(Q26749359)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27066465%20AND%20SRC:MED&resulttype=core&format=json

1 April 2020

title

Pathology of Podocytopathies Causing Nephrotic Syndrome in Children (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27066465%20AND%20SRC:MED&resulttype=core&format=json

1 April 2020

0 references

1 reference

Sarangarajan Ranganathan

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27066465%20AND%20SRC:MED&resulttype=core&format=json

1 April 2020

author name string

Sarangarajan Ranganathan

series ordinal

1

0 references

language of work or name

English

0 references

publication date

31 March 2016

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27066465%20AND%20SRC:MED&resulttype=core&format=json

1 April 2020

published in

Frontiers in pediatrics

2 references

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27066465%20AND%20SRC:MED&resulttype=core&format=json

1 April 2020

volume

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27066465%20AND%20SRC:MED&resulttype=core&format=json

1 April 2020

page(s)

32

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27066465%20AND%20SRC:MED&resulttype=core&format=json

Focal segmental glomerulosclerosis: molecular genetics and targeted therapies

1 April 2020

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4814732

Morphologic variants of focal segmental glomerulosclerosis and their significance.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4814732

IgA nephropathy with minimal change disease.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4814732

NPHS2 mutations in steroid-resistant nephrotic syndrome: a mutation update and the associated phenotypic spectrum

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4814732

Association of histologic variants in FSGS clinical trial with presenting features and outcomes

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4814732

Pathobiology of focal segmental glomerulosclerosis: new developments

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4814732

Genetics of focal segmental glomerulosclerosis and human immunodeficiency virus-associated collapsing glomerulopathy: the role of MYH9 genetic variation

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4814732

C1q nephropathy in the pediatric population: pathology and pathogenesis.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4814732

Very low birth weight is a risk factor for secondary focal segmental glomerulosclerosis

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4814732

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

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4814732

The spectrum of focal segmental glomerulosclerosis: new insights

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4814732

Current views on collapsing glomerulopathy

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4814732

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

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4814732

The spectrum of podocytopathies: a unifying view of glomerular diseases.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4814732

The podocyte's response to injury: role in proteinuria and glomerulosclerosis

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4814732

C1q nephropathy: a variant of focal segmental glomerulosclerosis.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4814732

Pathologic classification of focal segmental glomerulosclerosis

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4814732

Podocyte biology and response to injury

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4814732

Nephrotic syndrome: pathogenesis and management

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4814732

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

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4814732

Congenital nephrotic syndrome of Finnish type. Study of 75 patients

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4814732

Congenital nephrotic syndrome: prenatal diagnosis and genetic counselling by estimation of aminotic-fluid and maternal serum alpha-fetoprotein

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4814732

Pathology of the nephrotic syndrome in children: a report for the International Study of Kidney Disease in Children.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4814732

C1q nephropathy: a distinct pathologic entity usually causing nephrotic syndrome.

31 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4814732

Immunohistopathologic evaluation of C1q in 800 renal biopsy specimens.

31 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4814732

Do C1q or IgM nephropathies predict disease severity in children with minimal change nephrotic syndrome?

19 June 2018

1 reference

https://api.crossref.org/works/10.3389%2FFPED.2016.00032

C1q nephropathy in children: clinical characteristics and outcome.

21 January 2018

1 reference

https://api.crossref.org/works/10.3389%2FFPED.2016.00032

Genotype–phenotype associations in WT1 glomerulopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.3389%2FFPED.2016.00032

Mutation-dependent recessive inheritance of NPHS2-associated steroid-resistant nephrotic syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.3389%2FFPED.2016.00032

Novel human pathological mutations. Gene symbol: NPHS1. Disease: congenital nephrotic syndrome, Finnish type.

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4814732

Pathologic classification of focal segmental glomerulosclerosis: a working proposal

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4814732

Congenital nephrotic syndrome (NPHS1): features resulting from different mutations in Finnish patients

28 November 2018

1 reference

12 December 2020

Podocyte proteins in congenital and minimal change nephrotic syndrome

1 reference

12 December 2020

Minimal change variants: IgM nephropathy

1 reference

12 December 2020

Graft function 5-7 years after renal transplantation in early childhood

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

TRPC6 gene variants in Czech adult patients with focal segmental glomerulosclerosis and minimal change disease

1 reference

12 December 2020

Nephrotic syndrome in children: prediction of histopathology from clinical and laboratory characteristics at time of diagnosis. A report of the International Study of Kidney Disease in Children

1 reference

12 December 2020

Identifiers

DOI

10.3389/FPED.2016.00032

2 references

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27066465%20AND%20SRC:MED&resulttype=core&format=json

1 April 2020

1 reference

2 references

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27066465%20AND%20SRC:MED&resulttype=core&format=json

1 April 2020

2 references