Birth characteristics and Wilms tumors in children in the Nordic countries: A register‐based case–control study

J Schüz, LS Schmidt, P Kogner… - … journal of cancer, 2011 - Wiley Online Library
Little is known about causes of Wilms tumor. Because of the young age at diagnosis, several
studies have looked at various birth characteristics. We conducted a registry‐based case …

Congenital gastric teratoma in Wiedemann‐Beckwith syndrome

TC Falik‐Borenstein, JR Korenberg… - American journal of …, 1991 - Wiley Online Library
Wiedemann‐Beckwith syndrome (WBS) may be associated with abdominal tumors,
including Wilms tumor, adrenocortical carcinoma, hepatoblastoma, gonadoblastoma …

Introduction to the genetics of primary renal tumors in children

AG Knudson Jr - Medical and pediatric oncology, 1993 - Wiley Online Library
Wilms tumor can be explained only partially by the “two hit” model that was originally
developed for retinoblastoma. Heterogeneity of two kinds, operates. The first is that four …

Multiple genetic abnormalities of 11p15 in Wilms' tumor

AP Feinberg - Medical and Pediatric Oncology: The Official …, 1996 - Wiley Online Library
Wilms' tumor has served as a model of multiple genetic alterations in childhood cancer. This
review summarizes work in our laboratory identifying several of these alterations. These …

Familial Wiedemann-Beckwith syndrome and a second Wilms tumor locus both map to 11p15. 5.

A Koufos, P Grundy, K Morgan, KA Aleck… - American journal of …, 1989 - ncbi.nlm.nih.gov
Wilms tumor of the kidney occurs with increased frequency in association with two clinically
and cytogenetically distinct congenital syndromes, the Wiedemann-Beckwith syndrome …

Complete and incomplete forms of Beckwith-Wiedemann syndrome: their oncogenic potential.

C Sotelo-Avila, F Gonzalez-Crussi… - The Journal of …, 1980 - europepmc.org
The diagnosis of Beckwith-Wiedemann syndrome may be missed because of variable or
incomplete clinical expression. Recognition of such patients is important, however, because …

Positional cloning of genes involved in the Beckwith‐Wiedemann syndrome, hemihypertrophy, and associated childhood tumors

M Mannens, M Alders, B Redeker… - … : The Official Journal …, 1996 - Wiley Online Library
Abstract The Beckwith‐Wiedemann syndrome (BWS) is an overgrowth malformation
syndrome that occurs with an incidence of 1: 13,700 births. There is a striking incidence of …

Twenty‐five year follow‐up of childhood Wilms tumor: a report from the Childhood Cancer Survivor Study

AM Termuhlen, JM Tersak, Q Liu, Y Yasui… - Pediatric blood & …, 2011 - Wiley Online Library
Background Treatment cures over 90% of children with Wilms tumor (WT) who subsequently
risk late morbidity and mortality. This study describes the 25‐year outcomes of 5‐year WT …

Is nephron sparing surgery justified in Wilms tumor with Beckwith–Wiedemann syndrome or isolated hemihypertrophy?

A Scalabre, C Bergeron, F Brioude… - Pediatric blood & …, 2016 - Wiley Online Library
Background Patients with Beckwith–Wiedemann syndrome (BWS) or isolated
hemihypertrophy (HH) treated for a Wilms tumor (WT) carry an increased risk of developing …

Wilms tumor

AD Friedman - Pediatrics in Review, 2013 - publications.aap.org
Wilms tumor is responsible for 5% of pediatric malignant tumors or approximately 500 new
cases each year in the United States, with equivalent frequency in boys and girls. The …