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1. Associations of longitudinal height and weight with clinical outcomes in pediatric kidney replacement therapy: results from the ESPN/ERA Registry

Author

Bonthuis, Marjolein, Bakkaloglu, Sevcan A., Vidal, Enrico, Baiko, Sergey, Braddon, Fiona, Errichiello, Carmela, Francisco, Telma, Haffner, Dieter, Lahoche, Annie, Leszczyńska, Beata, Masalkiene, Jurate, Stojanovic, Jelena, Molchanova, Maria S., Reusz, George, Barba, Adela Rodriguez, Rosales, Alejandra, Tegeltija, Sanja, Ylinen, Elisa, Zlatanova, Galia, Harambat, Jérôme, and Jager, Kitty J.

Published
2023
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2. Metabolic Acidosis Is Associated With an Accelerated Decline of Allograft Function in Pediatric Kidney Transplantation

Author

Ariceta, Gema, Awan, Atif, Bakkaloğlu, Sevcan, Bonthuis, Marjolein, Robroeks, Charlotte Bootsma, Bouts, Antonia, Christian, Martin, Cornelissen, Marlies, Duzova, Ali, Esfandiar, Nasrin, Ghio, Luciana, Grenda, Ryszard, Guzzo, Isabella, Goni, Maria Herrero, Hogan, Julien, Hongsawong, Nattaphorn, Kanzelmeyer, Nele, Bayazit, Aysun Karabay, Aksoy, Gülşah Kaya, Knops, Noel, Kamphuis, Linda Koster, Erez, Daniella Levy, Lopez-Baez, Victor, Madrid, Alvaro, Marks, Stephen, Melk, Anette, Murer, Luisa, Pape, Lars, Peruzzi, Licia, Petrosyan, Edita, Preka, Evgenia, Printza, Nikoleta, Rachisan, Andreea Liana, Raes, Ann, Shenoy, Mohan, Soylemezoglu, Oguz, Strologo, Luca Dello, Teixeira, Ana, Topaloglu, Rezan, Weitz, Markus, Zieg, Jakub, Zlatanova, Galia, Patry, Christian, Harambat, Jerome, Ağbaş, Ayşe, Askiti, Varvara, Avramescu, Marina, Bacchetta, Justine, Bakkaloglu, Sevcan, Bontuis, Marjolein, Booth, Caroline, Dehoux, Laurene, Dizazzo, Giacomo, Drozdz, Dorota, Dursun, Ismail, Gessner, Michaela, Groothoff, Jaap, Guido, Giuliana, Klaus, Guenter, Koster-Kamphuis, Linda, Lalayiannis, Alexander, Leifheit-Nestler, Maren, Manish, Sinha, Matteucci, Chiara, Oh, Jun, Ozkaya, Ozan, Pietrement, Christine, Prytula, Agnieszka, Reusz, George, Schaefer, Franz, Schmitt, Claus Peter, Schön, Anne, Sever, Fatma Lale, Stabouli, Stella, Döven, Serra Sürmeli, Tondel, Camilla, Verrina, Enrico, Vidal, Enrico, Wallace, Dean, Arslan, Zainab, Bald, M., Fehrenbach, H., Haffner, D., Hansen, M., Hempel, C., John, U., Klaus, G., König, J., Lange-Sperandio, B., Müller, D., Oh, J., Pape, L., Pohl, M., Sauerstein, K., Schalk, G., Staude, H., Strotmann, P., Weber, L.T., Weitz, M., Berta, L., Heindl-Rusai, K., Shroff, Rukshana, van Gremberghe, Ineke, Krupka, Kai, Benetti, Elisa, Büyükkaragöz, Bahar, Kranz, Birgitta, Nalçacıoğlu, Hülya, Sellier-Leclerc, Anne-Laure, and Tönshoff, Burkhard

Published
2024
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3. A multicenter retrospective study of calcineurin inhibitors in nephrotic syndrome secondary to podocyte gene variants

Author

Malakasioti, Georgia, Iancu, Daniela, Milovanova, Anastasiia, Tsygin, Alexey, Horinouchi, Tomoko, Nagano, China, Nozu, Kandai, Kamei, Koichi, Fujinaga, Shuichiro, Iijima, Kazumoto, Kang, Hee Gyung, Sinha, Rajiv, Basu, Biswanath, Morello, William, Montini, Giovanni, Waters, Aoife, Boyer, Olivia, Yıldırım, Zeynep Yürük, Yel, Sibel, Dursun, İsmail, McCarthy, Hugh J., Vivarelli, Marina, Prikhodina, Larisa, Besouw, Martine T.P., Chan, Eugene Yu-hin, Huang, Wenyan, Kemper, Markus J., Loos, Sebastian, Prestidge, Chanel, Wong, William, Zlatanova, Galia, Ehren, Rasmus, Weber, Lutz T., Chehade, Hassib, Hooman, Nakysa, Tkaczyk, Marcin, Stańczyk, Małgorzata, Miligkos, Michael, and Tullus, Kjell

Published
2023
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5. Corrigendum to “A multicenter retrospective study of calcineurin inhibitors in nephrotic syndrome secondary to podocyte gene variants.” Kidney Int. 2023;103:962–972

Author

Malakasioti, Georgia, primary, Iancu, Daniela, additional, Milovanova, Anastasiia, additional, Tsygin, Alexey, additional, Horinouchi, Tomoko, additional, Nagano, China, additional, Nozu, Kandai, additional, Kamei, Koichi, additional, Fujinaga, Shuichiro, additional, Iijima, Kazumoto, additional, Kang, Hee Gyung, additional, Sinha, Rajiv, additional, Basu, Biswanath, additional, Morello, William, additional, Montini, Giovanni, additional, Waters, Aoife, additional, Boyer, Olivia, additional, Yıldırım, Zeynep Yürük, additional, Yel, Sibel, additional, Dursun, İsmail, additional, McCarthy, Hugh J., additional, Vivarelli, Marina, additional, Prikhodina, Larisa, additional, Besouw, Martine T.P., additional, Chan, Eugene Yu-hin, additional, Huang, Wenyan, additional, Kemper, Markus J., additional, Loos, Sebastian, additional, Prestidge, Chanel, additional, Wong, William, additional, Zlatanova, Galia, additional, Ehren, Rasmus, additional, Weber, Lutz T., additional, Chehade, Hassib, additional, Hooman, Nakysa, additional, Tkaczyk, Marcin, additional, Stańczyk, Małgorzata, additional, Miligkos, Michael, additional, Tullus, Kjell, additional, Malakasioti, Georgia, additional, Martins, Vitor Hugo, additional, Camilla, Roberta, additional, Gianoglio, Bruno, additional, Maxted, Andrew, additional, Tsimaratos, Michel, additional, Alpay, Harika, additional, Said-Conti, Valerie, additional, Meglič, Anamarija, additional, Bresso, Paula, additional, Coccia, Paula, additional, Mitsioni, Andromachi, additional, and Yap, Yok-Chin, additional

Published
2024
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7. Parathyroid hormone and phosphate homeostasis in patients with Bartter and Gitelman syndrome: an international cross-sectional study

Author

Verploegen, Maartje F A, Vargas-Poussou, Rosa, Walsh, Stephen B, Alpay, Harika, Amouzegar, Atefeh, Ariceta Iraola, Gema, Atmis, Bahriye, Bacchetta, Justine, Bárány, Peter, Baron, Stéphanie, Bayrakci, Umut Selda, Belge, Hendrica, Besouw, Martine, Blanchard, Anne, Bökenkamp, Arend, Boyer, Olivia, Burgmaier, Kathrin, Calò, Lorenzo A, Decramer, Stéphane, Devuyst, Olivier, van Dyck, Maria, Ferraro, Pietro Manuel, Fila, Marc, Francisco, Telma, Ghiggeri, Gian Marco, Gondra, Leire, Guarino, Stefano, Hooman, Nakysa, Hoorn, Ewout J, Houillier, Pascal, Kamperis, Konstantinos, Kari, Jameela A, Konrad, Martin, Levtchenko, Elena, Lucchetti, Laura, Lugani, Francesca, Marzuillo, Pierluigi, Mohidin, Barian, Neuhaus, Thomas J, Osman, Abdaldafae, Papizh, Svetlana, Perelló, Manel, Rookmaaker, Maarten B, Conti, Valerie Said, Santos, Fernando, Sawaf, Ghalia, Serdaroglu, Erkin, Szczepanska, Maria, Taroni, Francesca, Topaloglu, Rezan, Trepiccione, Francesco, Vidal, Enrico, Wan, Elizabeth R, Weber, Lutz, Yildirim, Zeynep Yuruk, Yüksel, Selçuk, Zlatanova, Galia, Bockenhauer, Detlef, Emma, Francesco, Nijenhuis, Tom, Universitat Autònoma de Barcelona, Institut Català de la Salut, [Verploegen MFA] Department of Nephrology, Radboud University Medical Center, Nijmegen, The Netherlands. [Vargas-Poussou R] Department of Genetics, Centre de Références MARHEA, Hôpital Européen Georges Pompidou Assistance Publique Hôpitaux de Paris, Paris, France. [Walsh SB] Department of Renal Medicine, University College London, London, UK. [Alpay H] Division of Paediatric Nephrology, Faculty of Medicine, Marmara University, Istanbul, Turkey. [Amouzegar A] Division of Nephrology, Department of Medicine, Firoozgar Clinical Research Development Center, Iran University of Medical Sciences, Tehran, Iran. [Ariceta G] Servei de Nefrologia Pediàtrica, Vall d’Hebron Hospital Universitari, Barcelona, Spain. [Perelló M] Servei de Nefrologia, Vall d’Hebron Hospital Universitari, Barcelona, Spain. Universitat Autònoma de Barcelona, Bellaterra, Spain, Vall d'Hebron Barcelona Hospital Campus, Verploegen M. F. A., Vargas-Poussou R., Walsh S. B., ALPAY H., Amouzegar A., Ariceta G., ATMIŞ B., Bacchetta J., Barany P., Baron S., et al., Verploegen, Maartje F A, Vargas-Poussou, Rosa, Walsh, Stephen B, Alpay, Harika, Amouzegar, Atefeh, Ariceta, Gema, Atmis, Bahriye, Bacchetta, Justine, Bárány, Peter, Baron, Stéphanie, Bayrakci, Umut Selda, Belge, Hendrica, Besouw, Martine, Blanchard, Anne, Bökenkamp, Arend, Boyer, Olivia, Burgmaier, Kathrin, Calò, Lorenzo A, Decramer, Stéphane, Devuyst, Olivier, van Dyck, Maria, Ferraro, Pietro Manuel, Fila, Marc, Francisco, Telma, Ghiggeri, Gian Marco, Gondra, Leire, Guarino, Stefano, Hooman, Nakysa, Hoorn, Ewout J, Houillier, Pascal, Kamperis, Konstantino, Kari, Jameela A, Konrad, Martin, Levtchenko, Elena, Lucchetti, Laura, Lugani, Francesca, Marzuillo, Pierluigi, Mohidin, Barian, Neuhaus, Thomas J, Osman, Abdaldafae, Papizh, Svetlana, Perelló, Manel, Rookmaaker, Maarten B, Conti, Valerie Said, Santos, Fernando, Sawaf, Ghalia, Serdaroglu, Erkin, Szczepanska, Maria, Taroni, Francesca, Topaloglu, Rezan, Trepiccione, Francesco, Vidal, Enrico, Wan, Elizabeth R, Weber, Lutz, Yildirim, Zeynep Yuruk, Yüksel, Selçuk, Zlatanova, Galia, Bockenhauer, Detlef, Emma, Francesco, Nijenhuis, Tom, and UCL - SSS/IREC/NEFR - Pôle de Néphrologie

Subjects
Internal Diseases, Hormones, Hormone Substitutes, and Hormone Antagonists::Hormones::Peptide Hormones::Parathyroid Hormone [CHEMICALS AND DRUGS], Homeòstasi, urologic and male genital diseases, Sağlık Bilimleri, İç Hastalıkları, Clinical Medicine (MED), Bartter syndomr, Transplantasyon, Gitelman Syndrome/complications, salt losing tubulopathies, Homeostasis, HYPERCALCIURIA, Klinik Tıp (MED), Child, enfermedades urogenitales masculinas::enfermedades urológicas::enfermedades renales::defectos congénitos del transporte tubular renal::síndrome de Gitelman [ENFERMEDADES], Klinik Tıp, Hyperparathyroidism, Tıp, Nefroloji, fenómenos fisiológicos::homeostasis [FENÓMENOS Y PROCESOS], Nephrology, Üroloji, Medicine, Gitelman syndrome, Ronyons - Malalties - Malformacions, Urology, CALCIUM, Phosphates, UROLOGY & NEPHROLOGY, Health Sciences, Humans, parathyroid hormone, HYPERPARATHYROIDISM, ÜROLOJİ VE NEFROLOJİ, hormonas, sustitutos de hormonas y antagonistas de hormonas::hormonas::hormonas peptídicas::hormona paratiroidea [COMPUESTOS QUÍMICOS Y DROGAS], phosphate, Transplantation, Internal Medicine Sciences, Male Urogenital Diseases::Urologic Diseases::Kidney Diseases::Renal Tubular Transport, Inborn Errors::Bartter Syndrome [DISEASES], Dahili Tıp Bilimleri, Hormones peptídiques, CLINICAL MEDICINE, GENE, Bartter syndrome, Male Urogenital Diseases::Urologic Diseases::Kidney Diseases::Renal Tubular Transport, Inborn Errors::Gitelman Syndrome [DISEASES], Renal disorders Radboud Institute for Molecular Life Sciences [Radboudumc 11], Cross-Sectional Studies, Calcium, Bartter Syndrome/complications, Physiological Phenomena::Homeostasis [PHENOMENA AND PROCESSES], enfermedades urogenitales masculinas::enfermedades urológicas::enfermedades renales::defectos congénitos del transporte tubular renal::síndrome de Bartter [ENFERMEDADES]
Abstract

European Reference Network for Rare Kidney Diseases (ERKNet) - European Union; Dutch Kidney Foundation [19OI06], Verploegen MFA, Vargas-Poussou R, Walsh SB, Alpay H, Amouzegar A, Ariceta G, Atmis B, Bacchetta J, Bárány P, Baron S, Bayrakci US, Belge H, Besouw M, Blanchard A, Bökenkamp A, Boyer O, Burgmaier K, Calò LA, Decramer S, Devuyst O, van Dyck M, Ferraro PM, Fila M, Francisco T, Ghiggeri GM, Gondra L, Guarino S, Hooman N, Hoorn EJ, Houillier P, Kamperis K, Kari JA, Konrad M, Levtchenko E, Lucchetti L, Lugani F, Marzuillo P, Mohidin B, Neuhaus TJ, Osman A, Papizh S, Perelló M, Rookmaaker MB, Conti VS, Santos F, Sawaf G, Serdaroglu E, Szczepanska M, Taroni F, Topaloglu R, Trepiccione F, Vidal E, Wan ER, Weber L, Yildirim ZY, Yüksel S, Zlatanova G, Bockenhauer D, Emma F, Nijenhuis T

Published
2022

8. C4 nephritic factor in patients with immune-complex-mediated membranoproliferative glomerulonephritis and C3-glomerulopathy

Author

Garam, Nóra, Prohászka, Zoltán, Szilágyi, Ágnes, Aigner, Christof, Schmidt, Alice, Gaggl, Martina, Sunder-Plassmann, Gere, Bajcsi, Dóra, Brunner, Jürgen, Dumfarth, Alexandra, Cejka, Daniel, Flaschberger, Stefan, Flögelova, Hana, Haris, Ágnes, Hartmann, Ágnes, Heilos, Andreas, Mueller, Thomas, Rusai, Krisztina, Arbeiter, Klaus, Hofer, Johannes, Jakab, Dániel, Sinkó, Mária, Szigeti, Erika, Bereczki, Csaba, Janko, Viktor, Kelen, Kata, Reusz, György S., Szabó, Attila J., Klenk, Nóra, Kóbor, Krisztina, Kojc, Nika, Knechtelsdorfer, Maarten, Laganovic, Mario, Lungu, Adrian Catalin, Meglic, Anamarija, Rus, Rina, Kersnik-Levart, Tanja, Macioniene, Ernesta, Miglinas, Marius, Pawłowska, Anna, Stompór, Tomasz, Podracka, Ludmila, Rudnicki, Michael, Mayer, Gert, Romana Rysava, Reiterova, Jana, Saraga, Marijan, Tomáš Seeman, Zieg, Jakub, Sládková, Eva, Szabó, Tamás, Capitanescu, Andrei, Stancu, Simona, Tisljar, Miroslav, Galesic, Kresimir, Tislér, András, Vainumäe, Inga, Windpessl, Martin, Zaoral, Tomas, Zlatanova, Galia, and Csuka, Dorottya

Published
2019
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9. Parathyroid hormone and phosphate homeostasis in patients with Bartter and Gitelman syndrome: an international cross-sectional study

Author

Verploegen, Maartje F. A., Vargas-Poussou, Rosa, Walsh, Stephen B., Alpay, Harika, Amouzegar, Atefeh, Ariceta, Gema, Atmis, Bahriye, Bacchetta, Justine, Barany, Peter, Baron, Stephanie, Bayrakci, Umut Selda, Belge, Hendrica, Besouw, Martine, Blanchard, Anne, Bokenkamp, Arend, Boyer, Olivia, Burgmaier, Kathrin, Calo, Lorenzo A., Decramer, Stephane, Devuyst, Olivier, van Dyck, Maria, Ferraro, Pietro Manuel, Fila, Marc, Francisco, Telma, Ghiggeri, Gian Marco, Gondra, Leire, Guarino, Stefano, Hooman, Nakysa, Hoorn, Ewout J., Houillier, Pascal, Kamperis, Konstantinos, Kari, Jameela A., Konrad, Martin, Levtchenko, Elena, Lucchetti, Laura, Lugani, Francesca, Marzuillo, Pierluigi, Mohidin, Barian, Neuhaus, Thomas J., Osman, Abdaldafae, Papizh, Svetlana, Perello, Manel, Rookmaaker, Maarten B., Conti, Valerie Said, Santos, Fernando, Sawaf, Ghalia, Serdaroglu, Erkin, Szczepanska, Maria, Taroni, Francesca, Topaloglu, Rezan, Trepiccione, Francesco, Vidal, Enrico, Wan, Elizabeth R., Weber, Lutz, Yildirim, Zeynep Yuruk, Yuksel, Selcuk, Zlatanova, Galia, Bockenhauer, Detlef, Emma, Francesco, Nijenhuis, Tom, Verploegen, Maartje F. A., Vargas-Poussou, Rosa, Walsh, Stephen B., Alpay, Harika, Amouzegar, Atefeh, Ariceta, Gema, Atmis, Bahriye, Bacchetta, Justine, Barany, Peter, Baron, Stephanie, Bayrakci, Umut Selda, Belge, Hendrica, Besouw, Martine, Blanchard, Anne, Bokenkamp, Arend, Boyer, Olivia, Burgmaier, Kathrin, Calo, Lorenzo A., Decramer, Stephane, Devuyst, Olivier, van Dyck, Maria, Ferraro, Pietro Manuel, Fila, Marc, Francisco, Telma, Ghiggeri, Gian Marco, Gondra, Leire, Guarino, Stefano, Hooman, Nakysa, Hoorn, Ewout J., Houillier, Pascal, Kamperis, Konstantinos, Kari, Jameela A., Konrad, Martin, Levtchenko, Elena, Lucchetti, Laura, Lugani, Francesca, Marzuillo, Pierluigi, Mohidin, Barian, Neuhaus, Thomas J., Osman, Abdaldafae, Papizh, Svetlana, Perello, Manel, Rookmaaker, Maarten B., Conti, Valerie Said, Santos, Fernando, Sawaf, Ghalia, Serdaroglu, Erkin, Szczepanska, Maria, Taroni, Francesca, Topaloglu, Rezan, Trepiccione, Francesco, Vidal, Enrico, Wan, Elizabeth R., Weber, Lutz, Yildirim, Zeynep Yuruk, Yuksel, Selcuk, Zlatanova, Galia, Bockenhauer, Detlef, Emma, Francesco, and Nijenhuis, Tom

Abstract

Background Small cohort studies have reported high parathyroid hormone (PTH) levels in patients with Bartter syndrome and lower serum phosphate levels have anecdotally been reported in patients with Gitelman syndrome. In this cross-sectional study, we assessed PTH and phosphate homeostasis in a large cohort of patients with salt-losing tubulopathies. Methods Clinical and laboratory data of 589 patients with Bartter and Gitelman syndrome were provided by members of the European Rare Kidney Diseases Reference Network (ERKNet) and the European Society for Paediatric Nephrology (ESPN). Results A total of 285 patients with Bartter syndrome and 304 patients with Gitelman syndrome were included for analysis. Patients with Bartter syndrome type I and II had the highest median PTH level (7.5 pmol/L) and 56% had hyperparathyroidism (PTH >7.0 pmol/L). Serum calcium was slightly lower in Bartter syndrome type I and II patients with hyperparathyroidism (2.42 versus 2.49 mmol/L; P = .038) compared to those with normal PTH levels and correlated inversely with PTH (r(s) -0.253; P = .009). Serum phosphate and urinary phosphate excretion did not correlate with PTH. Overall, 22% of patients had low serum phosphate levels (phosphate-standard deviation score < -2), with the highest prevalence in patients with Bartter syndrome type III (32%). Serum phosphate correlated with tubular maximum reabsorption of phosphate/glomerular filtration rate (TmP/GFR) (r(s) 0.699; P < .001), suggesting renal phosphate wasting. Conclusions Hyperparathyroidism is frequent in patients with Bartter syndrome type I and II. Low serum phosphate is observed in a significant number of patients with Bartter and Gitelman syndrome and appears associated with renal phosphate wasting.

Published
2022

10. FHR-5 Serum Levels and CFHR5 Genetic Variations in Patients With Immune Complex-Mediated Membranoproliferative Glomerulonephritis and C3-Glomerulopathy

Author

Garam, Nóra, primary, Cserhalmi, Marcell, additional, Prohászka, Zoltán, additional, Szilágyi, Ágnes, additional, Veszeli, Nóra, additional, Szabó, Edina, additional, Uzonyi, Barbara, additional, Iliás, Attila, additional, Aigner, Christof, additional, Schmidt, Alice, additional, Gaggl, Martina, additional, Sunder-Plassmann, Gere, additional, Bajcsi, Dóra, additional, Brunner, Jürgen, additional, Dumfarth, Alexandra, additional, Cejka, Daniel, additional, Flaschberger, Stefan, additional, Flögelova, Hana, additional, Haris, Ágnes, additional, Hartmann, Ágnes, additional, Heilos, Andreas, additional, Mueller, Thomas, additional, Rusai, Krisztina, additional, Arbeiter, Klaus, additional, Hofer, Johannes, additional, Jakab, Dániel, additional, Sinkó, Mária, additional, Szigeti, Erika, additional, Bereczki, Csaba, additional, Janko, Viktor, additional, Kelen, Kata, additional, Reusz, György S., additional, Szabó, Attila J., additional, Klenk, Nóra, additional, Kóbor, Krisztina, additional, Kojc, Nika, additional, Knechtelsdorfer, Maarten, additional, Laganovic, Mario, additional, Lungu, Adrian Catalin, additional, Meglic, Anamarija, additional, Rus, Rina, additional, Kersnik Levart, Tanja, additional, Macioniene, Ernesta, additional, Miglinas, Marius, additional, Pawłowska, Anna, additional, Stompór, Tomasz, additional, Podracka, Ludmila, additional, Rudnicki, Michael, additional, Mayer, Gert, additional, Rysava, Romana, additional, Reiterova, Jana, additional, Saraga, Marijan, additional, Seeman, Tomáš, additional, Zieg, Jakub, additional, Sládková, Eva, additional, Stajic, Natasa, additional, Szabó, Tamás, additional, Capitanescu, Andrei, additional, Stancu, Simona, additional, Tisljar, Miroslav, additional, Galesic, Kresimir, additional, Tislér, András, additional, Vainumäe, Inga, additional, Windpessl, Martin, additional, Zaoral, Tomas, additional, Zlatanova, Galia, additional, Józsi, Mihály, additional, and Csuka, Dorottya, additional

Published
2021
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11. CFHR5 Genetic Variations and Serum Levels in Patients with Immune-Complex-Mediated Membranoproliferative Glomerulonephritis and C3-Glomerulopathy

Author

Garam, Nóra, primary, Cserhalmi, Marcell, additional, Prohászka, Zoltán, additional, Szilágyi, Ágnes, additional, Veszeli, Nóra, additional, Szabó, Edina, additional, Uzonyi, Barbara, additional, Iliás, Attila, additional, Aigner, Christof, additional, Schmidt, Alice, additional, Gaggl, Martina, additional, Sunder-Plassmann, Gere, additional, Bajcsi, Dóra, additional, Brunner, Jürgen, additional, Dumfarth, Alexandra, additional, Cejka, Daniel, additional, Flaschberger, Stefan, additional, Flögelova, Hana, additional, Haris, Ágnes, additional, Hartmann, Ágnes, additional, Heilos, Andreas, additional, Mueller, Thomas, additional, Rusai, Krisztina, additional, Arbeiter, Klaus, additional, Hofer, Johannes, additional, Jakab, Dániel, additional, Sinkó, Mária, additional, Szigeti, Erika, additional, Bereczki, Csaba, additional, Janko, Viktor, additional, Kelen, Kata, additional, Reusz, György S., additional, Szabó, Attila J., additional, Klenk, Nóra, additional, Kóbor, Krisztina, additional, Kojc, Nika, additional, Knechtelsdorfer, Maarten, additional, Laganovic, Mario, additional, Lungu, Adrian Catalin, additional, Meglic, Anamarija, additional, Rus, Rina, additional, Kersnik-Levart, Tanja, additional, Macioniene, Ernesta, additional, Miglinas, Marius, additional, Pawłowska, Anna, additional, Stompór, Tomasz, additional, Podracka, Ludmila, additional, Rudnicki, Michael, additional, Mayer, Gert, additional, Rysava, Romana, additional, Reiterova, Jana, additional, Saraga, Marijan, additional, Seeman, Tomáš, additional, Zieg, Jakub, additional, Sládková, Eva, additional, Stajic, Natasa, additional, Szabó, Tamás, additional, Capitanescu, Andrei, additional, Stancu, Simona, additional, Tisljar, Miroslav, additional, Galesic, Kresimir, additional, Tislér, András, additional, Vainumäe, Inga, additional, Windpessl, Martin, additional, Zaoral, Tomas, additional, Zlatanova, Galia, additional, Józsi, Mihály, additional, and Csuka, Dorottya, additional

Published
2020
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12. Validation of distinct pathogenic patterns in a cohort of membranoproliferative glomerulonephritis patients by cluster analysis

Author

Garam, Nóra, primary, Prohászka, Zoltán, primary, Szilágyi, Ágnes, primary, Aigner, Christof, primary, Schmidt, Alice, primary, Gaggl, Martina, primary, Sunder-Plassmann, Gere, primary, Bajcsi, Dóra, primary, Brunner, Jürgen, primary, Dumfarth, Alexandra, primary, Cejka, Daniel, primary, Flaschberger, Stefan, primary, Flögelova, Hana, primary, Haris, Ágnes, primary, Hartmann, Ágnes, primary, Heilos, Andreas, primary, Mueller, Thomas, primary, Rusai, Krisztina, primary, Arbeiter, Klaus, primary, Hofer, Johannes, primary, Jakab, Dániel, primary, Sinkó, Mária, primary, Szigeti, Erika, primary, Bereczki, Csaba, primary, Janko, Viktor, primary, Kelen, Kata, primary, Reusz, György S, primary, Szabó, Attila J, primary, Klenk, Nóra, primary, Kóbor, Krisztina, primary, Kojc, Nika, primary, Knechtelsdorfer, Maarten, primary, Laganovic, Mario, primary, Lungu, Adrian Catalin, primary, Meglic, Anamarija, primary, Rus, Rina, primary, Kersnik-Levart, Tanja, primary, Macioniene, Ernesta, primary, Miglinas, Marius, primary, Pawłowska, Anna, primary, Stompór, Tomasz, primary, Podracka, Ludmila, primary, Rudnicki, Michael, primary, Mayer, Gert, primary, Rysava, Romana, primary, Reiterova, Jana, primary, Saraga, Marijan, primary, Seeman, Tomáš, primary, Zieg, Jakub, primary, Sládková, Eva, primary, Szabó, Tamás, primary, Capitanescu, Andrei, primary, Stancu, Simona, primary, Tisljar, Miroslav, primary, Galesic, Kresimir, primary, Tislér, András, primary, Vainumäe, Inga, primary, Windpessl, Martin, primary, Zaoral, Tomas, primary, Zlatanova, Galia, primary, and Csuka, Dorottya, primary

Published
2019
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16. Parathyroid hormone and phosphate homeostasis in patients with Bartter and Gitelman syndrome: an international cross-sectional study.

Author

Verploegen MFA, Vargas-Poussou R, Walsh SB, Alpay H, Amouzegar A, Ariceta G, Atmis B, Bacchetta J, Bárány P, Baron S, Bayrakci US, Belge H, Besouw M, Blanchard A, Bökenkamp A, Boyer O, Burgmaier K, Calò LA, Decramer S, Devuyst O, van Dyck M, Ferraro PM, Fila M, Francisco T, Ghiggeri GM, Gondra L, Guarino S, Hooman N, Hoorn EJ, Houillier P, Kamperis K, Kari JA, Konrad M, Levtchenko E, Lucchetti L, Lugani F, Marzuillo P, Mohidin B, Neuhaus TJ, Osman A, Papizh S, Perelló M, Rookmaaker MB, Conti VS, Santos F, Sawaf G, Serdaroglu E, Szczepanska M, Taroni F, Topaloglu R, Trepiccione F, Vidal E, Wan ER, Weber L, Yildirim ZY, Yüksel S, Zlatanova G, Bockenhauer D, Emma F, and Nijenhuis T

Subjects
Child, Humans, Parathyroid Hormone, Cross-Sectional Studies, Phosphates, Homeostasis, Calcium, Gitelman Syndrome complications, Bartter Syndrome complications, Hyperparathyroidism
Abstract

Background: Small cohort studies have reported high parathyroid hormone (PTH) levels in patients with Bartter syndrome and lower serum phosphate levels have anecdotally been reported in patients with Gitelman syndrome. In this cross-sectional study, we assessed PTH and phosphate homeostasis in a large cohort of patients with salt-losing tubulopathies., Methods: Clinical and laboratory data of 589 patients with Bartter and Gitelman syndrome were provided by members of the European Rare Kidney Diseases Reference Network (ERKNet) and the European Society for Paediatric Nephrology (ESPN)., Results: A total of 285 patients with Bartter syndrome and 304 patients with Gitelman syndrome were included for analysis. Patients with Bartter syndrome type I and II had the highest median PTH level (7.5 pmol/L) and 56% had hyperparathyroidism (PTH >7.0 pmol/L). Serum calcium was slightly lower in Bartter syndrome type I and II patients with hyperparathyroidism (2.42 versus 2.49 mmol/L; P = .038) compared to those with normal PTH levels and correlated inversely with PTH (rs -0.253; P = .009). Serum phosphate and urinary phosphate excretion did not correlate with PTH. Overall, 22% of patients had low serum phosphate levels (phosphate-standard deviation score < -2), with the highest prevalence in patients with Bartter syndrome type III (32%). Serum phosphate correlated with tubular maximum reabsorption of phosphate/glomerular filtration rate (TmP/GFR) (rs 0.699; P < .001), suggesting renal phosphate wasting., Conclusions: Hyperparathyroidism is frequent in patients with Bartter syndrome type I and II. Low serum phosphate is observed in a significant number of patients with Bartter and Gitelman syndrome and appears associated with renal phosphate wasting., (© The Author(s) 2022. Published by Oxford University Press on behalf of ERA.)

Published
2022
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