2019

Possible digenic disease in a caucasian family with COL4A3 and COL4A5 mutations.
Choi, M. ORCID: https://orcid.org/0000-0002-0286-1491, Anistan, Y.M., Eckardt, K.U. ORCID: https://orcid.org/0000-0001-8345-4371, Gollasch, M. ORCID: https://orcid.org/0000-0003-2797-1934 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., Konrad, M., Verkaart, S.A.J., Tkaczyk, M., Latta, F., Altmüller, J. ORCID: https://orcid.org/0000-0003-4372-1521, Thiele, H., Beck, B. ORCID: https://orcid.org/0000-0003-0495-7670, Schlingmann, K.P. and de Baaij, J.H.F. ORCID: https://orcid.org/0000-0003-2372-8486
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., Heintz, B. and Sieberth, H.G.
Nephron 81 : 256-263. 1 March 1999