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Literature DB >> 4316066

A syndrome of pseudohermaphroditism, Wilms' tumor, hypertension, and degenerative renal disease.

A Drash, F Sherman, W H Hartmann, R M Blizzard.

Abstract

Entities: Disease

Mesh：

Year: 1970 PMID： 4316066 DOI： 10.1016/s0022-3476(70)80409-7

Source DB: PubMed Journal: J Pediatr ISSN： 0022-3476 Impact factor: 4.406

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66 in total

Review 1. Frasier and Denys-Drash syndromes: different disorders or part of a spectrum?

Authors: A Koziell; R Grundy
Journal: Arch Dis Child Date: 1999-10 Impact factor: 3.791

Review 2. Wilms' tumor.

Authors: R P Warrier; O Regueira
Journal: Pediatr Nephrol Date: 1992-07 Impact factor: 3.714

3. A single base pair polymorphism in the WT1 gene detected by single-strand conformation polymorphism analysis.

Authors: N Groves; P N Baird; A Hogg; J K Cowell
Journal: Hum Genet Date: 1992-12 Impact factor: 4.132

Review 4. Candidate genes and potential targets for therapeutics in Wilms' tumour.

Authors: Christopher Blackmore; Max J Coppes; Aru Narendran
Journal: Clin Transl Oncol Date: 2010-09 Impact factor: 3.405

5. Two children with kidney disease. Demonstrated at the Royal College of Physicians of London.

Authors:
Journal: Br Med J Date: 1978-09-23

Review 6. Wilms tumor: what's new?

Authors: Tomás Acha García; Carlota Calvo Escribano; José Alfaro Gutiérrez; Paloma Galarón García; Mercedes Guibelalde del Castillo
Journal: Clin Transl Oncol Date: 2005-03 Impact factor: 3.405

7. Broad and unexpected phenotypic expression in Greek children with steroid-resistant nephrotic syndrome due to mutations in the Wilms' tumor 1 (WT1) gene.

Authors: Spyridon Megremis; Andromachi Mitsioni; Irene Fylaktou; Sofia Kitsiou Tzeli; Filadelfia Komianou; Constantinos J Stefanidis; Emmanuel Kanavakis; Joanne Traeger-Synodinos
Journal: Eur J Pediatr Date: 2011-04-16 Impact factor: 3.183