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The Journal of Rheumatology|February 16, 2021
Efficacy of Moderately Dosed Etoposide in Macrophage Activation Syndrome-Hemophagocytic LymphohistiocytosisAnnaCarin Horne, Tatiana von Bahr Greenwood, Samuel C C Chiang, et al.The Journal of Pediatrics|June 19, 2021
Additive Prognostic Impact of Gastrointestinal Involvement in Severe Multisystem Langerhans Cell HistiocytosisMilen Minkov, Ulrike Pötschger, Nirav Thacker, et al.Acta Paediatrica (Oslo, Norway : 1992)|April 24, 2012
The need for worldwide policy and action plans for rare diseasesJohn Forman, Domenica Taruscio, Virginia A Llera, et al.Pediatric Blood & Cancer|December 3, 2009
Clinical presentation of Griscelli syndrome type 2 and spectrum of RAB27A mutationsMarie Meeths, Yenan T Bryceson, Eva Rudd, et al.Journal of Medical Genetics|January 21, 2011
Genotype-phenotype study of familial haemophagocytic lymphohistiocytosis type 3Elena Sieni, Valentina Cetica, Alessandra Santoro, et al.Blood|April 17, 2013
Therapy prolongation improves outcome in multisystem Langerhans cell histiocytosisHelmut Gadner, Milen Minkov, Nicole Grois, et al.Pediatric Blood & Cancer|July 18, 2015
Spectrum of Atypical Clinical Presentations in Patients with Biallelic PRF1 Missense MutationsBianca Tesi, Samuel C C Chiang, Dalia El-Ghoneimy, et al.Nature Medicine|December 25, 2007
Langerhans cell histiocytosis reveals a new IL-17A-dependent pathway of dendritic cell fusionFabienne Coury, Nicola Annels, Aymeric Rivollier, et al.Blood Advances|August 12, 2020
Stem cell transplantation for children with hemophagocytic lymphohistiocytosis: results from the HLH-2004 studyElisabet Bergsten, AnnaCarin Horne, Ida Hed Myrberg, et al.British Journal of Haematology|December 19, 2014
Lack of bone lesions at diagnosis is associated with inferior outcome in multisystem langerhans cell histiocytosis of childhoodMaurizio Aricò, Itziar Astigarraga, Jorge Braier, et al.Pageof 17