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Defects of class-switch recombinationNOTARANGELO, Luigi D; LANZI, Gaetana; PERON, Sophie et al.Journal of allergy and clinical immunology. 2006, Vol 117, Num 4, pp 855-864, issn 0091-6749, 10 p.Article

c-Rel plays a key role in deficient activation of B cells from a non-X-linked hyper-IgM patientLU, Kristina T; SINQUETT, Frank L; DRYER, Rebecca L et al.Blood. 2006, Vol 108, Num 12, pp 3769-3776, issn 0006-4971, 8 p.Article

An unusual presentation of immunodeficiency with hyper-IgMUGUZ, Aysen; YILMAZ, Ertan; CIFTCIOGLU, M. Akif et al.Pediatric dermatology. 2001, Vol 18, Num 1, pp 48-50, issn 0736-8046Article

Cutaneous sarcoid-like granulomas in a patient with X-linked hyper-IgM syndromeGALLERANI, Isabella; DEGLI INNOCENTI, Damiano; CORONELLA, Giordana et al.Pediatric dermatology. 2004, Vol 21, Num 1, pp 39-43, issn 0736-8046, 5 p.Article

An imbalance of naive and memoryleffector subsets and altered expression of CD38 on T lymphocytes in two girls with hyper-IgM syndromeCOSTA-CARVALHO, B. T; VIANA, M. A; BRUNIALTI, M. K. C et al.Clinical and experimental immunology (Print). 2004, Vol 136, Num 2, pp 291-296, issn 0009-9104, 6 p.Article

Mutations in activation-induced cytidine deaminase in patients with hyper IgM syndromeMINEGISHI, Yoshiyuki; LAVOIE, Aubert; DURANDY, Anne et al.Clinical immunology (Orlando, Fla. Print). 2000, Vol 97, Num 3, pp 203-210, issn 1521-6616Article

Etude comparative de la voie d'activation CD40 des lymphocytes B, des monocytes et des cellules dendritiques chez l'homme : application à un déficit immunitaire héréditaire, le syndrome d'hyper-IgM de transmission autosomique récéssive = Comparative study of the CD40 activation pathway in human B cells, monocytes and dendritic cells : application in an immune deficiency the hyper-IgM syndrome with autosomal recessive inheritanceRevy, Patrick; Durandy, Anne.1999, 180 p.Thesis

X-linked hyper-IgM syndrome associated with a rapid course of multifocal leukoencephalopathyASCHERMANN, Zsuzsanna; GOMORI, Eva; KOVACS, Gabor G et al.Archives of neurology (Chicago). 2007, Vol 64, Num 2, pp 273-276, issn 0003-9942, 4 p.Article

JC virus granule cell neuronopathy in a child with CD40 ligand deficiencyHECHT, Jonathan H; GLENN, Orit A; WARA, Diane W et al.Pediatric neurology. 2007, Vol 36, Num 3, pp 186-189, issn 0887-8994, 4 p.Article

Hyper-IgM syndrome with CHARGE associationBAHILLO, Pilar; CANTERO, Teresa; SOLIS, Pilar et al.Pediatric allergy and immunology. 2003, Vol 14, Num 6, pp 487-489, issn 0905-6157, 3 p.Article

A novel activation-induced cytidine deaminase gene mutation in a Tunisian family with hyper IgM syndromeFIORINI, Claudia; JILANI, Sawssen; LOSI, Claretta Gioia et al.European journal of pediatrics. 2004, Vol 163, Num 12, pp 704-708, issn 0340-6199, 5 p.Article

X-linked hyper IgM syndromeSCHNEIDER, Lynda C.Clinical reviews in allergy and immunology. 2000, Vol 19, Num 2, pp 205-215, issn 1080-0549Article

Correction of X-linked hyper-IgM syndrome by allogeneic bone marrow transplantationTHOMAS, C; DE SAINT BASILE, G; LE DEIST, F et al.The New England journal of medicine. 1995, Vol 333, Num 7, pp 426-429, issn 0028-4793Article

Inducible CO-stimulator molecule, a candidate gene for defective isotype switching, is normal in patients with hyper-IgM syndrome of unknown molecular diagnosisLEE, Wen-I; QULI ZHU; GAMBINERI, Eleonora et al.Journal of allergy and clinical immunology. 2003, Vol 112, Num 5, pp 958-964, issn 0091-6749, 7 p.Article

Treatment of CD40 ligand deficiency by hematopoietic stem cell transplantation: a survey of the European experience, 1993-2002GENNERY, Andrew R; KHAWAJA, Khulood; FASTH, Anders et al.Blood. 2004, Vol 103, Num 3, pp 1152-1157, issn 0006-4971, 6 p.Article

Development of a rapid whole blood flow cytometry procedure for the diagnosis of X-linked Hyper-IgM syndrome patients and carriersO'GORMAN, M. R. G; ZAAS, D; PANIAGUA, M et al.Clinical immunology and immunopathology (Print). 1997, Vol 85, Num 2, pp 172-181, issn 0090-1229Article

A boy with X-linked hyper-IgM syndrome and natural killer cell deficiencyØSTENSTAD, R; GILIANI, S; MELLBYE, O. J et al.Clinical and experimental immunology (Print). 1997, Vol 107, Num 2, pp 230-234, issn 0009-9104Article

Absence of CD40-CD40 ligand interactions in X-linked hyper-IgM syndrome does not affect differentiation of T helper cell subsetsURONEN, H; CALLARD, R. E.Clinical and experimental immunology (Print). 2000, Vol 121, Num 2, pp 346-352, issn 0009-9104Article

Clinical, immunologic and genetic analysis of 29 patients with autosomal recessive hyper-IgM syndrome due to Activation-Induced Cytidine Deaminase deficiencyQUARTIER, Pierre; BUSTAMANTE, Jacinta; HORNEFF, Gerd et al.Clinical immunology (Orlando, Fla. Print). 2004, Vol 110, Num 1, pp 22-29, issn 1521-6616, 8 p.Article

Coexpression of normal and mutated CD40 ligand with deletion of a putative RNA lariat branchpoint sequence in X-linked hyper-IgM syndromeXIAOMEI ZHU; CHUNG, Isabel; O'GORMAN, Maurice R et al.Clinical immunology (Orlando, Fla. Print). 2001, Vol 99, Num 3, pp 334-339, issn 1521-6616Article

Circumscribed scleroderma in congenital rubella syndrome with hypogammaglobulinemiaESPANOL, T; PASCUAL, C; HUGUET, P et al.Allergy (Copenhagen). 1998, Vol 53, Num 10, pp 1005-1006, issn 0105-4538Article

Hyper-IgM syndrome with putative dominant negative mutation in activation-induced cytidine deaminaseKASAHARA, Yukiko; KANEKO, Hideo; FUKAO, Toshiyuki et al.Journal of allergy and clinical immunology. 2003, Vol 112, Num 4, pp 755-760, issn 0091-6749, 6 p.Article

CD154 deficiency and related syndromesBONILLA, Francisco A; GEHA, Raif S.Immunology and allergy clinics of North America. 2001, Vol 21, Num 1, issn 0889-8561, viii, 65-89 [26 p.]Article

Primary immune deficienciesBALLOW, Mark; STROBER, Warren.Clinical reviews in allergy and immunology. 2000, Vol 19, Num 2, issn 1080-0549, 137 p.Serial Issue