Antifungal susceptibility of yeasts isolated from anthropogenic watershed von Milanezi, Ana C M, Witusk, João P D, VAN DER Sand, Sueli T

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Chromosomal microarray analyses from 5778 patients with neurodevelopmental disorders and congenital anomalies in Brazil von Krepischi, Ana C. V., Villela, Darine, da Costa, Silvia Souza, Mazzonetto, Patricia C., Schauren, Juliana, Migliavacca, Michele P., Milanezi, Fernanda, Santos, Juliana G., Guida, Gustavo, Guarischi-Sousa, Rodrigo, Campana, Gustavo, Kok, Fernando, Schlesinger, David, Kitajima, Joao Paulo, Campagnari, Francine, Bertola, Debora R., Vianna-Morgante, Angela M., Pearson, Peter L., Rosenberg, Carla

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Regulation of Trypanosoma cruzi-Induced Myocarditis by Programmed Death Cell Receptor 1 von Gutierrez, Fredy R.S, Mariano, Flávia S, Oliveira, Carlo J.F, Pavanelli, Wander R, Guedes, Paulo M.M, Silva, Grace K, Campanelli, Ana P, Milanezi, Cristiane M, Azuma, Miyuki, Honjo, Tasuku, Teixeira, Mauro M, Aliberti, Julio C.S, Silva, João S

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Congenital chromoanagenesis in the routine postnatal chromosomal microarray analyses von Villela, Darine, Mazzonetto, Patricia C., Migliavacca, Michele P., Perrone, Eduardo, Guida, Gustavo, Milanezi, Maria Fernanda G., Jorge, Alexander A. L., Ribeiro‐Bicudo, Lucilene A., Kok, Fernando, Campagnari, Francine, Rosso‐Giuliani, Liane, Costa, Silvia Souza, Vianna‐Morgante, Angela M., Pearson, Peter L., Krepischi, Ana C. V., Rosenberg, Carla

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Low-pass whole genome sequencing is a reliable and cost-effective approach for copy number variant analysis in the clinical setting von Mazzonetto, Patricia C, Villela, Darine, da Costa, Silvia Souza, Krepischi, Ana C V, Milanezi, Fernanda, Migliavacca, Michele P, Pierry, Paulo M, Bonaldi, Adriano, Almeida, Luiz Gustavo D, De Souza, Camila Alves, Kroll, José Eduardo, Paula, Marcelo G, Guarischi-Sousa, Rodrigo, Scapulatempo-Neto, Cristovam, Rosenberg, Carla

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The IgG glycome of SARS-CoV-2 infected individuals reflects disease course and severity von Siekman, Sterre L, Pongracz, Tamas, Wang, Wenjun, Nouta, Jan, Kremsner, Peter G, da Silva-Neto, Pedro Vieira, Esen, Meral, Kreidenweiss, Andrea, Held, Jana, Trapé, Átila Alexandre, Fendel, Rolf, de Miranda Santos, Isabel Kinney Ferreira, Wuhrer, Manfred

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Mixed lineage kinase 3 gene mutations in mismatch repair deficient gastrointestinal tumours von Velho, Sérgia, Oliveira, Carla, Paredes, Joana, Sousa, Sónia, Leite, Marina, Matos, Paulo, Milanezi, Fernanda, Ribeiro, Ana Sofia, Mendes, Nuno, Licastro, Danilo, Karhu, Auli, Oliveira, Maria José, Ligtenberg, Marjolijn, Hamelin, Richard, Carneiro, Fátima, Lindblom, Annika, Peltomaki, Paivi, Castedo, Sérgio, Schwartz, Simó, Jordan, Peter, Aaltonen, Lauri A., Hofstra, Robert M.W., Suriano, Gianpaolo, Stupka, Elia, Fialho, Arsenio M., Seruca, Raquel

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A Novel MGP Gene Mutation Causing Keutel Syndrome in a Brazilian Patient von Perrone, Eduardo, Chen, Kelin, Ramos, Marco, Milanezi, Maria Fernanda, Nakano, Viviane, Falconi, Ariane, Silva, Juliana, Campos, Jamille, Silva, Celia M.C., Filho, Joao B.O., Perez, Ana B.A.

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Role of Interleukin (IL)-18 in experimental paracoccidioidomycosis von Panagio, Luciano A., Tristão, Fabrine S. M., Moreira, Ana P., Pereira, Marcelo S. F., Cavassani, Karen A., Milanezi, Cristiane M., Rossi, Marcos A., Silva, João S.

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