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Blood|August 26, 2016
Cytoskeletal abnormalities and neutrophil dysfunction in WDR1 deficiencyDouglas B Kuhns, Danielle L Fink, Uimook Choi, et al.Science Translational Medicine|April 22, 2016
Lentiviral hematopoietic stem cell gene therapy for X-linked severe combined immunodeficiencySuk See De Ravin, Xiaolin Wu, Susan Moir, et al.The New England Journal of Medicine|September 21, 2007
STAT3 mutations in the hyper-IgE syndromeSteven M Holland, Frank R DeLeo, Houda Z Elloumi, et al.Cell|February 10, 2015
Chromothriptic cure of WHIM syndromeDavid H McDermott, Ji-Liang Gao, Qian Liu, et al.Blood|February 14, 2014
A phase 1 clinical trial of long-term, low-dose treatment of WHIM syndrome with the CXCR4 antagonist plerixaforDavid H McDermott, Qian Liu, Daniel Velez, et al.Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America|December 25, 2014
Common severe infections in chronic granulomatous diseaseBeatriz E Marciano, Christine Spalding, Alan Fitzgerald, et al.The Journal of Allergy and Clinical Immunology|March 4, 2014
Recommendations for live viral and bacterial vaccines in immunodeficient patients and their close contacts, William T Shearer, Thomas A Fleisher, et al.Science Translational Medicine|February 7, 2024
Exonic knockout and knockin gene editing in hematopoietic stem and progenitor cells rescues RAG1 immunodeficiencyMaria Carmina Castiello, Chiara Brandas, Samuele Ferrari, et al.The New England Journal of Medicine|April 18, 2019
Lentiviral Gene Therapy Combined with Low-Dose Busulfan in Infants with SCID-X1Ewelina Mamcarz, Sheng Zhou, Timothy Lockey, et al.Blood|May 11, 2021
Long-term outcomes after gene therapy for adenosine deaminase severe combined immune deficiencyBryanna Reinhardt, Omar Habib, Kit L Shaw, et al.Pageof 19