Ghent University Academic Bibliography

Your filters: cql: author=" Bossuyt, Xavier" or (type any "bookEditor issueEditor" and editor=" Bossuyt, Xavier")

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AD hyper-IgE syndrome due to a novel loss-of-function mutation in STAT3 : a diagnostic pursuit won by clinical acuity

Leen Moens, Heidi Schaballie (UGent) , Barbara Bosch, Arnout Voet, Xavier Bossuyt, Jean-Laurent Casanova, Stephanie Boisson-Dupuis, Stuart G. Tangye and Isabelle Meyts

(2017) JOURNAL OF CLINICAL IMMUNOLOGY. 37(1). p.12-17
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- Journal Article
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Homozygous N-terminal missense mutation in TRNT1 leads to progressive B-cell immunodeficiency in adulthood

Glynis Frans, Leen Moens, Heidi Schaballie (UGent) , Greet Wuyts, Adrian Liston, Koen Poesen, Ann Janssens, Gillian I. Rice, Yanick J. Crow, Isabelle Meyts, et al.

(2017) JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY. 139(1). p.360-363.e6
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Fifth percentile cutoff values for antipneumococcal polysaccharide and anti-salmonella typhi Vi IgG describe a normal polysaccharide response

Heidi Schaballie (UGent) , Barbara Bosch, Rik Schrijvers, Marijke Proesmans, Kris De Boeck, Mieke Nelly Boon, Francois Vermeulen, Natalie Lorent, Doreen Dillaerts, Glynis Frans, et al.

(2017) FRONTIERS IN IMMUNOLOGY. 8.
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A novel hypomorphic mutation in STIM1 results in a late-onset immunodeficiency

Heidi Schaballie (UGent) , Remy Rodriguez, Emmanuel Martin, Leen Moens, Glynis Frans, Christelle Lenoir, Joris Dutre, Danielle Canioni, Xavier Bossuyt, Alain Fischer, et al.

(2015) JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY. 136(3). p.816-819.e4
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Hematopoietic stem cell transplantation rescues the immunologic phenotype and prevents vasculopathy in patients with adenosine deaminase 2 deficiency

Lien Van Eyck, Michael S. Hershfield, Diana Pombal, Susan J. Kelly, Nancy J. Ganson, Leen Moens, Glynis Frans, Heidi Schaballie (UGent) , Gert De Hertogh, James Dooley, et al.

(2015) JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY. 135(1). p.283-287.e5
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Gain-of-function mutations in signal transducer and activator of transcription 1 (STAT1) : chronic mucocutaneous candidiasis accompanied by enamel defects and delayed dental shedding

Glynis Frans, Leen Moens, Heidi Schaballie (UGent) , Lien Van Eyck, Heleen Borgers, Margareta Wuyts, Doreen Dillaerts, Edith Vermeulen, James Dooley, Bodo Grimbacher, et al.

(2014) JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY. 134(5). p.1209-1213

Academic Bibliography

AD hyper-IgE syndrome due to a novel loss-of-function mutation in STAT3 : a diagnostic pursuit won by clinical acuity

Homozygous N-terminal missense mutation in TRNT1 leads to progressive B-cell immunodeficiency in adulthood

Fifth percentile cutoff values for antipneumococcal polysaccharide and anti-salmonella typhi Vi IgG describe a normal polysaccharide response

A novel hypomorphic mutation in STIM1 results in a late-onset immunodeficiency

Hematopoietic stem cell transplantation rescues the immunologic phenotype and prevents vasculopathy in patients with adenosine deaminase 2 deficiency

Gain-of-function mutations in signal transducer and activator of transcription 1 (STAT1) : chronic mucocutaneous candidiasis accompanied by enamel defects and delayed dental shedding

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