يعرض 1 - 10 نتائج من 42 نتيجة بحث عن '"Gondra, Leire"', وقت الاستعلام: 1.22s تنقيح النتائج
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    دورية أكاديمية
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    دورية أكاديمية
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    دورية أكاديمية

    Alternate Title: Acidosis tubular renal distal hereditaria: correlación genotípica, evolución a largo plazo y nuevas perspectivas terapéuticas (Spanish; Castilian)

    المصدر: In NEFROLOGIA (English Edition) July-August 2021 41(4):383-390

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    دورية أكاديمية

    Alternate Title: Hereditary distal renal tubular acidosis: Genotypic correlation, evolution to long term, and new therapeutic perspectives (English)

    المصدر: In NEFROLOGÍA July-August 2021 41(4):383-390

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    دورية أكاديمية
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    دورية أكاديمية
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    المساهمون: 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, UCL - SSS/IREC/NEFR - Pôle de Néphrologie

    المصدر: 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

    مصطلحات موضوعية: 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]

    وصف الملف: Print; application/pdf

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