Michael Ludwig
Institut für Klinische Biochemie
Universität Bonn
Sigmund-Freud-Strasse 25
53105 Bonn
Germany
Name/email consistency: high
- Genome-wide linkage scan for bladder exstrophy-epispadias complex. Ludwig, M., Rüschendorf, F., Saar, K., Hübner, N., Siekmann, L., Boyadjiev, S.A., Reutter, H. Birth Defects Res. Part A Clin. Mol. Teratol. (2009)
- Bladder exstrophy-epispadias complex. Ludwig, M., Ching, B., Reutter, H., Boyadjiev, S.A. Birth Defects Res. Part A Clin. Mol. Teratol. (2009)
- Hypercalciuria in patients with CLCN5 mutations. Ludwig, M., Utsch, B., Balluch, B., Fründ, S., Kuwertz-Bröking, E., Bökenkamp, A. Pediatr. Nephrol. (2006)
- Recent advances in understanding the clinical and genetic heterogeneity of Dent's disease. Ludwig, M., Utsch, B., Monnens, L.A. Nephrol. Dial. Transplant. (2006)
- Functional evaluation of Dent's disease-causing mutations: implications for ClC-5 channel trafficking and internalization. Ludwig, M., Doroszewicz, J., Seyberth, H.W., Bökenkamp, A., Balluch, B., Nuutinen, M., Utsch, B., Waldegger, S. Hum. Genet. (2005)
- Pseudohypoaldosteronism type 1 and the genes encoding prostasin, alpha-spectrin, and Nedd4. Ludwig, M., Bidlingmaier, F., Reissinger, A. Int. J. Mol. Med. (2004)
- Four additional CLCN5 exons encode a widely expressed novel long CLC-5 isoform but fail to explain Dent's phenotype in patients without mutations in the short variant. Ludwig, M., Waldegger, S., Nuutinen, M., Bökenkamp, A., Reissinger, A., Steckelbroeck, S., Utsch, B. Kidney Blood Press. Res. (2003)









