Pathology and pathogenic pathways in fabry nephropathy
Author:
Publisher
Springer Science and Business Media LLC
Subject
Physiology (medical),Nephrology,Physiology
Link
https://link.springer.com/content/pdf/10.1007/s10157-021-02058-z.pdf
Reference57 articles.
1. Scriba K. Zur pathogenesis des angiokeratoma corporis diffusum Fabry mit cardio-vasorenalem symptomenkomplex. Verh Dtsch Ges Pathol. 1950;34:221–6.
2. Ferraz MJ, Kallemeijn WW, Mirzaian M, Moro DH, Marques D, Wisse D, et al. Gaucher disease and Fabry disease: new markers and insights in pathophysiology for two distinct glycosphingolipidoses. Biochim Biophys Acta. 2014;1841:811–25.
3. Rozenfeld P, Feriozzi S. Contribution of inflammation pathways to Fabry disease pathogenesis. Mol Gen Metab. 2017;122:19–27.
4. Tondel C, Kanai T, Larsen KK, Ito S, Politei JM, Warnock DG, Svarstad E. Foot process effacement is an early marker of nephropathy in young classic Fabry patients without albuminuria. Nephron. 2015;129:16–21.
5. Najafian B, Tondel C, Svarstand E, Gubler MC, Oliveira JP, Mauer M. Accumulation of globotriasylceramide in podocytes in Fabry nephropathy is associated with progressive podocyte loss. J Am Soc Nephrol. 2020;31:865–75. https://doi.org/10.1681/ASN.2019050497.
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