Failure To Detect Circulating Aspergillus Markers in a Patient with Chronic Granulomatous Disease and Invasive Aspergillosis

od Verweij, Paul E., Weemaes, Corry M., Curfs, Jo H. A. J., Bretagne, Stephane, Meis, Jacques F. G. M.
Wydane 2000

The DNMT3B DNA methyltransferase gene is mutated in the ICF immunodeficiency syndrome

od Hansen, R. Scott, Wijmenga, Cisca, Luo, Ping, Stanek, Ann M., Canfield, Theresa K., Weemaes, Corry M. R., Gartler, Stanley M.
Wydane 1999

IgM Augments Complement Bactericidal Activity with Serum from a Patient with a Novel CD79a Mutation

od Langereis, Jeroen D., Henriet, Stefanie S, Kuipers, Saskia, Weemaes, Corry M.R., van der Burg, Mirjam, de Jonge, Marien I., van der Flier, Michiel
Wydane w J Clin Immunol (2018)

Normal Numbers of Stem Cell Memory T Cells Despite Strongly Reduced Naive T Cells Support Intact Memory T Cell Compartment in Ataxia Telangiectasia

od Weitering, Thomas J., Melsen, Janine E., van Ostaijen-ten Dam, Monique M., Weemaes, Corry M. R., Schilham, Marco W., van der Burg, Mirjam
Wydane w Front Immunol (2021)

Hyper-Immunoglobulin A in the Hyperimmunoglobulinemia D Syndrome

od Klasen, Ina S., Göertz, Joop H. C., van de Wiel, Gertrude A. S., Weemaes, Corry M. R., van der Meer, Jos W. M., Drenth, Joost P. H.
Wydane 2001

Dilemma of Reporting Incidental Findings in Newborn Screening Programs for SCID: Parents’ Perspective on Ataxia Telangiectasia

od Blom, Maartje, Schoenaker, Michiel H. D., Hulst, Myrthe, de Vries, Martine C., Weemaes, Corry M. R., Willemsen, Michèl A. A. P., Henneman, Lidewij, van der Burg, Mirjam
Wydane w Front Immunol (2019)

Immunodeficiency in Bloom’s Syndrome

od Schoenaker, Michiel H. D., Henriet, Stefanie S., Zonderland, Jip, van Deuren, Marcel, Pan-Hammarström, Qiang, Posthumus-van Sluijs, Sandra J., Pico-Knijnenburg, Ingrid, Weemaes, Corry M. R., IJspeert, Hanna
Wydane w J Clin Immunol (2017)

Dysarthria in children and adults with ataxia telangiectasia

od Veenhuis, Stefanie J G, van OS, Nienke J H, van Gerven, Marjo H J C, van Haaften, Leenke, Mulder, Elisabeth H, Weemaes, Corry M R, Willemsen, Michèl A A P
Wydane w Dev Med Child Neurol (2021)

Classic ataxia-telangiectasia: the phenotype of long-term survivors

od van Os, Nienke J. H., van Deuren, Marcel, Weemaes, Corry M. R., van Gaalen, Judith, Hijdra, Helma, Taylor, Alexander M. R., van de Warrenburg, Bart P. C., Willemsen, Michèl A. A. P.
Wydane w J Neurol (2019)

Mutations in ZBTB24 Are Associated with Immunodeficiency, Centromeric Instability, and Facial Anomalies Syndrome Type 2

od de Greef, Jessica C., Wang, Jun, Balog, Judit, den Dunnen, Johan T., Frants, Rune R., Straasheijm, Kirsten R., Aytekin, Caner, van der Burg, Mirjam, Duprez, Laurence, Ferster, Alina, Gennery, Andrew R., Gimelli, Giorgio, Reisli, Ismail, Schuetz, Catharina, Schulz, Ansgar, Smeets, Dominique F.C.M., Sznajer, Yves, Wijmenga, Cisca, van Eggermond, Marja C., van Ostaijen-ten Dam, Monique M., Lankester, Arjan C., van Tol, Maarten J.D., van den Elsen, Peter J., Weemaes, Corry M., van der Maarel, Silvère M.
Wydane 2011