about
Podocyte pathology and nephropathy - sphingolipids in glomerular diseasesReceptor-mediated endocytosis of α-galactosidase A in human podocytes in Fabry diseaseMannose 6-phosphate receptor and sortilin mediated endocytosis of α-galactosidase A in kidney endothelial cellsSkin-impedance in Fabry Disease: a prospective, controlled, non-randomized clinical studyFabry nephropathy: a review - how can we optimize the management of Fabry nephropathy?Podocytes degrade endocytosed albumin primarily in lysosomesCharacterization of Fabry mice treated with recombinant adeno-associated virus 2/8-mediated gene transfer.Scoring system for renal pathology in Fabry disease: report of the International Study Group of Fabry Nephropathy (ISGFN).Dysregulated autophagy contributes to podocyte damage in Fabry's disease.Update on role of agalsidase alfa in management of Fabry disease.Lipid biology of the podocyte--new perspectives offer new opportunities.Curvilinear bodies in hydroxychloroquine-induced renal phospholipidosis resembling Fabry disease.Epithelial-Mesenchymal Transition in Kidney Tubular Epithelial Cells Induced by Globotriaosylsphingosine and GlobotriaosylceramideWeekly enzyme replacement therapy may slow decline of renal function in patients with Fabry disease who are on long-term biweekly dosing.Agalsidase benefits renal histology in young patients with Fabry disease.Fabry's Disease: Case Series and Review of LiteratureFibrosis: a key feature of Fabry disease with potential therapeutic implicationsApplication of regenerative medicine for kidney diseasesAgalsidase alfa and kidney dysfunction in Fabry disease.Renal complications of Fabry disease in childrenAltered dynamics of a lipid raft associated protein in a kidney model of Fabry diseaseLysosome dysfunction in the pathogenesis of kidney diseases.Characterization and phosphoproteomic analysis of a human immortalized podocyte model of Fabry disease generated using CRISPR/Cas9 technology.Genetic-Variation-Driven Gene-Expression Changes Highlight Genes with Important Functions for Kidney Disease.Renal variant of Fabry disease with sporadic GLA gene mutation: role of early renal biopsy.Sphingolipids and Redox Signaling in Renal Regulation and Chronic Kidney Diseases.Fabry disease: characterisation of the plasma proteome pre- and post-enzyme replacement therapy.Medullary thick ascending limb impairment in the GlatmTg(CAG-A4GALT) Fabry model mice.Variable phenotypic presentations of renal involvement in Fabry disease: a case series.
P2860
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P2860
description
2002 nî lūn-bûn
@nan
2002 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
2002 թվականի հունիսին հրատարակված գիտական հոդված
@hy
2002年の論文
@ja
2002年論文
@yue
2002年論文
@zh-hant
2002年論文
@zh-hk
2002年論文
@zh-mo
2002年論文
@zh-tw
2002年论文
@wuu
name
Renal pathology in Fabry disease.
@ast
Renal pathology in Fabry disease.
@en
Renal pathology in Fabry disease.
@nl
type
label
Renal pathology in Fabry disease.
@ast
Renal pathology in Fabry disease.
@en
Renal pathology in Fabry disease.
@nl
prefLabel
Renal pathology in Fabry disease.
@ast
Renal pathology in Fabry disease.
@en
Renal pathology in Fabry disease.
@nl
P2093
P1476
Renal pathology in Fabry disease
@en
P2093
Jeffrey B Kopp
Joseph Alroy
Sharda Sabnis
P304
P478
13 Suppl 2
P577
2002-06-01T00:00:00Z