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Journal of Clinical Immunology|May 6, 2016
Successful Hematopoietic Stem Cell Transplantation in a Patient with LPS-Responsive Beige-Like Anchor (LRBA) Gene MutationBianca Tesi, Peter Priftakis, Fredrik Lindgren, et al.European Journal of Cancer Care|December 16, 2014
Trismus, xerostomia and nutrition status in nasopharyngeal carcinoma survivors treated with radiationY-J Chen, S-C Chen, C-P Wang, et al.Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|October 26, 2006
Comparison of clinical outcomes and spectral Doppler indices of uterine and ovarian stromal arteries in women undergoing myomectomy with or without hypogastric arterial ligationH-C Fu, K-H Huang, C-W Tseng, et al.Frontiers in Immunology|January 25, 2014
An N-Terminal Missense Mutation in STX11 Causative of FHL4 Abrogates Syntaxin-11 Binding to Munc18-2Martha-Lena Müller, Samuel C C Chiang, Marie Meeths, et al.Journal of Pediatric Hematology/Oncology|July 11, 2017
A Case of Familial Hemophagocytic Lymphohistiocytosis Type 4 With Involvement of the Central Nervous System Complicated With InfarctSaliha Ciraci, Alper Ozcan, Mustafa M Ozdemir, et al.The Journal of Experimental Medicine|May 21, 2014
Transcriptional regulation of Munc13-4 expression in cytotoxic lymphocytes is disrupted by an intronic mutation associated with a primary immunodeficiencyFrank Cichocki, Heinrich Schlums, Hongchuan Li, et al.Blood|June 10, 2022
Quercetin ameliorates XIAP deficiency-associated hyperinflammationSamuel C C Chiang, Erika Owsley, Neelam Panchal, et al.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.Journal of Pediatric Hematology/Oncology|April 30, 2019
A Rare Case of Activated Phosphoinositide 3-Kinase Delta Syndrome (APDS) Presenting With Hemophagocytosis Complicated With Hodgkin LymphomaMurat Cansever, Natalia Zietara, Samuel C C Chiang, et al.Journal of Medical Genetics|May 3, 2013
A novel intellectual disability syndrome caused by GPI anchor deficiency due to homozygous mutations in PIGTMalin Kvarnung, Daniel Nilsson, Anna Lindstrand, et al.Pageof 11