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Publications tagged Hemo­phago­cytic Lympho­histio­cytosis

2020
J Clin Immunol
Neuroinflammatory Disease as an Isolated Manifestation of Hemophagocytic Lymphohistiocytosis.
A. Blincoe, M. Heeg, P. K. Campbell, M. Hines, A. Khojah, M. Klein-Gitelman, J. A. Talano, C. Speckmann, F. Touzot, A. Lankester, G. E. Legger, J. G. Riviere, M. Garcia-Prat, L. Alonso, M. C. Putti, K. Lehmberg, S. Maier, Y. El Chazli, M. A. Elmaksoud, I. Astigarraga, N. Kurjane, I. Bulina, V. Kenina, Y. Bryceson, J. Rascon, A. Lortie, G. Goldstein, C. Booth, A. Worth, E. Wassmer, E. G. Schmitt, J. T. Warren, J. J. Bednarski, S. Ali, K. Y. Chiang, J. Krueger, M. M. Henry, S. M. Holland, R. A. Marsh, S. Ehl, and E. Haddad.
DOI
2018
Pediatr Blood Cancer
Is an infectious trigger always required for primary hemophagocytic lymphohistiocytosis? Lessons from in utero and neonatal disease.
M. Heeg, S. Ammann, C. Klemann, M. Panning, V. Falcone, H. Hengel, K. Lehmberg, U. Zur Stadt, K. Wustrau, G. Janka, and S. Ehl.
DOI
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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