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1. Genotype–phenotype study of familial haemophagocytic lymphohistiocytosis type 3. Issue 5 (19th January 2011)

5. Is an infectious trigger always required for primary hemophagocytic lymphohistiocytosis? Lessons from in utero and neonatal disease. Issue 11 (1st August 2018)

7. Lack of bone lesions at diagnosis is associated with inferior outcome in multisystem langerhans cell histiocytosis of childhood. (18th December 2014)

8. Langerhans cell histiocytosis (LCH): Guidelines for diagnosis, clinical work‐up, and treatment for patients till the age of 18 years1. Issue 2 (25th October 2012)

10. Primary and secondary hemophagocytic lymphohistiocytosis have different patterns of T‐cell activation, differentiation and repertoire. Issue 2 (3rd January 2017)