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Revista De Enfermeria (Barcelona, Spain)|October 22, 2005
[Defects in immune system response by our organisms]Teresa EspañolExpert Review of Clinical Immunology|May 19, 2010
An update on treatment strategies for common variable immunodeficiencyDrahomíra Detková, Teresa EspañolJournal of Paediatrics and Child Health|September 15, 2007
Congenital rubella syndrome, hyper-IgM syndrome and autoimmunity in an 18-year-old girlPere Soler Palacin, Yolanda Castilla, Paula Garzón, et al.The Pediatric Infectious Disease Journal|July 28, 2009
Visceral leishmaniasis associated hemophagocytic syndrome in patients with chronic granulomatous diseaseAndrea Martín, Laura Marques, Pere Soler-Palacín, et al.Frontiers in Immunology|January 8, 2015
Primary immune deficiencies - principles of careHelen Chapel, Johan Prevot, Hubert Bobby Gaspar, et al.Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America|July 12, 2003
Clinical tuberculosis in 2 of 3 siblings with interleukin-12 receptor beta1 deficiencyIsabel Caragol, Miquel Raspall, Claire Fieschi, et al.Clinical Immunology (Orlando, Fla.)|January 10, 2002
Progressive neurodegeneration in patients with primary immunodeficiency disease on IVIG treatmentUlrike H M Ziegner, Roger H Kobayashi, Charlotte Cunningham-Rundles, et al.Plos One|April 22, 2009
Chronic granulomatous disease: the European experienceJ Merlijn van den Berg, Elsbeth van Koppen, Anders Ahlin, et al.The Journal of Allergy and Clinical Immunology|February 18, 2010
Mutations in STAT3 and diagnostic guidelines for hyper-IgE syndromeCristina Woellner, E Michael Gertz, Alejandro A Schäffer, et al.The Journal of Allergy and Clinical Immunology|October 5, 2016
Long-term outcomes of 176 patients with X-linked hyper-IgM syndrome treated with or without hematopoietic cell transplantationM Teresa de la Morena, David Leonard, Troy R Torgerson, et al.Pageof 1