Literature DB >> 4292870

[Association of an anatomo-pathological syndrome of male pseudohermaphroditism, Wilms' tumor, parenchymatous nephropathy and XX/XY mosaicism].

P Denys, P Malvaux, H Van Den Berghe, W Tanghe, W Proesmans.   

Abstract

Entities:  

Mesh：

Year:  1967        PMID： 4292870

Source DB:  PubMed          Journal:  Arch Fr Pediatr        ISSN： 0003-9764


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  45 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

2.  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

3.  WT1 gene mutations in three girls with nephrotic syndrome.

Authors:  Khalid Ismaili; Véronique Verdure; Katherina Vandenhoute; Françoise Janssen; Michelle Hall
Journal:  Eur J Pediatr       Date:  2007-06-01       Impact factor: 3.183

4.  Clinical and molecular characterization of patients with heterozygous mutations in wilms tumor suppressor gene 1.

Authors:  Anja Lehnhardt; Claartje Karnatz; Thurid Ahlenstiel-Grunow; Kerstin Benz; Marcus R Benz; Klemens Budde; Anja K Büscher; Thomas Fehr; Markus Feldkötter; Norbert Graf; Britta Höcker; Therese Jungraithmayr; Günter Klaus; Birgit Koehler; Martin Konrad; Birgitta Kranz; Carmen R Montoya; Dominik Müller; Thomas J Neuhaus; Jun Oh; Lars Pape; Martin Pohl; Brigitte Royer-Pokora; Uwe Querfeld; Reinhard Schneppenheim; Hagen Staude; Giuseppina Spartà; Kirsten Timmermann; Frauke Wilkening; Simone Wygoda; Carsten Bergmann; Markus J Kemper
Journal:  Clin J Am Soc Nephrol       Date:  2015-03-27       Impact factor: 8.237

5.  Molecular analysis of chromosome region 11p13 in patients with Drash syndrome.

Authors:  L Jadresic; R B Wadey; B Buckle; T M Barratt; C D Mitchell; J K Cowell
Journal:  Hum Genet       Date:  1991-03       Impact factor: 4.132

6.  A familial WT1 mutation associated with incomplete Denys-Drash syndrome.

Authors:  Chunhua Zhu; Fei Zhao; Weizhen Zhang; Hongmei Wu; Ying Chen; Guixia Ding; Aihua Zhang; Songming Huang
Journal:  Eur J Pediatr       Date:  2013-05-29       Impact factor: 3.183

7.  Nephropathy with Wilms tumour or gonadal dysgenesis: incomplete Denys-Drash syndrome or separate diseases?

Authors:  K Schmitt; B Zabel; G Tulzer; F Eitelberger; J Pelletier
Journal:  Eur J Pediatr       Date:  1995-07       Impact factor: 3.183

8.  A novel WT1 mutation in a 46,XY boy with congenital bilateral cryptorchidism, nystagmus and Wilms tumor.

Authors:  Monica Terenziani; Michele Sardella; Beatrice Gamba; Maria Adele Testi; Filippo Spreafico; Gianluigi Ardissino; Fausto Fedeli; Franca Fossati-Bellani; Paolo Radice; Daniela Perotti
Journal:  Pediatr Nephrol       Date:  2008-12-02       Impact factor: 3.714

Review 9.  Tumour suppressor gene mutations in humans and mice: parallels and contrasts.

Authors:  M L Hooper
Journal:  EMBO J       Date:  1998-12-01       Impact factor: 11.598

10.  Two cases of isolated diffuse mesangial sclerosis with WT1 mutations.

Authors:  Hyewon Hahn; Young Mi Cho; Young Seo Park; Han Wook You; Hae Il Cheong
Journal:  J Korean Med Sci       Date:  2006-02       Impact factor: 2.153
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