Laboratory evaluation of primary immunodeficiencies

per Oliveira, João B., Fleisher, Thomas A.
Publicat 2009

ALPS – Ten Lessons from an International Workshop on a Genetic Disease of Apoptosis

per Lenardo, Michael J., Oliveira, João B., Zheng, Lixin, Rao, V. Koneti
Publicat 2010

Critical role for BIM in T cell receptor restimulation-induced death

per Fleisher Thomas A, Dale Janet K, Zheng Lixin, Oliveira João B, Snow Andrew L, Lenardo Michael J
Publicat 2008-08-01

Critical role for BIM in T cell receptor restimulation-induced death

per Snow, Andrew L, Oliveira, João B, Zheng, Lixin, Dale, Janet K, Fleisher, Thomas A, Lenardo, Michael J
Publicat 2008

FAS Haploinsufficiency Is a Common Disease Mechanism in the Human Autoimmune Lymphoproliferative Syndrome

per Kuehn, Hye Sun, Caminha, Iusta, Niemela, Julie E., Rao, V. Koneti, Davis, Joie, Fleisher, Thomas A., Oliveira, João B.
Publicat 2011

Caspase-8 deficiency presenting as late-onset multi-organ lymphocytic infiltration with granulomas in two adult siblings

per Niemela, Julie, Kuehn, Hye Sun, Kelly, Corin, Zhang, Mingchang, Davies, Joie, Jose, Melendez, Dreiling, Jennifer, Kleiner, David, Calvo, Katherine, Oliveira, João B., Rosenzweig, Sergio D.
Publicat a J Clin Immunol (2015)

Revised diagnostic criteria and classification for the autoimmune lymphoproliferative syndrome (ALPS): report from the 2009 NIH International Workshop

per Oliveira, Joao B., Bleesing, Jack J., Dianzani, Umberto, Fleisher, Thomas A., Jaffe, Elaine S., Lenardo, Michael J., Rieux-Laucat, Frederic, Siegel, Richard M., Su, Helen C., Teachey, David T., Rao, V. Koneti
Publicat 2010

Somatic KRAS mutations associated with a human nonmalignant syndrome of autoimmunity and abnormal leukocyte homeostasis

per Niemela, Julie E., Lu, Lianghao, Fleisher, Thomas A., Davis, Joie, Caminha, Iusta, Natter, Marc, Beer, Laurel A., Dowdell, Kennichi C., Pittaluga, Stefania, Raffeld, Mark, Rao, V. Koneti, Oliveira, João B.
Publicat 2011

NRAS mutation causes a human autoimmune lymphoproliferative syndrome

per Oliveira, João B., Bidère, Nicolas, Niemela, Julie E., Zheng, Lixin, Sakai, Keiko, Nix, Cynthia P., Danner, Robert L., Barb, Jennifer, Munson, Peter J., Puck, Jennifer M., Dale, Janet, Straus, Stephen E., Fleisher, Thomas A., Lenardo, Michael J.
Publicat 2007

Anti-cytokine autoantibodies are associated with opportunistic infection in patients with thymic neoplasia

per Burbelo, Peter D., Browne, Sarah K., Sampaio, Elizabeth P., Giaccone, Giuseppe, Zaman, Rifat, Kristosturyan, Ervand, Rajan, Arun, Ding, Li, Ching, Kathryn H., Berman, Arlene, Oliveira, Joao B., Hsu, Amy P., Klimavicz, Caitlin M., Iadarola, Michael J., Holland, Steven M.
Publicat 2010

Loss-of-function of the protein kinase C δ (PKCδ) causes a B-cell lymphoproliferative syndrome in humans

per Kuehn, Hye Sun, Niemela, Julie E., Rangel-Santos, Andreia, Zhang, Mingchang, Pittaluga, Stefania, Stoddard, Jennifer L., Hussey, Ashleigh A., Evbuomwan, Moses O., Priel, Debra A. Long, Kuhns, Douglas B., Park, C. Lucy, Fleisher, Thomas A., Uzel, Gulbu, Oliveira, João B.
Publicat 2013

Relationship between age and blastocyst chromosomal ploidy analyzed by noninvasive preimplantation genetic testing for aneuploidies (niPGT-A)

per Vagnini, Laura D., Petersen, Claudia G., Renzi, Adriana, Dieamant, Felipe, Oliveira, João B.A., Oliani, Antonio H., Canas, Maria C.T., Nakano, Raul, Almodin, Carlos G., Marcondes, Condesmar, Ceschin, Alvaro, Amaral, Adelino, Soares, Jonathas B., Lopes, Joaquim, Franco, Antonio C., Franco Jr., Jose G.
Publicat a JBRA Assist Reprod (2020)

CD40 agonist antibody mediated improvement of chronic Cryptosporidium infection in patients with X- linked hyper IgM syndrome

per Fan, Xiying, Upadhyaya, Bhaskar, Wu, Liming, Koh, Christopher, Santín-Durán, Mónica, Pittaluga, Stefania, Uzel, Gulbu, Kleiner, David, Williams, Ester, Ma, Chi A., Bodansky, Aaron, Oliveira, Joao B., Edmonds, Pamela, Hornung, Ronald, Wong, Duane W., Fayer, Ronald, Fleisher, Tom, Heller, Theo, Prussin, Calman, Jain, Ashish
Publicat 2012

Immune dysregulation in human subjects with heterozygous germline mutations in CTLA4

per Kuehn, Hye Sun, Ouyang, Weiming, Lo, Bernice, Deenick, Elissa K., Niemela, Julie E., Avery, Danielle T., Schickel, Jean-Nicolas, Tran, Dat Q., Stoddard, Jennifer, Zhang, Yu, Frucht, David M., Dumitriu, Bogdan, Scheinberg, Phillip, Folio, Les R., Frein, Cathleen A., Price, Susan, Koh, Christopher, Heller, Theo, Seroogy, Christine M., Huttenlocher, Anna, Rao, V. Koneti, Su, Helen C., Kleiner, David, Notarangelo, Luigi D., Rampertaap, Yajesh, Olivier, Kenneth N., McElwee, Joshua, Hughes, Jason, Pittaluga, Stefania, Oliveira, Joao B., Meffre, Eric, Fleisher, Thomas A., Holland, Steven M., Lenardo, Michael J., Tangye, Stuart G., Uzel, Gulbu
Publicat a Science (2014)