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The Journal of Pediatrics|January 22, 2013
Differentiating macrophage activation syndrome in systemic juvenile idiopathic arthritis from other forms of hemophagocytic lymphohistiocytosisKai Lehmberg, Isabell Pink, Christine Eulenburg, et al.
Annals of Hematology|July 15, 2026
Simultaneous onset of familial hemophagocytic lymphohistiocytosis and T-cell large granular lymphocytic leukemia in an adultFriederike Dierks, Finn-Ole Paulsen, Kai Lehmberg, et al.
Arthritis Research & Therapy|June 12, 2012
Recent advances in the diagnosis and treatment of hemophagocytic lymphohistiocytosisSebastian Fn Bode, Kai Lehmberg, Andrea Maul-Pavicic, et al.
Zeitschrift Fur Geburtshilfe Und Neonatologie|July 8, 2016
Inherited Thrombotic Thrombocytopenic Purpura (Upshaw Schulman Syndrome) as Differential Diagnosis to Neonatal Septicaemia with Disseminated Intravascular Coagulation - a Case SeriesKai Lehmberg, Wolf A Hassenpflug, Ilka Klaassen, et al.
The Laryngoscope|June 1, 2012
Fulminant Epstein-Barr virus-associated hemophagocytic lymphohistiocytosisSilvia Bohne, Karim Kentouche, Iver Petersen, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 7, 2013
Syntaxin binding mechanism and disease-causing mutations in Munc18-2Yvonne Hackmann, Stephen C Graham, Stephan Ehl, et al.
Frontiers in Immunology|September 17, 2024
Case report: Granulocyte-macrophage colony-stimulating factor sargramostim did not rescue the neutrophil phenotype in two patients with JAGN1-mutant severe congenital neutropeniaSusan Farmand, Susanne Eva Aydin, Katharina Wustrau, et al.
Frontiers in Pediatrics|November 16, 2020
Tuberculosis-Associated HLH in an 8-Month-Old Infant: A Case Report and ReviewHolger Hauch, Susanne Skrzypek, Wilhelm Woessmann, et al.
Blood Advances|March 31, 2026
Digenic and Multigenic Heterozygous FHL Genotypes Are Common but Clinically Silent in the General PopulationOleg Borisov, Jasmin Mann, Kevin Kim Walz, et al.
Journal of Pediatric Gastroenterology and Nutrition|December 9, 2025
Acute severe cholestatic hepatitis and lymphopenia characterize pediatric hepatitis-associated aplastic anemiaDaniel Tegtmeyer, Sofia Tsaka, Kai Lehmberg, et al.
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