Ewa A. Bernatowska

Warsaw, MZ, Poland

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 33 publications

Intraoral and maxillofacial abnormalities in patients with autosomal dominant hyper-IgE syndrome.

Intraoral and maxillofacial abnormalities in patients with autosomal dominant hyper-IgE syndrome.

Journal: Central-European journal of immunology

Published: December 10, 2022

National experience with adenosine deaminase deficiency related SCID in Polish children.

National experience with adenosine deaminase deficiency related SCID in Polish children.

Journal: Frontiers in immunology

Published: September 30, 2022

Care of patients with inborn errors of immunity in thirty J Project countries between 2004 and 2021.

Care of patients with inborn errors of immunity in thirty J Project countries between 2004 and 2021.

Journal: Frontiers in immunology

Published: August 30, 2022

Correction to: A Multi-center, Open-Label, Single-Arm Trial to Evaluate the Efficacy, Pharmacokinetics, and Safety and Tolerability of IGSC 20% in Subjects with Primary Immunodeficiency.

Correction to: A Multi-center, Open-Label, Single-Arm Trial to Evaluate the Efficacy, Pharmacokinetics, and Safety and Tolerability of IGSC 20% in Subjects with Primary Immunodeficiency.

Journal: Journal of clinical immunology

Published: February 17, 2022

BCG Moreau Polish Substrain Infections in Patients With Inborn Errors of Immunity: 40 Years of Experience in the Department of Immunology, Children's Memorial Health Institute, Warsaw.

BCG Moreau Polish Substrain Infections in Patients With Inborn Errors of Immunity: 40 Years of Experience in the Department of Immunology, Children's Memorial Health Institute, Warsaw.

Journal: Frontiers in pediatrics

Published: December 19, 2021

Lack of relationship between 25-hydoxyvitamin D concentration and a titer of antibodies to hepatitis B surface antigen in children under 12 years of age.

Lack of relationship between 25-hydoxyvitamin D concentration and a titer of antibodies to hepatitis B surface antigen in children under 12 years of age.

Journal: PloS one

Published: September 25, 2021

A Multi‑Center, Open‑Label, Single‑Arm Trial to Evaluate the Efficacy, Pharmacokinetics, and Safety and Tolerability of IGSC 20% in Subjects with Primary Immunodeficiency.

A Multi‑Center, Open‑Label, Single‑Arm Trial to Evaluate the Efficacy, Pharmacokinetics, and Safety and Tolerability of IGSC 20% in Subjects with Primary Immunodeficiency.

Journal: Journal of clinical immunology

Published: March 09, 2021

Tumor Necrosis Factor Receptor-Associated Periodic Syndrome (TRAPS) with a New Pathogenic Variant in TNFRSF1A Gene in a Family of the Adult Male with Renal AA Amyloidosis-Diagnostic and Therapeutic Challenge for Clinicians.

Tumor Necrosis Factor Receptor-Associated Periodic Syndrome (TRAPS) with a New Pathogenic Variant in TNFRSF1A Gene in a Family of the Adult Male with Renal AA Amyloidosis-Diagnostic and Therapeutic Challenge for Clinicians.

Journal: Journal of clinical medicine

Published: December 30, 2020

Newborn Screening for SCID and Other Severe Primary Immunodeficiency in the Polish-German Transborder Area: Experience From the First 14 Months of Collaboration.

Newborn Screening for SCID and Other Severe Primary Immunodeficiency in the Polish-German Transborder Area: Experience From the First 14 Months of Collaboration.

Journal: Frontiers in immunology

Published: April 30, 2020

Interstitial Lung Disease in Children With Selected Primary Immunodeficiency Disorders-A Multicenter Observational Study.

Interstitial Lung Disease in Children With Selected Primary Immunodeficiency Disorders-A Multicenter Observational Study.

Journal: Frontiers in immunology

Published: April 30, 2020

Systemic Redox Imbalance in Patients with Chronic Granulomatous Disease.

Systemic Redox Imbalance in Patients with Chronic Granulomatous Disease.

Journal: Journal of clinical medicine

Published: April 06, 2020

The Clinical and Genetic Spectrum of 82 Patients With RAG Deficiency Including a c.256_257delAA Founder Variant in Slavic Countries.

The Clinical and Genetic Spectrum of 82 Patients With RAG Deficiency Including a c.256_257delAA Founder Variant in Slavic Countries.

Journal: Frontiers in immunology

Published: March 04, 2020

Showing 1-12 of 33

Last Updated: 09/26/2026