References
- Sebire NJ, Vujanic GM. Paediatric renal tumours: recent developments, new entities and pathological features. Histopathology 2009;54:516–28.
- Vadeyar S, Ramsay M, James D, et al. Prenatal diagnosis of congenital Wilms tumor (nephroblastoma) presenting as fetal hydrops. Ultrasound Obstet Gynecol 2000;16:80–3.
- Gutjahr P. Congenital Wilms tumors are mostly (benign) mesoblasticnephromas—significance of prenatally detected solid kidney tumors. Geburtshilfe Frauenheilkd 1991;51:124–6.
- Blute ML, Kelalis PP, Offord KP, et al. Bilateral Wilms tumor. J Urol 1987;138:968–73.
- Coppes MJ, de Kraker J, van Dijken PJ, et al. Bilateral Wilms tumor: long-term survival and some epidemiological features. J Clin Oncol 1989;7:310–15.
- Hennigar RA, O'Shea PA, et al. Clinicopathologic features of nephrogenic rests and nephroblastomatosis. Adv Anat Pathol 2001;8:276–89.
- Breslow N, Olshan A, Beckwith JB, et al. Epidemiology of Wilms tumor. Med Pediatr Oncol 1993;21:172–81.
- Greenberg F, Copeland K, Gresik MV. Expanding the spectrum of the Perlman syndrome. Am J Med Genet.1988;29:773–6.
- Desmet VJ. Ludwig symposium on biliary disorders—part I. Pathogenesis of ductal plate abnormalities. Mayo Clin Proc 1998;73:80–9.
- Davenport M, Tizzard SA, Underhill J, Mieli-Vergani G, Portmann B, Hadzic N. The biliary atresia splenic malformation syndrome: a 28-year single-center retrospective study. J Pediatr. 2006;149:393–400.