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Pediatric Cardiology|July 19, 2022
Into the Blue: First in Man Data on Diving Physiology in Fontan PatientsC Paech, R A Gebauer, M Weidenbach, et al.
European Journal of Immunology|March 15, 2011
Functional type 1 regulatory T cells develop regardless of FOXP3 mutations in patients with IPEX syndromeLaura Passerini, Sara Di Nunzio, Silvia Gregori, et al.
The Journal of Antimicrobial Chemotherapy|May 25, 2013
Age- and gender-related differences in teicoplanin levels in paediatric patientsVolker Strenger, Nora Hofer, Siegfried Rödl, et al.
Journal of Medical Genetics|January 17, 2014
A novel immunodeficiency syndrome associated with partial trisomy 19p13Markus G Seidel, Celia Duerr, Stavroula Woutsas, et al.
The Journal of Experimental Medicine|December 10, 2009
Nfil3/E4bp4 is required for the development and maturation of NK cells in vivoShintaro Kamizono, Gordon S Duncan, Markus G Seidel, et al.
Klinische Padiatrie|November 13, 2012
Fatal EBV infection and variable clinical manifestations in an XLP-1 pedigree - rapid diagnosis of primary immunodeficiencies may save livesD Sperl, M Benesch, C Urban, et al.
Surgery|February 27, 2024
Optimizing antibiotic management for patients with acute appendicitis: A quality improvement studyJason Beckermann, Maria E Linnaus, Hayden Swartz, et al.
Journal of Medical Genetics|November 10, 2019
Novel phenotypes observed in patients with ETV6-linked leukaemia/familial thrombocytopenia syndrome and a biallelic ARID5B risk allele as leukaemogenic cofactorAnna Karastaneva, Karin Nebral, Axel Schlagenhauf, et al.
The Journal of Allergy and Clinical Immunology|December 17, 2021
Phenotype, genotype, treatment, and survival outcomes in patients with X-linked inhibitor of apoptosis deficiencyLinlin Yang, Claire Booth, Carsten Speckmann, et al.
Frontiers in Immunology|September 12, 2019
Repertoire Sequencing of B Cells Elucidates the Role of UNG and Mismatch Repair Proteins in Somatic Hypermutation in HumansHanna IJspeert, Pauline A van Schouwenburg, Ingrid Pico-Knijnenburg, et al.
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