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Prenatal test for X-linked severe combined immunodeficiency by analysis of maternal X-chromosome inactivation and linkage analysisPUCK, J. M; KRAUSS, C. M; PUCK, S. M et al.The New England journal of medicine. 1990, Vol 322, Num 15, pp 1063-1066, issn 0028-4793Article

Chronic diarrhea in a 5 1/2-month-old infantMINGS, R; KNUTSEN, A. P; KRANTMAN, H et al.Annals of allergy. 1987, Vol 58, Num 5, pp 322-372, issn 0003-4738, 4 p.Article

X-linked agammaglobulinemia and the red blood cell determinants Xg and 12E7 are not closely linkedMENSINK, E. J. B. M; SCHOT, J. D. L; TIPPETT, P et al.Human genetics. 1984, Vol 68, Num 4, pp 303-309, issn 0340-6717Article

BRUTON'S AGAMMAGLOBULINEMIA: ETIOLOGY, DIAGNOSIS, AND CLINICAL MANAGEMENTKUMER K; NWANGWU PU.1981; CURR. THER. RES.; ISSN 0011-393X; USA; DA. 1981; VOL. 29; NO 2; PP. 335-342; BIBL. 12 REF.Article

X-LINKED LYMPHOPROLIFERATIVE SYNDROME REGISTRY REPORTHAMILTON JK; PAQUIN LA; SULLIVAN JL et al.1980; J. PEDIATR.; USA; DA. 1980; VOL. 96; NO 4; PP. 669-673; BIBL. 18 REF.Article

Lung transplantation in patients with X-linked agammaglobulinemiaMORALES, P; HERNANDEZ, D; VICENTE, R et al.Transplantation proceedings. 2003, Vol 35, Num 5, pp 1942-1943, issn 0041-1345, 2 p.Conference Paper

Neutropenia associated with X-linked agammaglobulinaemiaKOZLOWSKI, C; EVANS, D. I.Journal of clinical pathology. 1991, Vol 44, Num 5, pp 388-390, issn 0021-9746Article

Congenital X-linked hypogammaglobulinemia and asymptomatic hepatitis B antigen carrier stateWRAY, B. B; FAGUET, G. B; MIDDLETON, H. M. III et al.Journal of allergy and clinical immunology. 1985, Vol 76, Num 3, pp 507-510, issn 0091-6749Article

Serum IgG levels and complement activity in hypogammaglobulinaemic patients under substitution therapyPLEBANI, A; NOTARANGELO, L. D; DUSE, M et al.Clinical and experimental immunology (Print). 1984, Vol 58, Num 1, pp 193-198, issn 0009-9104Article

X-linked agammaglobulinemiaCONLEY, Mary Ellen; ROHRER, Jurg; MINEGISHI, Yoshiyuki et al.Clinical reviews in allergy and immunology. 2000, Vol 19, Num 2, pp 183-204, issn 1080-0549Article

Transcriptional regulatory elements within the first intron of Bruton's tyrosine kinaseROHRER, J; CONLEY, M. E.Blood. 1998, Vol 91, Num 1, pp 214-221, issn 0006-4971Article

Chronic Skin Lesions from a Patient with Bruton's X-Linked AgammaglobulinemiaSHARP, Susan E.Journal of clinical microbiology (Print). 2011, Vol 49, Num 2, issn 0095-1137, 483, 770 [2 p.]Article

Echovirus 11 arthritis in a patient with X-linked agammaglobulinemiaACKERSON, B. K; RAGHUNATHAN, R; KELLER, M. A et al.Pediatric infectious disease. 1987, Vol 6, Num 5, pp 485-488, issn 0277-9730Article

Mapping of a gene for X-linked agammaglobulinemia and evidence for genetic heterogeneityMENSINK, E. J. B. M; THOMPSON, A; SCHOT, J. D. L et al.Human genetics. 1986, Vol 73, Num 4, pp 327-332, issn 0340-6717Article

Coding-region alterations in BTK do not universally cause X-linked agammaglobulinemiaABBOTT, Jordan K; OCHS, Hans D; GELFAND, Erwin W et al.Journal of allergy and clinical immunology. 2013, Vol 132, Num 5, pp 1246-1248, issn 0091-6749, 3 p.Article

SEX-LINKED HYPOGAMMAGLOBULINEMIA AND AMYLOIDOSISPODJARNY E; MEKORI YA; BERNHAIM J et al.1982; ARCH. PATHOL. LAB. MED.; ISSN 0096-8528; USA; DA. 1982; VOL. 106; NO 9; PP. 447-448; BIBL. 14 REF.Article

IMMUNE DEFICIENCY IN THE X-LINKED LYMPHOPROLIFERATIVE SYNDROME. II: IMMUNOREGULATORY T CELL DEFECTSLINDSTEN T; SEELEY JK; BALLOW M et al.1982; JOURNAL OF IMMUNOLOGY; ISSN 0022-1767; USA; DA. 1982; VOL. 129; NO 6; PP. 2536-2540; BIBL. 25 REF.Article

PROGRESSIVE ENCEPHALOPATHY ASSOCIATED WITH X-LINKED AGAMMAGLOBULINEMIASACQUEGNA T; PAZZAGLIA P; BALDRATI A et al.1982; EUR. NEUROL.; ISSN 0014-3022; CHE; DA. 1982; VOL. 21; NO 2; PP. 107-111; BIBL. 9 REF.Article

DIE PHAENAKOPIE EINER PELGER-HUETSCHEN KERNANOMALIE BEI IDIOPATHISCHEM ANTIKOERPERMANGELSYNDROM. = LA PHENOCOPIE D'UNE ANOMALIE NUCLEAIRE DE PELGER-HUET DANS LE SYNDROME DE DEFICIT EN ANTICORPS IDIOPATHIQUERISTER M; BOTTCHER K; GRAMER H et al.1978; KLIN. PAEDIATR.; DTSCH.; DA. 1978; VOL. 190; NO 2; PP. 203-208; ABS. ANGL.; BIBL. 1 P. 1/2Article

CONSIDERAZIONI SU UN CASO DI IPOGAMMAGLOBULINEMIA CONGENITA (MALATTIA DI BRUTON). STUDIO CLINICO, ISTOLOGICO E ULTRASTRUTTURALE. = CONSIDERATIONS SUR UN CAS D'HYPOGAMMAGLOBULINEMIE CONGENITALE (MALADIE DE BRUTON). ETUDE CLINIQUE, HISTOLOGIQUE ET ULTRASTRUCTURALECATALDO F; VALENTINO B; VARRICA D et al.1977; PEDIATRIA; ITAL.; DA. 1977; VOL. 85; NO 1; PP. 84-105; ABS. FR. ANGL. ALLEM. ESP.; BIBL. 1 P.Article

DEFICIT IMMUNITAIRE AVEC MANIFESTATIONS ARTICULAIRES: A PROPOS D'UNE OBSERVATION CHEZ L'ENFANTPAYEN BERNARD.sd; FRA; DA. S.D.; 276; 120 P.; 30 CM; BIBL. 123 REF.; TH.: MED./LILLE/1978Thesis

BRUTON SYNDROME AND CELIAC DISEASEBONAMICO, Margherita; MAGLIOCCA, Fabio Massimo; MENNINI, Maurizio et al.Annals of allergy, asthma, & immunology. 2011, Vol 107, Num 1, pp 86-87, issn 1081-1206, 2 p.Article

X-linked agammaglobulinemia complicated with endobronchial tuberculosisKAWAKAMI, Chihiro; INOUE, Akiko; TAKITANI, Kimitaka et al.Acta paediatrica (Oslo). 2011, Vol 100, Num 3, pp 466-468, issn 0803-5253, 3 p.Article

Female agammaglobulinemia due to the Bruton tyrosine kinase deficiency caused by extremely skewed X-chromosome inactivationTAKADA, Hidetoshi; KANEGANE, Hirokazu; NOMURA, Akihiko et al.Blood. 2004, Vol 103, Num 1, pp 185-187, issn 0006-4971, 3 p.Article

Dermatofibrosarcoma protuberans in a patient with X-linked agammaglobulinaemiaYONG, P. F. K; GROSSE-KREUL, D; MAHER, J et al.Journal of clinical pathology. 2007, Vol 60, Num 10, pp 1162-1164, issn 0021-9746, 3 p.Article

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