(Q37156672)

18 August 2017

1 reference

title

Molecular pathology of nephrotic syndrome in childhood: a contemporary approach to diagnosis (English)

1 reference

18 August 2017

0 references

0 references

1 reference

Helen Liapis

1

1 reference

18 August 2017

1 July 2008

1 reference

Pediatric and Developmental Pathology

18 August 2017

1 reference

18 August 2017

11

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18 August 2017

4

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18 August 2017

154-163

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The origins and development of the concept of a "nephrotic syndrome".

18 August 2017

1 reference

https://api.crossref.org/works/10.2350%2F07-11-0375.1

Nephrotic syndrome in the 1st year of life

21 January 2018

1 reference

https://api.crossref.org/works/10.2350%2F07-11-0375.1

Changing patterns in the histopathology of idiopathic nephrotic syndrome in children

21 January 2018

1 reference

https://api.crossref.org/works/10.2350%2F07-11-0375.1

High incidence of initial and late steroid resistance in childhood nephrotic syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.2350%2F07-11-0375.1

A proposed taxonomy for the podocytopathies: a reassessment of the primary nephrotic diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.2350%2F07-11-0375.1

Cell biology of the glomerular podocyte

21 January 2018

1 reference

https://api.crossref.org/works/10.2350%2F07-11-0375.1

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

21 January 2018

1 reference

https://api.crossref.org/works/10.2350%2F07-11-0375.1

A mutation in the TRPC6 cation channel causes familial focal segmental glomerulosclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.2350%2F07-11-0375.1

Collapsing glomerulopathy in HIV and non-HIV patients: a clinicopathological and follow-up study

21 January 2018

1 reference

https://api.crossref.org/works/10.2350%2F07-11-0375.1

Bone morphogenetic protein-7 delays podocyte injury due to high glucose

21 January 2018

1 reference

https://api.crossref.org/works/10.2350%2F07-11-0375.1

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/10.2350%2F07-11-0375.1

Hereditary proteinuria syndromes and mechanisms of proteinuria

21 January 2018

1 reference

https://api.crossref.org/works/10.2350%2F07-11-0375.1

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

21 January 2018

1 reference

https://api.crossref.org/works/10.2350%2F07-11-0375.1

Respiratory chain deficiency presenting as congenital nephrotic syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.2350%2F07-11-0375.1

Proteinuria and prenatal diagnosis of congenital nephrosis in fetal carriers of nephrin gene mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.2350%2F07-11-0375.1

Recurrence of nephrotic syndrome in kidney grafts of patients with congenital nephrotic syndrome of the Finnish type: role of nephrin.

21 January 2018

1 reference

https://api.crossref.org/works/10.2350%2F07-11-0375.1

WT1 and glomerular diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.2350%2F07-11-0375.1

Cytomegalovirus-related congenital nephrotic syndrome with diffuse mesangial sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.2350%2F07-11-0375.1

Podocyte proteins in Galloway-Mowat syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.2350%2F07-11-0375.1

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/10.2350%2F07-11-0375.1

Expanding the clinical spectrum of Frasier syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.2350%2F07-11-0375.1

WT1 and PAX-2 podocyte expression in Denys-Drash syndrome and isolated diffuse mesangial sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.2350%2F07-11-0375.1

Human laminin beta2 deficiency causes congenital nephrosis with mesangial sclerosis and distinct eye abnormalities

21 January 2018

1 reference

https://api.crossref.org/works/10.2350%2F07-11-0375.1

Recessive missense mutations in LAMB2 expand the clinical spectrum of LAMB2-associated disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.2350%2F07-11-0375.1

Positional cloning uncovers mutations in PLCE1 responsible for a nephrotic syndrome variant that may be reversible

21 January 2018

1 reference

https://api.crossref.org/works/10.2350%2F07-11-0375.1

Focal and segmental glomerulosclerosis: varying biologic mechanisms underlie a final histopathologic end point

21 January 2018

1 reference

https://api.crossref.org/works/10.2350%2F07-11-0375.1

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

21 January 2018

1 reference

https://api.crossref.org/works/10.2350%2F07-11-0375.1

Broadening the spectrum of diseases related to podocin mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.2350%2F07-11-0375.1

Expression profile of nephrin, podocin, and CD2AP in Chinese children with MCNS and IgA nephropathy

21 January 2018

1 reference

https://api.crossref.org/works/10.2350%2F07-11-0375.1

Collapsing glomerulopathy in a 16-year-old girl with pulmonary tuberculosis: the role of systemic inflammatory mediators.

21 January 2018

1 reference

https://api.crossref.org/works/10.2350%2F07-11-0375.1

Idiopathic collapsing glomerulopathy in children

21 January 2018

1 reference

https://api.crossref.org/works/10.2350%2F07-11-0375.1

Idiopathic collapsing focal segmental glomerulosclerosis in pediatric patients

21 January 2018

1 reference

https://api.crossref.org/works/10.2350%2F07-11-0375.1

COQ2 nephropathy: a newly described inherited mitochondriopathy with primary renal involvement

21 January 2018

1 reference

https://api.crossref.org/works/10.2350%2F07-11-0375.1

Quinone-responsive multiple respiratory-chain dysfunction due to widespread coenzyme Q10 deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.2350%2F07-11-0375.1

Gene Expression Profiles of Podocyte-Associated Molecules as Diagnostic Markers in Acquired Proteinuric Diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.2350%2F07-11-0375.1

Expression of nephrin in acquired forms of nephrotic syndrome in childhood

21 January 2018

1 reference

https://api.crossref.org/works/10.2350%2F07-11-0375.1

WT1 mutations in nephrotic syndrome revisited. High prevalence in young girls, associations and renal phenotypes

21 January 2018

1 reference

https://api.crossref.org/works/10.2350%2F07-11-0375.1

21 January 2018

Identifiers

DOI

10.2350/07-11-0375.1

1 reference

18 August 2017

1 reference

PubMed ID

18462046