Zobrazeno 1 - 10
of 53
pro vyhledávání: '"Edyta Heropolitańska-Pliszka"'
Autor:
Ildikó Tar, Márta Szegedi, Ewa Krasuska-Sławińska, Edyta Heropolitańska-Pliszka, Ewa A. Bernatowska, Elif Öncü, Sevgi Keles, Sukru N. Guner, Ismail Reisli, Nevena Gesheva, Elissaveta Naumova, Lydie Izakovicova-Holla, Jiri Litzman, Igor Savchak, Larysa Kostyuchenko, Melinda Erdős
Publikováno v:
Central European Journal of Immunology, Vol 48, Iss 3, Pp 228-236 (2023)
Autosomal dominant hyper-IgE syndrome (AD-HIES) is an inborn error of immunity (IEI) caused by a dominant-negative mutation in the signal transducer and activator of transcription 3 (STAT 3). This disease is characterized by chronic eczematoid dermat
Externí odkaz:
https://doaj.org/article/c82a97b04920449189b05edd75f8ff55
Autor:
Ahmad Vosughimotlagh, Seyed Erfan Rasouli, Hosein Rafiemanesh, Molood Safarirad, Niusha Sharifinejad, Atossa Madanipour, Maria Marluce Dos Santos Vilela, Edyta Heropolitańska-Pliszka, Gholamreza Azizi
Publikováno v:
Allergy, Asthma & Clinical Immunology, Vol 19, Iss 1, Pp 1-11 (2023)
Abstract Objectives Immunoglobulin A deficiency (IgAD) is a common disease with an unknown genetic defect, characterized by the decreased or absent IgA with other isotypes normal, normal subclasses, and specific antibodies. Patients with this disorde
Externí odkaz:
https://doaj.org/article/f446e091947d4b5ab35b7924390b1fb6
Publikováno v:
Urology Case Reports, Vol 48, Iss , Pp 102409- (2023)
Chronic Granulomatous Disease is a primary immunodeficiency syndrome caused by a phagocytic defect, characterized by recurrent, life-threatening bacterial and fungal infections and an excessive inflammatory response. We present the case of a boy with
Externí odkaz:
https://doaj.org/article/6fbd91196c1c4c50a0fab3cab193c122
Autor:
Nel Dabrowska-Leonik, Agata Karolina Pastorczak, Katarzyna Bąbol-Pokora, Katarzyna Bernat-Sitarz, Barbara Piątosa, Edyta Heropolitańska-Pliszka, Magdalena M. Kacprzak, Krzysztof Kalwak, Katarzyna Gul, Mirjam van der Burg, Marek Ussowicz, Malgorzata Pac
Publikováno v:
Frontiers in Immunology, Vol 13 (2022)
DNA ligase I deficiency is an extremely rare primary immunodeficiency with only 6 patients reported in the literature. Most common manifestations include radiosensitivity, macrocytic anemia, lymphopenia with an increased percentage of gamma-delta T c
Externí odkaz:
https://doaj.org/article/d67e7697d6024300ac72134a47af7664
Autor:
Sylwia Kołtan, Marcin Ziętkiewicz, Elżbieta Grześk, Rafał Becht, Elżbieta Berdej-Szczot, Magdalena Cienkusz, Marlena Ewertowska, Edyta Heropolitańska-Pliszka, Natalia Krysiak, Aleksandra Lewandowicz-Uszyńska, Monika Mach-Tomalska, Aleksandra Matyja-Bednarczyk, Marcin Milchert, Katarzyna Napiórkowska-Baran, Karolina Pieniawska-Śmiech, Anna Pituch-Noworolska, Joanna Renke, Jacek Roliński, Iwona Rywczak, Agnieszka Stelmach-Gołdyś, Magdalena Strach, Hanna Suchanek, Joanna Sulicka-Grodzicka, Aleksandra Szczawińska-Popłonyk, Sławomir Tokarski, Ewa Więsik-Szewczyk, Beata Wolska-Kuśnierz, Krzysztof Zeman, Małgorzata Pac
Publikováno v:
Frontiers in Immunology, Vol 13 (2022)
At the beginning of the Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) pandemic, patients with inborn errors of immunity (IEI) appeared to be particularly vulnerable to a severe course of the disease. It quickly turned out that only som
Externí odkaz:
https://doaj.org/article/fc3c881aae5547c7bd5c03e1f7ec4269
Autor:
Edyta Heropolitańska-Pliszka, Barbara Piątosa, Anna Szmydki-Baran, Karolina Kuczborska, Karolina Miarka-Walczyk, Agata Pastorczak, Wojciech Młynarski, Łukasz Sędek, Tomasz Szczepański, Marek Ussowicz
Publikováno v:
Frontiers in Immunology, Vol 13 (2022)
GATA-binding protein 2 (GATA2) is a transcription factor responsible for the regulation of blood cell proliferation, differentiation, and maintenance in hematopoietic stem cells. Here, we describe successful bone marrow transplantation in a carrier o
Externí odkaz:
https://doaj.org/article/b7a6867f3b634d81a60bcc4b8ac3a81b
Autor:
Ewa Bernatowska, Małgorzata Pac, Edyta Heropolitańska-Pliszka, Barbara Pietrucha, Nel Dąbrowska-Leonik, Małgorzata Skomska-Pawliszak, Katarzyna Bernat-Sitarz, Katarzyna Krzysztopa-Grzybowska, Beata Wolska-Kuśnierz, Nadia Bohynikova, Ewa Augustynowicz, Ewa Augustynowicz-Kopeć, Maria Korzeniewska-Koseła, Anna Wieteska-Klimczak, Janusz Książyk, Teresa Jackowska, Mirjam van den Burg, Jean-Laurent Casanova, Capucine Picard, Bożena Mikołuć
Publikováno v:
Frontiers in Pediatrics, Vol 10 (2022)
ObjectiveWe aimed to assess BCG (Bacillus Calmette-Guérin) complications in patients with Inborn Errors of Immunity (IEI), according to the inherited disorders and associated immunological defects, as well as the different BCG substrains.MaterialWe
Externí odkaz:
https://doaj.org/article/9b346cafab36422a8915fa2ddf6637ff
Autor:
Małgorzata Sopińska, Karolina Kapusta, Edyta Heropolitańska-Pliszka, Anna Jung, Bolesław Kalicki
Publikováno v:
Pediatria i Medycyna Rodzinna, Vol 12, Iss 2, Pp 214-219 (2016)
Chromosome X-linked Bruton agammaglobulinemia is classified as a primary immunodeficiency disorder. It is a genetic condition associated with a mutation in the BTK gene encoding tyrosine kinase. It is characterised by the lack or only trace amounts
Externí odkaz:
https://doaj.org/article/67e953b0d2fd49b082f35c9355965575
Autor:
Barbara Pietrucha, Edyta Heropolitańska-Pliszka, Robert Geffers, Julia Enßen, Britta Wieland, Natalia Valerijevna Bogdanova, Thilo Dörk
Publikováno v:
Frontiers in Immunology, Vol 8 (2017)
Germline mutations in the RING finger protein gene RNF168 have been identified in a combined immunodeficiency disorder called RIDDLE syndrome. Since only two patients have been described with somewhat different phenotypes, there is need to identify f
Externí odkaz:
https://doaj.org/article/46da44d39ed2478495113d5eb9ee531a
Autor:
Monika Sztupecka-Rutkowska, Barbara Wojciechowska, Edyta Heropolitańska-Pliszka, Cezary Kowalewski, Karolina Rutkowska, Anna Walczak, Rafał Płoski, Katarzyna Woźniak
Background: Acrodermatitis enteropathica is a rare genetic metabolic disorder which results in poor absorption of zinc ions in digestive tract. Zinc is an important microelement in human body, that plays a crucial role in many metabolic and biochemic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bda65dcd6d7e174bba13c94e8edae168
https://doi.org/10.21203/rs.3.rs-2318276/v1
https://doi.org/10.21203/rs.3.rs-2318276/v1