Histopathologic and Ultrastructural Studies of Angiokeratoma Corporis Diffusum in Kanzaki Disease-Reference-Cited by-同舟云学术

Histopathologic and Ultrastructural Studies of Angiokeratoma Corporis Diffusum in Kanzaki Disease

Published:1995-01 Issue:1 Volume:22 Page:10-18
ISSN:0385-2407
Container-title:The Journal of Dermatology
language:en
Short-container-title:The Journal of Dermatology

Author:

Yokota Michiko¹,Koji Masato¹,Yotsumoto Shinichi¹²

Affiliation:

1. Department of Dermatology; Nagoya City University Medical School; Nagoya

2. Department of Dermatology; Kagoshima University Faculty of Medicine; Kagoshima Japan

Publisher

Wiley

Subject

Dermatology,General Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1346-8138.1995.tb03333.x/fullpdf

Reference24 articles.

1. Angiokeratoma corporis diffusum with glycopeptiduria due to deficient lysosomal α-N-acetylgalactosaminidase activity;Kanzaki;Arch Dermatol,1993

2. Novel lysosomal glycoaminoacid storage disease with angiokeratoma corporis diffusum;Kanzaki;Lancet,1989

3. Lysosomal α-N-acetylgalactosaminidase deficiency, the enzymatic defect in angiokeratoma corporis diffusum with glycopeptiduria;Kanzaki;J Clin Invest,1991

4. Isolation and characterization of major urinary amino acid O-glycosides and a dipeptide O-glycoside from a new lysosomal storage disorder (Kanzaki disease);Hirabayashi;J Biol Chem,1990

5. 104170 Alpha-galactosidase B, 0002 Kanzaki disease;McKusick,1992

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