(Q59416414)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18392643%20AND%20SRC:MED&resulttype=core&format=json

5 January 2020

title

NPHS2 screening with SURVEYOR in Hellenic children with steroid-resistant nephrotic syndrome (English)

1 reference

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5 January 2020

1 reference

Konstantinos Voskarides

1

1 reference

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5 January 2020

Constantinos Deltas

11

1 reference

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5 January 2020

9

Alkis Pierides

1 reference

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5 January 2020

Gregory Papagregoriou

3

object named as

Gregory Papagregoriou

1 reference

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5 January 2020

7

Avraam Elia

1 reference

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5 January 2020

10

Eleni Georgaki

1 reference

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5 January 2020

author name string

Christiana Makariou

2

1 reference

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5 January 2020

Nicolaos Stergiou

4

1 reference

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5 January 2020

Nicoletta Printza

5

1 reference

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5 January 2020

Efstathios Alexopoulos

6

1 reference

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5 January 2020

Fotis Papachristou

8

1 reference

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5 January 2020

publication date

5 April 2008

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5 January 2020

1 reference

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5 January 2020

volume

23

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5 January 2020

issue

8

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5 January 2020

page(s)

1373-1375

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https://scigraph.springernature.com/pub.10.1007/s00467-008-0804-3

5 January 2020

exact match

0 references

cites work

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

1 reference

12 December 2020

Analysis of NPHS2 mutations in Turkish steroid-resistant nephrotic syndrome patients

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

Podocin, a raft-associated component of the glomerular slit diaphragm, interacts with CD2AP and nephrin

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

Clinical and genetic evaluation of familial steroid-responsive nephrotic syndrome in childhood.

1 reference

12 December 2020

COL4A3/COL4A4 mutations producing focal segmental glomerulosclerosis and renal failure in thin basement membrane nephropathy

1 reference

12 December 2020

NPHS2 gene, nephrotic syndrome and focal segmental glomerulosclerosis: a HuGE review

1 reference

12 December 2020

Mutations in the Wilms' tumor 1 gene cause isolated steroid resistant nephrotic syndrome and occur in exons 8 and 9.

1 reference

12 December 2020

10.1007/S00467-008-0804-3

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18392643%20AND%20SRC:MED&resulttype=core&format=json

5 January 2020

1 reference