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Autor:
Georges Deschênes, Arnold Köckerling, Henny H. Lemmink, Willy M. Nillesen, Lisa M. Guay-Woodford, Dorthe K. Zimmermann, Lothar Károlyi, Christian Wieg, Lambertus P. van den Heuvel, Corinne Antignac, Karl-Heinz Grzeschik, Louis David, Christopher J. Wright, Pascal Saunier, Michele Deschaux, R. Vargas, Friedhelm Hildebrandt, Hannsjörg W. Seyberth, Andreas Ziegler, Nine V A M Knoers, Matthias Brandis, Lionel Forestier, Willem Proesmans, Emmanuel Cougoureux, Jean-Luc Alessandri, Steven C. Hebert, Manuela C. Koch, Martin Konrad, Delphine Feldmann, Gian Franco Rizzoni, Leo A. H. Monnens, Geneviève Jean, Gilbert Madrigal, Niaudet P, Frederique Lorridon, Martin Vollmer, Bernd Roth
Publikováno v:
Human molecular genetics. 6(1)
Inherited renal tubular disorders associated with hypokalemic alkalosis (Bartter-like syndromes) can be subdivided into at least three clinical phenotypes: (i) the hypocalciuric-hypomagnesemic Gitelman variant; (ii) the classic variant; and (iii) the