Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Bartter Syndrome/complications"'
Autor:
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
Publikováno v:
Verploegen, M F A, Vargas-Poussou, R, Walsh, S B, Alpay, H, Amouzegar, A, Ariceta, G, Atmis, B, Bacchetta, J, Bárány, P, Baron, S, Bayrakci, U S, Belge, H, Besouw, M, Blanchard, A, Bökenkamp, A, Boyer, O, Burgmaier, K, Calò, L A, Decramer, S, Devuyst, O, van Dyck, M, Ferraro, P M, Fila, M, Francisco, T, Ghiggeri, G M, Gondra, L, Guarino, S, Hooman, N, Hoorn, E J, Houillier, P, Kamperis, K, Kari, J A, Konrad, M, Levtchenko, E, Lucchetti, L, Lugani, F, Marzuillo, P, Mohidin, B, Neuhaus, T J, Osman, A, Papizh, S, Perelló, M, Rookmaaker, M B, Conti, V S, Santos, F, Sawaf, G, Serdaroglu, E, Szczepanska, M, Taroni, F, Topaloglu, R, Trepiccione, F, Vidal, E, Wan, E R, Weber, L, Yildirim, Z Y, Yüksel, S, Zlatanova, G, Bockenhauer, D, Emma, F & Nijenhuis, T 2022, ' Parathyroid hormone and phosphate homeostasis in patients with Bartter and Gitelman syndrome : an international cross-sectional study ', Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association-European Renal Association, vol. 37, no. 12, pp. 2474–2486 . https://doi.org/10.1093/ndt/gfac029
Nephrology Dialysis Transplantation, 37(12). Oxford University Press
Scientia
Nephrology, Dialysis, Transplantation, 37, 2474-2486
Nephrology Dialysis Transplantation, Vol. 37, no.12, p. 2474-2486 (2022)
Nephrology, Dialysis, Transplantation, 37, 12, pp. 2474-2486
WOS:000785626500001
Nephrology Dialysis Transplantation, 37(12). Oxford University Press
Scientia
Nephrology, Dialysis, Transplantation, 37, 2474-2486
Nephrology Dialysis Transplantation, Vol. 37, no.12, p. 2474-2486 (2022)
Nephrology, Dialysis, Transplantation, 37, 12, pp. 2474-2486
WOS:000785626500001
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,
Verploegen MFA, Vargas-Poussou R, Walsh SB, Alpay H, Amouzegar A, Ariceta G, Atmis B, Bacchetta J, Bárány P, Baron S, Bayrakci US,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c639689a475748116bfba4ef271c625c
https://lirias.kuleuven.be/handle/20.500.12942/691467
https://lirias.kuleuven.be/handle/20.500.12942/691467
Neonatal Bartter syndrome (NBS) is a rare autosomal recessive renal tubular disorder. This disease is characterized by hypokalemia, hypochloremia, and metabolic alkalosis that is often associated with failure to thrive and recurrent episodes of dehyd
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3566::2a7e0fab73ebe75fa98df84eface955b
Endocochlear potential depends on Cl− channels: mechanism underlying deafness in Bartter syndrome IV
Autor:
Thomas J. Jentsch, Nicola Strenzke, Hannes Maier, Adrian Muenscher, Corina E. Andreescu, Gesa Rickheit, Chris I. De Zeeuw, Anselm A. Zdebik
Publikováno v:
The EMBO journal, 27(21): 2809-2942
Human Bartter syndrome IV is an autosomal recessive disorder characterized by congenital deafness and severe renal salt and fluid loss. It is caused by mutations in BSND, which encodes barttin, a beta-subunit of ClC-Ka and ClC-Kb chloride channels. I
Nephrol Dial Transplant
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_____10561::32aa682a59677fc311fcd1d272563ba5
http://olympias.lib.uoi.gr/jspui/handle/123456789/21083
http://olympias.lib.uoi.gr/jspui/handle/123456789/21083
Autor:
Satoshi Gando, Tomoyuki Sato, Yosihiro Takeyama, Izumi Matubara, Yuji Morimoto, Mineji Hayakawa
Publikováno v:
Intensive care medicine. 26(11):1711