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Clinical Immunology (Orlando, Fla.)|November 14, 2006
Coronary artery aneurysms in patients with hyper IgE recurrent infection syndromeJennifer C Ling, Alexandra F Freeman, Ahmed M Gharib, et al.Atherosclerosis|February 8, 2017
Coronary atherosclerosis and dilation in hyper IgE syndrome patients: Depiction by magnetic resonance vessel wall imaging and pathological correlationKhaled Z Abd-Elmoniem, Nadine Ramos, Saami K Yazdani, et al.Journal of Clinical Immunology|June 27, 2013
B-cell lymphoma in a patient with complete interferon gamma receptor 1 deficiencyHannelore I Bax, Alexandra F Freeman, Victoria L Anderson, et al.Nuclear Medicine and Biology|April 2, 2013
The use of 14C-FIAU to predict bacterial thymidine kinase presence: implications for radiolabeled FIAU bacterial imagingKristin L Peterson, William C Reid, Alexandra F Freeman, et al.Journal of the Pediatric Infectious Diseases Society|December 28, 2018
Hematopoietic Stem Cell Transplantation in Primary Immunodeficiencies Beyond Severe Combined ImmunodeficiencyAlexandra F FreemanPediatrics|April 18, 2007
Brain abnormalities in patients with hyperimmunoglobulin E syndromeAlexandra F Freeman, Christina J Collura-Burke, Nicholas J Patronas, et al.Frontiers in Pediatrics|March 16, 2017
DOCK 8 Deficiency, EBV+ Lymphomatoid Granulomatosis, and Intrafamilial Variation in PresentationVictoria R Dimitriades, Vincent Devlin, Stefania Pittaluga, et al.Arthritis and Rheumatism|December 14, 2011
Brief report: genotype, phenotype, and clinical course in five patients with PAPA syndrome (pyogenic sterile arthritis, pyoderma gangrenosum, and acne)Andrew P Demidowich, Alexandra F Freeman, Douglas B Kuhns, et al.Archives of Dermatology|September 21, 2011
Cutaneous manifestations of DOCK8 deficiency syndromeEmily Y Chu, Alexandra F Freeman, Huie Jing, et al.Journal of Clinical Immunology|June 17, 2015
IL2RG reversion event in a common lymphoid progenitor leads to delayed diagnosis and milder phenotypeAmy P Hsu, Stefania Pittaluga, Bianca Martinez, et al.Pageof 67