Zobrazeno 1 - 10
of 29
pro vyhledávání: '"Irena Bałasz Chmielewska"'
Autor:
Katarzyna Kiliś-Pstrusińska, Anna Medyńska, Piotr Adamczyk, Irena Bałasz-Chmielewska, Ryszard Grenda, Agnieszka Kluska-Jóźwiak, Beata Leszczyńska, Ilona Olszak-Szczot, Monika Miklaszewska, Maria Szczepańska, Marcin Tkaczyk, Anna Wasilewska, Katarzyna Zachwieja, Maria Zajączkowska, Helena Ziólkowska, Ilona Zagożdżon, Danuta Zwolińska
Publikováno v:
Annals of Agricultural and Environmental Medicine, Vol 21, Iss 876253, Pp 876-881 (2014)
[b]introduction and objective.[/b] Chronic kidney disease (CKD) in children burdens life of patients and their families. Little is known about parents` assessment of families’ social situation. However, the knowledge of the details of a patient’s
Externí odkaz:
https://doaj.org/article/bf76c0c937404c57a7ac65457bafb9f4
Anxiety in Children and Adolescents with Chronic Kidney Disease - Multicenter National Study Results
Autor:
Katarzyna Kiliś-Pstrusińska, Anna Medyńska, Piotr Adamczak, Irena Bałasz- Chmielewska, Ryszard Grenda, Agnieszka Kluska-Jóźwiak, Beata Leszczyńska, Ilona Olszak-Szot, Monika Miklaszewska, Maria Szczepańska, Marcin Tkaczyk, Anna Wasilewska, Katarzyna Zachwieja, Maria Zajączkowska, Helena Ziółkowska, Ilona Zagożdżon, Danuta Zwolińska
Publikováno v:
Kidney & Blood Pressure Research, Vol 37, Iss 6, Pp 579-587 (2013)
Background/Aims: Chronic medical illness is a significant risk factor for the development of psychiatric disorders. The aims of the study were: to investigate the level of anxiety in children with chronic kidney disease (CKD) and to identify factors
Externí odkaz:
https://doaj.org/article/958cb7184eea44d6a7b57da9e7d35c99
Autor:
Anna Jander, Ryszard Wierciński, Irena Bałasz-Chmielewska, Monika Miklaszewska, Katarzyna Zachwieja, Halina Borzęcka, Jacek Zachwieja, Irena Olszak-Szot, Dariusz Kubicki, Helena Ziółkowska, Jacek Rubik, Maria Szczepańska, Dariusz Runowski, Wojciech Fendler, Marcin Tkaczyk
Publikováno v:
Pediatria i Medycyna Rodzinna, Vol 7, Iss 2, Pp 156-163 (2011)
Wstęp: Choć czynniki stymulujące erytropoezę (ESA) są stosowane od wielu lat w leczeniu niedokrwistości nerkopochodnej u chorych ze schyłkową niewydolnością nerek, niewiele jest badań oceniających skuteczność takiego leczenia u dzieci
Externí odkaz:
https://doaj.org/article/73abbb20a08d476fa95f4763732cbe3c
Autor:
Stefania Drovandi, Beata S. Lipska-Ziętkiewicz, Fatih Ozaltin, Francesco Emma, Bora Gulhan, Olivia Boyer, Agnes Trautmann, Szymon Ziętkiewicz, Hong Xu, Qian Shen, Jia Rao, Korbinian M. Riedhammer, Uwe Heemann, Julia Hoefele, Sarah L. Stenton, Alexey N. Tsygin, Kar-Hui Ng, Svitlana Fomina, Elisa Benetti, Manon Aurelle, Larisa Prikhodina, Anne M. Schijvens, Mansoureh Tabatabaeifar, Maciej Jankowski, Sergey Baiko, Jianhua Mao, Chunyue Feng, Fang Deng, Caroline Rousset-Rouviere, Małgorzata Stańczyk, Irena Bałasz-Chmielewska, Marc Fila, Anne M. Durkan, Tanja Kersnik Levart, Ismail Dursun, Nasrin Esfandiar, Dorothea Haas, Anna Bjerre, Ali Anarat, Marcus R. Benz, Saeed Talebi, Nakysa Hooman, Gema Ariceta, Franz Schaefer, Lina Maria Serna Higuita, Alaleh Gheissari, Nazym Nigmatullina, Marcin Tkaczyk, Halina Borzecka, Radovan Bogdanovic, Sevgi Mir, Thomas Klopstock, Holger Prokisch, Cornelia Kornblum, Cui-Hua Liu, Shu-Zhen Sun, Yang Dong, Xiao-Wen Wang, Jiang-Wei Luan
Publikováno v:
Kidney Int. 102, 592-603 (2022)
Scientia
Scientia
Coenzyme Q10; Mitochondria; Steroid-resistant nephrotic syndrome Coenzima Q10; Mitocondrias; Síndrome nefrótico resistente a los esteroides Coenzim Q10; Mitocondris; Síndrome nefròtic resistent als esteroides Primary Coenzyme Q10 deficiency is a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a4e1e37391fef1cc876f8e121f4381fe
http://hdl.handle.net/10852/99032
http://hdl.handle.net/10852/99032
Autor:
Stefania Drovandi, Beata S. Lipska-Ziętkiewicz, Fatih Ozaltin, Francesco Emma, Bora Gulhan, Olivia Boyer, Agnes Trautmann, Hong Xu, Qian Shen, Jia Rao, Korbinian M. Riedhammer, Uwe Heemann, Julia Hoefele, Sarah L. Stenton, Alexey N. Tsygin, Kar-Hui Ng, Svitlana Fomina, Elisa Benetti, Manon Aurelle, Larisa Prikhodina, Michiel F. Schreuder, Mansoureh Tabatabaeifar, Maciej Jankowski, Sergey Baiko, Jianhua Mao, Chunyue Feng, Cuihua Liu, Shuzhen Sun, Fang Deng, Xiaowen Wang, Stéphanie Clavé, Małgorzata Stańczyk, Irena Bałasz-Chmielewska, Marc Fila, Anne M. Durkan, Tanja Kersnik Levart, Ismail Dursun, Nasrin Esfandiar, Dorothea Haas, Anna Bjerre, Ali Anarat, Marcus R. Benz, Saeed Talebi, Nakysa Hooman, Gema Ariceta, Franz Schaefer, Lina Maria Serna Higuita, Alaleh Gheissari, Nazym Nigmatullina, Marcin Tkaczyk, Halina Borzecka, Radovan Bogdanovic, Sevgi Mir, Thomas Klopstock, Holger Prokisch, Cornelia Kornblum, Cui-Hua Liu, Shu-Zhen Sun, Yang Dong, Xiao-Wen Wang, Jiang-Wei Luan
Publikováno v:
Kidney International, 102, 3, pp. 604-612
Kidney Int. 102, 604-612 (2022)
Kidney International, 102, 604-612
Kidney Int. 102, 604-612 (2022)
Kidney International, 102, 604-612
Contains fulltext : 283144.pdf (Publisher’s version ) (Open Access) Primary Coenzyme Q10 (CoQ(10)) deficiency is an ultra-rare disorder caused by defects in genes involved in CoQ(10) biosynthesis leading to multidrug-resistant nephrotic syndrome as
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b84c27b3e90b69a46a805c20918a32ef
http://hdl.handle.net/10852/100389
http://hdl.handle.net/10852/100389
Publikováno v:
Pediatric nephrology (Berlin, Germany). 33(12)
Treatment of steroid resistant nephrotic syndrome is still a challenge for physicians. There are a growing number of studies exploring genetic background of steroid-resistant glomerulopathies. We present the case of a 4-year-old girl with steroid-res
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::49dff57a0e2a53999b19a3c2c3808e09
https://pubmed.ncbi.nlm.nih.gov/30588546
https://pubmed.ncbi.nlm.nih.gov/30588546
Autor:
Maria Szczepańska, Joanna Ksiazek, Mieczysław Litwin, Beata S. Lipska, Marcin Tkaczyk, Elzbieta Kuzma-Mroczkowska, Aleksandra Zurowska, Janusz Limon, Magdalena Silska, Anna Medyńska, Anna Wasilewska, Franz Schaefer, L Morzuch, Tomasz Jarmoliński, Kacper Wasielewski, Irena Bałasz-Chmielewska, Halina Borzecka, Agnieszka Firszt-Adamczyk, Ewa Gacka, Dorota Drozdz, Dominika Vetter
Publikováno v:
Journal of Applied Genetics; Vol 54
Journal of Applied Genetics
Journal of Applied Genetics
Hereditary nephrotic syndrome is caused by mutations in a number of different genes, the most common being NPHS2. The aim of the study was to identify the spectrum of NPHS2 mutations in Polish patients with the disease. A total of 141 children with s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::192bbe7f41c322b378e6b5769a91dc48
https://doi.org/10.1007/s13353-013-0147-z
https://doi.org/10.1007/s13353-013-0147-z
Autor:
Monika Miklaszewska, Maria SzczepaŃska, Irena Bałasz-Chmielewska, Wojciech Fendler, Katarzyna Zachwieja, Halina Borzecka, Jacek Zachwieja, Jacek Rubik, Anna Jander, Helena Ziółkowska, Dariusz Kubicki, Irena Olszak-Szot, Dariusz Runowski, Marcin Tkaczyk, Ryszard WierciŃski
Publikováno v:
Scandinavian Journal of Urology and Nephrology. 46:375-380
Erythropoiesis-stimulating agents (ESAs) are applied as a standard therapy in children with anaemia in chronic kidney disease. The aim of this study was to describe the efficacy and details of ESA treatment in a population of dialysed children in Pol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2982795cb8ff0b6f3dfd21d1f36a0bf6
https://doi.org/10.3109/00365599.2012.685492
https://doi.org/10.3109/00365599.2012.685492
Autor:
Ilona Zagozdzon, Irena Bałasz-Chmielewska, Ryszard Wierciński, Katarzyna Zachwieja, Iga Załuska-Leśniewska, Hanna Kipigroch, Hanna Boguszewska-Bączkowska, Barbara Kołłątaj, Ewa Stefaniak, Joanna Latoszyńska, Anna Jander, Beata Leszczyńska, Marcin Tkaczyk, Irena Makulska
Publikováno v:
Archives of Medical Science. 3:414-419
INTRODUCTION Peritoneal dialysis (PD) is a preferred method of renal replacement therapy for end-stage renal disease in children. Recent advances have allowed chronic PD to be provided to children of all ages and sizes. MATERIAL AND METHODS The study
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1b4a3636453e449e3d57c88efc111fef
https://doi.org/10.5114/aoms.2010.14265
https://doi.org/10.5114/aoms.2010.14265
Autor:
Aleksandra Żurowska, Marcin Tkaczyk, Irena Bałasz-Chmielewska, Anna Jander, Jacek A Pietrzyk, Dorota Drozdz, Piotr Skrzypczyk, Maria Roszkowska-Blaim
Publikováno v:
Publons
Purpose To evaluate the effect of hypertension (HTN) and antihypertensive medications (AHM) on residual renal function (RRF) in children on CAPD and APD. Material/methods We retrospectively evaluated underlying kidney disease, systolic and diastolic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::10f3db038a6f508cd6269ad12da6f0e2
https://ruj.uj.edu.pl/xmlui/handle/item/96809
https://ruj.uj.edu.pl/xmlui/handle/item/96809