Stephan Borte

Syndromic Inborn Errors of Immunity in TREC-Newborn Screening: 5-year Experience from the German Screening Program

Conversion of monoclonal IgG to dimeric and secretory IgA restores neutralizing ability and prevents infection of Omicron lineages

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

Genomic characterization of lymphomas in patients with inborn errors of immunity

Point-of-care bulk testing for SARS-CoV-2 by combining hybridization capture with improved colorimetric LAMP

Gut Microbiota Perturbation in IgA Deficiency Is Influenced by IgA-Autoantibody Status

The German National Registry of Primary Immunodeficiencies (2012–2017)

Impaired polysaccharide responsiveness without agammaglobulinaemia in three patients with hypomorphic mutations in <i>Bruton Tyrosine Kinase</i>—No detection by newborn screening for primary immunodeficiencies

Microcephaly, short stature, and limb abnormality disorder due to novel autosomal biallelic DONSON mutations in two German siblings

Combined immunodeficiency and Epstein-Barr virus–induced B cell malignancy in humans with inherited CD70 deficiency

Newborn Screening for Severe Primary Immunodeficiency Diseases in Sweden—a 2-Year Pilot TREC and KREC Screening Study

The Extended Clinical Phenotype of 26 Patients with Chronic Mucocutaneous Candidiasis due to Gain-of-Function Mutations in STAT1

Novel mutations in TNFRSF7/CD27: Clinical, immunologic, and genetic characterization of human CD27 deficiency

Prospective neonatal screening for severe T‐ and B‐lymphocyte deficiencies in Seville

SYK expression endows human ZAP70-deficient CD8 T cells with residual TCR signaling

Clinical picture and treatment of 2212 patients with common variable immunodeficiency

RAC2 loss-of-function mutation in 2 siblings with characteristics of common variable immunodeficiency

Eight-color immunophenotyping of T-, B-, and NK-cell subpopulations for characterization of chronic immunodeficiencies

Eight color immunophenotyping of T-, B- and NK-cell subpopulations for characterization of chronic immunodeficiencies

The Case for Mandatory Newborn Screening for Severe Combined Immunodeficiency (SCID)

Deficiency of Innate and Acquired Immunity Caused by an <i>IKBKB</i> Mutation

The German national registry for primary immunodeficiencies (PID)

Guidelines for newborn screening of primary immunodeficiency diseases