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Date |
Item TypeArticle
Possible digenic disease in a caucasian family with COL4A3 and COL4A5 mutations.
Choi, M., Anistan, Y.M., Eckardt, K.U., Gollasch, M. and Nickel, P.
Nephron 141
(3): 213-218.
March 2019
A de novo KCNA1 mutation in a patient with tetany and hypomagnesemia.
van der Wijst, J., Konrad, M., Verkaart, S.A.J., Tkaczyk, M., Latta, F., Altmüller, J., Thiele, H., Beck, B., Schlingmann, K.P. and de Baaij, J.H.F.
Nephron 139
(4): 359-366.
August 2018
Letter
Bronchial stenosis and extensive bronchiectasis due to Wegener's granulomatosis.
Woywodt, A. and Goebel, U.
Nephron 85
: 366-367.
1 August 2000
Editorial
VCAM-1, ICAM-1, and E-selectin in IgA nephropathy and Schonlein-Henoch syndrome: Differences between tissue expression and serum concentration.
Mrowka, C., Heintz, B. and Sieberth, H.G.
Nephron 81
: 256-263.
1 March 1999
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