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Results 1-5 of 5 (Search time: 0.034 seconds).
Issue DateTitleAuthor(s)
2019Whole exome sequencing of Chagas disease cardiomyopathy families reveals accumulation of rare variants in mitochondrial and inflammation-associated genesCUNHA-NETO, E.; MARQUET, S.; FRADE, A. Farage; FERREIRA, A. Mota; OUARHACHE, M.; IANNI, B.; FERREIRA, L. Rodrigues Pinto; RIGAUD, V. Oliveira-Carvalho; ALMEIDA, R. Ribeiro; CANDIDO, D.; TORRES, M.; GALLARDO, F.; FERNANDES, R.; MADY, C.; BUCK, P.; CARDOSO, C.; SANTOS-JUNIOR, O. R.; OLIVEIRA, L. C.; OLIVEIRA, C. D. L.; NUNES, M. do Carmo; ABEL, L.; KALIL, J.; RIBEIRO, A. L. P.; SABINO, E. C.; CHEVILLARD, C.
2012HLA Class I Deficiency Resembling Wegener's Granulomatosis: Report of Two CasesALMEIDA, Lais Pinto de; LEITE, Olavo Henrique Munhoz; NICODEMO, Antonio Carlos; ORII, Noemia Mie; DIAS, Alana dos Santos; MORAES-VASCONCELOS, Dewton de
2012DEVELOPMENT OF A BIOLOGIC DRESSING FOR THE TREATMENT OF SKIN ULCERS ASSOCIATED TO HLA CLASS I DEFICIENCYMORAES-VASCONCELOS, D.; PAGGIARO, A. O.; ISAAC, C.; RIBEIRO, R. L.; NICODEMO, A. C.
2016MCM4 DEFICIENCY: A RARE VARIANT OF IMMUNODEFICIENCY OF NK CELLS ASSOCIATED TO PROPORTIONATE NANISM AND ADRENAL INSUFFICIENCY. DESCRIPTION OF THE FIRST CASE IN BRAZILMORAES-VASCONCELOS, Dewton; RIBEIRO, Roberto; RIGATO, Paula Ordonhez; PINICHI, Paula; AOKI, Valeria; TAKAOKA, Roberto; DUARTE, Alberto Jose da Silva; SABINO, Ester Cerdeira
2014Histopathological Characterization of HLA Class I Deficiency GranulomatosisVASCONCELOS, D. Moraes; MORTARI, N.; LEITE, O. H. M.; NISIDA, I.; NICODEMO, A. C.; PAGLIARI, C.; SLEIMAN, M.; ZIMMER, J.; DUARTE, M. I. S.
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