Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Beata Bienias"'
Autor:
Alper Soylu, Elke Wühl, Max C. Liebau, Guillaume Dorval, Wanja Bernhardt, Rukshana Shroff, Salim Caliskan, Laura Massella, Gordana Miloševski-Lomić, Ludwig Patzer, Juan David Gonzalez Rodriguez, Klaus Zerres, Katarzyna Taranta-Janusz, Francisco de la Cerda Ojeda, Bahriye Atmis, Bodo B. Beck, Jens König, Nadejda Ranguelov, Claudia Kowalewska, Jörg Dötsch, Florian Erger, Augustina Jankauskiene, Alberto Caldas Afonso, Markus Feldkoetter, Svetlana Papizh, Olivia Boyer, Jérôme Harambat, Franziska Grundmann, Matthias Galiano, Jun Oh, Claire Dossier, Jacques Lombet, Dieter Haffner, Gema Ariceta, Raphael Schild, Ismail Dursun, Ibrahim Gökce, Stella Stabouli, Marcus R. Benz, Rina Rus, Martin Bald, Michaela Gessner, Mieczysław Litwin, Neveen A. Soliman, Djalila Mekahli, Francesco Emma, Nurver Akinci, Loai A. Eid, Cengiz Candan, Alev Yilmaz, Anja Buescher, Lale Sever, Barbara Uetz, Julia Thumfart, Donald Wurm, Beata Bienias, Nadina Ortiz-Bruechle, Ali Duzova, Germana Longo, Przemysław Sikora, Oliver Gross, Susanne Schaefer, Yılmaz Tabel, Sabine Ponsel, Karsten Häffner, Franz Schaefer, Antonio Mastrangelo, Ana Teixeira, Bruno Ranchin, Günter Klaus, Maria Szczepańska, Claudia Dafinger, Andreea Rachisan, Monika Miklaszewska, Aurélie De Mul, Hulya Nalcacioglu, Sevgi Mir, Denis Morin, Katarzyna Zachwieja, Bärbel Lange-Sperandio, William Morello, Marc Fila, Jan Halbritter, Houweyda Jilani, Ute Derichs, Aurelia Morawiec-Knysak, Laure Collard, Małgorzata Stańczyk, Felix Lechner, Francesca Mencarelli, Jakub Zieg, Oliver Dunand, Klaus Arbeiter, Kathrin Burgmaier, Carsten Bergmann, Ilona Zagozdzon, Tomáš Seeman, Larisa Prikhodina, Nakysa Hooman, Lutz T. Weber, Björn Buchholz, Leonie Brinker, Nathalie Godefroid, Simone Wygoda, Hagen Staude
Publikováno v:
Kidney international, Vol. 100, no.3, p. 650-659 (2021)
Autosomal recessive polycystic kidney disease (ARPKD) is a severe disease of early childhood that is clinically characterized by fibrocystic changes of the kidneys and the liver. The main cause of ARPKD are variants in the PKHD1 gene encoding the lar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4a8d4bc309906dd46993a944c7188b5c
https://hdl.handle.net/20.500.12831/6664
https://hdl.handle.net/20.500.12831/6664
Akademický článek
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Autor:
Karolina Kalicka, Anna Wieczorkiewicz-Płaza, Beata Bienias, Katarzyna Bernat-Sitarz, Przemysław Sikora
Publikováno v:
Annales Academiae Medicae Silesiensis. 71:104-108
Zespół autoimmunolimfoproliferacyjny (ALPS) jest zespołem genetycznym o autosomalnym dominującym lub recesywnym sposobie dziedziczenia, charakteryzującym się łagodną limfoproliferacją oraz autoimmunizacją. Większość pacjentów z tą chor
Autor:
Piero Stratta, David Jayne, Fabio Sallustio, Alina Casian, Jingyuan Xie, Cristiane B. Dias, Serena Simeone, John Feehally, Hong Ren, Patrícia Cotovio, Derya Özmen, Byung Yoon Yang, Harin Rhee, Xiangmei Chen, Rosanna Coppo, Rachel B Jones, Jean Pierre Fauvel, Derya Guler, Hee Yeon Jung, Grazia Serino, Isao Ohsawa, George Efstratiadis, Claire Kennedy, Afroditi Pantzaki, Claudia Yuste, I. De Simone, Jadwiga Małdyk, Michael R. Clarkson, G. B. Visciano, Wenhu Liu, Krzysztof Kiryluk, Shubha Bellur, Beata Bienias, Jing Xu, Carlos Botelho, Özlem Yilmaz, Yuansheng Xie, François Berthoux, Rui Toledo Barros, Ali G. Gharavi, Emilie Kalbacher, Manuel Praga, Wenge Li, Shuwei Duan, Christos Bantis, Chunhua Zhou, Soo Bong Lee, Ligia C. Battaini, F. Ferrario, Noshaba Naz, George Toulkeridis, Cristina Silva, Stratis Kasimatis, Ying Zheng, Kyung Hoon Kim, Owen Kwon, Dóra Bajcsi, Weiming Wang, Viktoria Woronik, Pedro Maia, György Ábrahám, Kálmán Polner, Denis Fouque, Katarzyna Gadomska-Prokop, Yoshio Shimizu, Chan-Duck Kim, Federico Mecacci, Brigitte MacGregor, Sun-Hee Park, Dong Won Lee, Karina Lopes, Shanmai Guo, Rona M Smith, Aikaterini Papagianni, Leticia Jorge, Xiaoxia Pan, Guangyan Cai, Roman Stankiewicz, Il Young Kim, Yavuz Doǧan, Cristina Izzo, Ian Roberts, Hesham Mohey, A. Pani, Zhi-Qiang Huang, Jan Novak, Benedek Ronaszeki, Anindya Banerjee, Mark Canney, Haner Direskeneli, Lide Lun, Michel Ducher, Hakki Arikan, G. Fogazzi, Rui Toledo-Barros, Francesco Paolo Schena, Norella C T Kong, Armando Carreira, Denise Malheiro, Cristina Jironda, Yasuhiko Tomino, Anna Wasilewska, Xuemei Li, Francois Combarnous, Yong-Xi Chen, Myrthes Toledo-Barros, Halim Abdul Gafor, Philip H. Bredin, Ekaterina S Stolyarevich, Bruce A. Julian, Elena Romoli, Eun Young Seong, Jianrong Zhang, Salih Kavukçu, Ryszard Grenda, V. Terraneo, Maria Roszkowska-Blaim, Jie Wu, Koshi Yamada, Maria Júlia Correia Lima Nepomuceno Araújo, Colin Reily, Péter Légrády, Hitoshi Suzuki, Małgorzata Mizerska-Wasiak, Peter A. Merkel, Ihm Soo Kwak, Arzu Velioglu, Serdar Nalcaci, Nan Chen, Elisa Lazzarich, Yusuke Suzuki, Ga Young Park, Giorgio Mello, C. Sarcina, Shamsul Azhar Shah, Elena Zakharova, Sabah Mohamed Alharazy, Roberta Camilla, Satoshi Horikoshi, Marlyn Mohammad, Jin Lee, Yaping Wang, Cristiane Bitencourt Dias, Mehmet Koc, Lectícia Barbosa Jorge, Gurdal Birdal, Mário Campos, Terence Cook, Francisco Ferrer, C. Pozzi, F. Rastelli, Maria Skoularopoulou, Calogero Cirami, Francesco Pesce, Alfons Segarra, Agnieszka Rybi-Szumińska, Pingyan Shen, Luca Vergano, Cetin Ozener, Mrityunjay Hiremath, Jang-Hee Cho, Zsolt Balla, Roberta Fenoglio, Shuwen Liu, Maria Stangou, Hiyori Suzuki, Mamiko Shimamoto, Yeşim Öztürk, Serhan Tuglular, Elisabetta Radin, Małgorzata Zajaczkowska, Liam Plant, Enrico Eugenio Minetti, Rivera F, Marco Quaglia, Zhao-Hui Wang, Stéphan Troyanov, Arbaiyah Bain, Daniel C. Cattran, Yaser Shah, Ya Li, Blandine Laurent, Christophe Mariat, Maria Guedes Marques, Wen Zhang, Béla Iványi, Sharon Cox, Alper Soylu, Min Ji Shin, Laura Morando, Yong-Lim Kim, Xiaoyan Zhang, Seiji Nagamachi, Vivian L. Onusic, Michelle Lewin, Zoltán Rakonczay, Andrea Airoldi, Agnieszka Firszt-Adamczyk, Pamela Gallo, Zina Moldoveanu, Ágnes Haris, Milan Raska, Ji-Young Choi, Sandor Sonkodi
Publikováno v:
Nephrology Dialysis Transplantation. 28:i175-i184
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:
Roman Stankiewicz, Jadwiga Małdyk, Agnieszka Firszt-Adamczyk, Ryszard Grenda, Agnieszka Pukajło-Marczyk, Jacek J Pietrzyk, Małgorzata Zajaczkowska, Karolina Cichoń-Kawa, Maria Szczepańska, Magdalena Drozyńska-Duklas, Agnieszka Rybi-Szumińska, Agnieszka Turczyn, Danuta Zwolińska, Beata Bienias, Anna Wasilewska, Małgorzata Pańczyk-Tomaszewska, Katarzyma Gadomska-Prokop, Aleksandra Zurowska, Monika Miklaszewska, Małgorzata Mizerska-Wasiak
Publikováno v:
Nephrology Dialysis Transplantation. 31:i329-i330
Autor:
Monika Pawlak-Bratkowska, Anna Jakubowska, Maria Roszkowska-Blaim, Malgorzata Zajgzkowska, Piotr Skrzypczyk, Zofia Wawer, Katarzyna Kilis-Pstrusinska, Marcin Tkaczyk, Małgorzata Pańczyk-Tomaszewska, Marta Szczepaniak, Beata Bienias
Publikováno v:
Clinical nephrology. 81(3)
The aim of the study was to assess idiopathic nephrotic syndrome (INS) relapse rate, co-morbidities, and social status of adults diagnosed with INS in childhood.A written questionnaire was sent to 118 adults treated for INS in childhood. In 61 (51.7%
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:
Beata Bienias, Przemysław Sikora, Ewelina Ksiazek, Andrzej Borzecki, Marek Majewski, Halina Borzecka, Małgorzata Zajaczkowska
Publikováno v:
Urinary Tract Infections
Post-inflammatory nephropathy is a progressive renal scarring which may be a consequence of one or more episodes of acute pyelonephritis. Macroscopically, post-inflammatory nephropathy leads to gradual decrease in kidney size and deformity and dilati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ddcc196cff89b36a876db67d9c5ff6de
http://www.intechopen.com/articles/show/title/post-inflammatory-nephropathy
http://www.intechopen.com/articles/show/title/post-inflammatory-nephropathy