Browsing by Author Klaver, S.

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2014First report of the Hyper-IgM Syndrome registry of the Latin American Society for Immunodeficiencies: novel mutations, unique infections, and outcomesCabral-Marques, O.; Klaver, S.; Pinto-Mariz, F.; Aldave, J. C.; Berron-Ruiz, L.; Goudouris, E.; Ascendino, E. H.; Roxo, P.; Schimke, L. F.; Lima, S.; Rosario, N. A.; Pereira, P. V. S.; BaptistellaGrota, M.; Falcai, A.; King, A.; Khan, T. A.; Vilela, M. M. D.; Santos-Argumedo, L.; Raccio, A. G.; Di Giovanni, D.; Vargas-Hernandez, A.; Seminario, G.; Bezrodnik, L.; Moreira, I.; Ferreira, J. F.; Moura, L. D.; de Carvalho, E.; di Gesu, R. S. W.; Tavares, F. S.; Weber, C. W.; Valente, C. F. C.; Mansour, E.; Porras, O.; Kuntze, G.; Galicchio, M.; Talesnik, E.; Torgerson, T. R.; Carvalho, B. T. C.; Durandy, A.; Staines-Boone, T.; Sorensen, R.; Grumach, A. S.; Calderon, W. O. C.; Zarate-Hernandez, M. D.; Espinosa-Rosales, F.; Ochs, H. D.; Neto, A. C.-Artigo
2012MOLECULAR-GENETIC DEFECTS IN AICDA GENE CONFIRMS CLINICAL SPECTRUM OF AUTOSOMAL HYPER IGM SYNDROME IN BRAZILIAN PATIENTSKlaver, S.; Carvalho, B.; Tavares, F.; Lima, S.; Ferreira, J.; Mansur, E.; Roxo-Junior, P.; Durandy, A.; Condino-Neto, A.-Artigo de periódico
2012Molecular-genetic defects in the AICDA gene confirms clinical spectrum of autosomal Hyper IgM Syndrome in Brazilian patientsKlaver, S.; Carvalho, B.; Tavares, F.; Lima, S.; Ferreira, J.; Mansur, E.; Roxo-Junior, P.; Durandy, A.; Condino-Neto, A.-Artigo