Angiokeratoma corporis diffusum in a patient with normal enzyme activities
- 29 February 1984
- journal article
- case report
- Published by Elsevier in Journal of the American Academy of Dermatology
- Vol. 10 (2) , 384-387
- https://doi.org/10.1016/s0190-9622(84)80012-2
Abstract
No abstract availableKeywords
This publication has 8 references indexed in Scilit:
- Angiokeratoma corporis diffusum with features of a mucopolysaccharidosis.Journal of Medical Genetics, 1980
- Adult type neuronal storage disease with neuraminidase deficiencyAnnals of Neurology, 1979
- Macular cherry-red spots and myoclonus with dementia: Coexistent neuraminidase and β-galactosidase deficienciesBiochemical and Biophysical Research Communications, 1978
- ANGIOKERATOMA CORPORIS DIFFUSUM AND LYSOSOMAL ENZYME DEFICIENCYThe Lancet, 1974
- GENETIC HETEROGENEITY IN FUCOSIDOSISThe Lancet, 1973
- GENETIC HETEROGENEITY IN FUCOSIDOSISThe Lancet, 1973
- Angiokeratoma Corporis Diffusum With a-L-Fucosidese DeficiencyArchives of Dermatology, 1973
- Deficiency of α-L-FucosidaseScience, 1972