Search Results - "Marin, Maria Lucia C."

High rate of clinical recurrence in patients with Vogt–Koyanagi–Harada disease treated with early high-dose corticosteroids by Sakata, Viviane M., da Silva, Felipe T., Hirata, Carlos E., Marin, Maria Lucia C., Rodrigues, Helcio, Kalil, Jorge, Costa, Rogerio A., Yamamoto, Joyce H.

“…Purpose To analyse the rate of clinical recurrences in Brazilian patients with Vogt–Koyanagi–Harada (VKH) disease after early high-dose corticosteroid…”
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MHC Variants Associated With Symptomatic Versus Asymptomatic SARS-CoV-2 Infection in Highly Exposed Individuals by Castelli, Erick C, de Castro, Mateus V, Naslavsky, Michel S, Scliar, Marilia O, Silva, Nayane S B, Andrade, Heloisa S, Souza, Andreia S, Pereira, Raphaela N, Castro, Camila F B, Mendes-Junior, Celso T, Meyer, Diogo, Nunes, Kelly, Matos, Larissa R B, Silva, Monize V R, Wang, Jaqueline Y T, Esposito, Joyce, Coria, Vivian R, Bortolin, Raul H, Hirata, Mario H, Magawa, Jhosiene Y, Cunha-Neto, Edecio, Coelho, Verônica, Santos, Keity S, Marin, Maria Lucia C, Kalil, Jorge, Mitne-Neto, Miguel, Maciel, Rui M B, Passos-Bueno, Maria Rita, Zatz, Mayana

“…Despite the high number of individuals infected by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) who develop coronavirus disease 2019 (COVID-19)…”
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Autoimmune hepatitis, HLA and extended haplotypes by Oliveira, Lea Campos, Porta, Gilda, Marin, Maria Lucia C, Bittencourt, Paulo Lisboa, Kalil, Jorge, Goldberg, Anna Carla

“…Abstract Autoimmune hepatitis (AIH) is a chronic inflammatory liver disease. Characteristic liver-infiltrating immune cells in portal and periportal areas,…”
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HLA-G is upregulated in advanced endometriosis by Rached, Marici R., Coelho, Verônica, Marin, Maria Lúcia C., Pincerato, Kátia, Fujita, André, Kalil, Jorge E., Abrão, Maurício S.

“…To assess whether the HLA-G immunomodulatory protein is potentially involved in the pathophysiology of endometriosis or disease progression. Cross-sectional…”
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Identification of multiple HLA-A0201-restricted cruzipain and FL-160 CD8 + epitopes recognized by T cells from chronically Trypanosoma cruzi-infected patients by Fonseca, Simone G., Moins-Teisserenc, Hélène, Clave, Emmanuel, Ianni, Bárbara, Nunes, Vera Lopes, Mady, Charles, Iwai, Leo K., Sette, Alessandro, Sidney, John, Marin, Maria Lúcia C., Goldberg, Anna Carla, Guilherme, Luiza, Charron, Dominique, Toubert, Antoine, Kalil, Jorge, Cunha-Neto, Edecio

“…Chronic Chagas disease occurs in 16 million individuals chronically infected by the protozoan Trypanosoma cruzi in Latin America, and may lead to a dilated…”
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Identification of multiple HLA-A0201-restricted cruzipain and FL-160 CD8 super(+) epitopes recognized by T cells from chronically Trypanosoma cruzi- infected patients by Fonseca, Simone G, Moins-Teisserenc, Helene, Clave, Emmanuel, Ianni, Barbara, Nunes, Vera Lopes, Mady, Charles, Iwai, Leo K, Sette, Alessandro, Sidney, John, Marin, Maria Lucia C, Goldberg, Anna Carla, Guilherme, Luiza, Charron, Dominique, Toubert, Antoine, Kalil, Jorge, Cunha-Neto, Edecio

“…Chronic Chagas disease occurs in 16 million individuals chronically infected by the protozoan Trypanosoma cruzi in Latin America, and may lead to a dilated…”
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A novel missense mutation, GLY424SER, in Brazilian patients with 21-hydroxylase deficiency by BILLERBECK, A. E. C, BACHEGA, T. A. S. S, FRAZZATTO, E. T, NISHI, M. Y, GOLDBERG, A. C, MARIN, M. L. C, MADUREIRA, G, MONTE, O, ARNHOLD, I. J. P, MENDONCA, B. B

“…A previous screening of 17 mutations in 130 Brazilian patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency did not identify mutations…”
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A Novel Missense Mutation, GLY424SER, in Brazilian Patients with 21-Hydroxylase Deficiency1 by Billerbeck, Ana Elisa C, Bachega, Tânia A. S. S, Frazzatto, Eliana T, Nishi, Mirian Yumie, Goldberg, Anna Carla, Marin, Maria Lucia C, Madureira, Guiomar, Monte, Osmar, Arnhold, Ivo J. P, Mendonca, Berenice B

“…A previous screening of 17 mutations in 130 Brazilian patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency did not identify mutations…”
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A Novel Missense Mutation, GLY424SER, in Brazilian Patients with 21-Hydroxylase Deficiency 1 by Billerbeck, Ana Elisa C., Bachega, Tânia A. S. S., Frazzatto, Eliana T., Nishi, Mirian Yumie, Goldberg, Anna Carla, Marin, Maria Lucia C., Madureira, Guiomar, Monte, Osmar, Arnhold, Ivo J. P., Mendonca, Berenice B.

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