1. Fabry's disease (a-galacto- Since then two cases in which there were cardiac manifestations have been enzymologically studied." In these cases, however, hemizygotic Fabry's disease was diagnosed from the dermal findings, proteinuria, and family history. The mechanism of the occurrence of Fabry's disease as a sex linked recessive hereditary condition in females had been sidase A deficiency);Desnic, R.J.; Sweeley, C.C.,1983
2. A differential staining of semithin sections of epon-embedded tissue and a short review on the optical microscopy of plastic-embedded tissue;Kurotaki, M.;Acta anat Nippon,1972
3. Fabry cardiomyopathy in the female confirmed by endomyocardial biopsy;Broadbent, J.C.; Edwards, W.D.; Gordon, H.; Hartzler, G.O.; Krawisz, J.E.
4. Fabry's in a heterozygous women;Rodorignez, F.H.; Hoffmann, E.O.; Ordinario, A.T.; Baliga, M.;Arch Pathol Lab Med,1985
5. Enzymic diagnosis of sphingolipidosis;Suzuki, K.,1978