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Frontiers in Pediatrics|November 7, 2022
Infections and immune dysregulation in ataxia-telangiectasia children with hyper-IgM and non-hyper-IgM phenotypes: A single-center experienceAleksandra Szczawińska-Popłonyk, Katarzyna Tąpolska-Jóźwiak, Eyal Schwartzmann, et al.
Frontiers in Pediatrics|April 11, 2022
Immune Dysregulation in Pediatric Common Variable Immunodeficiency: Implications for the Diagnostic ApproachAleksandra Szczawińska-Popłonyk, Katarzyna Ta Polska-Jóźwiak, Eyal Schwartzmann, et al.
Frontiers in Pediatrics|January 17, 2022
Case Report: Autoimmune Lymphoproliferative Syndrome vs. Chronic Active Epstein-Barr Virus Infection in Children: A Diagnostic ChallengeAleksandra Szczawińska-Popłonyk, Elzbieta Grześk, Eyal Schwartzmann, et al.
Allergologia Et Immunopathologia|July 5, 2022
Clinical and immunological assessment of APDS2 with features of the SHORT syndrome related to a novel mutation in PIK3R1 with reduced penetranceAleksandra Szczawińska-Popłonyk, Katarzyna Bernat-Sitarz, Eyal Schwartzmann, et al.
European Journal of Pediatrics|December 23, 2021
The pediatric common variable immunodeficiency - from genetics to therapy: a reviewAleksandra Szczawinska-Poplonyk, Eyal Schwartzmann, Ewelina Bukowska-Olech, et al.
International Journal of Molecular Sciences|May 13, 2023
Chromosome 22q11.2 Deletion Syndrome: A Comprehensive Review of Molecular Genetics in the Context of Multidisciplinary Clinical ApproachAleksandra Szczawińska-Popłonyk, Eyal Schwartzmann, Zuzanna Chmara, et al.
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