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. Population prevalence of diagnosed primary immunodeficiency diseases in the United States. J Clin Immunol. 2007; 27: 497–502. 4 Jonkman-Berk BM, van den Berg JM, Ten Berge IJ, et al

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2017 Dec 11] 2 Picard C, Bobby Gaspar H, Al-Herz W, et al. International Union of Immunological Societies: 2017 Primary Immunodeficiency Diseases Committee report on inborn

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Hematológia–Transzfuziológia
Authors: Livia Vida, Gábor Ottóffy, Barnabás Rózsai, József Stankovics, Beáta Tóth, Zoltán Nyúl, and Béla Kajtár

, Bousfiha A, et al. Primary immunodeficiency diseases: an update on the classification from the international union of immunological societies expert committee for primary immunodeficiency 2015. J

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TREC testing of newborns with severe combined immunodeficiency and other primary immunodeficiency diseases. Mol Genet Metab Rep. 2014; 1: 324–333. 21 Kalman L

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with primary immunodeficiency disease. Ther. Clin. Risk Manag., 2010, 6 , 1–10. Ochs H. D. Subcutaneous immunglobulin replacement therapy in the treatment of patients with primary

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Orvosi Hetilap
Authors: Melinda Erdős, Beáta Tóth, Pálma Juhász, Mohamed Mahdi, and László Maródi

282 Maródi, L., Casanova, J. L.: Primary immunodeficiency diseases: The J Project. Lancet, 2009, 373 , 2179–2181. Casanova J. L

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Acta Microbiologica et Immunologica Hungarica
Authors: Elham Rayzan, Gholamreza Pouladfar, Nima Parvaneh, Mohammad Shahrooei, Zahra Aryan, and Nima Rezaei

adenine dinucleotide phosphate PID :primary immunodeficiency disease CBC :complete blood cell count

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References 1 Picard C, Al-Herz W, Bousfiha A, et al. Primary immunodeficiency diseases: an update on the classification from the International Union of Immunological

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Picard C, Bobby Gaspar H, Al-Herz W, et al. International Union of Immunological Societies: 2017 Primary Immunodeficiency Diseases Committee report on inborn errors of immunity. J Clin Immunol. 2018; 38: 96

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Acta Microbiologica et Immunologica Hungarica
Authors: Gulay Korukluoglu, Umit Ozdemirer, Fatma Bayrakdar, Zehra Unal, Yasemin Cosgun, Tunca Atak, Hulya Karademirtok, Isil Ata, and Fatih Kara

-to-person transmission in the community exists; 2) iVDPVs, when they are isolated from persons with primary immunodeficiency diseases (PIDs); and 3) aVDPVs, when they are clinical isolates from persons with no known immunodeficiency and no evidence of transmission, or

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