(Q53928610)

22 May 2018

title

Clinical, histopathologic, and genetic studies in nine families with focal segmental glomerulosclerosis. (English)

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22 May 2018

focal segmental glomerulosclerosis

main subject

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Kesha Rana

1

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22 May 2018

Nicole Isbel

2

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22 May 2018

Mark Buzza

3

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22 May 2018

Hayat Dagher

4

1 reference

22 May 2018

Paul Henning

5

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22 May 2018

Gad Kainer

6

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22 May 2018

Judy Savige

7

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22 May 2018

publication date

1 June 2003

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22 May 2018

American Journal of Kidney Diseases

published in

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22 May 2018

volume

41

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22 May 2018

issue

6

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22 May 2018

page(s)

1170-1178

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22 May 2018

Clinical and genetic heterogeneity in familial focal segmental glomerulosclerosis

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0272-6386%2803%2900347-0

7 January 2021

Circulating factor associated with increased glomerular permeability to albumin in recurrent focal segmental glomerulosclerosis

1 reference

https://api.crossref.org/works/10.1016%2FS0272-6386%2803%2900347-0

7 January 2021

Mapping a gene (SRN1) to chromosome 1q25-q31 in idiopathic nephrotic syndrome confirms a distinct entity of autosomal recessive nephrosis.

1 reference

https://api.crossref.org/works/10.1016%2FS0272-6386%2803%2900347-0

7 January 2021

Linkage of a Gene Causing Familial Focal Segmental Glomerulosclerosis to Chromosome 11 and Further Evidence of Genetic Heterogeneity

1 reference

https://api.crossref.org/works/10.1016%2FS0272-6386%2803%2900347-0

7 January 2021

A locus for inherited focal segmental glomerulosclerosis maps to chromosome 19q13

1 reference

https://api.crossref.org/works/10.1016%2FS0272-6386%2803%2900347-0

7 January 2021

Evidence for the genetic heterogeneity of nephropathic phenotypes associated with Denys-Drash and Frasier syndromes

1 reference

https://api.crossref.org/works/10.1016%2FS0272-6386%2803%2900347-0

7 January 2021

A case of mitochondrial cytopathy with a typical point mutation for MELAS, presenting with severe focal-segmental glomerulosclerosis as main clinical manifestation.

1 reference

https://api.crossref.org/works/10.1016%2FS0272-6386%2803%2900347-0

7 January 2021

A case of craniomandibular dermatodysostosis associated with focal glomerulosclerosis

1 reference

https://api.crossref.org/works/10.1016%2FS0272-6386%2803%2900347-0

7 January 2021

Another autosomal recessive form of focal glomerulosclerosis with neurological findings

1 reference

https://api.crossref.org/works/10.1016%2FS0272-6386%2803%2900347-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0272-6386%2803%2900347-0

7 January 2021

Mutations in ACTN4, encoding alpha-actinin-4, cause familial focal segmental glomerulosclerosis

1 reference

https://api.crossref.org/works/10.1016%2FS0272-6386%2803%2900347-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0272-6386%2803%2900347-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0272-6386%2803%2900347-0

7 January 2021

Congenital nephrotic syndrome in mice lacking CD2-associated protein

1 reference

https://api.crossref.org/works/10.1016%2FS0272-6386%2803%2900347-0

7 January 2021

Proteinuria and perinatal lethality in mice lacking NEPH1, a novel protein with homology to NEPHRIN

1 reference

https://api.crossref.org/works/10.1016%2FS0272-6386%2803%2900347-0

7 January 2021

FAT is a component of glomerular slit diaphragms

1 reference

https://api.crossref.org/works/10.1016%2FS0272-6386%2803%2900347-0

7 January 2021

Hematuria: a simple method for identifying glomerular bleeding.

1 reference

https://api.crossref.org/works/10.1016%2FS0272-6386%2803%2900347-0

7 January 2021

Clinical and pathologic features of familial focal segmental glomerulosclerosis

1 reference

https://api.crossref.org/works/10.1016%2FS0272-6386%2803%2900347-0

7 January 2021

Focal glomerular sclerosis: contrasting clinical patterns in children and adults

1 reference

https://api.crossref.org/works/10.1016%2FS0272-6386%2803%2900347-0

7 January 2021

Absence of nephritogenic GBM antigen(s) in some patients with hereditary nephritis

1 reference

https://api.crossref.org/works/10.1016%2FS0272-6386%2803%2900347-0

7 January 2021

10.1016/S0272-6386(03)00347-0

Identifiers

DOI

1 reference

22 May 2018

1 reference

22 May 2018