NPHS2 screening with SURVEYOR in Hellenic children with steroid-resistant nephrotic syndrome (Q59416414)

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title

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

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Konstantinos Voskarides

1

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Constantinos Deltas

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9

Alkis Pierides

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Gregory Papagregoriou

3

object named as

Gregory Papagregoriou

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Avraam Elia

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10

Eleni Georgaki

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author name string

Christiana Makariou

2

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Nicolaos Stergiou

4

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Nicoletta Printza

5

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Efstathios Alexopoulos

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Fotis Papachristou

8

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publication date

5 April 2008

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volume

23

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issue

8

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page(s)

1373-1375

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

5 January 2020

exact match

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cites work

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

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12 December 2020

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

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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

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5 January 2020

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