(Q46558317)

23 December 2017

title

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

1 reference

23 December 2017

1 reference

3

Eero Kajantie

1 reference

23 December 2017

author name string

Anne-Tiina Lahdenkari

1

1 reference

23 December 2017

Maija Suvanto

2

1 reference

23 December 2017

Olli Koskimies

4

1 reference

23 December 2017

Marjo Kestilä

5

1 reference

23 December 2017

Hannu Jalanko

6

1 reference

23 December 2017

publication date

21 June 2005

1 reference

23 December 2017

published in

Pediatric Nephrology

1 reference

23 December 2017

volume

20

1 reference

23 December 2017

issue

8

1 reference

23 December 2017

page(s)

1073-1080

1 reference

23 December 2017

https://scigraph.springernature.com/pub.10.1007/s00467-005-1965-y

exact match

0 references

cites work

A podocentric view of nephrology

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS00467-005-1965-Y

Cell biology of the glomerular podocyte

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS00467-005-1965-Y

High incidence of minimal change nephrotic syndrome in Asians

21 January 2018

1 reference

12 December 2020

Mutation spectrum in the nephrin gene (NPHS1) in congenital nephrotic syndrome

1 reference

12 December 2020

The nephrotic syndrome. Its incidence and implications for the community

1 reference

12 December 2020

No evidence for genotype/phenotype correlation in NPHS1 and NPHS2 mutations.

1 reference

12 December 2020

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

1 reference

12 December 2020

Steroid-sensitive nephrotic syndrome: from childhood to adulthood

1 reference

12 December 2020

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

1 reference

12 December 2020

Increased interleukin-12 release from peripheral blood mononuclear cells in nephrotic phase of minimal change nephrotic syndrome

1 reference

12 December 2020

Podocin mutations in sporadic focal-segmental glomerulosclerosis occurring in adulthood

1 reference

12 December 2020

Podocytes are firmly attached to glomerular basement membrane in kidneys with heavy proteinuria

1 reference

12 December 2020

Positionally cloned gene for a novel glomerular protein--nephrin--is mutated in congenital nephrotic syndrome

1 reference

12 December 2020

Steroid-responsive nephrotic syndrome and allergy: immunological studies

1 reference

12 December 2020

What has the immune system got against the glomerular podocyte?

1 reference

12 December 2020

Prevalence, genetics, and clinical features of patients carrying podocin mutations in steroid-resistant nonfamilial focal segmental glomerulosclerosis.

1 reference

12 December 2020

NPHS2 mutations in late-onset focal segmental glomerulosclerosis: R229Q is a common disease-associated allele

1 reference

12 December 2020

T cells and minimal change disease

1 reference

12 December 2020

The incidence of atopy in steroid-responsive nephrotic syndrome: clinical and immunological parameters

1 reference

12 December 2020

Identification of the first gene locus (SSNS1) for steroid-sensitive nephrotic syndrome on chromosome 2p.

1 reference

12 December 2020

Nephrin gene (NPHS1) in patients with minimal change nephrotic syndrome (MCNS).

1 reference

12 December 2020

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

1 reference

12 December 2020

Nephrotic syndrome: from toddlers to twenties

1 reference

12 December 2020

The familial nephrotic syndrome. I. A European survey

1 reference

12 December 2020

Heterozygous NPHS1 or NPHS2 mutations in responsive nephrotic syndrome and the multifactorial origin of proteinuria

1 reference

12 December 2020

Determinants of vascular permeability in the kidney glomerulus.

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Genotype/phenotype correlations of NPHS1 and NPHS2 mutations in nephrotic syndrome advocate a functional inter-relationship in glomerular filtration

1 reference

12 December 2020

Mutations in NPHS2 encoding podocin are a prevalent cause of steroid-resistant nephrotic syndrome among Israeli-Arab children

1 reference

12 December 2020

Not all in the family: mutations of podocin in sporadic steroid-resistant nephrotic syndrome

1 reference

12 December 2020

Structure of the human type IV collagen gene COL4A3 and mutations in autosomal Alport syndrome.

1 reference

12 December 2020

Incidence and prevalence of asthma and allergic rhinitis: a cohort study of Finnish adolescents.

1 reference

12 December 2020

Corticosteroid therapy in nephrotic syndrome: a meta-analysis of randomised controlled trials.

1 reference

12 December 2020

NPHS2 R229Q functional variant is associated with microalbuminuria in the general population

1 reference

12 December 2020

Long-term outcome of primary nephrotic syndrome

1 reference

12 December 2020

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

1 reference

12 December 2020

T-lymphocyte populations and cytokines in childhood nephrotic syndrome

1 reference

12 December 2020

Recent approaches to the pathogenesis of minimal-change nephrotic syndrome

1 reference

12 December 2020

Influence of age at onset on the outcome of steroid-sensitive nephrotic syndrome

1 reference

12 December 2020

Role of nephrin in proteinuric renal diseases.

1 reference

12 December 2020

The role of podocytes in glomerular pathobiology

1 reference

12 December 2020

Th1 and Th2 cytokine mRNA profiles in childhood nephrotic syndrome: evidence for increased IL-13 mRNA expression in relapse

1 reference

12 December 2020

Molecular basis of the functional podocin-nephrin complex: mutations in the NPHS2 gene disrupt nephrin targeting to lipid raft microdomains

1 reference

12 December 2020

Broadening the spectrum of diseases related to podocin mutations

1 reference

12 December 2020

CD2-associated protein haploinsufficiency is linked to glomerular disease susceptibility

1 reference

12 December 2020

Congenital nephrotic syndrome in mice lacking CD2-associated protein

1 reference

12 December 2020

Long-term outcome for children with minimal-change nephrotic syndrome

1 reference

12 December 2020

10.1007/S00467-005-1965-Y

Identifiers

DOI

1 reference

23 December 2017

1 reference

23 December 2017