Zoekresultaten - Têmis Maria Félix

Evaluation of functioning and associated factors in children and adolescents with osteogenesis imperfecta door Arthur Cherem Netto Fernandes, Têmis Maria Félix

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CARACTERÍSTICAS CLÍNICAS E PADRÃO DE FRATURAS NO MOMENTO DO DIAGNÓSTICO DE OSTEOGÊNESE IMPERFEITA EM CRIANÇAS door Evelise Brizola, Marina Bauer Zambrano, Bruna de Souza Pinheiro, Ana Paula Vanz, Têmis Maria Félix

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TGFA/Taq I polymorphism and environmental factors in non-syndromic oral clefts in Southern Brazil door Liliane Todeschini de Souza, Thayne Woycinck Kowalski, Ana Paula Vanz, Roberto Giugliani, Têmis Maria Félix

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ID247 Jornada Assistencial de Valor do RARAS (JAV RARAS): Aspectos metodológicos da análise de aderência aos PCDTs door Myrianne Barbosa, Cláudia Lorea, Camila Azevedo, Luana Lopes, Alef Almeida, Temis Felix, Gabriel Ogata, Marcelo Nita, Têmis Maria Félix

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Challenges and recommendations to increasing the use of exome sequencing and whole genome sequencing for diagnosing rare diseases in Brazil: an expert perspective door Têmis Maria Félix, Carolina Fischinger Moura de Souza, João Bosco Oliveira, Mariana Rico-Restrepo, Edmar Zanoteli, Mayana Zatz, Roberto Giugliani

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The Minimum Data Set for Rare Diseases: Systematic Review door Filipe Andrade Bernardi, Bibiana Mello de Oliveira, Diego Bettiol Yamada, Milena Artifon, Amanda Maria Schmidt, Victória Machado Scheibe, Domingos Alves, Têmis Maria Félix

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Does universal newborn hearing screening impact the timing of deafness treatment? door Marina Faistauer, Alice Lang Silva, Daniela de Oliveira Ruiz Dominguez, Renata Bohn, Têmis Maria Félix, Sady Selaimen da Costa, Letícia Petersen Schmidt Rosito

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Genomic imbalances in syndromic congenital heart disease, door Miriam Coelho Molck, Milena Simioni, Társis Paiva Vieira, Ilária Cristina Sgardioli, Fabíola Paoli Monteiro, Josiane Souza, Agnes Cristina Fett-Conte, Têmis Maria Félix, Isabella Lopes Monlléo, Vera Lúcia Gil-

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Genomic imbalances in syndromic congenital heart disease door Miriam Coelho Molck, Milena Simioni, Társis Paiva Vieira, Ilária Cristina Sgardioli, Fabíola Paoli Monteiro, Josiane Souza, Agnes Cristina Fett-Conte, Têmis Maria Félix, Isabella Lopes Monlléo, Vera Lúcia Gil-

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Health-related quality of life of children and adolescents with osteogenesis imperfecta: a cross-sectional study using PedsQL™ door Ana Paula Vanz, Juliana van de Sande Lee, Bruna Pinheiro, Marina Zambrano, Evelise Brizola, Neusa Sicca da Rocha, Ida Vanessa D. Schwartz, Maria Marlene de Souza Pires, Têmis Maria Félix

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Genomic imbalances in syndromic congenital heart disease door Miriam Coelho Molck, Milena Simioni, Társis Paiva Vieira, Ilária Cristina Sgardioli, Fabíola Paoli Monteiro, Josiane Souza, Agnes Cristina Fett‐Conte, Têmis Maria Félix, Isabella Lopes Monlléo, Vera Lúcia Gil‐da‐Silva‐Lopes

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Lista de anomalias congênitas prioritárias para vigilância no âmbito do Sistema de Informações sobre Nascidos Vivos do Brasil door Augusto César Cardoso-, Ana Cláudia Medeiros-, João Matheus Bremm, Ronaldo Fernandes Santos Alves, Valdelaine Etelvina Miranda de Araújo, Júlio Cesar Loguercio Leite, Lavínia Schuler-Faccini, Maria Teresa Vieira Sanseverino, Simone de Menezes Karam, Têmis Maria Félix, Mariana Bertol Leal, Eduardo Marques Macário, Arnaldo Correia de Medeiros, Giovanny Vinícius Araújo de França

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Achondroplasia in Latin America: practical recommendations for the multidisciplinary care of pediatric patients door Juan Llerena, Chong Ae Kim, Virginia Fano, Pablo Rosselli, Paulo Ferrez Collett-Solberg, Paula Frassinetti Vasconcelos de Medeiros, Mariana del Pino, Débora Bertola, Charles Marques Lourenço, Denise Pontes Cavalcanti, Têmis Maria Félix, Antonio Rosa-Bellas, Norma Teresa Rossi, Fanny Cortes, Flávia Abreu, Nicolette Cavalcanti, Maria Cecilia Hervias Ruz, Wagner Baratela

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