A female heterozygous patient with fabry's disease with renal accumulation of trihexosylceramide detected with a monoclonal antibody-Reference-Cited by-同舟云学术

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A female heterozygous patient with fabry's disease with renal accumulation of trihexosylceramide detected with a monoclonal antibody

Published:1995-12 Issue:6 Volume:26 Page:952-955
ISSN:0272-6386
Container-title:American Journal of Kidney Diseases
language:en
Short-container-title:American Journal of Kidney Diseases

Author:

Fukushima Masaki,Tsuchiyama Yoshinori,Nakato Tatsuaki,Yokoi Toru,Ikeda Hiroshi,Yoshida Soichiro,Kusumoto Toru,Itoh Kohji,Sakuraba Hitoshi

Publisher

Elsevier BV

Subject

Nephrology

Reference17 articles.

1. Fabry's disease: Alpha galactosidase A deficiency;Desnick,1983

2. Fabry's disease: A correlative clinical, morphologic, and biochemical study;Bagdade;Lab Invest,1986

3. Clinicopathologic, enzymatic, and genetic features in a case of Fabry's disease;Burkholder;Arch Pathol Lab Med,1980

4. Angiokeratoma corporis diffusum universale (Fabry's disease) in female subjects;Burda;Am J Med,1967

5. Early renal changes in hemizygous and heterozygous patients with Fabry's disease;Gubler;Kidney Int,1978

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1. X Chromosome Inactivation in Carriers of Fabry Disease: Review and Meta-Analysis;International Journal of Molecular Sciences;2021-07-17

2. A heterozygous female with Fabry disease due to a novel α-galactosidase A mutation exhibits a unique synaptopodin distribution in vacuolated podocytes;Clinical Nephrology;2015-05-01

3. Identification and Expression Analysis of Zebrafish Glypicans during Embryonic Development;PLoS ONE;2013-11-14

4. Genetic Abnormalities in Glomerular Function;Seldin and Giebisch's The Kidney;2013

5. Immunohistochemical diagnosis of Fabry nephropathy and localisation of globotriaosylceramide deposits in paraffin-embedded kidney tissue sections;Virchows Archiv;2011-12-29

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