Zobrazeno 1 - 10
of 54
pro vyhledávání: '"Beata, Bieniaś"'
Publikováno v:
Pediatria Polska, Vol 97, Iss 1, Pp 61-65 (2022)
Bardet-Biedl syndrome (BBS) is a rare, autosomal recessive multi-system ciliopathy. Its diagnosis is based on a constellation of characteristic clinical symptoms that appear in childhood, including kidney defects, obesity, retinal dystrophy, polydact
Externí odkaz:
https://doaj.org/article/6e136d7acd1d4a99a44732ad3c4536fe
Autor:
Małgorzata Mizerska-Wasiak, Agnieszka Turczyn, Karolina Cichoń-Kawa, Jadwiga Małdyk, Monika Miklaszewska, Dorota Drożdż, Beata Bieniaś, Przemysław Sikora, Magdalena Drożyńska-Duklas, Aleksandra Żurowska, Maria Szczepańska, Małgorzata Pańczyk-Tomaszewska
Publikováno v:
Pediatric Rheumatology Online Journal, Vol 19, Iss 1, Pp 1-9 (2021)
Abstract The aim of the study was to investigate the relationship between the severity of typical clinical symptoms, severity of histopathological lesions in kidney biopsies in IgA vasculitis nephritis (IgAVN) and to propose indications for kidney bi
Externí odkaz:
https://doaj.org/article/22973b637a5345ed8f6a21b85239c3a1
Autor:
Małgorzata Mizerska-Wasiak, Łukasz Gajewski, Karolina Cichoń-Kawa, Agata Siejko, Jadwiga Małdyk, Anna Spława-Neyman, Jacek Zachwieja, Agnieszka Firszt-Adamczyk, Roman Stankiewicz, Magdalena Drożyńska-Duklas, Aleksandra Żurowska, Beata Bieniaś, Przemysław Sikora, Agnieszka Pukajło-Marczyk, Danuta Zwolińska, Maria Szczepańska, Monika Pawlak-Bratkowska, Marcin Tkaczyk, Anna Stelmaszczyk-Emmel, Małgorzata Pańczyk-Tomaszewska
Publikováno v:
Central European Journal of Immunology, Vol 46, Iss 2, Pp 199-209 (2021)
Externí odkaz:
https://doaj.org/article/606b128ada404e9cae92b6573742f45d
Autor:
Raphael Schild, Simeon Dupont, Jérôme Harambat, Enrico Vidal, Ayşe Balat, Csaba Bereczki, Beata Bieniaś, Per Brandström, Francoise Broux, Silvia Consolo, Ivana Gojkovic, Jaap W Groothoff, Kristine Hommel, Holger Hubmann, Fiona E M Braddon, Tatiana E Pankratenko, Fotios Papachristou, Lucy A Plumb, Ludmila Podracka, Sylwester Prokurat, Anna Bjerre, Carolina Cordinhã, Juuso Tainio, Enkelejda Shkurti, Giuseppina Spartà, Karel Vondrak, Kitty J Jager, Jun Oh, Marjolein Bonthuis
Publikováno v:
Clinical Kidney Journal. 16:745-755
Background Data on comorbidities in children on kidney replacement therapy (KRT) are scarce. Considering their high relevance for prognosis and treatment, this study aims to analyse the prevalence and implications of comorbidities in European childre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1e53d903a21cda4dcfb5152a896835d1
https://doi.org/10.1093/ckj/sfad008
https://doi.org/10.1093/ckj/sfad008
Autor:
Magdalena Maria Woźniak, Paweł Osemlak, Aikaterini Ntoulia, Halina Borzęcka, Beata Bieniaś, Agnieszka Brodzisz, Grzegorz Jędrzejewski, Anna Drelich-Zbroja, Maciej Powerski, Maciej Pech, Andrzej Paweł Wieczorek
Publikováno v:
Journal of Ultrasonography, Vol 18, Iss 73, Pp 120-125 (2018)
Background: By now, two-dimensional contrast-enhanced voiding urosonography (ceVUS) has become a well-established method for the diagnosis and treatment monitoring of vesicoureteral reflux in children, particularly after the recent approval for thi
Externí odkaz:
https://doaj.org/article/ad9034e6ce5a4d49ad7ab801f23fd5f5
Autor:
Beata S Lipska-Ziętkiewicz, Jutta Gellermann, Olivia Boyer, Olivier Gribouval, Szymon Ziętkiewicz, Jameela A Kari, Mohamed A Shalaby, Fatih Ozaltin, Jiri Dusek, Anette Melk, Aysun K Bayazit, Laura Massella, Lidia Hyla-Klekot, Sandra Habbig, Astrid Godron, Maria Szczepańska, Beata Bieniaś, Dorota Drożdż, Rasha Odeh, Wioletta Jarmużek, Katarzyna Zachwieja, Agnes Trautmann, Corinne Antignac, Franz Schaefer, PodoNet Consortium
Publikováno v:
PLoS ONE, Vol 12, Iss 8, p e0180926 (2017)
Schimke immuno-osseous dysplasia (SIOD) is a rare multisystem disorder with early mortality and steroid-resistant nephrotic syndrome (SRNS) progressing to end-stage kidney disease. We hypothesized that next-generation gene panel sequencing may unsurf
Externí odkaz:
https://doaj.org/article/ea42cc11ba6a483999137f6d15f84b6c
Autor:
Przemysław Sikora, Ryszard Grenda, Małgorzata Kowalczyk, Beata Kieć-Wilk, Beata Bieniaś, Jacek Rubik, Maciej Szymczak, Hanna Nosek, Paulina Surowiec, Thorsten Marquardt, Bodo B. Beck, Marcin Zaniew
Publikováno v:
Polish archives of internal medicine. 132(11)
Nephropathic cystinosis (NC) is a rare, autosomal recessive disorder leading to lysosomal accumulation of cystine. It is caused by mutations in the CTNS gene encoding a cystine cotransporter cystinosin. The infantile (INC) and juvenile (JNC) forms ar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2a78398f0cab7161362ffb5ec50d6886
https://pubmed.ncbi.nlm.nih.gov/36426771
https://pubmed.ncbi.nlm.nih.gov/36426771
Autor:
Irena Wikiera-Magott, Beata Bieniaś, Małgorzata Pańczyk-Tomaszewska, Beata Banaszak, Małgorzata Barabasz, Anna Wieczorkiewicz-Płaza, Hanna Szymanik-Grzelak, Magdalena Drożyńska-Duklas, Marcin Tkaczyk
Publikováno v:
Advances in Medical Sciences. 66:128-137
The aim of the study was to evaluate the clinical course and pathomorphological correlations in Polish children with the diagnosis of lupus nephritis (LN).We retrospectively analyzed the medical records of 39 children hospitalized due to LN in 7 pedi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fc1b4f636dc4128ff414afd139eae7f8
https://doi.org/10.1016/j.advms.2021.01.004
https://doi.org/10.1016/j.advms.2021.01.004
Autor:
Jadwiga Małdyk, Beata Bieniaś, Małgorzata Pańczyk-Tomaszewska, Karolina Cichoń-Kawa, Maria Szczepańska, Magdalena Drożyńska-Duklas, Przemysław Sikora, Monika Miklaszewska, Aleksandra Żurowska, Dorota Drozdz, Małgorzata Mizerska-Wasiak, Agnieszka Turczyn
Publikováno v:
Pediatric Rheumatology Online Journal, Vol 19, Iss 1, Pp 1-9 (2021)
Pediatric Rheumatology Online Journal
Pediatric Rheumatology Online Journal
Abstract The aim of the study was to investigate the relationship between the severity of typical clinical symptoms, severity of histopathological lesions in kidney biopsies in IgA vasculitis nephritis (IgAVN) and to propose indications for kidney bi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f30198b57ca449daf2dd5203bc1f612d
https://doi.org/10.1186/s12969-021-00616-z
https://doi.org/10.1186/s12969-021-00616-z
Autor:
Dorota Drozdz, Anna Medyńska, Anna Moczulska, Magdalena Silska-Dittmar, Przemysław Sikora, Aleksandra Żurowska, Danuta Ostalska-Nowicka, Ilona Olszak-Szot, Beata Bieniaś, Jacek Zachwieja, Marcin Tkaczyk, Roman Stankiewicz, Danuta Zwolińska, Lidia Hyla-Klekot, Anna Rogowska-Kalisz, Grażyna Kucharska, Magdalena Drozyńska-Duklas
Publikováno v:
Clinical and Experimental Pharmacology and Physiology. 46:313-321
The aim of the study was a multicenter analysis of the efficacy and safety of a non-standard immunosuppressive therapy with rituximab (Rtx) in children with steroid-resistant nephrotic syndrome (SRNS) with particular emphasis on the possibility of pe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::87e5d42e9acd6cef44c079b50cf29f0b
https://doi.org/10.1111/1440-1681.13046
https://doi.org/10.1111/1440-1681.13046