(Q44795813)

English

NPHS2 mutation associated with recurrence of proteinuria after transplantation

scientific article published on 10 March 2004

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

6 December 2017

NPHS2 mutation associated with recurrence of proteinuria after transplantation (English)

1 reference

Europe PubMed Central

PubMed publication ID

6 December 2017

author name string

Heiko Billing

1

1 reference

Europe PubMed Central

PubMed publication ID

6 December 2017

Dominik Müller

2

1 reference

Europe PubMed Central

PubMed publication ID

6 December 2017

Rainer Ruf

3

1 reference

Europe PubMed Central

PubMed publication ID

6 December 2017

Anne Lichtenberger

4

1 reference

Europe PubMed Central

PubMed publication ID

6 December 2017

Friedhelm Hildebrandt

5

1 reference

Europe PubMed Central

PubMed publication ID

6 December 2017

Christian August

6

1 reference

Europe PubMed Central

PubMed publication ID

6 December 2017

Uwe Querfeld

7

1 reference

Europe PubMed Central

PubMed publication ID

6 December 2017

Dieter Haffner

8

1 reference

Europe PubMed Central

PubMed publication ID

6 December 2017

publication date

10 March 2004

1 reference

Europe PubMed Central

PubMed publication ID

6 December 2017

Pediatric Nephrology

1 reference

Europe PubMed Central

PubMed publication ID

6 December 2017

19

1 reference

Europe PubMed Central

PubMed publication ID

6 December 2017

5

1 reference

Europe PubMed Central

PubMed publication ID

6 December 2017

561-564

1 reference

Europe PubMed Central

PubMed publication ID

6 December 2017

Genetic models: clues for understanding the pathogenesis of idiopathic nephrotic syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/15015071

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Serum glomerular permeability activity in patients with podocin mutations (NPHS2) and steroid-resistant nephrotic syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/15015071

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/15015071

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/15015071

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/15015071

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Recurrence of focal segmental glomerulosclerosis after renal transplantation in patients with mutations of podocin

1 reference

https://pubmed.ncbi.nlm.nih.gov/15015071

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Recurrent focal segmental glomerulosclerosis in grafts treated with plasma exchange and increased immunosuppression

1 reference

https://pubmed.ncbi.nlm.nih.gov/15015071

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/15015071

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/15015071

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Co-localization of nephrin, podocin, and the actin cytoskeleton: evidence for a role in podocyte foot process formation

1 reference

https://pubmed.ncbi.nlm.nih.gov/15015071

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S00467-003-1408-6

1 reference

Europe PubMed Central

PubMed publication ID

6 December 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

6 December 2017

ResearchGate publication ID

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