(Q57980374)

Luigi Bisceglia

2

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Gianluca Caridi

Gianluca Caridi

5

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Gian Marco Ghiggeri

Gian Marco Ghiggeri

10

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Giancarlo Barbano

6

Giancarlo Barbano

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Filippo Aucella

1

Filippo Aucella

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Francesco Perfumo

8

Francesco Perfumo

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Loreto Gesualdo

9

Loreto Gesualdo

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author name string

Patrizia De Bonis

3

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Gerolamo Mattioli

Identification of constitutional WT1 mutations, in patients with isolated diffuse mesangial sclerosis, and analysis of genotype/phenotype correlations by use of a computerized mutation database

7

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publication date

15 August 2006

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published in

Pediatric Nephrology

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volume

21

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issue

10

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page(s)

1393-1398

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cites work

1 reference

12 December 2020

Cyclosporine in patients with steroid-resistant nephrotic syndrome: an open-label, nonrandomized, retrospective study

1 reference

12 December 2020

Fine structure analysis of the WT1 gene in sporadic Wilms tumors

1 reference

12 December 2020

Mother-to-child transmitted WT1 splice-site mutation is responsible for distinct glomerular diseases

1 reference

12 December 2020

Alport syndrome–like basement membrane changes in frasier syndrome: an electron microscopy study

1 reference

12 December 2020

WT1 splice site mutation in a 46,XX female with minimal-change nephrotic syndrome and Wilms' tumour

1 reference

12 December 2020

Constitutional mutations in the WT1 gene in patients with Denys-Drash syndrome

1 reference

12 December 2020

NPHS2 (Podocin) mutations in nephrotic syndrome. Clinical spectrum and fine mechanisms

1 reference

12 December 2020

WT1-mediated growth suppression of Wilms tumor cells expressing a WT1 splicing variant.

1 reference

12 December 2020

Prevalence of WT1 mutations in a large cohort of patients with steroid-resistant and steroid-sensitive nephrotic syndrome.

1 reference

12 December 2020

Frasier syndrome: a cause of focal segmental glomerulosclerosis in a 46,XX female.

1 reference

12 December 2020

Isolation and characterization of a zinc finger polypeptide gene at the human chromosome 11 Wilms' tumor locus

1 reference

12 December 2020

WT1 nephropathy in a girl with normal karyotype (46,XX)

1 reference

12 December 2020

Prospective, controlled trial of cyclophosphamide therapy in children with nephrotic syndrome. Report of the International study of Kidney Disease in Children

1 reference

12 December 2020

Primary nephrotic syndrome in children: clinical significance of histopathologic variants of minimal change and of diffuse mesangial hypercellularity. A Report of the International Study of Kidney Disease in Children

1 reference

12 December 2020

Two splice variants of the Wilms' tumor 1 gene have distinct functions during sex determination and nephron formation

1 reference

12 December 2020

The genomic organization and expression of the WT1 gene

1 reference

12 December 2020

Frasier syndrome is caused by defective alternative splicing of WT1 leading to an altered ratio of WT1 +/-KTS splice isoforms.

1 reference

12 December 2020

Donor splice-site mutations in WT1 are responsible for Frasier syndrome

1 reference

12 December 2020

Exon 9 mutations in the WT1 gene, without influencing KTS splice isoforms, are also responsible for Frasier syndrome

1 reference

12 December 2020

Broadening the spectrum of diseases related to podocin mutations

1 reference

12 December 2020

Mutations in the Wilms' tumor 1 gene cause isolated steroid resistant nephrotic syndrome and occur in exons 8 and 9.

1 reference

12 December 2020