Browse by Journal Title

2019

Possible digenic disease in a caucasian family with COL4A3 and COL4A5 mutations.
Choi, M. and Anistan, Y.M. and Eckardt, K.U. and Gollasch, M. and Nickel, P.
Nephron 141 (3): 213-218. March 2019

2018

A de novo KCNA1 mutation in a patient with tetany and hypomagnesemia.
van der Wijst, J. and Konrad, M. and Verkaart, S.A.J. and Tkaczyk, M. and Latta, F. and Altmüller, J. and Thiele, H. and Beck, B. and Schlingmann, K.P. and de Baaij, J.H.F.
Nephron 139 (4): 359-366. August 2018

2000

Bronchial stenosis and extensive bronchiectasis due to Wegener's granulomatosis.
Woywodt, A. and Goebel, U.
Nephron 85 : 366-367. 1 August 2000

1999

VCAM-1, ICAM-1, and E-selectin in IgA nephropathy and Schonlein-Henoch syndrome: Differences between tissue expression and serum concentration.
Mrowka, C. and Heintz, B. and Sieberth, H.G.
Nephron 81 : 256-263. 1 March 1999