Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Dominique Chaveau"'
Autor:
Maria Mileva, Sandrine Lemoine, Christiane Mousson, Elsa Seys, Rosa Vargas-Poussou, Mathilde Cailliez, Gwenaëlle Roussey-Kesler, Aurélia Bertholet-Thomas, Paul Cozette, Theresa Kwon, Anne Blanchard, Guylhène Bourdat-Michel, Pauline Krug, Jean Sébastien Borde, Jacques Teulon, Christophe Simian, Laurence Dubourg, Robert Novo, Isabelle Vrillon, Bertrand Knebelmann, Brigitte Llanas, Djamal Djeddi, Dominique Chaveau, Stephen B. Walsh, Olga Andrini, François Nobili, Jean Daniel Delbet, Marc Fila, Georges Deschênes, Mathilde Keck, Ferielle Louillet, Lamisse Mansour-Hendili, Elodie Merieau, Stéphane Decramer, Noémie Jourde-Chiche, Marie-Pierre Lavocat, Pierre-Yves Courand, Luisa Mota-Vieira, Guillaume Bobrie
Publikováno v:
Journal of the American Society of Nephrology
Journal of the American Society of Nephrology, American Society of Nephrology, 2017, 28 (8), pp.2540-2552. ⟨10.1681/ASN.2016101057⟩
Journal of the American Society of Nephrology, 2017, 28 (8), pp.2540-2552. ⟨10.1681/ASN.2016101057⟩
Journal of the American Society of Nephrology, American Society of Nephrology, 2017, 28 (8), pp.2540-2552. ⟨10.1681/ASN.2016101057⟩
Journal of the American Society of Nephrology, 2017, 28 (8), pp.2540-2552. ⟨10.1681/ASN.2016101057⟩
Bartter syndrome type 3 is a clinically heterogeneous hereditary salt-losing tubulopathy caused by mutations of the chloride voltage-gated channel Kb gene (CLCNKB), which encodes the ClC-Kb chloride channel involved in NaCl reabsorption in the renal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8e23d089a59dee73a738b2794aa5789a
https://hal-amu.archives-ouvertes.fr/hal-01787263/document
https://hal-amu.archives-ouvertes.fr/hal-01787263/document
Autor:
Tevfik Ecder, Andreas L. Serra, Yannick Le Meur, Dominique Chaveau, Ron T. Gansevoort, Olivier Devuyst, Rudolf P. Wüthrich, Kai-Uwe Eckardt, Giuseppe Remuzzi, Anna Köttgen, Richard Sandford, Klemens Budde, Albert C.M. Ong, Katja Petzold, Vladimir Tesar, Laura Rotar, Roser Torra, Yves Pirson
Publikováno v:
Nephrology, Dialysis, Transplantation, 29, 26-32. Oxford University Press
NEPHROLOGY DIALYSIS TRANSPLANTATION
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname
Nephrology dialysis transplantation : official publication of the European Dialysis and Transplant
NEPHROLOGY DIALYSIS TRANSPLANTATION
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname
Nephrology dialysis transplantation : official publication of the European Dialysis and Transplant
Background. Autosomal dominant polycystic kidney disease (ADPKD) is the most common monogenic inherited kidney disease, affecting an estimated 600 000 individuals in Europe. The disease is characterized by age-dependent development of a multiple cyst
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e1adad08a8c9496530e141f5b6ef865c
https://research.rug.nl/en/publications/c6f78759-02ad-4fad-bd0b-d4b51d66343b
https://research.rug.nl/en/publications/c6f78759-02ad-4fad-bd0b-d4b51d66343b
Autor:
Andreas L. Serra, Laura Rotar, Rudolf P. Wthrich, Yannick Le Meur, Klemens Budde, Vladimir Tesar, Olivier Devuyst, Kai-Uwe Eckardt, Roser Torra, Ron T. Gansevoort, Dominique Chaveau, Richard Sandford, Giuseppe Remuzzi, Albert C.M. Ong, Anna Köttgen, Yves Pirson, Katja Petzold, Tevfik Ecder
Publikováno v:
Nephrology Dialysis Transplantation. 29:2353-2353
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c53bdb27b0b1202a77959e5fe4f8e742
https://doi.org/10.1093/ndt/gfu358
https://doi.org/10.1093/ndt/gfu358
