Heterozygous COL4A3 Variants in Histologically Diagnosed Focal Segmental Glomerulosclerosis.

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Heterozygous COL4A3 Variants in Histologically Diagnosed Focal Segmental Glomerulosclerosis.

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2018 nî lūn-bûn

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2018年の論文

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年学术文章

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Heterozygous COL4A3 Variants i ...... Segmental Glomerulosclerosis.

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Heterozygous COL4A3 Variants i ...... Segmental Glomerulosclerosis.

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Heterozygous COL4A3 Variants i ...... Segmental Glomerulosclerosis.

@en

Heterozygous COL4A3 Variants i ...... Segmental Glomerulosclerosis.

@nl

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Heterozygous COL4A3 Variants i ...... Segmental Glomerulosclerosis.

@en

Heterozygous COL4A3 Variants i ...... Segmental Glomerulosclerosis.

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P1476

Heterozygous COL4A3 Variants i ...... Segmental Glomerulosclerosis.

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Christoph Schmaderer

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Claudius Küchle

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Dagmar Wahl

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Hanns-Georg Klein

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Julia Hoefele

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Korbinian M Riedhammer

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Lutz Renders

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Maike Büttner-Herold

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Matthias C Braunisch

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Pierre-Maurice Herr

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P2860

COL4A3/COL4A4 mutations producing focal segmental glomerulosclerosis and renal failure in thin basement membrane nephropathy

Treatment of primary FSGS in adults

Thin basement membrane nephropathy

Alport syndrome. An inherited disorder of renal, ocular, and cochlear basement membranes.

Hereditary nephrotic syndrome: a systematic approach for genetic testing and a review of associated podocyte gene mutations.

Autosomal-dominant Alport syndrome: natural history of a disease due to COL4A3 or COL4A4 gene.

A single-gene cause in 29.5% of cases of steroid-resistant nephrotic syndrome.

Rare hereditary COL4A3/COL4A4 variants may be mistaken for familial focal segmental glomerulosclerosis

GSDS 2.0: an upgraded gene feature visualization server.

Safety and Efficacy of the ACE-Inhibitor Ramipril in Alport Syndrome: The Double-Blind, Randomized, Placebo-Controlled, Multicenter Phase III EARLY PRO-TECT Alport Trial in Pediatric Patients.

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171

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scholarly article

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10.3389/FPED.2018.00171

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P478

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P577

2018-06-12T00:00:00Z

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29946535

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6007128

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