Ghent University Academic Bibliography

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Machine learning–assisted diagnosis classification of primary immune dysregulation using IDDA2.1 phenotype profiling

Malte Schwitzkowski, Sai Pavan Kumar Veeranki, Benedikt N. Seidel, Gerhard Kindle, Stephan Rusch, Dalia Abd Elaziz, Sohilla Lofty M. Abdelkader, Avigaelle Abitbol, Hassan Abolhassani, Lalash Abrahim, et al.

(2026) JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY. 157(2). p.470-485
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Recommendations for transitioning young people with primary immunodeficiency disorders and autoinflammatory diseases to adult care

Muskan Israni, Eliska Alderson, Nizar Mahlaoui, Laura Obici, Linda Rossi-Semerano, Helen Lachmann, Mojca Zajc Avramovič, Aurelien Guffroy, Virgil Dalm, Rachel Rimmer, et al.

(2025) JOURNAL OF CLINICAL IMMUNOLOGY. 45(1).
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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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Autoantibodies against type I IFNs in humans with alternative NF-κB pathway deficiency

Tom Le Voyer, Audrey V. Parent, Xian Liu, Axel Cederholm, Adrian Gervais, Jérémie Rosain, Tina Nguyen, Malena Perez Lorenzo, Elze Rackaityte, Darawan Rinchai, et al.

(2023) NATURE. 623(7988). p.803-813
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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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Outcome of hematopoietic stem cell transplantation for adenosine deaminase-deficient severe combined immunodeficiency

Amel Hassan, Claire Booth, Alex Brightwell, Zoe Allwood, Paul Veys, Kanchan Rao, Manfred Hönig, Wilhelm Friedrich, Andrew Gennery, Mary Slatter, et al.

(2012) BLOOD. 120(17). p.3615-3624
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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

Machine learning–assisted diagnosis classification of primary immune dysregulation using IDDA2.1 phenotype profiling

Recommendations for transitioning young people with primary immunodeficiency disorders and autoinflammatory diseases to adult care

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

Autoantibodies against type I IFNs in humans with alternative NF-κB pathway deficiency

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

Outcome of hematopoietic stem cell transplantation for adenosine deaminase-deficient severe combined immunodeficiency

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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