Literature DB >> 10330366

Evidence for the genetic heterogeneity of nephropathic phenotypes associated with Denys-Drash and Frasier syndromes.

A B Koziell, R Grundy, T M Barratt, P Scambler.   

Abstract

Entities:  

Mesh：

Year:  1999        PMID： 10330366      PMCID： PMC1377922          DOI： 10.1086/302409

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN： 0002-9297            Impact factor:   11.025


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  4 in total

1.  Novel mutations in the inverted formin 2 gene of Chinese families contribute to focal segmental glomerulosclerosis.

Authors:  Jingyuan Xie; Xu Hao; Evren U Azeloglu; Hong Ren; Zhaohui Wang; Jun Ma; Jian Liu; Xiaodan Ma; Weiming Wang; Xiaoxia Pan; Wen Zhang; Fang Zhong; Yifu Li; Guoyu Meng; Krzysztof Kiryluk; John Cijiang He; Ali G Gharavi; Nan Chen
Journal:  Kidney Int       Date:  2015-06-03       Impact factor: 10.612

Review 2.  WT1 and glomerular diseases.

Authors:  Patrick Niaudet; Marie-Claire Gubler
Journal:  Pediatr Nephrol       Date:  2006-08-23       Impact factor: 3.714

3.  Pediatric onco-nephrology: time to spread the word : Part I: early kidney involvement in children with malignancy.

Authors:  Arwa Nada; Jennifer G Jetton
Journal:  Pediatr Nephrol       Date:  2020-11-27       Impact factor: 3.714

4.  Long-term kidney function in children with Wilms tumour and constitutional WT1 pathogenic variant.

Authors:  Maria Pia Falcone; Kathryn Pritchard-Jones; Jesper Brok; William Mifsud; Richard D Williams; Kayo Nakata; Suzanne Tugnait; Reem Al-Saadi; Lucy Side; John Anderson; Catriona Duncan; Stephen D Marks; Detlef Bockenhauer; Tanzina Chowdhury
Journal:  Pediatr Nephrol       Date:  2021-10-04       Impact factor: 3.651
  4 in total

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