Endocrinol (Paris). 2007. PMID: 17499572 Review. French.
Delineation of late onset hypoventilation associated with hypothalamic dysfunction syndrome.
De Pontual L, Trochet D, Caillat-Zucman S, Abou Shenab OA, Bougneres P, Crow Y, Cunningham S, Esteva B, Heberle LC, Leger J, Pinto G, Polak M, Shafik MH, Straus C, Trang H, Munnich A, Lyonnet S, Desguerre I, Amiel J. De Pontual L, et al. Among authors: polak m. Pediatr Res. 2008 Dec;64(6):689-94. doi: 10.1203/PDR.0b013e318187dd0e. Pediatr Res. 2008. PMID: 18670370
Steroidogenic factor-1 (SF-1) gene mutation as a frequent cause of primary amenorrhea in 46,XY female adolescents with low testosterone concentration.
Philibert P, Leprieur E, Zenaty D, Thibaud E, Polak M, Frances AM, Lespinasse J, Raingeard I, Servant N, Audran F, Paris F, Sultan C. Philibert P, et al. Among authors: polak m. Reprod Biol Endocrinol. 2010 Mar 19;8:28. doi: 10.1186/1477-7827-8-28. Reprod Biol Endocrinol. 2010. PMID: 20302644 Free PMC article.
1,133 results