kw.\*:("Duncan disease")
Results 1 to 25 of 43
Selection :
Molecular and cellular pathogenesis of X-linked lymphoproliferative diseaseNICHOLS, Kim E; MA, Cindy S; CANNONS, Jennifer L et al.Immunological reviews. 2005, Vol 203, pp 180-199, issn 0105-2896, 20 p.Article
Using flow cytometry to screen patients for X-linked lymphoproliferative disease due to SAP deficiency and XIAP deficiencyMARSH, Rebecca A; BLEESING, Jack J; FILIPOVICH, Alexandra H et al.Journal of immunological methods. 2010, Vol 362, Num 1-2, pp 1-9, issn 0022-1759, 9 p.Article
Simultaneous manifestation of fulminant infectious mononucleosis with haemophagocytic syndrome and B-cell lymphoma in X-linked lymphoproliferative diseaseHIIGLE, Boris; ASTIGARRAGA, Itziar; HENTER, Jan-Inge et al.European journal of pediatrics. 2007, Vol 166, Num 6, pp 589-593, issn 0340-6199, 5 p.Article
X-linked lymphoproliferative disease associated with hypogammaglobulinemia and growth-hormone deficiencyALANGARI, Abdullah; ABOBAKER, Abdullah; KANEGANE, Hirokazu et al.European journal of pediatrics. 2006, Vol 165, Num 3, pp 165-167, issn 0340-6199, 3 p.Article
Allogeneic stem cell transplantation in X-linked lymphoproliferative disease : two cases in one family and review of the literatureLANKESTER, A. C; VISSER, L. F. A; HARTWIG, N. G et al.Bone marrow transplantation (Basingstoke). 2005, Vol 36, Num 2, pp 99-105, issn 0268-3369, 7 p.Article
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
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
Factors involved in the generation of memory CDo8+ T cells in patients with X-linked lymphoproliferative disease (XLP)BELMONTE, L; PARODI, C; BARE, P et al.Clinical and experimental immunology (Print). 2007, Vol 147, Num 3, pp 456-464, issn 0009-9104, 9 p.Article
Epstein-barr virus : the impact of scientific advances on clinical practiceWILLIAMS, Hilary; CRAWFORD, Dorothy H.Blood. 2006, Vol 107, Num 3, pp 862-869, issn 0006-4971, 8 p.Article
Treatment of primary Epstein-Barr virus infection in patients with X-linked lymphoproliferative disease using B-cell-directed therapyMILONE, Michael C; TSAI, Donald E; HODINKA, Richard L et al.Blood. 2005, Vol 105, Num 3, pp 994-996, issn 0006-4971, 3 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
Rapid detection of intracellular SH2D1A protein in cytotoxic lymphocytes from patients with X-linked lymphoproliferative disease and their family membersTABATA, Yasuhiro; VILLANUEVA, Joyce; LEE, Susan Molleran et al.Blood. 2005, Vol 105, Num 8, pp 3066-3071, issn 0006-4971, 6 p.Article
X-linked lymphoproliferative disease in an adultHOSHINO, Takumi; KANEGANE, Hirokazu; DOKI, Noriko et al.International journal of hematology. 2005, Vol 82, Num 1, pp 55-58, issn 0925-5710, 4 p.Article
Loss of circulating CD27+ memory B cells and CCR4+T cells occurring in association with elevated EBV loads in XLP patients surviving primary EBV infectionMALBRAN, Alejandro; BELMONTE, Liliana; DE BRACCO, Maria M et al.Blood. 2004, Vol 103, Num 5, pp 1625-1631, issn 0006-4971, 7 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 (TFH) 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
XIAP deficiency in humans causes an X-linked lymphoproliferative syndromeRIGAUD, Stéphanie; FONDANECHE, Marie-Claude; FISCHER, Alain et al.Nature (London). 2006, Vol 444, Num 7115, pp 110-114, issn 0028-0836, 5 p.Article
Impaired Ig class switch in mice deficient for the X-linked lymphoproliferative disease gene SapAL-ALEM, Umaima; CUILING LI; FOREY, Nathalie et al.Blood. 2005, Vol 106, Num 6, pp 2069-2075, issn 0006-4971, 7 p.Article
Cell surface receptors Ly-9 and CD84 recruit the X-linked lymphoproliferative disease gene product SAPSAYOS, Joan; MARTIN, Margarita; CHEN, Alice et al.Blood. 2001, Vol 97, Num 12, pp 3867-3874, issn 0006-4971Article
Correlation of mutations of the SH2D1A gene and Epstein-Barr virus infection with clinical phenotype and outcome in X-linked lymphoproliferative diseaseSUMEGI, Janos; DALI HUANG; GROSS, Thomas G et al.Blood. 2000, Vol 96, Num 9, pp 3118-3125, issn 0006-4971Article
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