Results 151 to 160 of about 3,736 (191)
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Metachromatische Leukodystrophie (Sulfatid-Lipidose)
1976Die metachromatische Leukodystrophie ist eine angeborene, familiar auftretende progressive Entmarkungskrankheit des Gehirns, deren Ursache ein Enzymdefekt im katabolen Stoffwechsel physiologischer Myelinlipide darstellt. Neben dieser genetisch-meta-bolischen Leukodystrophie mit bereits bekanntem Stoffwechseldefekt gibt es noch weitere angeborene ...
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Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine, 1958
S. Aronson, A. Saifer, G. Perle, B. Volk
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S. Aronson, A. Saifer, G. Perle, B. Volk
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Role of apolipoprotein E variants in lipoprotein glomerulopathy and other renal lipidoses
Clinical and Experimental Nephrology, 2001T. Saito +3 more
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Ceroid Lipofuscinosis; Miscellaneous Lipidoses
1975This disease, like Tay-Sachs disease, was initially recognized by its fundoscopic manifestations (Batten, 1903). In the first report on its cerebral lesions Spielmeyer (1905) noticed the pigmentary nature of some of the material deposited in the neurons and thought that the disease differed from Tay-Sachs disease in its later onset and longer duration.
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Biochemical, psychometric, and neuropsychological studies in heterozygotes for various lipidoses
Human Genetics, 1980Helene Christomanou +4 more
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FINE STRUCTURAL LOCALIZATION OF TWO HYDROLYTIC ENZYMES IN THE CEREBELLUM OF CHILDREN WITH LIPIDOSES
, 1966B. J. Wallace +3 more
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Drug-induced lipidoses of the cornea and conjunctiva
International ophtalmology, 1981D. D’Amico, K. Kenyon
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