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The impact of thalidomide use in birth defects in Brazil.
Sales Luiz Vianna F, Kowalski TW, Fraga LR, Sanseverino MT, Schuler-Faccini L. Sales Luiz Vianna F, et al. Eur J Med Genet. 2017 Jan;60(1):12-15. doi: 10.1016/j.ejmg.2016.09.015. Epub 2016 Sep 13. Eur J Med Genet. 2017. PMID: 27638330
Prenatal exposure to misoprostol and vascular disruption defects: a case-control study.
Vargas FR, Schuler-Faccini L, Brunoni D, Kim C, Meloni VF, Sugayama SM, Albano L, Llerena JC Jr, Almeida JC, Duarte A, Cavalcanti DP, Goloni-Bertollo E, Conte A, Koren G, Addis A. Vargas FR, et al. Am J Med Genet. 2000 Dec 11;95(4):302-6. doi: 10.1002/1096-8628(20001211)95:4<302::aid-ajmg2>3.0.co;2-b. Am J Med Genet. 2000. PMID: 11186881
New cases of thalidomide embryopathy in Brazil.
Schuler-Faccini L, Soares RC, de Sousa AC, Maximino C, Luna E, Schwartz IV, Waldman C, Castilla EE. Schuler-Faccini L, et al. Birth Defects Res A Clin Mol Teratol. 2007 Sep;79(9):671-2. doi: 10.1002/bdra.20384. Birth Defects Res A Clin Mol Teratol. 2007. PMID: 17676592
p53 signaling pathway polymorphisms associated to recurrent pregnancy loss.
Fraga LR, Dutra CG, Boquett JA, Vianna FS, Gonçalves RO, Paskulin DD, Costa OL, Ashton-Prolla P, Sanseverino MT, Schuler-Faccini L. Fraga LR, et al. Mol Biol Rep. 2014 Mar;41(3):1871-7. doi: 10.1007/s11033-014-3036-6. Epub 2014 Jan 17. Mol Biol Rep. 2014. PMID: 24435975
199 results