An Overlapping Syndrome of Allergy and Immune Deficiency in Children

por Szczawinska-Poplonyk, Aleksandra
Publicado 2012

Development of Mucosal Immunity in Children: A Rationale for Sublingual Immunotherapy?

por Szczawinska-Poplonyk, Aleksandra
Publicado 2012

The B-cell compartment in antibody-deficient infants and young children – developing common variable immunodeficiency or transient immune maturation?

por Szczawinska-Poplonyk, Aleksandra, Tapolska-Jozwiak, Katarzyna, Samara, Husam
Publicado 2016

Granulomatous Liver Disease in Ataxia-Telangiectasia With the Hyper-IgM Phenotype: A Case Report

por Szczawińska-Popłonyk, Aleksandra, Ossowska, Lidia, Jończyk-Potoczna, Katarzyna
Publicado 2020

Imaging in children with ataxia-telangiectasia—The radiologist’s approach

por Jończyk-Potoczna, Katarzyna, Potoczny, Jakub, Szczawińska-Popłonyk, Aleksandra
Publicado 2022

A Novel CDC42 Mutation in an 11-Year Old Child Manifesting as Syndromic Immunodeficiency, Autoinflammation, Hemophagocytic Lymphohistiocytosis, and Malignancy: A Case Report

por Szczawinska-Poplonyk, Aleksandra, Ploski, Rafal, Bernatowska, Ewa, Pac, Malgorzata
Publicado 2020

Immune Dysregulation in Pediatric Common Variable Immunodeficiency: Implications for the Diagnostic Approach

por Szczawińska-Popłonyk, Aleksandra, Ta̧polska-Jóźwiak, Katarzyna, Schwartzmann, Eyal, Popłonyk, Natalia
Publicado 2022

Infections and immune dysregulation in ataxia-telangiectasia children with hyper-IgM and non-hyper-IgM phenotypes: A single-center experience

por Szczawińska-Popłonyk, Aleksandra, Tąpolska-Jóźwiak, Katarzyna, Schwartzmann, Eyal, Pietrucha, Barbara
Publicado 2022

Pulmonary manifestation of immunoglobulin G4-related disease in a 7-year-old immunodeficient boy with Epstein-Barr virus infection: a case report

por Szczawinska-Poplonyk, Aleksandra, Wojsyk-Banaszak, Irena, Jonczyk-Potoczna, Katarzyna, Breborowicz, Anna
Publicado 2016

Hyper Ig E syndrome (Job syndrome, HIES) – radiological images of pulmonary complications on the basis of three cases

por Jończyk-Potoczna, Katarzyna, Szczawińska-Popłonyk, Aleksandra, Warzywoda, Małgorzata, Bręborowicz, Anna, Pawlak, Bogdan
Publicado 2012

Case Report: Autoimmune Lymphoproliferative Syndrome vs. Chronic Active Epstein-Barr Virus Infection in Children: A Diagnostic Challenge

por Szczawińska-Popłonyk, Aleksandra, Grześk, Elzbieta, Schwartzmann, Eyal, Materna-Kiryluk, Anna, Małdyk, Jadwiga
Publicado 2021

Fatal respiratory distress syndrome due to coronavirus infection in a child with severe combined immunodeficiency

por Szczawinska‐Poplonyk, Aleksandra, Jonczyk‐Potoczna, Katarzyna, Breborowicz, Anna, Bartkowska‐Sniatkowska, Alicja, Figlerowicz, Magdalena
Publicado 2012

The hyperimmunoglobulin E syndrome - clinical manifestation diversity in primary immune deficiency

por Szczawinska-Poplonyk, Aleksandra, Kycler, Zdzislawa, Pietrucha, Barbara, Heropolitanska-Pliszka, Edyta, Breborowicz, Anna, Gerreth, Karolina
Publicado 2011

Factors causing oral and skin pathological features in the hyperimmunoglobulin E syndrome patient including the environmental component: a review of the literature and own experien...

por Gerreth, Karolina, Szczawinska-Poplonyk, Aleksandra, Kycler, Zdzislawa, Adamski, Zygmunt, Borysewicz-Lewicka, Maria, Breborowicz, Anna
Publicado 2020

Cytomegalovirus pneumonia as the first manifestation of severe combined immunodeficiency

por Szczawińska-Popłonyk, Aleksandra, Jończyk-Potoczna, Katarzyna, Ossowska, Lidia, Bręborowicz, Anna, Bartkowska-Śniatkowska, Alicja, Wachowiak, Jacek
Publicado 2014

Cutaneous and systemic granulomatosis in ataxia-telangiectasia: a clinico-pathological study

por Szczawińska-Popłonyk, Aleksandra, Olejniczak, Katarzyna, Tąpolska-Jóźwiak, Katarzyna, Boruczkowski, Maciej, Jończyk-Potoczna, Katarzyna, Małdyk, Jadwiga, Bręborowicz, Anna
Publicado 2020

Case report: The cardio-facio-cutaneous syndrome due to a novel germline mutation in MAP2K1: A multifaceted disease with immunodeficiency and short stature

por Szczawińska-Popłonyk, Aleksandra, Popłonyk, Natalia, Niedziela, Marek, Sowińska-Seidler, Anna, Sztromwasser, Paweł, Jamsheer, Aleksander, Obara-Moszyńska, Monika
Publicado 2022

The clinical phenotype with gastrostomy and abdominal wall infection in a pediatric patient with Takenouchi-Kosaki syndrome due to a heterozygous c.191A > G (p.Tyr64Cys) variant in...

por Szczawińska-Popłonyk, Aleksandra, Popłonyk, Natalia, Badura-Stronka, Magdalena, Juengling, Jerome, Huhn, Kerstin, Biskup, Saskia, Bancerz, Bartłomiej, Walkowiak, Jarosław
Publicado 2023

Chromosome 22q11.2 Deletion Syndrome: A Comprehensive Review of Molecular Genetics in the Context of Multidisciplinary Clinical Approach

por Szczawińska-Popłonyk, Aleksandra, Schwartzmann, Eyal, Chmara, Zuzanna, Głukowska, Antonina, Krysa, Tomasz, Majchrzycki, Maksymilian, Olejnicki, Maurycy, Ostrowska, Paulina, Babik, Joanna
Publicado 2023

The pediatric common variable immunodeficiency — from genetics to therapy: a review

por Szczawinska-Poplonyk, Aleksandra, Schwartzmann, Eyal, Bukowska-Olech, Ewelina, Biernat, Michal, Gattner, Stanislaw, Korobacz, Tomasz, Nowicki, Filip, Wiczuk-Wiczewska, Monika
Publicado 2021