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Publications from 2017

2017
J Allergy Clin Immunol
Hemophagocytic lymphohistiocytosis as presenting manifestation of profound combined immunodeficiency due to an ORAI1 mutation.
C. Klemann, S. Ammann, M. Heizmann, S. Fuchs, S. F. Bode, M. Heeg, H. Fuchs, K. Lehmberg, U. Zur Stadt, C. Roll, T. Vraetz, C. Speckmann, M. R. Lorenz, K. Schwarz, J. Rohr, S. Feske, and S. Ehl.
DOI
2017
Eur J Immunol
Primary and secondary hemophagocytic lymphohistiocytosis have different patterns of T-cell activation, differentiation and repertoire.
S. Ammann, K. Lehmberg, U. Zur Stadt, G. Janka, A. Rensing-Ehl, C. Klemann, M. Heeg, S. Bode, I. Fuchs, S. Ehl, and H. L. H. s. o. t. GPOH.
DOI

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