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Clinical Immunology (Orlando, Fla.)|November 27, 2007
Clinical features, long-term follow-up and outcome of a large cohort of patients with Chronic Granulomatous Disease: an Italian multicenter studyBaldassarre Martire, Roberto Rondelli, Annarosa Soresina, et al.
Clinical Immunology (Orlando, Fla.)|September 10, 2002
Clinical, immunological, and molecular analysis in a large cohort of patients with X-linked agammaglobulinemia: an Italian multicenter studyAlessandro Plebani, Annarosa Soresina, Roberto Rondelli, et al.
The Journal of Pediatrics|March 25, 2014
Clinical features and follow-up in patients with 22q11.2 deletion syndromeCaterina Cancrini, Pamela Puliafito, Maria Cristina Digilio, et al.
Science Immunology|September 17, 2021
Combined immunodeficiency with autoimmunity caused by a homozygous missense mutation in inhibitor of nuclear factor 𝛋B kinase alpha (IKKα)Wayne Bainter, Vassilios Lougaris, Jacqueline G Wallace, et al.
Journal of Clinical Immunology|April 21, 2022
The Impact of SARS-CoV-2 Infection in Patients with Inborn Errors of Immunity: the Experience of the Italian Primary Immunodeficiencies Network (IPINet)Giuliana Giardino, Cinzia Milito, Vassilios Lougaris, et al.
The Journal of Allergy and Clinical Immunology. in Practice|March 30, 2019
Immunophenotype Anomalies Predict the Development of Autoimmune Cytopenia in 22q11.2 Deletion SyndromeDavide Montin, Agostina Marolda, Francesco Licciardi, et al.
The Journal of Allergy and Clinical Immunology|December 2, 2024
Consensus of the Italian Primary Immunodeficiency Network on the use and interpretation of genetic testing for diagnosing inborn errors of immunityGiuliana Giardino, Gigliola Di Matteo, Silvia Giliani, et al.
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