Zobrazeno 1 - 10
of 16
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:
Marta Badeńska, Małgorzata Pac, Andrzej Badeński, Karolina Rutkowska, Justyna Czubilińska-Łada, Rafał Płoski, Nadezda Bohynikova, Maria Szczepańska
Publikováno v:
International Journal of Molecular Sciences, Vol 25, Iss 8, p 4486 (2024)
Idiopathic nephrotic syndrome is the most common chronic glomerular disease in children. Treatment with steroids is usually successful; however, in a small percentage of patients, steroid resistance is observed. The most frequent histologic kidney fe
Externí odkaz:
https://doaj.org/article/f167116cc7324ad0b39e6a09508c69f9
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, Vol 24, Iss 8, p 6993 (2023)
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://doaj.org/article/0dcb7dd36bee456a889f35a594d4a190
Autor:
Andrzej Badeński, Marta Badeńska, Elżbieta Świętochowska, Agnieszka Didyk, Aurelia Morawiec-Knysak, Maria Szczepańska
Publikováno v:
International Journal of Molecular Sciences, Vol 23, Iss 20, p 12312 (2022)
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://doaj.org/article/daf00f6a794943beb604682834bdbed1
Autor:
Anna Bogdał, Andrzej Badeński, Małgorzata Pac, Anna Wójcicka, Marta Badeńska, Agnieszka Didyk, Elżbieta Trembecka-Dubel, Nel Dąbrowska-Leonik, Małgorzata Walaszczyk, Natalia Matysiak, Aurelia Morawiec-Knysak, Tomasz Szczepański, Maria Szczepańska
Publikováno v:
International Journal of Molecular Sciences, Vol 22, Iss 17, 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://doaj.org/article/56ac6f502f07478e8e3a83839cd2157e
Autor:
Bartosz Chmiela, Omar Bjanid, Maria Szczepańska, Piotr Adamczyk, Marta Badeńska, Grzegorz Kudela, Grzegorz Moskal, Andrzej Badeński
Publikováno v:
Pediatric Nephrology (Berlin, Germany)
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