(Q54563047)

1 June 2018

title

Mutational analysis of NPHS2 and WT1 in frequently relapsing and steroid-dependent nephrotic syndrome. (English)

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4

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author name string

Rasheed Gbadegesin

1

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Bernward Hinkes

2

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Christopher Vlangos

3

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Jinhong Liu

5

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Jeff Hopcian

6

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Friedhelm Hildebrandt

7

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publication date

10 January 2007

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1 June 2018

published in

Pediatric Nephrology

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1 June 2018

volume

22

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issue

4

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page(s)

509-513

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1 June 2018

Clinical features and outcome of childhood minimal change nephrotic syndrome: is genetics involved?

cites work

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12 December 2020

Patients with mutations in NPHS2 (podocin) do not respond to standard steroid treatment of nephrotic syndrome.

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12 December 2020

NPHS2, encoding the glomerular protein podocin, is mutated in autosomal recessive steroid-resistant nephrotic syndrome

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12 December 2020

Predicting the response to cytotoxic therapy for childhood nephrotic syndrome: superiority of response to corticosteroid therapy over histopathologic patterns.

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12 December 2020

Nephrotic syndrome in childhood.

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12 December 2020

A gene mutated in nephronophthisis and retinitis pigmentosa encodes a novel protein, nephroretinin, conserved in evolution

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12 December 2020

NPHS2 mutation analysis shows genetic heterogeneity of steroid-resistant nephrotic syndrome and low post-transplant recurrence.

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12 December 2020

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

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12 December 2020

Corticosteroid therapy for nephrotic syndrome in children

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12 December 2020

Structure of the gene for congenital nephrotic syndrome of the finnish type (NPHS1) and characterization of mutations

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12 December 2020

Novel mutations in NPHS2 detected in both familial and sporadic steroid-resistant nephrotic syndrome

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12 December 2020

In situ evaluation of podocin in normal and glomerular diseases

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12 December 2020

The number of podocyte slit diaphragms is decreased in minimal change nephrotic syndrome.

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12 December 2020

NPHS2 gene, nephrotic syndrome and focal segmental glomerulosclerosis: a HuGE review

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12 December 2020

Broadening the spectrum of diseases related to podocin mutations

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12 December 2020

Long versus standard prednisone therapy for initial treatment of idiopathic nephrotic syndrome in children. Arbeitsgemeinschaft für Pädiatrische Nephrologie

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12 December 2020

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

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12 December 2020

10.1007/S00467-006-0377-Y

Identifiers

DOI

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1 June 2018

release_bydh7nhswjb45lmrllm6tmkcpu

Fatcat ID

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Fatcat

https://api.fatcat.wiki/v0/release/bydh7nhswjb45lmrllm6tmkcpu

24 November 2022

mapped directly with Wikidata item

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1 June 2018