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PreviewIssue DateTitleAuthor(s)AdvisorType
2015A new compound heterozygosis for inactivating mutations in the glucokinase gene as cause of permanent neonatal diabetes mellitus (PNDM) in double-first cousinsEsquiaveto-Aun, Adriana Mangue; De Mello, Maricilda Palandi; Vanti Macedo Paulino, Maria Fernanda; Minicucci, Walter Jose; Guerra-Junior, Gil; Valente De Lemos-Marini, Sofia Helena-Artigo
2019Association of the CFH Y402H polymorphism with the 1-year response of exudative AMD to intravitreal Anti-VEGF treatment in the brazilian populationMedina, F. M. C.; Da Motta, A. A. L.; Takahashi, W. Y.; Carricondo, P. C.; Dos Santos Motta, M. M.; Melo, M. B.; Vasconcellos, J. P. C.-Artigo
2015Pharmacogenetic effect of complement factor H gene polymorphism in response to the initial intravitreal injection of bevacizumab for wet age-related macular degenerationMedina, Flavio Mac Cord; Lopes da Motta, Augusto Alves; Takahashi, Walter Y.; Carricondo, Pedro Carlos; dos Santos Motta, Mario Martins; Melo, Monica B.; Vasconcellos, Jose Paulo C.-Artigo
2016A case of 46,XY DSD due to a novel mutation in the HSD17B3 genePetroli, R.J.; Soardi, F.C.; Mazzola, T.; Michelato, Dd.P.; Vieira Goes, L.C.; Lima do Nascimento, D.L.; Palandi de Mello, M.; Lopes Monlleó, I.-Outro documento
2018Discrete virilization in girls with the classic form of congenital adrenal hyperplasia: the importance of a detailed genital examination at birthChagas, Letícia Santos Silva; Guerra-Junior, Gil; De-Melo, Maricilda Palandi; Lemos-Marini, Sofia Helena Valente-Outro documento
2016Molecular analysis of NR5A1 gene in a cohort of 96 brazilian patients with 46, XY DSD revealed nine novel mutationsCampos Fabbri, H.; Hiort, O.; Guerra Junior, G.; Maciel-Guerra, A.; Ribeiro de Andrade, J.G.; Maia Costa de Queiroz, C.; Lopes Monlleó, I.; Carvalho Castro, J.; Werner, R.; Palandi de Mello, M.-Outro documento
2014Social network analysis metrics and their application in microbiological network studiesSilva, Juliana Saragiotto; Stoppe, Nancy de Castro; Torres, Tatiana Teixeira; Ottoboni, Laura Maria Mariscal; Saraiva, Antonio Mauro-Artigo
2016A novel CYP21A2 mutation identified a patient with classical 21-hydroxylase deficiencyMichelato, Dd.P.; Petroli, R.J.; Santos, L.Gd.; Monlleó, I.L.; Mello, M.Pd.-Outro documento
2019Contribution of the GSTP1 c.313A > G variant to hearing loss risk in patients exposed to platin chemotherapy during childhoodLiberman, P. H. P.; Goffi-Gomez, M. V. S.; Schultz, C.; Jacob, P. L.; de Paula, C. A. A.; Sartorato, E. L.; Torrezan, G. T.; Ferreira, E. N.; Carraro, D. M.-Artigo
2019DNA methylation profile in placentas of sickle cell anemia womenGil, Gislene; Ananina, Galina; Maschietto, Mariana; Baptista, Leticia; Costa, Sueli; Costa, Fernando; Costa, Maria; Melo, Monica-Artigo