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Primary immunodeficiency diseases associated with increased susceptibility to viral infections and malignanciesREZAEI, Nima; HEDAYAT, Mona; AGHAMOHAMMADI, Asghar et al.Journal of allergy and clinical immunology. 2011, Vol 127, Num 6, pp 1329-1341, issn 0091-6749, 13 p.Article

Diagnosing XLP1 in patients with hemophagocytic lymphohistiocytosisMEAZZA, Raffaella; TUBEROSA, Claudia; MONTIN, Davide et al.Journal of allergy and clinical immunology. 2014, Vol 134, Num 6, pp 1381-1387, issn 0091-6749, 7 p.Article

X-linked lymphoproliferative disease due to SAP/SH2D1A deficiency: a multicenter study on the manifestations, management and outcome of the diseaseBOOTH, Claire; GILMOUR, Kimberly C; KERRIGAN, Hilary et al.Blood. 2011, Vol 117, Num 1, pp 53-62, issn 0006-4971, 10 p.Article

Impaired Epstein-Barr virus-specific CD8⁺ T-cell function in X-linked lymphoproliferative disease is restricted to SLAM family―positive B-cell targetsHISLOP, Andrew D; PALENDIRA, Umaimainthan; LEESE, Alison M et al.Blood. 2010, Vol 116, Num 17, pp 3249-3257, issn 0006-4971, 9 p.Article

Importance and mechanism of `switch' function of SAP family adaptersVEILLETTE, André; ZHONGJUN DONG; PEREZ-QUINTERO, Luis-Alberto et al.Immunological reviews. 2009, Vol 232, pp 229-239, issn 0105-2896, 11 p.Article

Epstein-Barr virus persistence in the absence of conventional memory B cells : IgM⁺IgD⁺CD27⁺ B cells harbor the virus in X-linked lymphoproliferative disease patientsCHAGANTI, Sridhar; MA, Cindy S; BELL, Andrew I et al.Blood. 2008, Vol 112, Num 3, pp 672-679, issn 0006-4971, 8 p.Article

Treatment of Epstein Barr virus-induced haemophagocytic lymphohistiocytosis with rituximab-containing chemo-immunotherapeutic regimensCHELLAPANDIAN, Deepakbabu; DAS, Rupali; ZELLEY, Kristin et al.British journal of haematology. 2013, Vol 162, Num 3, pp 376-382, issn 0007-1048, 7 p.Article

Clinical similarities and differences of patients with X-linked lymphoproliferative syndrome type 1 (XLP-1/SAP deficiency) versus type 2 (XLP-2/XIAP deficiency)PACHLOPNIK SCHMID, Jana; CANIONI, Danielle; GALICIER, Lionel et al.Blood. 2011, Vol 117, Num 5, pp 1522-1529, issn 0006-4971, 8 p.Article

Increased lymphocyte viability after non-stimulated peripheral blood mononuclear cell (PBMC) culture in patients with X-linked lymphoproliferative disease (XLP)BELMONTE, Liliana; PARODI, Cecilia; BASTON, Mariela et al.Clinical immunology (Orlando, Fla. Print). 2009, Vol 133, Num 1, pp 86-94, issn 1521-6616, 9 p.Article

Primary immunodeficiencies predisposed to Epstein-Barr virus-driven haematological diseasesPARVANEH, Nima; FILIPOVICH, Alexandra H; BORKHARDT, Arndt et al.British journal of haematology. 2013, Vol 162, Num 5, pp 573-586, issn 0007-1048, 14 p.Article

SAP expression in invariant NKT cells is required for cognate help to support B-cell responsesDETRE, Cynthia; KESZEI, Marton; NINGHAI WANG et al.Blood. 2012, Vol 120, Num 1, pp 122-129, issn 0006-4971, 8 p.Article

CD4+ T Lymphocytes with follicular helper phenotype (T_FH) in patients with SH2D1A deficiency (XLP)CORAGLIA, Ana; FELIPPO, Martha; SCHIERLOH, Pablo et al.Clinical immunology (Orlando, Fla. Print). 2011, Vol 141, Num 3, pp 357-364, issn 1521-6616, 8 p.Article

Allogeneic stem cell transplantation as immunotherapy for X-linked lymphoproliferative disease-associated cerebral T-cell lymphomaGOODYER, Matthew; SARGENT, Jeremy; BOND, Jonathan et al.British journal of haematology. 2013, Vol 163, Num 1, pp 133-135, issn 0007-1048, 3 p.Article

Clinical features and outcome of X-linked lymphoproliferative syndrome type 1 (SAP deficiency) in Japan identified by the combination of flow cytometric assay and genetic analysisKANEGANE, Hirokazu; XI YANG; TERUI, Kiminori et al.Pediatric allergy and immunology. 2012, Vol 23, Num 5, pp 488-493, issn 0905-6157, 6 p.Article

Stable low-level donor-cell engraftment in a patient with X-linked lymphoproliferative disease following matched unrelated allo-SCTHASLAM, K; MOLLOY, K; LANGABEER, S et al.Bone marrow transplantation (Basingstoke). 2011, Vol 46, Num 9, pp 1263-1264, issn 0268-3369, 2 p.Article

XIAP deficiency: a unique primary immunodeficiency best classified as X-linked familial hemophagocytic lymphohistiocytosis and not as X-linked lymphoproliferative diseaseMARSH, Rebecca A; MADDEN, Lisa; KITCHEN, Brenda J et al.Blood. 2010, Vol 116, Num 7, pp 1079-1082, issn 0006-4971, 4 p.Article

Chronic Active Gastritis in X-linked Lymphoproliferative DiseaseROUGEMONT, Anne-Laure; FOURNET, Jean-Christophe; MARTIN, Steven R et al.The American journal of surgical pathology. 2008, Vol 32, Num 2, pp 323-328, issn 0147-5185, 6 p.Article

Patients with X-linked lymphoproliferative disease due to BIRC4 mutation have normal invariant natural killer T-cell populationsMARSH, Rebecca A; VILLANUEVA, Joyce; KIM, Mi-Ok et al.Clinical immunology (Orlando, Fla. Print). 2009, Vol 132, Num 1, pp 116-123, issn 1521-6616, 8 p.Article