Enterovirus antibody titers after IVIG replacement in agammaglobulinemic childrenGALAMA, J. M. D; GIELEN, M; WEEMAES, C. M. R et al.Clinical microbiology and infection. 2000, Vol 6, Num 11, pp 630-632, issn 1198-743XArticle

Skin manifestations in congenital deficiency of leucocyte-adherence glycoproteins (CDLG)VAN DE KERKHOF, P. C. M; WEEMAES, C. M. R.British journal of dermatology (1951). 1990, Vol 129, Num 3, pp 395-401, issn 0007-0963, 7 p.Article

Ataxia―telangiectasia patients presenting with hyper-IgM syndromeNOORDZIJ, J. G; WULFFRAAT, N. M; HARALDSSON, A et al.Archives of disease in childhood. 2009, Vol 94, Num 6, pp 448-449, issn 0003-9888, 2 p.Article

Neuromuscular abnormalities in taxia telangiectasia : A clinical, electrophysiological and muscle ultrasound studyVERHAGEN, M. M. M; VAN ALFEN, N; PILLEN, S et al.Neuropediatrics. 2007, Vol 38, Num 3, pp 117-121, issn 0174-304X, 5 p.Article

Clinical and virologic response to combination treatment with indinavir, zidovudine, and lamivudine in children with human immunodeficiency virus-1 infection : A multicenter study in The NetherlandsVAN RASSUM, A. M. C; NIESTERS, H. G. M; HOP, W. C. J et al.The Journal of pediatrics. 2000, Vol 136, Num 6, pp 780-788, issn 0022-3476Article

Cerebrospinal fluid examinations in cryptogenic West and Lennox-Gastaut syndrome before and after intravenous immunoglobulin administrationVAN ENGELEN, B. G. M; RENIER, W. O; WEEMAES, C. M. R et al.Epilepsy research. 1994, Vol 18, Num 2, pp 139-147, issn 0920-1211Article

Immunoglobulin G, A and M light chain ratio in childrenHARALDSSON, A; WEEMAES, C. M. R; KOCK-JANSEN, M. J. H et al.Annals of clinical biochemistry. 1992, Vol 29, pp 271-274, issn 0004-5632, 3Article

Increased expression of interleukin-13 but not interleukin-4 in CD4⁺ cells from patients with the hyper-IgE syndromeGUDMUNDSSON, K. O; SIGURJONSSON, O. E; GUDMUNDSSON, S et al.Clinical and experimental immunology (Print). 2002, Vol 128, Num 3, pp 532-537, issn 0009-9104Article

High-dose intravenous immunoglobulin treatment in cryptogenic West and Lennox-Gastaut syndrome ; and add-on studyVAN ENGELEN, B. G. M; RENIER, W. O; WEEMAES, C. M. R et al.European journal of pediatrics. 1994, Vol 153, Num 10, pp 762-769, issn 0340-6199Article

ICF syndrome : a new case and review of the literatureSMEETS, D. F. C. M; MOOG, U; WEEMAES, C. M. R et al.Human genetics. 1994, Vol 94, Num 3, pp 240-246, issn 0340-6717Article

Light chain ratios and concentrations of serum immunoglobulins in children with epilepsyHARALDSSON, A; VAN ENGELEN, B. G. M; RENIER, W. O et al.Epilepsy research. 1992, Vol 13, Num 3, pp 255-260, issn 0920-1211Article

Immunological studies in the hyper-immunoglobulin D syndromeHARALDSSON, A; WEEMAES, C. M. R; DE BOER, A. W et al.Journal of clinical immunology. 1992, Vol 12, Num 6, pp 424-428, issn 0271-9142Article

Familial selective IgA deficiency with circulating Anti-IgA antibodies : a distinct group of patients ?DE LAAT, P. C. J; WEEMAES, C. M. R; BAKKEREN, J. A. J. M et al.Clinical immunology and immunopathology (Print). 1991, Vol 58, Num 1, pp 92-101, issn 0090-1229, 10 p.Article

Critical aneurysmal dilatation of the thoracic aorta in young adolescents with variant hyperimmunoglobulin e syndromeVAN DER MEER, J. W. M; WEEMAES, C. M. R; VAN KRIEKEN, J. H et al.Journal of internal medicine. 2006, Vol 259, Num 6, pp 615-618, issn 0954-6820, 4 p.Article

Distal spinal muscular atrophy as a major feature in adult-onset ataxia telangiectasiaHIEL, J. A. P; VAN ENGELEN, B. G. M; LAST, J. I et al.Neurology. 2006, Vol 67, Num 2, pp 346-349, issn 0028-3878, 4 p.Article

Common variable immunodeficiency (CVID) in a family : an autosomal dominant mode of inheritanceNIJENHUIS, T; KLASEN, I; WEEMAES, C. M. R et al.Netherlands journal of medicine. 2001, Vol 59, Num 3, pp 134-139, issn 0300-2977Article

Serologic HLA typing in cryptogenic Lennox-Gastaut syndromeVAN ENGELEN, B. G. M; DE WAAL, L. P; WEEMAES, C. M. R et al.Epilepsy research. 1994, Vol 17, Num 1, pp 43-47, issn 0920-1211Article

Immunoglobulin G, A, and M light chain ratios in some humoral immunological disordersHARALDSSON, A; JAMINON, M; BAKKEREN, J. A. J. M et al.Scandinavian journal of immunology (Print). 1992, Vol 36, Num 1, pp 57-61, issn 0300-9475Article

Clinical manifestations in selective IgA deficiency in childhood : a follow-up reportDE LAAT, P. C. J; WEEMAES, C. M. R; GONERA, R et al.Acta paediatrica scandinavica. 1991, Vol 80, Num 8-9, pp 798-804, issn 0001-656XArticle

Nephelometry of the kappa/lambda light-chain ratio in serum of normal and diseased childrenRENCKENS, A. L. J. M; JANSEN, M. J. H; VAN MUNSTER, P. J. J et al.Clinical chemistry (Baltimore, Md.). 1986, Vol 32, Num 12, pp 2147-2149, issn 0009-9147Article

Clinical spectrum of immunodeficiency, centromeric instability and facial dysmorphism (ICF syndrome)HAGLEITNER, M. M; LANKESTER, A; DE GROOT, R et al.Journal of medical genetics. 2008, Vol 45, Num 2, pp 93-99, issn 0022-2593, 7 p.Article

Increased urinary leukotriene E₄ during febrile attacks in the hyperimmunoglobulinaemia D and periodic fever syndromeFRENKEL, J; WILLEMSEN, M. A. A. P; WEEMAES, C. M. R et al.Archives of disease in childhood. 2001, Vol 85, Num 2, pp 158-159, issn 0003-9888Article

CD4 deficiency in myelodysplastic syndrome with monosomy 7WEEMAES, C. M. R; PREIJERS, F; DE VAAN, G. A. M et al.European journal of pediatrics. 1996, Vol 155, Num 2, pp 96-98, issn 0340-6199Conference Paper

Light chain ratios and concentrations of immunoglobulins G, A, and M in childhood common acute lymphoblastic leukemiaHARALDSSON, A; DE VAAN, G. A. M; VAN DIJK, W. J et al.Pediatric hematology and oncology. 1994, Vol 11, Num 1, pp 83-90, issn 0888-0018Article

Absent thumb, immune, disorder, and congenital anemia presenting with hydrops fetalisSEMMEKROT, B. A; HARALDSSON, A; WEEMAES, C. M. R et al.American journal of medical genetics. 1992, Vol 42, Num 5, pp 736-740, issn 0148-7299Article