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The New England Journal of Medicine|December 31, 2010
Residual NADPH oxidase and survival in chronic granulomatous diseaseDouglas B Kuhns, W Gregory Alvord, Theo Heller, et al.
Clinical Gastroenterology and Hepatology : the Official Clinical Practice Journal of the American Gastroenterological Association|November 8, 2015
Gastrointestinal Features of Chronic Granulomatous Disease Found During EndoscopySajneet K Khangura, Natasha Kamal, Nancy Ho, et al.
Blood Advances|January 18, 2019
NCF1 (p47phox)-deficient chronic granulomatous disease: comprehensive genetic and flow cytometric analysisDouglas B Kuhns, Amy P Hsu, David Sun, et al.
Human Gene Therapy|March 20, 2021
Preclinical Optimization and Safety Studies of a New Lentiviral Gene Therapy for p47phox-Deficient Chronic Granulomatous DiseaseAndrea Schejtman, Winston Vetharoy, Uimook Choi, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|October 8, 2014
An AAVS1-targeted minigene platform for correction of iPSCs from all five types of chronic granulomatous diseaseRandall K Merling, Colin L Sweeney, Jessica Chu, et al.
Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America|March 4, 2011
Geosmithia argillacea: an emerging cause of invasive mycosis in human chronic granulomatous diseaseSuk See De Ravin, Malliswari Challipalli, Victoria Anderson, et al.
The Journal of Infectious Diseases|May 12, 2026
Cryptosporidiosis in inborn errors of immunity: a single center cohort and review of the literatureChen Wang, Evgenii Filippov, Amir Seyedmousavi, et al.
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