Clinical and pathological phenotype of genetic causes of focal segmental glomerulosclerosis in adults. (Q54985317)

14 June 2018

title

Clinical and pathological phenotype of genetic causes of focal segmental glomerulosclerosis in adults. (English)

1 reference

14 June 2018

focal segmental glomerulosclerosis

main subject

1 reference

Nicola Lepori

1

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14 June 2018

Ladan Zand

2

1 reference

14 June 2018

Sanjeev Sethi

3

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14 June 2018

Gema Fernandez-Juarez

4

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14 June 2018

Fernando C Fervenza

5

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14 June 2018

publication date

9 January 2018

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14 June 2018

Clinical kidney journal / an academic journal of the ERA-EDTA (European Renal Association - European Dialysis and Transplant Association)

published in

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14 June 2018

volume

11

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14 June 2018

page(s)

179-190

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14 June 2018

issue

2

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14 June 2018

Creative Commons Attribution-NonCommercial 4.0 International

copyright license

start time

10 January 2018

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

cites work

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16 June 2018

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16 June 2018

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16 June 2018

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16 June 2018

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16 June 2018

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TRPC6 mutational analysis in a large cohort of patients with focal segmental glomerulosclerosis.

13 August 2018

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Kidney transplantation for primary focal segmental glomerulosclerosis: outcomes and response to therapy for recurrence.

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Clinical and epidemiological assessment of steroid-resistant nephrotic syndrome associated with the NPHS2 R229Q variant

13 August 2018

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Podocyte foot process effacement as a diagnostic tool in focal segmental glomerulosclerosis.

13 August 2018

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Nephrotic syndrome in the first year of life: two thirds of cases are caused by mutations in 4 genes (NPHS1, NPHS2, WT1, and LAMB2).

13 August 2018

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Mutational and Biological Analysis of alpha-actinin-4 in focal segmental glomerulosclerosis.

13 August 2018

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

13 August 2018

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A Case of Familial Kidney Disease

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Crossref

https://api.crossref.org/works/10.1093%2FCKJ%2FSFX143

Mutations in PLCE1 are a major cause of isolated diffuse mesangial sclerosis (IDMS)

21 January 2018

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Spectrum of disease in familial focal and segmental glomerulosclerosis

30 November 2018

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12 December 2020

Congenital focal segmental glomerulosclerosis associated with beta4 integrin mutation and epidermolysis bullosa

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12 December 2020

Molecular Analysis of NPHS2 and ACTN4 Genes in a Series of 33 Italian Patients Affected by Adult-Onset Nonfamilial Focal Segmental Glomerulosclerosis

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12 December 2020

Recessive NPHS2 (Podocin) mutations are rare in adult-onset idiopathic focal segmental glomerulosclerosis

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12 December 2020

Early coenzyme Q10 supplementation in primary coenzyme Q10 deficiency

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12 December 2020

Nephrin mutations cause childhood- and adult-onset focal segmental glomerulosclerosis

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12 December 2020

Mutations in podocyte genes are a rare cause of primary FSGS associated with ESRD in adult patients

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12 December 2020

COL4A3 mutations cause focal segmental glomerulosclerosis

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12 December 2020

Collagen (COL4A) mutations are the most frequent mutations underlying adult focal segmental glomerulosclerosis

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12 December 2020

Identifiers

DOI

10.1093/CKJ/SFX143

1 reference

14 June 2018

PMCID

5888331

1 reference

14 June 2018

PubMed ID

29644057

1 reference

14 June 2018