Early Markers of Tubulointerstitial Fibrosis in Children With Idiopathic Nephrotic Syndrome: Preliminary Report von Bieniaś, Beata, Zajączkowska, Małgorzata, Borzęcka, Halina, Sikora, Przemysław, Wieczorkiewicz-Płaza, Anna, Wilczyńska, Barbara

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What has changed in the prevalence of hypertension in dialyzed children during the last decade? von Tkaczyk, Marcin, Stańczyk, Małgorzata, Miklaszewska, Monika, Zachwieja, Katarzyna, Wierciński, Ryszard, Stankiewicz, Roman, Firszt-Adamczyk, Agnieszka, Zachwieja, Jacek, Borzęcka, Halina, Zagożdżon, Ilona, Leszczyńska, Beata, Medyńska, Anna, Adamczyk, Piotr, Szczepańska, Maria, Fendler, Wojciech

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3D/4D contrast-enhanced urosonography (ceVUS) in children – is it superior to the 2D technique? von Woźniak, Magdalena Maria, Osemlak, Paweł, Ntoulia, Aikaterini, Borzęcka, Halina, Bieniaś, Beata, Brodzisz, Agnieszka, Jędrzejewski, Grzegorz, Drelich-Zbroja, Anna, Powerski, Maciej, Pech, Maciej, Wieczorek, Andrzej Paweł

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Bilateral slipped capital femoral epiphysis in a male adolescent with familial hypomagnesemia with hypercalciuria and nephrocalcinosis (FHHNC), chronic renal failure, and severe hy... von Sikora, Przemysław, Zajączkowska, Małgorzata, Raganowicz, Tomasz, Borzęcka, Halina, Gregosiewicz, Andrzej, Konrad, Martin

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2D/3D/4D contrast-enhanced voiding urosonography in the diagnosis and monitoring of treatment of vesicoureteral reflux in children - can it replace voiding cystourethrography? von Woźniak, Magdalena Maria, Pawelec, Agata, Wieczorek, Andrzej Paweł, Zajączkowska, Maria Małgorzata, Borzęcka, Halina, Nachulewicz, Paweł

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Two-dimensional (2D), three-dimensional static (3D) and real-time (4D) contrast enhanced voiding urosonography (ceVUS) versus voiding cystourethrography (VCUG) in children with ves... von Woźniak, Magdalena Maria, Wieczorek, Andrzej Paweł, Pawelec, Agata, Brodzisz, Agnieszka, Zajączkowska, Maria Małgorzata, Borzęcka, Halina, Nachulewicz, Paweł

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Acute renal failure due to bilateral xanthine urolithiasis in a boy with Lesch-Nyhan syndrome von Sikora, Przemysław, Pijanowska, Monika, Majewski, Marek, Bieniaś, Beata, Borzecka, Halina, Zajczkowska, Małgorzata

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Genetic screening in adolescents with steroid-resistant nephrotic syndrome von Lipska, Beata S., Iatropoulos, Paraskevas, Maranta, Ramona, Caridi, Gianluca, Ozaltin, Fatih, Anarat, Ali, Balat, Ayse, Gellermann, Jutta, Trautmann, Agnes, Erdogan, Ozlem, Saeed, Bassam, Emre, Sevinc, Bogdanovic, Radovan, Azocar, Marta, Balasz-Chmielewska, Irena, Benetti, Elisa, Caliskan, Salim, Mir, Sevgi, Melk, Anette, Ertan, Pelin, Baskin, Esra, Jardim, Helena, Davitaia, Tinatin, Wasilewska, Anna, Drozdz, Dorota, Szczepanska, Maria, Jankauskiene, Augustina, Higuita, Lina Maria Serna, Ardissino, Gianluigi, Ozkaya, Ozan, Kuzma-Mroczkowska, Elzbieta, Soylemezoglu, Oguz, Ranchin, Bruno, Medynska, Anna, Tkaczyk, Marcin, Peco-Antic, Amira, Akil, Ipek, Jarmolinski, Tomasz, Firszt-Adamczyk, Agnieszka, Dusek, Jiri, Simonetti, Giacomo D., Gok, Faysal, Gheissari, Alaleh, Emma, Francesco, Krmar, Rafael T., Fischbach, Michel, Printza, Nikoleta, Simkova, Eva, Mele, Caterina, Ghiggeri, Gian Marco, Schaefer, Franz

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Color Doppler dynamic tissue perfusion measurement: a novel tool in the assessment of renal parenchymal perfusion in children with vesicoureteral reflux von Woźniak, Magdalena M, Scholbach, Thomas M, Scholbach, Jakob, Pawelec, Agata, Nachulewicz, Paweł, Wieczorek, Andrzej P, Brodzisz, Agnieszka, Zajączkowska, Maria M, Borzęcka, Halina

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Antihypertensive treatment prescription in pediatric dialysis patients in Poland: A comparison between two nationwide studies 2003/2004-2013 von Wróblewski, Krzysztof, Hincz, Karolina, Miklaszewska, Monika, Zachwieja, Katarzyna, Wierciński, Ryszard, Stankiewicz, Roman, Firszt-Adamczyk, Agnieszka, Zachwieja, Jacek, Borzęcka, Halina, Ziółkowska, Helena, Medyńska, Anna, Zwolińska, Danuta, Szczepańska, Maria, Stańczyk, Małgorzata, Zagożdżon, Ilona, Leszczyńska, Beata, Adamczyk, Piotr, Tkaczyk, Marcin

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Juvenile nephronophtisis, short stature, partial adontia and skeletal abnormalities—a new syndromic association von Sikora, Przemysław, Majewski, Marek, Kandzierski, Grzegorz, Zajączkowska, Małgorzata, Borzęcka, Halina, Korolczuk, Agnieszka, Kozlowski, Kazimierz

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Long-Term Outcome of Steroid-Resistant Nephrotic Syndrome in Children von Trautmann, Agnes, Schnaidt, Sven, Lipska-Ziętkiewicz, Beata S, Bodria, Monica, Ozaltin, Fatih, Emma, Francesco, Anarat, Ali, Melk, Anette, Azocar, Marta, Oh, Jun, Saeed, Bassam, Gheisari, Alaleh, Caliskan, Salim, Gellermann, Jutta, Higuita, Lina Maria Serna, Jankauskiene, Augustina, Drozdz, Dorota, Mir, Sevgi, Balat, Ayse, Szczepanska, Maria, Paripovic, Dusan, Zurowska, Alexandra, Bogdanovic, Radovan, Yilmaz, Alev, Ranchin, Bruno, Baskin, Esra, Erdogan, Ozlem, Remuzzi, Giuseppe, Firszt-Adamczyk, Agnieszka, Kuzma-Mroczkowska, Elzbieta, Litwin, Mieczyslaw, Murer, Luisa, Tkaczyk, Marcin, Jardim, Helena, Wasilewska, Anna, Printza, Nikoleta, Fidan, Kibriya, Simkova, Eva, Borzecka, Halina, Staude, Hagen, Hees, Katharina, Schaefer, Franz

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Leczenie czynnikami pobudzającymi erytropoezę u dzieci z przewlekłą chorobą nerek w 3.-5. stadium – wyniki ogólnopolskiego badania wieloośrodkowego Polskiego Towarzystwa Nefrologii... von 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

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Variation of the clinical spectrum and genotype-phenotype associations in Coenzyme Q10 deficiency associated glomerulopathy von Drovandi, Stefania, Lipska-Ziętkiewicz, Beata S., Ozaltin, Fatih, Emma, Francesco, Gulhan, Bora, Boyer, Olivia, Trautmann, Agnes, Ziętkiewicz, Szymon, Xu, Hong, Shen, Qian, Rao, Jia, Riedhammer, Korbinian M., Heemann, Uwe, Hoefele, Julia, Stenton, Sarah L., Tsygin, Alexey N., Ng, Kar-Hui, Fomina, Svitlana, Benetti, Elisa, Aurelle, Manon, Prikhodina, Larisa, Schijvens, Anne M., Tabatabaeifar, Mansoureh, Jankowski, Maciej, Baiko, Sergey, Mao, Jianhua, Feng, Chunyue, Deng, Fang, Rousset-Rouviere, Caroline, Stańczyk, Małgorzata, Bałasz-Chmielewska, Irena, Fila, Marc, Durkan, Anne M., Levart, Tanja Kersnik, Dursun, Ismail, Esfandiar, Nasrin, Haas, Dorothea, Bjerre, Anna, Anarat, Ali, Benz, Marcus R., Talebi, Saeed, Hooman, Nakysa, Ariceta, Gema, Baiko, Sergey, Serna Higuita, Lina Maria, Schaefer, Franz, Trautmann, Agnes, Tabatabaeifar, Mansoureh, Gheissari, Alaleh, Hooman, Nakysa, Benetti, Elisa, Emma, Francesco, Nigmatullina, Nazym, Lipska-Ziętkiewicz, Beata S., Bałasz-Chmielewska, Irena, Tkaczyk, Marcin, Stańczyk, Małgorzata, Borzecka, Halina, Tsygin, Alexey N., Prikhodina, Larisa, Bogdanovic, Radovan, Anarat, Ali, Ozaltin, Fatih, Mir, Sevgi, Fomina, Svitlana, Klopstock, Thomas, Prokisch, Holger, Kornblum, Cornelia, Xu, Hong, Shen, Qian, Rao, Jia, Liu, Cui-Hua, Sun, Shu-Zhen, Deng, Fang, Dong, Yang, Wang, Xiao-Wen, Luan, Jiang-Wei, Schaefer, Franz

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Spectrum of steroid-resistant and congenital nephrotic syndrome in children: the PodoNet registry cohort von Trautmann, Agnes, Bodria, Monica, Ozaltin, Fatih, Gheisari, Alaleh, Melk, Anette, Azocar, Marta, Anarat, Ali, Caliskan, Salim, Emma, Francesco, Gellermann, Jutta, Oh, Jun, Baskin, Esra, Ksiazek, Joanna, Remuzzi, Giuseppe, Erdogan, Ozlem, Akman, Sema, Dusek, Jiri, Davitaia, Tinatin, Özkaya, Ozan, Papachristou, Fotios, Firszt-Adamczyk, Agnieszka, Urasinski, Tomasz, Testa, Sara, Krmar, Rafael T, Hyla-Klekot, Lidia, Pasini, Andrea, Özcakar, Z Birsin, Sallay, Peter, Cakar, Nilgun, Galanti, Monica, Terzic, Joelle, Aoun, Bilal, Caldas Afonso, Alberto, Szymanik-Grzelak, Hanna, Lipska, Beata S, Schnaidt, Sven, Schaefer, Franz

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Oral Coenzyme Q10 supplementation leads to better preservation of kidney function in steroid-resistant nephrotic syndrome due to primary Coenzyme Q10 deficiency von Drovandi, Stefania, Lipska-Ziętkiewicz, Beata S., Ozaltin, Fatih, Emma, Francesco, Gulhan, Bora, Boyer, Olivia, Trautmann, Agnes, Xu, Hong, Shen, Qian, Rao, Jia, Riedhammer, Korbinian M., Heemann, Uwe, Hoefele, Julia, Stenton, Sarah L., Tsygin, Alexey N., Ng, Kar-Hui, Fomina, Svitlana, Benetti, Elisa, Aurelle, Manon, Prikhodina, Larisa, Schreuder, Michiel F., Tabatabaeifar, Mansoureh, Jankowski, Maciej, Baiko, Sergey, Mao, Jianhua, Feng, Chunyue, Liu, Cuihua, Sun, Shuzhen, Deng, Fang, Wang, Xiaowen, Clavé, Stéphanie, Stańczyk, Małgorzata, Bałasz-Chmielewska, Irena, Fila, Marc, Durkan, Anne M., Levart, Tanja Kersnik, Dursun, Ismail, Esfandiar, Nasrin, Haas, Dorothea, Bjerre, Anna, Anarat, Ali, Benz, Marcus R., Talebi, Saeed, Hooman, Nakysa, Ariceta, Gema, Baiko, Sergey, Serna Higuita, Lina Maria, Schaefer, Franz, Trautmann, Agnes, Tabatabaeifar, Mansoureh, Gheissari, Alaleh, Hooman, Nakysa, Benetti, Elisa, Emma, Francesco, Nigmatullina, Nazym, Lipska-Ziętkiewicz, Beata S., Bałasz-Chmielewska, Irena, Tkaczyk, Marcin, Stańczyk, Małgorzata, Borzecka, Halina, Tsygin, Alexey N., Prikhodina, Larisa, Bogdanovic, Radovan, Anarat, Ali, Ozaltin, Fatih, Mir, Sevgi, Fomina, Svitlana, Klopstock, Thomas, Prokisch, Holger, Kornblum, Cornelia, Xu, Hong, Shen, Qian, Rao, Jia, Liu, Cui-Hua, Sun, Shu-Zhen, Deng, Fang, Dong, Yang, Wang, Xiao-Wen, Luan, Jiang-Wei, Schaefer, Franz

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ADCK4-Associated Glomerulopathy Causes Adolescence-Onset FSGS von Korkmaz, Emine, Lipska-Ziętkiewicz, Beata S, Boyer, Olivia, Gribouval, Olivier, Fourrage, Cecile, Tabatabaei, Mansoureh, Schnaidt, Sven, Gucer, Safak, Kaymaz, Figen, Arici, Mustafa, Dinckan, Ayhan, Mir, Sevgi, Bayazit, Aysun K, Emre, Sevinc, Balat, Ayse, Rees, Lesley, Shroff, Rukshana, Bergmann, Carsten, Mourani, Chebl, Antignac, Corinne, Ozaltin, Fatih, Schaefer, Franz

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Exploring the Clinical and Genetic Spectrum of Steroid Resistant Nephrotic Syndrome: The PodoNet Registry von Trautmann, Agnes, Lipska-Ziętkiewicz, Beata S, Schaefer, Franz

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Sonocystografia mikcyjna 2D/3D/4D w diagnostyce i monitorowaniu leczenia odpływów pęcherzowo- -moczowodowych u dzieci – czy może zastąpić rentgenowską cystouretrografię mikcyjną?... von Woźniak, Magdalena Maria, Pawelec, Agata, Wieczorek, Andrzej Paweł, Zajączkowska, Maria Małgorzata, Borzęcka, Halina, Nachulewicz, Paweł

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Genotype–phenotype associations in WT1 glomerulopathy von Lipska, Beata S., Ranchin, Bruno, Iatropoulos, Paraskevas, Gellermann, Jutta, Melk, Anette, Ozaltin, Fatih, Caridi, Gianluca, Seeman, Tomas, Tory, Kalman, Jankauskiene, Augustina, Zurowska, Aleksandra, Szczepanska, Maria, Wasilewska, Anna, Harambat, Jerome, Trautmann, Agnes, Peco-Antic, Amira, Borzecka, Halina, Moczulska, Anna, Saeed, Bassam, Bogdanovic, Radovan, Kalyoncu, Mukaddes, Simkova, Eva, Erdogan, Ozlem, Vrljicak, Kristina, Teixeira, Ana, Azocar, Marta, Schaefer, Franz

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