Otros artículos de Fabia Lima Vilarino
Lerner TG, Bianco B, Teles JS, Vilarino FL, Christofolini DM, Barbosa CP. Analysis of CTLA4 gene variant in infertile Brazilian women with and without endometriosis. Int J Immunogenet 38(3):259-62, 2011.
Teles JS, Bianco B, Vilarino FL, André GM, Christofolini DM, Barbosa CP. Association of FCRL3 C-169T promoter single-nucleotide polymorphism with idiopathic infertility and infertility-related endometriosis. J Reprod Immunol 89(2):212-5, 2011.
André GM, Barbosa CP, Teles JS, Vilarino FL, Christofolini DM, Bianco B. Analysis of FOXP3 polymorphisms in infertile women with and without endometriosis. Fertil Steril 95(7):2223-7, 2011.
Gonçalves-Filho RP, Brandes A, Christofolini DM, Lerner TG, Bianco B, Barbosa CP. Plasminogen activator inhibitor-1 4G/5G polymorphism in infertile women with and without endometriosis. Acta Obstet Gynecol Scand 90(5):473-7, 2011.
Cordts EB, Christofolini DM, Dos Santos AA, Bianco B, Barbosa CP. Genetic aspects of premature ovarian failure: a literature review. Arch Gynecol Obstet 283(3):635-43, 2011.
Bianco B, Verreschi IT, Oliveira KC, Guedes AD, Galera BB, Galera MF, Barbosa CP, Lipay MV. PTPN22 polymorphism is related to autoimmune disease risk in patients with Turner syndrome. Scand J Immunol 72(3):256-9, 2010.
Barbosa CP, Souza AM, Bianco B, Christofolini D, Bach FA, Lima GR. Frequency of endometriotic lesions in peritoneum samples from asymptomatic fertile women and correlation with CA125 values. Sao Paulo Med J 127(6):342-5, 2009.
Bianco B, Oliveira KC, Guedes AD, Barbosa CP, Lipay MV, Verreschi IT. OCT4 gonadal gene expression related to the presence of Y-chromosome sequences in Turner syndrome. Fertil Steril 94(6):2347-9, 2010.
Gomes FM, Bianco B, Teles JS, Christofolini DM, de Souza AM, Guedes AD, Barbosa CP. PTPN22 C1858T polymorphism in women with endometriosis. Am J Reprod Immunol 63(3):227-32, 2010.
Bianco B, Christofolini DM, Mafra FA, Brandes A, Zulli K, Barbosa CP. +1730 G/A polymorphism of the estrogen receptor beta gene (ERbeta) may be an important genetic factor predisposing to endometriosis. Acta Obstet Gynecol Scand 88(12):1397-401, 2009.
Para comunicarse con Fabia Lima Vilarino mencionar a SIIC como
referencia:
bianca.bianco@hotmail.com
Autora invitada
18 de mayo, 2011
Descripción aprobada
30 de mayo, 2011
Reedición siicsalud
7 de junio, 2021