Hasil Pencarian - Fernanda Milanezi

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  1. 1
    Carcinoma da mama de tipo basal.

    Carcinoma da mama de tipo basal. oleh Fátima Silva, Sílvia Carvalho, Fernanda Milanezi, Fernando C Schmitt

    Diterbitkan 2008-10-01
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  2. 2
    Invasive medullary thymoma associated with myasthenia gravis: an unusual case Miastenia gravis em um paciente com timoma medular invasivo: relato de caso

    Invasive medullary thymoma associated with myasthenia gravis: an unusual case Miastenia gravis em um paciente com timoma medular invasivo: relato de caso oleh JORGE S. REIS FILHO, MARIA FERNANDA MILANEZI, CHRISTIANO G. MOREIRA, LINEU C. WERNECK, PAULO BOSCARDIN, SERGIO OSSAMU IOSHII, FERNANDO C. SCHMITT

    Diterbitkan 2000-12-01
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  3. 3
    Leigh syndrome in a patient with a novel C12orf65 pathogenic variant: case report and literature review

    Leigh syndrome in a patient with a novel C12orf65 pathogenic variant: case report and literature review oleh Eduardo Perrone, Thiago R. Cavole, Manuella G. Oliveira, Luiza do A. Virmond, Marina de França B. Silva, Maria de Fatima F. Soares, Simone Brasil de O. Iglesias, Ariane Falconi, Juliana S. Silva, Viviane Nakano, Maria Fernanda Milanezi, Carmen Silvia C. Mendes, Marco Antonio Curiati, Cecília Micheletti

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  4. 4
    A Benchmark of In-House Homologous Recombination Repair Deficiency Testing Solutions for High-Grade Serous Ovarian Cancer Diagnosis

    A Benchmark of In-House Homologous Recombination Repair Deficiency Testing Solutions for High-Grade Serous Ovarian Cancer Diagnosis oleh Rodrigo Guarischi-Sousa, José Eduardo Kroll, Adriano Bonaldi, Paulo Marques Pierry, Darine Villela, Camila Alves Souza, Juliana Santos Silva, Matheus Carvalho Bürger, Felipe Azevedo Oliveira, Marcelo Gomes de Paula, Fabiana Marcelino Meliso, Luiz Gustavo de Almeida, Priscilla Morais Monfredini, Ana Gabriela de Oliveira, Fernanda Milanezi, Cristovam Scapulatempo-Neto, Guilherme Lopes Yamamoto

    Diterbitkan 2023-10-01
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  5. 5
    Chromosomal microarray analyses from 5778 patients with neurodevelopmental disorders and congenital anomalies in Brazil

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

    Diterbitkan 2022-09-01
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