Search Results - "JC Leite"

LINFOHISTIOCITOSE HEMOFAGOCÍTICA SECUNDÁRIA À INFECÇÃO POR MICOBACTÉRIA COMO PRIMEIRA MANIFESTAÇÃO CLÍNICA DE SÍNDROME MONOMAC EM PACIENTE COM MUTAÇÃO DE GATA2 − RELATO DE CASO by LB Anastacio, PDT Oliveira, LL Paula, JC Leite, AL Costa

“…Objetivo: Descrição de um caso de linfohistiocitose hemofagocítica (LHH) secundária a infecção por micobactéria em um paciente portador da síndrome de…”
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DOENÇA DE CLASTLEMAN MULTICÊNTRICA COM SÍNDROME TAFRO (IMCD-TAFRO) − RELATO DE CASO by LB Anastacio, PDT Oliveira, JC Leite, LL Paula, HM Oliveira

“…Objetivo: Descrição de um caso de Doença de Clastleman Multicêntrica (DCM) com Síndrome TAFRO associada. Material e métodos: Relato de caso descritivo,…”
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Factors associated with adherence to antiretroviral therapy in HIV/AIDS patients: a cross-sectional study in Southern Brazil by Pinheiro, C A T, de-Carvalho-Leite, J C, Drachler, M L, Silveira, V L

“…A cross-sectional study was conducted on HIV-infected adults being treated with antiretroviral drugs at a reference service in Southern Brazil. Participants…”
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Immunogenicity and Safety of an Inactivated Hepatitis A Vaccine in Children With Down Syndrome by Ferreira, Cristina Targa, Leite, J??lio C??sar, Taniguchi, Adriano, Vieira, Sandra Maria, Pereira-Lima, Jorge, Silveira, Themis Reverbel da

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Application of X-ray scanning and tomography to evaluate the filtercake removal efficiency by Lopes, R.T, Oliveira, L.F.de, Miranda, C.R, Leite, J.C

“…The removal of the filtercake formed during the drilling operation is essential for a successful cementing job. Nowadays, the use of synthetic base fluids…”
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Detection of Organic Acidemias in Brazil by Wajner, Moaçir, Raymond, Kimiyo, Barschak, Alethéa, Luft, Ana Paula, Ferreira, Gustavo, Domingues, Gislane, Chiochetta, Marina, Sirtori, Lisana, Goulart, Laureci, Pulrolnik, Vânia, Pires, Ricardo, Grillo, Eugênio, Lohr, Alfredo, Funayama, Carolina, Sanseverino, Maria Teresa, Longuercio-Leite, Júlio César, Coelho, Janice C, Giugliani, Roberto, Regla-Vargas, Carmen

“…Organic acidurias or organic acidemias are inherited metabolic disorders in which organic acids (carboxylic acids) accumulate in tissues and physiologic fluids…”
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