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AJKD Atlas of Renal Pathology: Fabry nephropathy.

作者信息

Najafian Behzad, Fogo Agnes B, Lusco Mark A, Alpers Charles E

机构信息

Department of Pathology, University of Washington, Seattle, WA.

Department of Pathology, Microbiology and Immunology, Vanderbilt University, Nashville, TN.

出版信息

Am J Kidney Dis. 2015 Nov;66(5):e35-6. doi: 10.1053/j.ajkd.2015.08.006.

DOI:10.1053/j.ajkd.2015.08.006

PMID:26498420

Abstract

摘要

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相似文献

AJKD Atlas of Renal Pathology: Fabry nephropathy.

Am J Kidney Dis. 2015 Nov;66(5):e35-6. doi: 10.1053/j.ajkd.2015.08.006.

Unusual myelinoid bodies in minimal change renal disease.

Pathology. 2006 Feb;38(1):72-4. doi: 10.1080/00313020500466529.

When foots come first: early signs of podocyte injury in Fabry nephropathy without proteinuria.

Nephron. 2015;129(1):3-5. doi: 10.1159/000369307. Epub 2015 Jan 15.

Myeloid bodies in patients without clinical Fabry's disease.

Arch Pathol Lab Med. 1980 Jan;104(1):14-6.

Foot process effacement is an early marker of nephropathy in young classic Fabry patients without albuminuria.

Nephron. 2015;129(1):16-21. doi: 10.1159/000369309. Epub 2014 Dec 17.

AJKD Atlas of Renal Pathology: Sickle Cell Nephropathy.

Am J Kidney Dis. 2016 Jul;68(1):e1-3. doi: 10.1053/j.ajkd.2016.05.003.

Clinical parameters, LysoGb3, podocyturia, and kidney biopsy in children with Fabry disease: is a correlation possible?

Pediatr Nephrol. 2018 Nov;33(11):2095-2101. doi: 10.1007/s00467-018-4006-3. Epub 2018 Jul 9.

Clinical course and pathological findings of two late-onset Fabry hemizygous patients including mulberry cell counts after enzyme replacement therapy.

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AJKD Atlas of Renal Pathology: Karyomegalic Nephropathy.

Am J Kidney Dis. 2016 Jul;68(1):e7. doi: 10.1053/j.ajkd.2016.05.002.

Renal pathological changes in Fabry disease.

J Inherit Metab Dis. 2001;24 Suppl 2:66-70; discussion 65. doi: 10.1023/a:1012423924648.

引用本文的文献

Genetics in Kidney Diseases.

Adv Kidney Dis Health. 2025 Jan;32(1):33-40. doi: 10.1053/j.akdh.2024.10.003.

When should the nephrologist think about genetics in patients with glomerular diseases?

Clin Kidney J. 2025 Feb 13;18(3):sfaf044. doi: 10.1093/ckj/sfaf044. eCollection 2025 Mar.

ANCA-negative pauci-immune crescentic glomerulonephritis associated with Fabry disease: lesson for the clinical nephrologist.

J Nephrol. 2023 Apr;36(3):635-638. doi: 10.1007/s40620-022-01533-4. Epub 2023 Feb 16.

Genetic Susceptibility to Chronic Kidney Disease: Links, Risks and Management.

Int J Nephrol Renovasc Dis. 2023 Jan 5;16:1-15. doi: 10.2147/IJNRD.S363041. eCollection 2023.

LMX1B-associated nephropathy that showed myelin figures on electron microscopy.

CEN Case Rep. 2021 Nov;10(4):588-591. doi: 10.1007/s13730-021-00612-y. Epub 2021 Jun 2.

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Can J Kidney Health Dis. 2021 Jan 19;8:2054358120985627. doi: 10.1177/2054358120985627. eCollection 2021.

A case of female Fabry disease revealed by renal biopsy.

CEN Case Rep. 2020 Feb;9(1):24-29. doi: 10.1007/s13730-019-00420-5. Epub 2019 Sep 21.

TFEB-driven lysosomal biogenesis is pivotal for PGC1α-dependent renal stress resistance.

JCI Insight. 2019 Mar 14;5(8):126749. doi: 10.1172/jci.insight.126749.

Clinical parameters, LysoGb3, podocyturia, and kidney biopsy in children with Fabry disease: is a correlation possible?

Pediatr Nephrol. 2018 Nov;33(11):2095-2101. doi: 10.1007/s00467-018-4006-3. Epub 2018 Jul 9.