Alexander Leiss-Piller

Disease Progression of WHIM Syndrome in an International Cohort of 66 Pediatric and Adult Patients

Shannon M. McNulty, J. Walter, H. Kanegane, 2022, Journal of Clinical Immunology.

Hypomorphic Mutations in the BCR Signalosome Lead to Selective Immunoglobulin M Deficiency and Impaired B-cell Homeostasis

M. Eibl, H. Wolf, M. Fischer, 2018, Front. Immunol..

SCID and Other Inborn Errors of Immunity with Low TRECs — the Brazilian Experience

J. Walter, H. Ochs, T. Torgerson, 2022, Journal of Clinical Immunology.

Case Report: Meningoencephalitis With Thrombotic Occlusive Vasculopathy in a Young EBV-Naïve Boy Is Associated With a Novel SH2D1A Mutation

J. Hainfellner, W. Schmidt, M. Eibl, 2021, Frontiers in Immunology.

The Clinical and Genetic Spectrum of 82 Patients With RAG Deficiency Including a c.256_257delAA Founder Variant in Slavic Countries

M. van der Burg, L. Notarangelo, J. Walter, 2020, Frontiers in Immunology.

Case Report: A Novel IL2RG Frame-Restoring Rescue Mutation Mimics Early T Cell Engraftment Following Haploidentical Hematopoietic Stem Cell Transplantation in a Patient With X-SCID

M. Eibl, H. Wolf, A. Lawitschka, 2021, Frontiers in Immunology.

Biallelic Cys141Tyr variant of SEL1L is associated with neurodevelopmental disorders, agammaglobulinemia, and premature death

L. Danišovič, Denisa Weis, R. Feichtinger, 2023, The Journal of clinical investigation.