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European Journal of Immunology|December 8, 2016
Primary and secondary hemophagocytic lymphohistiocytosis have different patterns of T-cell activation, differentiation and repertoireSandra Ammann, Kai Lehmberg, Udo Zur Stadt, et al.
Acta Paediatrica (Oslo, Norway : 1992)|October 25, 2011
Risk factors for early death in children with haemophagocytic lymphohistiocytosisHelena Trottestam, Elisabet Berglöf, AnnaCarin Horne, et al.
Pediatric Blood & Cancer|August 3, 2018
Is an infectious trigger always required for primary hemophagocytic lymphohistiocytosis? Lessons from in utero and neonatal diseaseMaximilian Heeg, Sandra Ammann, Christian Klemann, et al.
Annals of Hematology|November 27, 2012
Administration of recombinant erythropoietin alone does not improve the phenotype in iron refractory iron deficiency anemia patientsKai Lehmberg, Regine Grosse, Martina U Muckenthaler, et al.
Blood Advances|October 7, 2022
MAP kinase activating death domain deficiency is a novel cause of impaired lymphocyte cytotoxicityKerstin Schütze, Miriam Groß, Kerstin Cornils, et al.
Haematologica|October 29, 2013
Treosulfan-based conditioning regimen for children and adolescents with hemophagocytic lymphohistiocytosisKai Lehmberg, Michael H Albert, Rita Beier, et al.
Molecular and Cellular Pediatrics|June 30, 2026
Diagnostic value of basic and extended procedures in pediatric fever of unknown origin - results of a nation-wide surveillance studyMira Katarina Bienioschek, Alice Lejeune, Gonza Ngoumou, et al.
Frontiers in Immunology|May 27, 2021
Case Report: Hemophagocytic Lymphohistiocytosis and Non-Tuberculous Mycobacteriosis Caused by a Novel GATA2 VariantThomas Mika, Deepak Vangala, Matthias Eckhardt, et al.
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