Browsing by Author Secolin, R

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Showing results 1 to 16 of 16
PreviewIssue DateTitleAuthor(s)AdvisorType
2003Magnetic resonance imaging abnormalities in familial temporal lobe epilepsy with auditory aurasKobayashi, E; Santos, NF; Torres, FR; Secolin, R; Sardinha, LAC; Lopez-Cendes, I; Cendes, F-Artigo de periódico
2010Family-based association study for bipolar affective disorderSecolin, R; Banzato, CEM; Oliveira, MCM; Bittar, MFR; Santos, ML; Dalgalarrondo, P; Lopes-Cendes, I-Artigo de periódico
2008LINKGEN: A new algorithm to process data in genetic linkage studiesSecolin, R; Rocha, CS; Torres, FR; Santos, ML; Maurer-Morelli, CV; Santos, NF; Lopes-Cendes, I-Artigo de periódico
2013Refinement of chromosome 3p22.3 region and identification of a susceptibility gene for bipolar affective disorderSecolin, R; Banzato, CEM; Mella, LFB; Santos, ML; Dalgalarrondo, P; Lopes-Cendes, I-Artigo de periódico
2012Genetic association study between Interleukin 10 gene and dental implant lossPigossi, SC; Alvim-Pereira, F; Montes, CC; Finoti, LS; Secolin, R; Trevilatto, PC; Scarel-Caminaga, RM-Artigo de periódico
2013Genetic interaction of GSH metabolic pathway genes in cystic fibrosisMarson, FAD; Bertuzzo, CS; Secolin, R; Ribeiro, AF; Ribeiro, JD-Artigo de periódico
2008Population analysis of the alpha hemoglobin stabilizing protein (AHSP) gene identifies sequence variants that alter expression and functiondos Santos, CO; Zhou, S; Secolin, R; Wang, X; Cunha, AF; Higgs, DR; Kwiatkowski, JL; Thein, SL; Gallagher, PG; Costa, FF; Weiss, MJ-Artigo de periódico
2013Study of candidate genes for dyslexia in Brazilian individualsSvidnicki, MCCM; Salgado, CA; Lima, RF; Ciasca, SM; Secolin, R; Pomilio, MCA; Junqueira, PA; Pinto, MS; Pereira, MM; Sartorato, EL-Artigo de periódico
2014SLC23A2-05 (rs4987219) and KRAS-LCS6 (rs61764370) polymorphisms in patients with squamous cell carcinoma of the head and neckSantiago, MB; Marson, FAD; Secolin, R; Ribeiro, JD; Lima, CSP; Bertuzzo, CS-Artigo de periódico
2012The periodized resistance training promotes similar changes in lipid profile in middle-aged men and womenLibardi, CA; Bonganha, V; Conceicao, MS; De Souza, GV; Bernardes, CF; Secolin, R; Madruga, VA; Chacon-Mikahil, MPT-Artigo de periódico
2006THE SCN2A gene is not a likely candidate for familial mesial temporal lobe epilepsyMaurer-Morelli, CV; Secolin, R; Marchesini, RB; Santos, NF; Kobayashi, E; Cendes, F; Lopes-Cendes, I-Artigo de periódico
2013Association between IL8 haplotypes and pathogen levels in chronic periodontitisFinoti, LS; Corbi, SCT; Anovazzi, G; Teixeira, SRL; Steffens, JP; Secolin, R; Kim, YJ; Orrico, SRP; Cirelli, JA; Mayer, MPA; Scarel-Caminaga, RM-Artigo de periódico
2011Association of matrix metalloproteinase gene polymorphism with temporomandibular joint degenerationPlanello, AC; Campos, MIG; Meloto, CB; Secolin, R; Rizatti-Barbosa, CM; Line, SRP; de Souza, AP-Artigo de periódico
2014Polymorphisms Of Cell Cycle Control Genes Influence The Development Of Sporadic Medullary Thyroid Carcinoma.Barbieri, R B; Bufalo, N E; Secolin, R; Assumpção, L V M; Maciel, R M B; Cerutti, J M; Ward, L S-Artigo de periódico
2014Tshr Intronic Polymorphisms (rs179247 And Rs12885526) And Their Role In The Susceptibility Of The Brazilian Population To Graves' Disease And Graves' Ophthalmopathy.Bufalo, N E; Dos Santos, R B; Marcello, M A; Piai, R P; Secolin, R; Romaldini, J H; Ward, L S-Artigo de periódico
2013Study Of Candidate Genes For Dyslexia In Brazilian Individuals.Svidnicki, M C C M; Salgado, C A; Lima, R F; Ciasca, S M; Secolin, R; Pomilio, M C A; Junqueira, P A; Pinto, M S; Pereira, M M; Sartorato, E L-Artigo de periódico