Lista de obras - Malgorzata Pac - Dominio Público Uruguay

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

scientific article published on 13 March 2020

Antioxidant Defense, Redox Homeostasis, and Oxidative Damage in Children With Ataxia Telangiectasia and Nijmegen Breakage Syndrome

scientific article published on 27 September 2019

B cell subsets in healthy children: reference values for evaluation of B cell maturation process in peripheral blood

artículo científico publicado en 2010

BCG 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 Immunodeficiency

scientific article published on 20 November 2019

Clinical efficacy of intravenous immunoglobulin in patients with severe inflammatory chest disease and IgG3 subclass deficiency

artículo científico publicado en 1991

Clinical heterogeneity and diagnostic delay of autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy syndrome

artículo científico publicado en 2011

Clinical immunology Disseminated Mycobacterium tuberculosis complex infection in a girl with partial dominant IFN-γ receptor 1 deficiency

scholarly article by Malgorzata Pac et al published 2012 in Central-European Journal of Immunology

Common variable immune deficiency in children--clinical characteristics varies depending on defect in peripheral B cell maturation

artículo científico publicado en 2013

Comparison of Selected Parameters of Redox Homeostasis in Patients with Ataxia-Telangiectasia and Nijmegen Breakage Syndrome.

artículo científico publicado en 2017

Comprehensive activities to increase recognition of primary immunodeficiency and access to immunoglobulin replacement therapy in Poland.

artículo científico publicado en 2016

Disseminated bacillus Calmette-Guérin infection and immunodeficiency

artículo científico publicado en 2007

Efficacy and safety of hizentra®, a new 20% immunoglobulin preparation for subcutaneous administration, in pediatric patients with primary immunodeficiency

artículo científico publicado en 2011

EuroFlow Standardized Approach to Diagnostic Immunopheneotyping of Severe PID in Newborns and Young Children

scientific article published on 19 March 2020

Gastrointestinal disorders next to respiratory infections as leading symptoms of X-linked agammaglobulinemia in children - 34-year experience of a single center.

artículo científico publicado en 2016

Genetic and demographic features of X-linked agammaglobulinemia in Eastern and Central Europe: a cohort study.

artículo científico publicado en 2009

Genetic characteristics of eighty-seven patients with the Wiskott-Aldrich syndrome.

artículo científico publicado en 2010

Genetic defects in PI3Kδ affect B-cell differentiation and maturation leading to hypogammaglobulineamia and recurrent infections.

artículo científico publicado en 2017

Incomplete penetrance for isolated congenital asplenia in humans with mutations in translated and untranslated RPSA exons

Incomplete penetrance for isolated congenital asplenia in humans with mutations in translated and untranslated exons

article published in the Proceedings of the National Academy of Sciences of the United States of America

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

scientific article published on 27 August 2020

Juvenile idiopathic arthritis in a child with nijmegen breakage syndrome

artículo científico publicado en 2014

Loss of juxtaposition of RAG-induced immunoglobulin DNA ends is implicated in the precursor B-cell differentiation defect in NBS patients.

artículo científico publicado en 2010

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

scientific article published on 16 October 2020

Nijmegen Breakage Syndrome: Clinical and Immunological Features, Long-Term Outcome and Treatment Options - a Retrospective Analysis.

artículo científico publicado en 2015

Nijmegen breakage syndrome: Long-term monitoring of viral and immunological biomarkers in peripheral blood before development of malignancy.

artículo científico publicado en 2010

Oxidative stress, mitochondrial abnormalities and antioxidant defense in Ataxia-telangiectasia, Bloom syndrome and Nijmegen breakage syndrome

artículo científico publicado en 2016

Progressive bronchiectasis and CMC in a patient with STAT1 GOF - a rare case of primary immunodeficiency

scientific article published on 01 January 2020

Pulmonary lymphomatoid granulomatosis in Griscelli syndrome type 2

scientific article published on 23 November 2011

Replacement therapy with subcutaneous immunoglobulin in primary immunodeficiency in children

artículo científico publicado el 1 de junio de 2011

Revisiting human IL-12Rβ1 deficiency: a survey of 141 patients from 30 countries

artículo científico publicado en 2010

Systemic Redox Imbalance in Patients with Chronic Granulomatous Disease

artículo científico publicado en 2020

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

artículo científico publicado en 2020

The defect in humoral immunity in patients with Nijmegen breakage syndrome is explained by defects in peripheral B lymphocyte maturation.

artículo científico publicado en 2012

The patients’ organisations of children with primary immunodeficiency in Poland.

artículo científico publicado en 2010

Thymus transplantation for complete DiGeorge syndrome: European experience.

artículo científico publicado en 2017

Vitamin D deficiency in children with recurrent respiratory infections, with or without immunoglobulin deficiency.

artículo científico publicado en 2017

Wiskott-Aldrich Syndrome protein deficiency perturbs the homeostasis of B-cell compartment in humans

artículo científico publicado en 2013

[Ataxia telangiectasia syndrome: clinical picture and immunological abnormalities]

artículo científico publicado en 2004

[Chronic neutropenia - experience from the Department of Immunology, Children's Memorial Health Institute]

artículo científico publicado en 2007

[Diagnosis and treatment of aspergillosis in the patients with chronic granulomatous disease].

artículo científico publicado en 2006

Lista de obras de Malgorzata Pac

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

Antioxidant Defense, Redox Homeostasis, and Oxidative Damage in Children With Ataxia Telangiectasia and Nijmegen Breakage Syndrome

B cell subsets in healthy children: reference values for evaluation of B cell maturation process in peripheral blood

BCG 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 Immunodeficiency

Clinical efficacy of intravenous immunoglobulin in patients with severe inflammatory chest disease and IgG3 subclass deficiency

Clinical heterogeneity and diagnostic delay of autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy syndrome

Clinical immunology Disseminated Mycobacterium tuberculosis complex infection in a girl with partial dominant IFN-γ receptor 1 deficiency

Common variable immune deficiency in children--clinical characteristics varies depending on defect in peripheral B cell maturation

Comparison of Selected Parameters of Redox Homeostasis in Patients with Ataxia-Telangiectasia and Nijmegen Breakage Syndrome.

Comprehensive activities to increase recognition of primary immunodeficiency and access to immunoglobulin replacement therapy in Poland.

Disseminated bacillus Calmette-Guérin infection and immunodeficiency

Efficacy and safety of hizentra®, a new 20% immunoglobulin preparation for subcutaneous administration, in pediatric patients with primary immunodeficiency

EuroFlow Standardized Approach to Diagnostic Immunopheneotyping of Severe PID in Newborns and Young Children

Gastrointestinal disorders next to respiratory infections as leading symptoms of X-linked agammaglobulinemia in children - 34-year experience of a single center.

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.

Genetic defects in PI3Kδ affect B-cell differentiation and maturation leading to hypogammaglobulineamia and recurrent infections.

Incomplete penetrance for isolated congenital asplenia in humans with mutations in translated and untranslated RPSA exons

Incomplete penetrance for isolated congenital asplenia in humans with mutations in translated and untranslated exons

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

Juvenile idiopathic arthritis in a child with nijmegen breakage syndrome

Loss of juxtaposition of RAG-induced immunoglobulin DNA ends is implicated in the precursor B-cell differentiation defect in NBS patients.

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

Nijmegen Breakage Syndrome: Clinical and Immunological Features, Long-Term Outcome and Treatment Options - a Retrospective Analysis.

Nijmegen breakage syndrome: Long-term monitoring of viral and immunological biomarkers in peripheral blood before development of malignancy.

Oxidative stress, mitochondrial abnormalities and antioxidant defense in Ataxia-telangiectasia, Bloom syndrome and Nijmegen breakage syndrome

Progressive bronchiectasis and CMC in a patient with STAT1 GOF - a rare case of primary immunodeficiency

Pulmonary lymphomatoid granulomatosis in Griscelli syndrome type 2

Replacement therapy with subcutaneous immunoglobulin in primary immunodeficiency in children

Revisiting human IL-12Rβ1 deficiency: a survey of 141 patients from 30 countries

Systemic Redox Imbalance in Patients with Chronic Granulomatous Disease

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

The defect in humoral immunity in patients with Nijmegen breakage syndrome is explained by defects in peripheral B lymphocyte maturation.

The patients’ organisations of children with primary immunodeficiency in Poland.

Thymus transplantation for complete DiGeorge syndrome: European experience.

Vitamin D deficiency in children with recurrent respiratory infections, with or without immunoglobulin deficiency.

Wiskott-Aldrich Syndrome protein deficiency perturbs the homeostasis of B-cell compartment in humans

[Ataxia telangiectasia syndrome: clinical picture and immunological abnormalities]

[Chronic neutropenia - experience from the Department of Immunology, Children's Memorial Health Institute]

[Diagnosis and treatment of aspergillosis in the patients with chronic granulomatous disease].