PAEDIATRIC ONCOLOGY
Karolinska University Hospital
Estocolmo, SueciaPublications in collaboration with researchers from Karolinska University Hospital (12)
2024
2021
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Additive Prognostic Impact of Gastrointestinal Involvement in Severe Multisystem Langerhans Cell Histiocytosis
Journal of Pediatrics, Vol. 237, pp. 65-70.e3
2020
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Neuroinflammatory Disease as an Isolated Manifestation of Hemophagocytic Lymphohistiocytosis
Journal of Clinical Immunology, Vol. 40, Núm. 6, pp. 901-916
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Stem cell transplantation for children with hemophagocytic lymphohistiocytosis: Results from the HLH-2004 study
Blood Advances, Vol. 4, Núm. 15, pp. 3754-3766
2018
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Recommendations for the Use of Etoposide-Based Therapy and Bone Marrow Transplantation for the Treatment of HLH: Consensus Statements by the HLH Steering Committee of the Histiocyte Society
Journal of Allergy and Clinical Immunology: In Practice, Vol. 6, Núm. 5, pp. 1508-1517
2017
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Confirmed efficacy of etoposide and dexamethasone in HLH treatment: Long-Term results of the cooperative HLH-2004 study
Blood, Vol. 130, Núm. 25, pp. 2728-2738
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Development and Initial Validation of the Macrophage Activation Syndrome/Primary Hemophagocytic Lymphohistiocytosis Score, a Diagnostic Tool that Differentiates Primary Hemophagocytic Lymphohistiocytosis from Macrophage Activation Syndrome
Journal of Pediatrics, Vol. 189, pp. 72-78.e3
2016
2015
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Lack of bone lesions at diagnosis is associated with inferior outcome in multisystem langerhans cell histiocytosis of childhood
British Journal of Haematology, Vol. 169, Núm. 2, pp. 241-248
2014
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Performance of current guidelines for diagnosis of macrophage activation syndrome complicating systemic juvenile idiopathic arthritis
Arthritis and Rheumatology, Vol. 66, Núm. 10, pp. 2871-2880
2013
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Therapy prolongation improves outcome in multisystem Langerhans cell histiocytosis
Blood, Vol. 121, Núm. 25, pp. 5006-5014
2007
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Simultaneous manifestation of fulminant infectious mononucleosis with haemophagocytic syndrome and B-cell lymphoma in X-linked lymphoproliferative disease
European Journal of Pediatrics, Vol. 166, Núm. 6, pp. 589-593