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- W2000254245 abstract "• Fifteen patients with lysosomal storage diseases were studied. Diagnoses of their illnesses included infantile Gaucher disease; Krabbe disease; Niemann-Pick disease, type A; glycogen storage disease, type 2; Fabry disease, Jansky-Bielschowsky and Spielmeyer-Vogt types of amaurotic idiocy, GM<sub>,</sub>gangliosidosis, type 1; Hurler disease; and Sanfilippo disease, types A and B. We carried out ultrastructural examinations of skin biopsy specimens that were taken to establish a cultured fibroblast line on each patient. We found diagnostic storage inclusions in all patients except those with infantile Gaucher disease, Krabbe disease, and Spielmeyer-Vogt disease. This technique can be carried out on a specimen obtained by a primary physician on an out-patient basis, thus avoiding major surgery." @default.
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- W2000254245 date "1975-09-01" @default.
- W2000254245 modified "2023-10-16" @default.
- W2000254245 title "Lysosomal Storage Disorders" @default.
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- W2000254245 doi "https://doi.org/10.1001/archneur.1975.00490510048002" @default.
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