Ghent University Academic Bibliography

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Your filters: cql: author="Hauck, Fabian" or (type any "bookEditor journalEditor issueEditor" and editor="Hauck, Fab...

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Humans with inherited MyD88 and IRAK-4 deficiencies are predisposed to hypoxemic COVID-19 pneumonia

Ana García-García, Rebeca Pérez de Diego, Carlos Flores, Darawan Rinchai, Jordi Solé-Violán, Àngela Deyà-Martínez, Blanca García-Solis, José M. Lorenzo-Salazar, Elisa Hernández-Brito, Anna-Lisa Lanz, et al.

(2023) JOURNAL OF EXPERIMENTAL MEDICINE. 220(5).
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Activated phosphoinositide 3-kinase δ syndrome : update from the ESID Registry and comparison with other autoimmune-lymphoproliferative inborn errors of immunity

Maria Elena Maccari, Martin Wolkewitz, Charlotte Schwab, Tiziana Lorenzini, Jennifer W. Leiding, Nathalie Aladjdi, Hassan Abolhassani, Wadih Abou-Chahla, Alessandro Aiuti, Saba Azarnoush, et al.

(2023) JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY. 152(4). p.984-996.e10
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Coronavirus disease 2019 in patients with inborn errors of immunity : an international study

Isabelle Meyts, Giorgia Bucciol, Isabella Quinti, Bénédicte Neven, Alain Fischer, Elena Seoane, Eduardo Lopez-Granados, Carla Gianelli, Angel Robles-Marhuenda, Pierre-Yves Jeandel, et al.

(2021) JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY. 147(5). p.520-531
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Initial presenting manifestations in 16,486 patients with inborn errors of immunity include infections and noninfectious manifestations

Julian Thalhammer, Gerhard Kindle, Alexandra Nieters, Stephan Rusch, Mikko R.J. Seppänen, Alain Fische, Bodo Grimbacher, David Edgar, Matthew Buckland, Nizar Mahlaoui, et al.

(2021) JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY. 148(5). p.1332-1341.e5
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Current understanding and future research priorities in malignancy associated with inborn errors of immunity and DNA repair disorders : the perspective of an interdisciplinary working group

Simon Bomken, Jutte van der Werff Ten Bosch, Andishe Attarbaschi, Chris M. Bacon, Arndt Borkhardt, Kaan Boztug, Ute Fischer, Fabian Hauck, Roland P. Kuiper, Tim Lammens (UGent) , et al.

(2018) FRONTIERS IN IMMUNOLOGY. 9.
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Clinical similarities and differences of patients with X-linked lymphoproliferative syndrome type 1 (XLP-1/SAP deficiency) versus type 2 (XLP-2/XIAP deficiency)

Jana Pachlopnik Schmid, Danielle Canioni, Despina Moshous, Fabien Touzot, Nizar Mahlaoui, Fabian Hauck, Hirokazu Kanegane, Eduardo Lopez-Granados, Ester Mejstrikova, Isabelle Pellier, et al.

(2011) BLOOD. 117(5). p.1522-1529

Academic Bibliography

Humans with inherited MyD88 and IRAK-4 deficiencies are predisposed to hypoxemic COVID-19 pneumonia

Activated phosphoinositide 3-kinase δ syndrome : update from the ESID Registry and comparison with other autoimmune-lymphoproliferative inborn errors of immunity

Coronavirus disease 2019 in patients with inborn errors of immunity : an international study

Initial presenting manifestations in 16,486 patients with inborn errors of immunity include infections and noninfectious manifestations

Current understanding and future research priorities in malignancy associated with inborn errors of immunity and DNA repair disorders : the perspective of an interdisciplinary working group

Clinical similarities and differences of patients with X-linked lymphoproliferative syndrome type 1 (XLP-1/SAP deficiency) versus type 2 (XLP-2/XIAP deficiency)

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