Literature DB >> 8381254

Diffuse mesangial sclerosis: a congenital glomerulopathy with nephrotic syndrome.

R Habib1, M C Gubler, C Antignac, M F Gagnadoux.   

Abstract

Entities:  

Mesh：

Year:  1993        PMID： 8381254

Source DB:  PubMed          Journal:  Adv Nephrol Necker Hosp        ISSN： 0084-5957


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  13 in total

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

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Review 3.  PAX2 in human kidney malformations and disease.

Authors:  Lyndsay A Harshman; Patrick D Brophy
Journal:  Pediatr Nephrol       Date:  2011-12-03       Impact factor: 3.714

Review 4.  The etiology of congenital nephrotic syndrome: current status and challenges.

Authors:  Jing-Jing Wang; Jian-Hua Mao
Journal:  World J Pediatr       Date:  2016-03-09       Impact factor: 2.764

Review 5.  The podocyte as a target: cyclosporin A in the management of the nephrotic syndrome caused by WT1 mutations.

Authors:  Constantinos J Stefanidis; Uwe Querfeld
Journal:  Eur J Pediatr       Date:  2011-02-08       Impact factor: 3.183

Review 6.  WT1 and glomerular diseases.

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7.  Atypical clinical presentation of a WT1-related syndrome associated with a novel exon 6 gene mutation.

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Review 8.  The Genetics of Nephrotic Syndrome.

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9.  Advillin acts upstream of phospholipase C ϵ1 in steroid-resistant nephrotic syndrome.

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Journal:  J Clin Invest       Date:  2017-10-23       Impact factor: 14.808

Review 10.  The renal biopsy in the genomic era.

Authors:  Helen Liapis; Joseph P Gaut
Journal:  Pediatr Nephrol       Date:  2012-11-21       Impact factor: 3.714
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