WorldCat Identities

van der Burg, Mirjam

Overview
Works: 15 works in 15 publications in 1 language and 67 library holdings
Roles: Editor, Other, Author, Contributor
Publication Timeline
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Most widely held works by Mirjam van der Burg
Application of Cytometry in Primary Immunodeficiencies by T Kalina( )

1 edition published in 2020 in English and held by 34 WorldCat member libraries worldwide

This eBook is a collection of articles from a Frontiers Research Topic. Frontiers Research Topics are very popular trademarks of the Frontiers Journals Series: they are collections of at least ten articles, all centered on a particular subject. With their unique mix of varied contributions from Original Research to Review Articles, Frontiers Research Topics unify the most influential researchers, the latest key findings and historical advances in a hot research area! Find out more on how to host your own Frontiers Research Topic or contribute to one as an author by contacting the Frontiers Editorial Office: frontiersin.org/about/contact
Recombination processes during human B-cell differentiation by Mirjam van der Burg( Book )

1 edition published in 2002 in English and held by 7 WorldCat member libraries worldwide

Editorial: Application of cytometry in primary immunodeficiencies by T Kalina( )

1 edition published in 2020 in English and held by 3 WorldCat member libraries worldwide

PRKDC mutations associated with immunodeficiency, granuloma and aire-dependent autoimmunity by Alexandre Belot( )

1 edition published in 2014 in English and held by 2 WorldCat member libraries worldwide

Low T Cell Numbers Resembling T−B+ SCID in a Patient with Wiskott-Aldrich Syndrome and the Outcome of Two Hematopoietic Stem Cell Transplantations by Deniz Cagdas( )

1 edition published in 2016 in English and held by 2 WorldCat member libraries worldwide

Correction to: Circulating T Cells of Patients with Nijmegen Breakage Syndrome Show Signs of Senescence by Ruud W. J Meijers( )

1 edition published in 2018 in English and held by 2 WorldCat member libraries worldwide

Disturbed B-lymphocytes selection in autoimmune lymphoproliferative syndrome by Aleš Janda( )

1 edition published in 2015 in English and held by 2 WorldCat member libraries worldwide

Circulating T Cells of Patients with Nijmegen Breakage Syndrome Show Signs of Senescence by Ruud W. J Meijers( )

1 edition published in 2016 in English and held by 2 WorldCat member libraries worldwide

An essential role for the Zn2+ transporter ZIP7 in B cell development by Consuelo Anzilotti( )

1 edition published in 2019 in English and held by 2 WorldCat member libraries worldwide

The presence of CLL-associated stereotypic B cell receptors in the normal BCR repertoire from healthy individuals increases with age by Alice F Muggen( )

1 edition published in 2019 in English and held by 2 WorldCat member libraries worldwide

Cost-effectiveness of newborn screening for severe combined immunodeficiency by Catharina P. B Van der Ploeg( )

1 edition published in 2019 in English and held by 2 WorldCat member libraries worldwide

IgM Augments Complement Bactericidal Activity with Serum from a Patient with a Novel CD79a Mutation by Jeroen D Langereis( )

1 edition published in 2018 in English and held by 2 WorldCat member libraries worldwide

An infant with ZAP-70 deficiency with disseminated mycobacterial disease by Saliha Esenboga( )

1 edition published in 2015 in English and held by 2 WorldCat member libraries worldwide

ImmunoGlobulin galaxy (IGGalaxy) for simple determination and quantitation of immunoglobulin heavy chain rearrangements from NGS by Michael J Moorhouse( )

1 edition published in 2014 in English and held by 2 WorldCat member libraries worldwide

Long-Term Follow-Up of Newborns with 22q11 Deletion Syndrome and Low TRECs by Jenny Lingman Framme( )

1 edition published in 2022 in English and held by 1 WorldCat member library worldwide

Background: Population-based neonatal screening using T-cell receptor excision circles (TRECs) identifies infants with profound T lymphopenia, as seen in cases of severe combined immunodeficiency, and in a subgroup of infants with 22q11 deletion syndrome (22q11DS). Purpose: To investigate the long-term prognostic value of low levels of TRECs in newborns with 22q11DS. Methods: Subjects with 22q11DS and low TRECs at birth (22q11Low, N=10), matched subjects with 22q11DS and normal TRECs (22q11Normal, N=10), and matched healthy controls (HC, N=10) were identified. At follow-up (median age 16 years), clinical and immunological characterizations, covering lymphocyte subsets, immunoglobulins, TRECs, T-cell receptor repertoires, and relative telomere length (RTL) measurements were performed. Results: At follow-up, the 22q11Low group had lower numbers of naïve T-helper cells, naïve T-regulatory cells, naïve cytotoxic T cells, and persistently lower TRECs compared to healthy controls. Receptor repertoires showed skewed V-gene usage for naïve T-helper cells, whereas for naïve cytotoxic T cells, shorter RTL and a trend towards higher clonality were found. Multivariate discriminant analysis revealed a clear distinction between the three groups and a skewing towards Th17 differentiation of T-helper cells, particularly in the 22q11Low individuals. Perturbations of B-cell subsets were found in both the 22q11Low and 22q11Normal group compared to the HC group, with larger proportions of naïve B cells and lower levels of memory B cells, including switched memory B cells. Conclusions: This long-term follow-up study shows that 22q11Low individuals have persistent immunologic aberrations and increased risk for immune dysregulation, indicating the necessity of lifelong monitoring. Clinical Implications: This study elucidates the natural history of childhood immune function in newborns with 22q11DS and low TRECs, which may facilitate the development of programs for long-term monitoring and therapeutic choices
 
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Alternative Names
Van der Burg, Mirjam

Languages
English (15)