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Bergstralh, E. J., Monico, C. G., Lieske, J. C., Herges, R. M., Langman, C. B., Hoppe, B. and Milliner, D. S. (2010). Transplantation Outcomes in Primary Hyperoxaluria. Am. J. Transplant., 10 (11). S. 2493 - 2502. HOBOKEN: WILEY. ISSN 1600-6143
Haas, C. S., Nitschke, M., Menne, J., Guthoff, M., Gaeckler, A., Bruck, H., Pape, L., Vester, U., Wuehl, E., Billing, H., Herbst, R., Thaiss, F., Hoppe, B., Weber, L. T., Zschiedrich, S., Feldkamp, T., Oh, J., Bald, M., Schroeppel, B., Holle, J. B., Jabs, W., Beckermann, J., Budde, K., Faulhaber-Walter, R. and Schaefer, F. (2019). Characteristics of Patients with atypical haemolytic-uremic Syndrome (aHUS) in Germany Data from the Global aHUS Registry. Nephrologe, 14 (6). S. 496 - 505. HEIDELBERG: SPRINGER HEIDELBERG. ISSN 1862-0418
Matoussevitch, V., Gawenda, M., Konner, K., Taylan, C., Kuhr, K., Reichert, V., Hoppe, B. and Brunkwall, J. (2015). Native dialysis shunts in children and adolescents. A single center analysis. Gefasschirurgie, 20 (1). S. 32 - 39. HEIDELBERG: SPRINGER HEIDELBERG. ISSN 1434-3932
Matthies, J., Huenseler, C., Ehren, R., Volland, R., Koerber, F., Hoppe, B., Weber, L. T. and Habbig, S. (2016). Extrarenal Manifestations in Shigatoxin-associated Haemolytic Uremic Syndrome. Klinische Padiatr., 228 (4). S. 181 - 189. STUTTGART: GEORG THIEME VERLAG KG. ISSN 1439-3824
Mehler, K., Taylan, C., Vierzig, A., Gottschalk, I., Hoppe, B., Kribs, A., Weber, L. T. and Habbig, S. (2016). Prenatal, neonatal and nephrological management of children with renal oligohydramnios. Pediatr. Nephrol., 31 (10). S. 1790 - 1792. NEW YORK: SPRINGER. ISSN 1432-198X
Waffenschmidt, L., Schneider, S., Altmueller, J., Thiele, H., Weber, S., Roesch, W., Merz, W. M., Feldkotter, M., Hoppe, B., Schalk, G., Zaniew, M., Reutter, H., Schreuder, M. F., Beckers, G. M. A., van Wijk, J. A. E. and Hilger, A. C. (2020). ZSCAN12, a candidate gene for congenital lower urinary tract obstruction (LUTO). Eur. J. Hum. Genet., 28 (SUPPL 1). S. 221 - 223. LONDON: SPRINGERNATURE. ISSN 1476-5438