M. Hönig

DOCK8 Deficiency: Clinical and Immunological Phenotype and Treatment Options - a Review of 136 Patients

J. Orange, A. Schulz, R. Geha, 2015, Journal of Clinical Immunology.

Prospective Newborn Screening for SCID in Germany: A First Analysis by the Pediatric Immunology Working Group (API)

A. Schulz, S. Ehl, R. Krüger, 2023, Journal of Clinical Immunology.

Successful Haploidentical Hematopoietic Stem Cell Transplantation in a Patient with SCID due to CD3ε Deficiency: Need for IgG-Substitution 6 Years Later

U. Pannicke, K. Schwarz, A. Schulz, 2014, Klinische Pädiatrie.

A multimorphic mutation in IRF4 causes human autosomal dominant combined immunodeficiency

U. Pannicke, K. Schwarz, J. Casanova, 2023, Science Immunology.

Long-term outcome and lineage-specific chimerism in 194 patients with Wiskott-Aldrich syndrome treated by hematopoietic cell transplantation in the period 1980-2009: an international collaborative study

A. Fischer, A. Schulz, W. Friedrich, 2011 .

Hematopoietic Stem Cell Transplantation for Severe Combined Immunodeficiency

W. Friedrich, M. Hönig, A. Schulz, 2011, Klinische Pädiatrie.

[Newborn screening for severe combined immunodeficiencies (SCID) in Germany].

Sujal Ghosh, C. Schütz, M. Hönig, 2023, Bundesgesundheitsblatt, Gesundheitsforschung, Gesundheitsschutz.