(Q35088316)

English

Mutated podocin manifesting as CMV-associated congenital nephrotic syndrome

scientific article

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

Mutated podocin manifesting as CMV-associated congenital nephrotic syndrome (English)

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

congenital disorder

0 references

author name string

Yaacov Frishberg

1

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

Choni Rinat

2

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

Sofia Feinstein

3

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

Rachel Becker-Cohen

4

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

Orli Megged

5

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

Yechiel Schlesinger

6

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

publication date

26 February 2003

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

Pediatric Nephrology

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

18

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

3

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

273-275

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/12644922

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fatal congenital cytomegalovirus infection acquired by an intra-uterine transfusion

1 reference

https://pubmed.ncbi.nlm.nih.gov/12644922

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/12644922

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Infantile nephrosis; clinical, biochemical, and morphologic studies of the syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/12644922

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/12644922

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/12644922

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Congenital nephrosis and neonatal cytomegalovirus infection: a clinical association

1 reference

https://pubmed.ncbi.nlm.nih.gov/12644922

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Nephrotic syndrome in a mother and her infant: relationship with cytomegalovirus infection

1 reference

https://pubmed.ncbi.nlm.nih.gov/12644922

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Nephrotic syndrome in early infancy as a manifestation of congenital syphilis

1 reference

https://pubmed.ncbi.nlm.nih.gov/12644922

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Congenital nephrotic syndrome associated with congenital toxoplasmosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/12644922

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S00467-003-1079-3

0 references

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

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