Genetic mutational testing of Chinese children with familial hematuria with biopsy‑proven FSGS. (Q47401355)

23 February 2018

title

Genetic mutational testing of Chinese children with familial hematuria with biopsy‑proven FSGS. (English)

1 reference

23 February 2018

author name string

Yongzhen Li

1

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23 February 2018

Ying Wang

2

1 reference

23 February 2018

Qingnan He

3

1 reference

23 February 2018

Xiqiang Dang

4

1 reference

23 February 2018

Yan Cao

5

1 reference

23 February 2018

Xiaochuan Wu

6

1 reference

23 February 2018

Shuanghong Mo

7

1 reference

23 February 2018

Xiaoxie He

8

1 reference

23 February 2018

Zhuwen Yi

9

1 reference

23 February 2018

publication date

10 November 2017

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23 February 2018

Molecular Medicine Reports

published in

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23 February 2018

volume

17

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23 February 2018

issue

1

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23 February 2018

page(s)

1513-1526

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23 February 2018

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LMX1B mutations cause hereditary FSGS without extrarenal involvement

22 May 2018

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Haematuria: the forgotten CKD factor?

22 May 2018

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22 May 2018

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CD2AP mutations are associated with sporadic nephrotic syndrome and focal segmental glomerulosclerosis (FSGS).

22 May 2018

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NPHS2 variation in focal and segmental glomerulosclerosis

22 May 2018

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Familial focal segmental glomerulosclerosis associated with an ACTN4 mutation and paternal germline mosaicism

22 May 2018

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Array-based gene discovery with three unrelated subjects shows SCARB2/LIMP-2 deficiency causes myoclonus epilepsy and glomerulosclerosis

22 May 2018

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22 May 2018

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22 May 2018

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22 May 2018

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Persistent asymptomatic isolated microscopic hematuria in Israeli adolescents and young adults and risk for end-stage renal disease

14 August 2018

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

14 August 2018

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Clinico-pathological correlations in 127 patients in 11 large pedigrees, segregating one of three heterozygous mutations in the COL4A3/ COL4A4 genes associated with familial haematuria and significant late progression to proteinuria and chronic kidn

14 August 2018

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Podocyte depletion causes glomerulosclerosis: diphtheria toxin-induced podocyte depletion in rats expressing human diphtheria toxin receptor transgene.

14 August 2018

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Mitochondrial tRNALeu(UUR) mutation in a patient with steroid-resistant nephrotic syndrome and focal segmental glomerulosclerosis

14 August 2018

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Asymptomatic isolated microscopic haematuria: long-term follow-up

14 August 2018

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Clinical and pathologic features of focal segmental glomerulosclerosis with mitochondrial tRNALeu(UUR) gene mutation

14 August 2018

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

14 August 2018

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Podocyte depletion and glomerulosclerosis have a direct relationship in the PAN-treated rat

14 August 2018

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Mitochondrial encephalomyopathies preceded by de-Toni-Debré-Fanconi syndrome or focal segmental glomerulosclerosis

1 December 2018

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12 December 2020

Renal biopsy diagnosis in children presenting with haematuria

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12 December 2020

Mitochondrial DNA point mutations detected in four cases of sudden infant death syndrome

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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

Red cell traverse through thin glomerular basement membranes

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12 December 2020

Mitochondrial DNA mutations in focal segmental glomerulosclerosis lesions

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Possible role of mtDNA mutations in sudden infant death

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12 December 2020

Nephrotic syndrome and aberrant expression of laminin isoforms in glomerular basement membranes for an infant with Herlitz junctional epidermolysis bullosa

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

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Chapter 6: Idiopathic focal segmental glomerulosclerosis in adults

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COL4A3 mutations cause focal segmental glomerulosclerosis

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Identifiers

DOI

10.3892/MMR.2017.8023

1 reference

23 February 2018

PMC publication ID

5780091

1 reference

23 February 2018

PubMed publication ID

29138824

1 reference

23 February 2018