Browsing by Author Secolin, R.

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Showing results 1 to 14 of 14
PreviewIssue DateTitleAuthor(s)AdvisorType
2012Evidence that polymorphisms in detoxification genes modulate the susceptibility for sporadic medullary thyroid carcinomaBarbieri, R. B.; Bufalo, N. E.; Secolin, R.; Silva, A. C. N.; Assumpcao, L. V. M.; Maciel, R. M. B.; Cerutti, J. M.; Ward, L. S.-Artigo de periódico
2012Evidence that polymorphisms in detoxification genes modulate the susceptibility for sporadic medullary thyroid carcinomaBarbieri, R. B.; Bufalo, N. E.; Secolin, R.; Silva, A. C. N.; Assumpcao, L. V. M.; Maciel, R. M. B.; Cerutti, J. M.; Ward, L. S.-Artigo
2018Genetic variation in CFH predicts phenytoin-induced maculopapular exanthema in European-descent patientsMcCormack, M.; Gui, H.S.; Ingason, A.; Speed, D.; Wright, G.E.B.; Zhang, E.J.; Secolin, R.; Yasuda, C.; Kwok, M.; Wolking, S.; Becker, F.; Rau, S.; Avbersek, A.; Heggeli, K.; Leu, C.; Depondt, C.; Sills, G.J.; Marson, A.G.; Auce, P.; Br-Artigo
2018Genetic variant RS2383207 is associated with susceptibility to large artery atherosclerosis ischemic stroke in brazilian populationFerreira, L.E.; Silva, J.T. da; Secolin, R.; Lopes-Cendes, I.; Cabral, N.; Franca, P.-Outros documentos
2017Is cerebral microbleed prevalence relevant as a biomarker in amnestic mild cognitive impairment and mild Alzheimer's disease?Rabelo, A.G.B.; Teixeira, C.V.L.; Magalhães, T.N.C.; Carletti-Cassani, A.F.M.K.; Amato Filho, A.C.S.; Joaquim, H.P.G.; Talib, L.L.; Forlenza, O.; Ribeiro, P.A.O.; Secolin, R.; Lopes-Cendes, I.; Cendes, F.; Balthazar, M.L.F.-Artigo
2014SLC23A2-05 (rs4987219) and KRAS-LCS6 (rs61764370) polymorphisms in patients with squamous cell carcinoma of the head and neckMarson, F. A. D.; Ribeiro, J. D.; Santiago, M. B.; Lima, C. S. P.; Secolin, R.; Bertuzzo, C. S.-Artigo
2015Identifying patients with pharmacoresistant epilepsy using a plasma-based testAvansini, S.; Lima, B.; Secolin, R.; Santos, M.; Coan, A. C.; Vieira, A.; Carvalho, B.; Alvim, M.; Torres, F.; Silva, L.; Rogerio, F.; Cendes, F.; Lopes-Cendes, I.-Outros documentos
2018Dysregulation of NEUROG2 plays a key role in focal cortical dysplasiaAvansini, S.H.; Torres, F.R.; Vieira, A.S.; Dogini, D.B.; Rogerio, F.; Coan, A.C.; Morita, M.E.; Guerreiro, M.M.; Yasuda, C.L.; Secolin, R.; Carvalho, B.S.; Borges, M.G.; Almeida, V.S.; Araujo, P.A.O.R.; Queiroz, L.; Cendes, F.; Lopes-Cend-Artigo
2017Determining the burden of copy number variation in patients with epilepsyAraujo, T. K. de; Torres, F.; Secolin, R.; Alvim, M. K. M.; Rocha, C. S.; Morita, M.; Yasuda, C. L.; Carvalho, B. S.; Cendes, F.; Lopes-Cendes, I.-Outros documentos
2017A prediction algorithm for drug response in patients with mesial temporal lobe epilepsy based on clinical and genetic informationSilva-Alves, M.S.; Secolin, R.; Carvalho, B.S.; Yasuda, C.L.; Bilevicius, E.; Alvim, M.K.M.; Santos, R.O.; Maurer-Morelli, C.V.; Cendes, F.; Lopes-Cendes, I.-Artigo
2016Functional single nucleotide polymorphisms in Il2 and Il10 alter predisposition Tomantle Cell Lymphoma, as well as its progression and imune antitumour responseMendonca, G.; Rocha, R.; Secolin, R.; Nonogaki, S.; Delamain, M.; Alves, A.; Colleoni, G.; Soares, F.; Lima, C.; Vassallo, J.-Outro documento
2016Family-based genetic association for molar-incisor hypomineralizationJeremias, F.; Pierri, Ricardo A.G.P.; Souza, J.F.; Fragelli, C.M.B.; Restrepo, M.; Finote, L.S.; Bussaneli, D.G.; Cordeiro, R.C.L.; Secolin, R.; Maurer, C.V.M.; Caminaga, R.M.S.; Santos-Pinto, L.-Artigo
2014Clinical outcomes of periodontal therapy are not influenced by the ATC /TTC haplotype in the IL 8 geneCorbi, S. C. T.; Finoti, L. S.; Anovazzi, G.; Tanaka, M. H.; Kim, Y. J.; Secolin, R.; Marcaccini, A. M.; Gerlach, R. F.; Orrico, S. R. P.; Cirelli, J. A.; Scarel-Caminaga, R. M.-Artigo
2015TSHR intronic polymorphisms (rs179247 and rs12885526) and their role in the susceptibility of the Brazilian population to Graves’ disease and Graves’ ophthalmopathyBufalo, N. E.; dos Santos, R. B.; Marcello, M. A.; Piai, R. P.; Secolin, R.; Romaldini, J. H.; Ward, L. S.-Artigo