Results 151 to 160 of about 3,736 (191)
Some of the next articles are maybe not open access.

Metachromatische Leukodystrophie (Sulfatid-Lipidose)

1976
Die 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 ...
openaire   +1 more source

Cerebrospinal Fluid Enzymes in Central Nervous System Lipidoses∗ (with particular reference to Amaurotic Family Idiocy)

Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine, 1958
S. Aronson, A. Saifer, G. Perle, B. Volk
semanticscholar   +1 more source

Role of apolipoprotein E variants in lipoprotein glomerulopathy and other renal lipidoses

Clinical and Experimental Nephrology, 2001
T. Saito   +3 more
semanticscholar   +1 more source

Cerebral Lipidoses

Annual Review of Medicine, 1970
openaire   +2 more sources

Ceroid Lipofuscinosis; Miscellaneous Lipidoses

1975
This 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.
openaire   +1 more source

Biochemical, psychometric, and neuropsychological studies in heterozygotes for various lipidoses

Human Genetics, 1980
Helene Christomanou   +4 more
semanticscholar   +1 more source

Drug-induced lipidoses of the cornea and conjunctiva

International ophtalmology, 1981
D. D’Amico, K. Kenyon
semanticscholar   +1 more source

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