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British Journal of Clinical Pharmacology|June 28, 2021
Model-informed precision dosing for alemtuzumab in paediatric and young adult patients undergoing allogeneic haematopoietic cell transplantationMin Dong, Chie Emoto, Tsuyoshi Fukuda, et al.
Blood Advances|June 17, 2020
Frequency and spectrum of disease-causing variants in 1892 patients with suspected genetic HLH disordersVanessa Gadoury-Levesque, Lei Dong, Rui Su, et al.
Pediatric Blood & Cancer|October 28, 2016
Salvage therapy for refractory hemophagocytic lymphohistiocytosis: A review of the published experienceRebecca A Marsh, Michael B Jordan, Julie-An Talano, et al.
The Journal of Allergy and Clinical Immunology. Global|June 12, 2025
STAT6 gain-of-function disease: p.D519N is a new disease-causing variant that responds well to dupilumab treatmentSimran Samra, Eleanor Cook, Jessica Wilson, et al.
Pediatric Blood & Cancer|March 25, 2015
Hemophagocytic lymphohistiocytosis in a female patient due to a heterozygous XIAP mutation and skewed X chromosome inactivationJennifer R Holle, Rebecca A Marsh, Anna Maria Holdcroft, et al.
Cytometry. Part B, Clinical Cytometry|March 12, 2014
Clinical flow cytometric screening of SAP and XIAP expression accurately identifies patients with SH2D1A and XIAP/BIRC4 mutationsCarrie E Gifford, Elizabeth Weingartner, Joyce Villanueva, et al.
Biology of Blood and Marrow Transplantation : Journal of the American Society for Blood and Marrow Transplantation|December 3, 2014
Outcomes of donor lymphocyte infusion for treatment of mixed donor chimerism after a reduced-intensity preparative regimen for pediatric patients with nonmalignant diseasesHilary L Haines, Jack J Bleesing, Stella M Davies, et al.
Cytometry. Part B, Clinical Cytometry|August 26, 2015
Clinical Flow Cytometric Screening of SAP and XIAP Expression Accurately Identifies Patients with SH2D1A and XIAP/BIRC4 MutationsCarrie E Gifford, Elizabeth Weingartner, Joyce Villanueva, et al.
Biology of Blood and Marrow Transplantation : Journal of the American Society for Blood and Marrow Transplantation|February 5, 2016
A Reduced-Intensity Conditioning Regimen for Patients with Dyskeratosis Congenita Undergoing Hematopoietic Stem Cell TransplantationAdam S Nelson, Rebecca A Marsh, Kasiani C Myers, et al.
Biology of Blood and Marrow Transplantation : Journal of the American Society for Blood and Marrow Transplantation|April 18, 2015
Peripheral Blood CD38 Bright CD8+ Effector Memory T Cells Predict Acute Graft-versus-Host DiseasePooja Khandelwal, Adam Lane, Vijaya Chaturvedi, et al.
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