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Blood|July 24, 2024
Diagnostic guidelines for familial hemophagocytic lymphohistiocytosis revisitedJan-Inge Henter, Elena Sieni, Julia Eriksson, et al.Blood|January 9, 2016
Mutations in AP3D1 associated with immunodeficiency and seizures define a new type of Hermansky-Pudlak syndromeSandra Ammann, Ansgar Schulz, Ingeborg Krägeloh-Mann, et al.Pediatric Blood & Cancer|July 4, 2020
Risk factors for mixed chimerism in children with hemophagocytic lymphohistiocytosis after reduced toxicity conditioningKatharina Wustrau, Johann Greil, Karl-Walter Sykora, et al.Journal of Clinical Immunology|September 29, 2021
Reduced-Intensity/Reduced-Toxicity Conditioning Approaches Are Tolerated in XIAP Deficiency but Patients Fare Poorly with Acute GVHDDanielle E Arnold, Rofida Nofal, Connor Wakefield, et al.Clinical Immunology (Orlando, Fla.)|November 27, 2019
Distinct molecular response patterns of activating STAT3 mutations associate with penetrance of lymphoproliferation and autoimmunitySabine Jägle, Maximilian Heeg, Sarah Grün, et al.Frontiers in Immunology|May 2, 2017
Differences in Granule Morphology yet Equally Impaired Exocytosis among Cytotoxic T Cells and NK Cells from Chediak-Higashi Syndrome PatientsSamuel C C Chiang, Stephanie M Wood, Bianca Tesi, et al.Cancer|December 7, 2018
A multicenter study of patients with multisystem Langerhans cell histiocytosis who develop secondary hemophagocytic lymphohistiocytosisDeepak Chellapandian, Melissa R Hines, Rui Zhang, et al.Blood Advances|May 9, 2020
Targeted busulfan-based reduced-intensity conditioning and HLA-matched HSCT cure hemophagocytic lymphohistiocytosisMatthias Felber, Colin G Steward, Karim Kentouche, et al.Blood|November 8, 2012
Allogeneic hematopoietic cell transplantation for XIAP deficiency: an international survey reveals poor outcomesRebecca A Marsh, Kanchan Rao, Prakash Satwani, et al.Blood|March 16, 2025
Beyond genotype: challenges in predicting disease risk for carriers of biallelic perforin variantsOliver Wegehaupt, Oleg Borisov, Elena Sieni, et al.Pageof 9