The 11q Terminal Deletion Disorder Jacobsen Syndrome is a Syndromic Primary Immunodeficiency

Por Dalm, Virgil A. S. H., Driessen, Gertjan J. A., Barendregt, Barbara H., van Hagen, Petrus M., van der Burg, Mirjam
Publicado no J Clin Immunol (2015)

A reversion of an IL2RG mutation in combined immunodeficiency providing competitive advantage to the majority of CD8(+) T cells

Por Kuijpers, Taco W., van Leeuwen, Ester M.M., Barendregt, Barbara H., Klarenbeek, Paul, aan de Kerk, Daan J., Baars, Paul A., Jansen, Machiel H., de Vries, Niek, van Lier, René A.W., van der Burg, Mirjam
Publicado em 2013

A new type of radiosensitive T(–)B(–)NK(+) severe combined immunodeficiency caused by a LIG4 mutation

Por van der Burg, Mirjam, van Veelen, Lieneke R., Verkaik, Nicole S., Wiegant, Wouter W., Hartwig, Nico G., Barendregt, Barbara H., Brugmans, Linda, Raams, Anja, Jaspers, Nicolaas G.J., Zdzienicka, Malgorzata Z., van Dongen, Jacques J.M., van Gent, Dik C.
Publicado em 2006

Common variable immunodeficiency and idiopathic primary hypogammaglobulinemia: two different conditions within the same disease spectrum

Por Driessen, Gertjan J., Dalm, Virgil A.S.H., van Hagen, P. Martin, Grashoff, H. Anne, Hartwig, Nico G., van Rossum, Annemarie M. C., Warris, Adilia, de Vries, Esther, Barendregt, Barbara H., Pico, Ingrid, Posthumus, Sandra, van Zelm, Menno C., van Dongen, Jacques J.M., van der Burg, Mirjam
Publicado em 2013

B-cell development and functions and therapeutic options in adenosine deaminase–deficient patients

Por Brigida, Immacolata, Sauer, Aisha V., Ferrua, Francesca, Giannelli, Stefania, Scaramuzza, Samantha, Pistoia, Valentina, Castiello, Maria Carmina, Barendregt, Barbara H., Cicalese, Maria Pia, Casiraghi, Miriam, Brombin, Chiara, Puck, Jennifer, Müller, Klaus, Notarangelo, Lucia Dora, Montin, Davide, van Montfrans, Joris M., Roncarolo, Maria Grazia, Traggiai, Elisabetta, van Dongen, Jacques J. M., van der Burg, Mirjam, Aiuti, Alessandro
Publicado no J Allergy Clin Immunol (2014)