(Q62937781)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16810518%20AND%20SRC:MED&resulttype=core&format=json

26 December 2019

title

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

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16810518%20AND%20SRC:MED&resulttype=core&format=json

26 December 2019

1 reference

7

1 reference

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26 December 2019

Mustafa Tekin

9

1 reference

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26 December 2019

author name string

Nermin Uncu

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16810518%20AND%20SRC:MED&resulttype=core&format=json

26 December 2019

Banu Acar

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16810518%20AND%20SRC:MED&resulttype=core&format=json

26 December 2019

Mesiha Ekim

8

1 reference

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26 December 2019

Z Birsin Ozçakar

1

1 reference

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26 December 2019

F Başak Cengiz

2

1 reference

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26 December 2019

Nilgün Cakar

3

1 reference

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26 December 2019

Nazli Kara

5

1 reference

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26 December 2019

Fatoş Yalçinkaya

10

1 reference

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26 December 2019

publication date

30 June 2006

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26 December 2019

1 reference

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26 December 2019

volume

21

1 reference

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26 December 2019

issue

8

1 reference

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26 December 2019

page(s)

1093-1096

1 reference

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https://scigraph.springernature.com/pub.10.1007/s00467-006-0116-4

26 December 2019

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

The primary nephrotic syndrome in children. Identification of patients with minimal change nephrotic syndrome from initial response to prednisone. A report of the International Study of Kidney Disease in Children

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

Three siblings with steroid-resistant nephrotic syndrome: new NPHS2 mutations in a Turkish family.

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

The genetic basis of FSGS and steroid-resistant nephrosis

1 reference

12 December 2020

Infantile steroid-resistant nephrotic syndrome associated with double homozygous mutations of podocin

1 reference

12 December 2020

NPHS2 mutations in sporadic steroid-resistant nephrotic syndrome in Japanese children

1 reference

12 December 2020

NPHS2 mutation analysis shows genetic heterogeneity of steroid-resistant nephrotic syndrome and low post-transplant recurrence.

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Mutations in NPHS2 in sporadic steroid-resistant nephrotic syndrome in Chinese children.

1 reference

12 December 2020

Broadening the spectrum of diseases related to podocin mutations

1 reference

12 December 2020