Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Marta Badeńska"'
Autor:
Aleksandra Gliwińska, Marta Badeńska, Marta Dworak, Elżbieta Świętochowska, Andrzej Badeński, Omar Bjanid, Elżbieta Trembecka-Dubel, Aurelia Morawiec-Knysak, Maria Szczepańska
Publikováno v:
BMC Nephrology, Vol 25, Iss 1, Pp 1-13 (2024)
Abstract Patients suffering from chronic kidney disease (CKD) are particularly placed at risk of multiorgan complications. One of them is malnutrition, which adds up to a higher mortality factor among them. This study was designed to determine the us
Externí odkaz:
https://doaj.org/article/8fc2d859f2744633a118943a055f19a2
Autor:
Martyna Szuster, Julia Gajewska, Artur Janek, Jagoda Perlikowska, Andrzej Badeński, Marta Badeńska, Tomasz Szczepański, Aneta Pobudejska-Pieniążek
Publikováno v:
Pediatria Polska, Vol 99, Iss 2, Pp 123-127 (2024)
Externí odkaz:
https://doaj.org/article/c01ae2a94d4d4bc9b8816aa91e6a7e82
Autor:
Grażyna Waśka, Weronika Fijałkowska, Marta Badeńska, Andrzej Badeński, Agnieszka Książek, Renata Tomaszewska, Elżbieta Trembecka-Dubel, Maria Szczepańska
Publikováno v:
Pediatria Polska, Vol 98, Iss 2, Pp 170-175 (2023)
Acquired thrombotic thrombocytopaenic purpura (TTP) in children is a rare immune-mediated haematological disease (iTTP) in which active thrombus formation and multiorgan symptoms resulting from ischaemia of specific organs occurs. A 16-year-old girl
Externí odkaz:
https://doaj.org/article/355aebf51cc44a4fac0e981fc8168485
Autor:
Andrzej Badeński, Marta Badeńska, Magdalena Mierzwa, Małgorzata Stojewska, Grażyna Deja, Maria Szczepańska, Katarzyna Ziora
Publikováno v:
Pediatria Polska, Vol 97, Iss 2, Pp 151-155 (2022)
Autoimmune polyendocrine syndromes (APS) include a diverse group of clinical conditions, characterized by functional impairment of many endocrine glands. Type 2 APS is characterized by the mandatory presence of Addison’s disease, which may be assoc
Externí odkaz:
https://doaj.org/article/462c3c996a794cbb9dc21ab321033739
Autor:
Andrzej Badeński, Marta Badeńska, Elżbieta Świętochowska, Artur Janek, Aleksandra Gliwińska, Aurelia Morawiec-Knysak, Maria Szczepańska
Publikováno v:
International Journal of Molecular Sciences; Volume 24; Issue 8; Pages: 6993
Idiopathic nephrotic syndrome (INS) is a chronic glomerular disease in children, characterized by severe proteinuria, hypoalbuminemia, and/or presence of edema and hyperlipidemia. The pathogenesis, however, has not been yet established. The clinical
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f7a1cf44259120888a82bdc76f1f0b1a
https://doi.org/10.3390/ijms24086993
https://doi.org/10.3390/ijms24086993
Autor:
Bartosz Chmiela, Omar Bjanid, Maria Szczepańska, Piotr Adamczyk, Marta Badeńska, Grzegorz Kudela, Grzegorz Moskal, Andrzej Badeński
Publikováno v:
Pediatric Nephrology (Berlin, Germany)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3e77b6b5393105c1115ecd058852462e
https://doi.org/10.1007/s00467-020-04709-x
https://doi.org/10.1007/s00467-020-04709-x
Autor:
Maria Szczepańska, Anna Bogdał, Marta Badeńska, Aleksandra Gliwińska, Olga Kupczyk, Andrzej Badeński, Omar Bjanid, Justyna Czubilińska-Łada
Publikováno v:
Pediatria Polska. 95:184-190
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a501da76ec2e74bbb6e6b57197e98a82
https://doi.org/10.5114/polp.2020.100877
https://doi.org/10.5114/polp.2020.100877
Autor:
Andrzej Badeński, Marta Badeńska, Elżbieta Trembecka-Dubel, Ewa Grzywna-Rozenek, Ewa Kluczewska, Maria Szczepańska
Publikováno v:
Paediatria Croatica. 65
Background: Schimke immuno-osseous dysplasia (SIOD, OMIM 242900) is a rare, autosomal recessive, pleiotropic disease caused by mutations in the SMARCAL1 gene. SIOD is characterized by a triad of symptoms, i.e., progressive kidney disease due to focal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::64c10199d33fc6776859e88bf5ff7cd8
https://doi.org/10.13112/pc.2021.34
https://doi.org/10.13112/pc.2021.34
Autor:
Andrzej Badeński, Marta Badeńska, Elżbieta Świętochowska, Agnieszka Didyk, Aurelia Morawiec-Knysak, Maria Szczepańska
Publikováno v:
International Journal of Molecular Sciences; Volume 23; Issue 20; Pages: 12312
Idiopathic nephrotic syndrome (INS) is a chronic disease affecting children in early childhood. It is characterized by proteinuria, hypoalbuminemia, edema and hyperlipidemia. To date, the diagnosis is usually established at an advanced stage of prote
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f5e3f9fb7f651f0f2cc04f7f23409605
https://doi.org/10.3390/ijms232012312
https://doi.org/10.3390/ijms232012312
Autor:
Maria Szczepańska, Nel Dąbrowska-Leonik, Anna Bogdał, Aurelia Morawiec-Knysak, Małgorzata Walaszczyk, Andrzej Badeński, Małgorzata Pac, Anna Wojcicka, Agnieszka Didyk, Elżbieta Trembecka-Dubel, Natalia Matysiak, Marta Badeńska, Tomasz Szczepański
Publikováno v:
International Journal of Molecular Sciences
International Journal of Molecular Sciences, Vol 22, Iss 9479, p 9479 (2021)
International Journal of Molecular Sciences, Vol 22, Iss 9479, p 9479 (2021)
Hemolytic uremic syndrome (HUS) is defined by the triad of microangiopathic hemolytic anemia, thrombocytopenia, and acute kidney injury (AKI). Atypical HUS (aHUS), distinguished by its etiology, is caused by uncontrolled overactivation of the alterna
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2bcc369f9c31e6e892c0b7db870fce07
https://doi.org/10.3390/ijms22179479
https://doi.org/10.3390/ijms22179479