Genetic polymorphisms and protein levels in vocal fold leukoplakia: a systematic review von Campello, C P, Lima-Silva, M F B, Lima, E L S de, Nunes, G R S, Silva, H A M, Dellalibera, E, Britto, L R P B de, Lemos, C A A, Muniz, M T C

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High tumor necrosis factor-α/interleukin-10 ratio is associated with hepatocellular carcinoma in patients with chronic hepatitis C von Aroucha, D.C.B.L., do Carmo, R.F., Moura, P., Silva, J.L.A., Vasconcelos, L.R.S., Cavalcanti, M.S.M., Muniz, M.T.C., Aroucha, M.L., Siqueira, E.R.F., Cahú, G.G.O.M., Pereira, L.M.M.B., Coêlho, M.R.C.D.

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MTP -493G/T gene polymorphism is associated with steatosis in hepatitis C-infected patients von Siqueira, E R F, Oliveira, C P M S, Correa-Giannella, M L, Stefano, J T, Cavaleiro, A M, Fortes, M A H Z, Muniz, M T C, Silva, F S, Pereira, L M M B, Carrilho, F J

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Using artificial neural networks to select the parameters for the prognostic of mild cognitive impairment and dementia in elderly individuals von Lins, A.J.C.C., Muniz, M.T.C., Garcia, A.N.M., Gomes, A.V., Cabral, R.M., Bastos-Filho, C.J.A.

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57 Interaction between RFC1 and MTHFR genes polymorphisms and risk of paediatric acute lymphoblastic leukemia with common somatic alterations von Emerenciano, M, Faro, A.J, Gonçalves, B.A.A, Zanrosso, C.W, Muniz, M.T.C, Pombo-de-Oliveira, M.S

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Effect of chromosome constitution variations on the expression of Turner phenotype von Bispo, A V S, Dos Santos, L O, Burégio-Frota, P, Galdino, M B, Duarte, A R, Leal, G F, Araújo, J, Gomes, B, Soares-Ventura, E M, Muniz, M T C, Santos, N

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Case Report New cytogenetic aberrations found in a case of aggressive retinoblastoma von Barros, J.E.X.S., Soares-Ventura, E.M., Santos, N., Amaral, B.A.S., Oliveira, F.M., Vera Cruz, R.S., Morais, V.L.L., Marques-Salles, T.J., Muniz, M.T.C.

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MTP -493G/T gene polymorphism is associated with steatosis in hepatitis C-infected patients von E.R.F. Siqueira, C.P.M.S. Oliveira, M.L. Correa-Giannella, J.T. Stefano, A.M. Cavaleiro, M.A.H.Z. Fortes, M.T.C. Muniz, F.S. Silva, L.M.M.B. Pereira, F.J. Carrilho

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Case Report Identification of a de novo inv dup(X)(pter→ q22) by multicolor banding in a girl with Turner syndrome von Burgio-Frota, P., Valena, L., Leal, G.F., Duarte, A.R., Bispo-Brito, A.V.S., Soares-Ventura, E.M., Marques-Salles, T.J., Nogueira, M.T.M.C., Muniz, M.T.C., Silva, M.L.M., Hunstig, F., Liehr, T., Santos, N.

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