(Q51458849)

5 April 2018

title

Discordant expression of a new WT1 gene mutation in a family with monozygotic twins presenting with congenital nephrotic syndrome. (English)

1 reference

5 April 2018

author

Michal Malina

2

1 reference

5 April 2018

author name string

Filip Fencl

1

1 reference

5 April 2018

Veronika Stará

3

1 reference

5 April 2018

Jakub Zieg

4

1 reference

5 April 2018

Dana Mixová

5

1 reference

5 April 2018

Tomáš Seeman

6

1 reference

5 April 2018

Květa Bláhová

7

1 reference

5 April 2018

publication date

26 May 2011

1 reference

5 April 2018

European Journal of Pediatrics

published in

1 reference

5 April 2018

volume

171

1 reference

5 April 2018

issue

1

1 reference

5 April 2018

page(s)

121-124

1 reference

5 April 2018

https://scigraph.springernature.com/pub.10.1007/s00431-011-1497-3

exact match

0 references

cites work

Immunosuppression and renal outcome in congenital and pediatric steroid-resistant nephrotic syndrome

1 reference

https://api.crossref.org/works/10.1007%2FS00431-011-1497-3

Genotype/phenotype correlation in nephrotic syndrome caused by WT1 mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00431-011-1497-3

Pulmonary dysplasia, Denys-Drash syndrome and Wilms tumor 1 gene mutation in twins

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00431-011-1497-3

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00431-011-1497-3

Successful treatment of steroid-resistant nephrotic syndrome associated with WT1 mutations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00431-011-1497-3

Nephrotic syndrome in the first year of life: two thirds of cases are caused by mutations in 4 genes (NPHS1, NPHS2, WT1, and LAMB2).

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00431-011-1497-3

The many facets of the Wilms' tumour gene, WT1

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00431-011-1497-3

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00431-011-1497-3

New insights into the function of the Wilms tumor suppressor gene WT1 in podocytes

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00431-011-1497-3

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00431-011-1497-3

Germline mutations in the Wilms' tumor suppressor gene are associated with abnormal urogenital development in Denys-Drash syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00431-011-1497-3

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00431-011-1497-3

Novel familial WT1 read-through mutation associated with Wilms tumor and slow progressive nephropathy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00431-011-1497-3

Frequency and Heritability ofWT1Mutations in Nonsyndromic Wilms' Tumor Patients: A UK Children’s Cancer Study Group Study

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00431-011-1497-3

A novel mutation of the WT1 gene (a tumor suppressor gene for Wilms' tumor) in a patient with Denys-Drash syndrome

21 January 2018

1 reference

12 December 2020

The nephropathy associated with male pseudohermaphroditism and Wilms' tumor (Drash syndrome): a distinctive glomerular lesion--report of 10 cases

1 reference

12 December 2020

Inherited WT1 mutation in Denys-Drash syndrome

1 reference

12 December 2020

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

1 reference

12 December 2020

A newly identified exonic mutation of the WT1 gene in a patient with Denys-Drash syndrome.

1 reference

12 December 2020

Denys-Drash syndrome with neonatal renal failure in monozygotic twins due to c.1097G>A mutation in the WT1 gene

1 reference

12 December 2020

10.1007/S00431-011-1497-3

Identifiers

DOI

1 reference

5 April 2018

PubMed ID

21614510

1 reference

5 April 2018