Showing 1 - 6 results of 6 for search 'Camila Simoes', query time: 0.01s Refine Results
  1. 1
    Identification of a novel SACS gene mutation leading to spastic ataxia Charlevoix-Saguenay type: a case report

    Identification of a novel SACS gene mutation leading to spastic ataxia Charlevoix-Saguenay type: a case report by Víctor Raggio, Andrea Rey, Camila Simoes, Florencia Birriel, Soledad Rodriguez, Kateryn Bentancor, Alejandra Tapié, Lucía Spangenberg

    Published 2025-08-01
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  2. 2
    New perspectives for the Annelida collection (National Museum/UFRJ) database: using data visualization to analyze and manage biological collections

    New perspectives for the Annelida collection (National Museum/UFRJ) database: using data visualization to analyze and manage biological collections by Camila Simões Martins de Aguiar Messias, Carlos Cesar de Oliveira Fonseca, Monique Cristina dos Santos, Asla M. Sá, Joana Zanol

    Published 2024-04-01
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  3. 3
    New perspectives for the Annelida collection (National Museum/UFRJ) database: using data visualization to analyze and manage biological collections

    New perspectives for the Annelida collection (National Museum/UFRJ) database: using data visualization to analyze and manage biological collections by Camila Simões Martins de Aguiar Messias, Carlos Cesar de Oliveira Fonseca, Monique Cristina dos Santos, Asla M. Sá, Joana Zanol

    Published 2024-04-01
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  4. 4
    Opposite effects of systemic and local conditional CD11c+ myeloid cell depletion during bleomycin‐induced inflammation and fibrosis in mice

    Opposite effects of systemic and local conditional CD11c+ myeloid cell depletion during bleomycin‐induced inflammation and fibrosis in mice by Gabriel Augusto Oliveira Lopes, Braulio Henrique Freire Lima, Camila Simões Freitas, Andiara Cardoso Peixoto, Frederico Marianetti Soriani, Geovanni Dantas Cassali, Bernhard Ryffel, Mauro Martins Teixeira, Fabiana Simão Machado, Remo Castro Russo

    Published 2024-11-01
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  5. 5
    WCN24-864 Alport Syndrome: genetic variants, phenotypes of kidney disease and association with End Stage Kidney Disease in a Uruguayan Cohort

    WCN24-864 Alport Syndrome: genetic variants, phenotypes of kidney disease and association with End Stage Kidney Disease in a Uruguayan Cohort by Federico Yandian, Lucía Spangenberg, Víctor Raggio, Nicolás Dell´Oca, Lucía Urquiola, Santiago Fontenla, Fernanda Domínguez, Camila Simoes, Jessica Segarra, Lucía Facal, Paula Parnizari, Jimena Cabrera, José Tort, Óscar Noboa, Hugo Naya, José Boggia

    Published 2024-04-01
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  6. 6
    Blue light-emitting diode phototherapy presents in vitro efficacy against distinct Leishmania species and is therapeutic against tegumentary leishmaniasis in BALB/c mice

    Blue light-emitting diode phototherapy presents in vitro efficacy against distinct Leishmania species and is therapeutic against tegumentary leishmaniasis in BALB/c mice by Breno Luiz Pimenta, Breno Luiz Pimenta, Daniela Pagliara Lage, Camila Simões de Freitas, Danniele Luciana Vale, Karolina Oliveira de Melo Falcão, Saulo Samuel Gonçalves Dias, Raquel Soares Bandeira Câmara, Isabela Amorim Gonçalves Pereira, Ana Luiza Silva, Lauro de Assis Duarte Júnior, Lauro de Assis Duarte Júnior, Miguel Angel Chavez-Fumagalli, Rodrigo Fernando Bianchi, Eduardo Antonio Ferraz Coelho, Eduardo Antonio Ferraz Coelho, André Talvani, André Talvani

    Published 2025-05-01
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