C Uschkereit, N Perez, C de Torres, M Kuff, J … - British Medical Journal, 2007 - jmg.bmj.com We describe a patient with a novel WT1 pS50X germ line mutation, who developed
bilateral Wilms tumours, both with stromal-type histology. Both tumours showed
loss of the wild type WT1 allele (loss of heterozygosity (LOH)) and a ... Cited by 7 - Related articles - BL Direct - All 5 versions
- ►bmj.com R Shibata, A Hashiguchi, J Sakamoto, T … - British Medical Journal, 2002 - jmg.bmj.com Wilms tumour (WT) is the most common malignant neoplasm of the kidney in
childhood and accounts for approximately 8% of all childhood solid tumours. 1, 2
Fetal rhabdomyomatous nephroblastoma (FRN) is a histological variant of WT ... Cited by 4 - Related articles - All 5 versions
D Perotti, P Mondini, M Terenziani, F Spreafico … - Journal of Pediatric Hematology/Oncology, 2005 - journals.lww.com Summary: The WT1 gene is responsible for two different genetic conditions
characterized by genitourinary anomalies and suscepti- bility to Wilms tumor
(WT): the WAGR syndrome and the Denys- Drash syndrome. Although only ... Cited by 7 - Related articles - All 4 versions
R Fukuzawa, RW Heathcott, M Sano, IM … - Pediatric and Developmental Pathology, 2004 - Springer 1 Department of Biochemistry, Cancer Genetics Laboratory, University of Otago,
PO Box 56, Dunedin, New Zealand 2 Department of Pathology, Nihon University
School of Medicine, 30-1 Ohyaguchi-kamimachi, Itabashi-ku, Tokyo173-8610, ... Cited by 19 - Related articles - BL Direct - All 4 versions
R Shibata, A Takata, A Hashiguchi, A … - Pathology international, 2003 - interscience.wiley.com To clarify a characteristic of bilateral Wilms' tumor (WT), we examined the
clinical and histological features, chemotherapy response and mutations in
Wilms' tumor suppressor gene (WT1) in five patients. Deoxyribonucleic acid ... Cited by 6 - Related articles - BL Direct - All 5 versions
RT Lugtenberg, K Cransberg, WJ Loos, A … - Cancer Chemotherapy and Pharmacology, 2008 - Springer Page 1. Cancer Chemother Pharmacol (2008) 62:1039–1044 DOI 10.1007/s00280-
008-0694-x 123 ORIGINAL ARTICLE Topotecan distribution ... Related articles - All 2 versions
S Uccini, D Perotti, C Colarossi, A … - Pediatric blood & cancer, 2008 - ncbi.nlm.nih.gov BACKGROUND: This study investigated the genetic events leading to tumorigenesis
in a patient affected with WAGR syndrome who developed multiple distinct Wilms
tumors (WTs). PROCEDURE AND RESULTS: At 1 year of age, the child developed ... Related articles
AB Garavaglia - Medical and Pediatric Oncology - interscience.wiley.com It is also possible that your web browser is not configured or not able to
display style sheets. In this case, although the visual presentation will be
degraded, the site should continue to be functional. We recommend using the ... Related articles
A CA - CA A Cancer Journal for Clinicians - interscience.wiley.com A long-term follow-up study was performed for 71 patients (International Society
of Pediatric Oncology Study 9/Society for Pediatric Oncology; n = 77 tumors)
with known molecular genetic status. Eight patients had bilateral disease, ... Related articles
