dc.contributor | Vall d'Hebron Barcelona Hospital Campus |
dc.contributor.author | Verploegen, Maartje |
dc.contributor.author | Vargas-Poussou, Rosa |
dc.contributor.author | Walsh, Stephen B. |
dc.contributor.author | Alpay, Harika |
dc.contributor.author | Amouzegar, Atefeh |
dc.contributor.author | Perelló Carrascosa, Manel |
dc.contributor.author | Ariceta Iraola, Gema |
dc.date.accessioned | 2022-12-05T09:37:46Z |
dc.date.available | 2022-12-05T09:37:46Z |
dc.date.issued | 2022-12 |
dc.identifier.citation | Verploegen MFA, Vargas-Poussou R, Walsh SB, Alpay H, Amouzegar A, Ariceta G, et al. Parathyroid hormone and phosphate homeostasis in patients with Bartter and Gitelman syndrome: an international cross-sectional study. Nephrol Dial Transplant. 2022 Dec;37(12):2474–86. |
dc.identifier.issn | 1460-2385 |
dc.identifier.uri | https://hdl.handle.net/11351/8605 |
dc.description | Síndrome de Bartter; Hormona paratiroïdal; Fosfat |
dc.description.sponsorship | This project has been supported by the European Reference Network for Rare Kidney Diseases (ERKNet), which is partly co-funded by the European Union within the framework of the Third Health Programme ‘ERN-2016-Framework Partnership Agreement 2017–2021’. This work is generated within the European Society for Paediatric Nephrology working group on inherited renal disorders. This work was supported by an Innovation Grant 19OI06 from the Dutch Kidney Foundation (to T.N.). |
dc.language.iso | eng |
dc.publisher | Oxford University Press |
dc.relation.ispartofseries | Nephrology, Dialysis, Transplantation;37(12) |
dc.rights | Attribution 4.0 International |
dc.rights.uri | http://creativecommons.org/licenses/by/4.0/ |
dc.source | Scientia |
dc.subject | Ronyons - Malalties - Malformacions |
dc.subject | Hormones peptídiques |
dc.subject | Homeòstasi |
dc.subject.mesh | Parathyroid Hormone |
dc.subject.mesh | Gitelman Syndrome |
dc.subject.mesh | Bartter Syndrome |
dc.subject.mesh | Homeostasis |
dc.title | Parathyroid hormone and phosphate homeostasis in patients with Bartter and Gitelman syndrome: an international cross-sectional study |
dc.type | info:eu-repo/semantics/article |
dc.identifier.doi | 10.1093/ndt/gfac029 |
dc.subject.decs | hormona paratiroidea |
dc.subject.decs | síndrome de Gitelman |
dc.subject.decs | síndrome de Bartter |
dc.subject.decs | homeostasis |
dc.relation.publishversion | https://doi.org/10.1093/ndt/gfac029 |
dc.type.version | info:eu-repo/semantics/publishedVersion |
dc.audience | Professionals |
dc.contributor.organismes | Institut Català de la Salut |
dc.contributor.authoraffiliation | [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 |
dc.identifier.pmid | 35137195 |
dc.identifier.wos | 000785626500001 |
dc.rights.accessrights | info:eu-repo/semantics/openAccess |