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An Enzymological Approach to the Lipidoses
Enzyme, 2017 The abnormal enzymology of Gaucher’s disease, metachromatic leukodystrophy, Fabry’s disease and Tay-Sachs disease is considered in light of recent experiments with highly purified enzymes from human sources. Structural, catalytic, and immunological properties of the enzymes involved are compared with their normal counterparts. The use of purified human
J F, Tallman, P G, Pentchev, R O, Brady
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, 1967 The lipidoses, as covered by this book,are inborn errors of metabolism, although some of them may be rather strongly subjected to modification by exogenous influences. Their exact classification depends largely on clinical, morphological, and particularly biochemical criteria.
W. Fuhrmann
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Lipidoses, Histiocytoses, and Hyperlipoproteinemias
, 2005 Donald Resnick, Mark J. Kransdorf
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