about
Genetic and demographic features of X-linked agammaglobulinemia in Eastern and Central Europe: a cohort study.Genetic characteristics of eighty-seven patients with the Wiskott-Aldrich syndrome.Thymus transplantation for complete DiGeorge syndrome: European experience.Revisiting human IL-12Rβ1 deficiency: a survey of 141 patients from 30 countries.Efficacy and safety of hizentra®, a new 20% immunoglobulin preparation for subcutaneous administration, in pediatric patients with primary immunodeficiencyCommon variable immune deficiency in children--clinical characteristics varies depending on defect in peripheral B cell maturation.Oxidative stress, mitochondrial abnormalities and antioxidant defense in Ataxia-telangiectasia, Bloom syndrome and Nijmegen breakage syndrome.Wiskott-Aldrich Syndrome protein deficiency perturbs the homeostasis of B-cell compartment in humans.Comprehensive activities to increase recognition of primary immunodeficiency and access to immunoglobulin replacement therapy in Poland.Gastrointestinal disorders next to respiratory infections as leading symptoms of X-linked agammaglobulinemia in children - 34-year experience of a single center.Genetic defects in PI3Kδ affect B-cell differentiation and maturation leading to hypogammaglobulineamia and recurrent infections.Nijmegen Breakage Syndrome: Clinical and Immunological Features, Long-Term Outcome and Treatment Options - a Retrospective Analysis.Loss of juxtaposition of RAG-induced immunoglobulin DNA ends is implicated in the precursor B-cell differentiation defect in NBS patients.Disseminated bacillus Calmette-Guérin infection and immunodeficiencyThe patients’ organisations of children with primary immunodeficiency in Poland.Juvenile idiopathic arthritis in a child with nijmegen breakage syndrome.Vitamin D deficiency in children with recurrent respiratory infections, with or without immunoglobulin deficiency.Comparison of Selected Parameters of Redox Homeostasis in Patients with Ataxia-Telangiectasia and Nijmegen Breakage Syndrome.The defect in humoral immunity in patients with Nijmegen breakage syndrome is explained by defects in peripheral B lymphocyte maturation.B cell subsets in healthy children: reference values for evaluation of B cell maturation process in peripheral blood.Nijmegen breakage syndrome: Long-term monitoring of viral and immunological biomarkers in peripheral blood before development of malignancy.[Diagnosis and treatment of aspergillosis in the patients with chronic granulomatous disease].Clinical immunology Disseminated Mycobacterium tuberculosis complex infection in a girl with partial dominant IFN-γ receptor 1 deficiencyIncomplete penetrance for isolated congenital asplenia in humans with mutations in translated and untranslated exonsIncomplete penetrance for isolated congenital asplenia in humans with mutations in translated and untranslated RPSA exonsClinical heterogeneity and diagnostic delay of autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy syndromeClinical efficacy of intravenous immunoglobulin in patients with severe inflammatory chest disease and IgG3 subclass deficiency[Ataxia telangiectasia syndrome: clinical picture and immunological abnormalities][Chronic neutropenia - experience from the Department of Immunology, Children's Memorial Health Institute]Pulmonary lymphomatoid granulomatosis in Griscelli syndrome type 2[Replacement therapy with subcutaneous immunoglobulin in primary immunodeficiency in children]Antioxidant Defense, Redox Homeostasis, and Oxidative Damage in Children With Ataxia Telangiectasia and Nijmegen Breakage SyndromeA Novel CDC42 Mutation in an 11-Year Old Child Manifesting as Syndromic Immunodeficiency, Autoinflammation, Hemophagocytic Lymphohistiocytosis, and Malignancy: A Case ReportBCG Moreau Vaccine Safety Profile and NK Cells-Double Protection Against Disseminated BCG Infection in Retrospective Study of BCG Vaccination in 52 Polish Children with Severe Combined ImmunodeficiencyEuroFlow Standardized Approach to Diagnostic Immunopheneotyping of Severe PID in Newborns and Young Children
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P50
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researcher ORCID ID = 0000-0003-2071-3297
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Malgorzata Pac
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Malgorzata Pac
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P31
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0000-0003-2071-3297