Immunosuppression and antimicrobial drugs: Effects on rat intestinal microflora by Bertazzoni Minelli, E., Benini, A., Soardi, E.

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A recurrent de novo splice site variant involving DNM1 exon 10a causes developmental and epileptic encephalopathy through a dominant-negative mechanism by Parthasarathy, Shridhar, Ruggiero, Sarah McKeown, Gelot, Antoinette, Soardi, Fernanda C, Ribeiro, Bethânia F R, Pires, Douglas E V, Ascher, David B, Schmitt, Alain, Rambaud, Caroline, Represa, Alfonso, Xie, Hongbo M, Lusk, Laina, Wilmarth, Olivia, McDonnell, Pamela Pojomovsky, Juarez, Olivia A, Grace, Alexandra N, Buratti, Julien, Mignot, Cyril, Gras, Domitille, Nava, Caroline, Pierce, Samuel R, Keren, Boris, Kennedy, Benjamin C, Pena, Sergio D J, Helbig, Ingo, Cuddapah, Vishnu Anand

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Inhibition of CYP21A2 Enzyme Activity Caused by Novel Missense Mutations Identified in Brazilian and Scandinavian Patients by Soardi, F. C., Barbaro, M., Lau, I. F., Lemos-Marini, S. H. V., Baptista, M. T. M., Guerra-Junior, G., Wedell, A., Lajic, S., de Mello, M. P.

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Molecular evidence of bovine herpesvirus 1 and 5 in cattle with suspected rabies in Rio Grande do Sul state, Brazil by Rodenbusch, C.R., Ferreira, J.C., Cunha, D.L.B.W., Roehe, P.M., Soardi, M.A., Costa, E.F., Almeida, L.L.

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Familial STAG2 germline mutation defines a new human cohesinopathy by Soardi, Fernanda C., Machado-Silva, Alice, Linhares, Natália D., Zheng, Ge, Qu, Qianhui, Pena, Heloísa B., Martins, Thaís M. M., Vieira, Helaine G. S., Pereira, Núbia B., Melo-Minardi, Raquel C., Gomes, Carolina C., Gomez, Ricardo S., Gomes, Dawidson A., Pires, Douglas E. V., Ascher, David B., Yu, Hongtao, Pena, Sérgio D. J.

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The novel p.E89K mutation in the SRY gene inhibits DNA binding and causes the 46, XY disorder of sex development by Cunha, J L, Soardi, F C, Bernardi, R D, Oliveira, LEC, Benedetti, CE, Guerra-Junior, G, Maciel-Guerra, A T, de Mello, MP

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The novel p.E89K mutation in the SRY gene inhibits DNA binding and causes the 46,XY disorder of sex development by Cunha, J L, Soardi, F C, Bernardi, R D, Oliveira, L E C, Benedetti, C E, Guerra-Junior, G, Maciel-Guerra, A T, de Mello, M P

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Molecular diagnosis of 5α-reductase type II deficiency in Brazilian siblings with 46,XY disorder of sex development by Leme de Calais, Flávia Leme, Soardi, Fernanda Caroline, Petroli, Reginaldo José, Lusa, Ana Letícia Gori, de Paiva E Silva, Roberto Benedito, Maciel-Guerra, Andréa Trevas, Guerra-Júnior, Gil, de Mello, Maricilda Palandi

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H28+C Insertion in the CYP21 Gene: A Novel Frameshift Mutation in a Brazilian Patient with the Classical Form of 21-Hydroxylase Deficiency by Lau, Ivy F., Soardi, Fernanda C., Lemos-Marini, Sofia H. V., Guerra Jr, Gil, Baptista, Maria Tereza M., De Mello, Maricilda P.

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Molecular Diagnosis of 5[alpha]-Reductase Type II Deficiency in Brazilian Siblings with 46,XY Disorder of Sex Development by Calais, Flavia Leme de, Soardi, Fernanda Caroline, Petroli, Reginaldo Jose, Lusa, Ana Letícia Gori, Paiva, Roberto Benedito de, Silva, e, Maciel-Guerra, Andrea Trevas, Guerra-Júnior, Gil, Mello, Maricilda Palandi de

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A Thomson's Principle for Infinite, Nonlinear Resistive Networks by De Michele, L., Soardi, P. M.

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Limitação de suporte de vida em três unidades de terapia intensiva pediátrica do sul do Brasil by Lago, Patrícia M., Piva, Jefferson, Kipper, Délio, Garcia, Pedro Celiny, Pretto, Cristiane, Giongo, Mateus, Branco, Ricardo, Bueno, Fernanda, Traiber, Cristiane, Araújo, Taisa, Wortmann, Daniela, Librelato, Graziela, Soardi, Deise

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