Results 101 to 110 of about 3,138 (148)
Physiological Reviews, 1946 Gerhard Schmidt. Volume 26, page 275: Lipins and Lipidoses, by S. J. Thannhauser and The Sentence beginning on line 22 (page 301) should read as follows: They are all a part of the syndrome under discussion. The organs which may be involved singly or in various combinations in the syndrome (essential xanthomatosis of the normocholesteremic type ...
S J Thannhauser
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Journal of Medicinal Chemistry, 1968 Contributors to this book are American (Burton, Cornwell, Kinsell, and Kritchevsky), Canadian (Rossiter), German (Fuhrmann, Kahlke, Schettler, Schlierf, Stoffel, and Wagener) and Israelian (Shapiro). The volume represents a solid text combining American clarity with German thoroughness. Two main parts deal with lipids and with lipidoses.
Erik Ask-Upmark
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Lipidomics in diagnosis of lipidoses
Sub-Cellular Biochemistry, 2008 A review is presented of the major clinical features of a number of glycolipidoses including Fabry, Gaucher, Tay-Sachs, metachromatic leukodystrophy as well as CeroidLipofucinosis and Sjogren-Larsson syndrome. The possibilities offered by lipidomics for diagnosis and follow-up after enzyme replacement therapy are presented from a practical perspective.
Peter J Quinn, P J Quinn
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Serum Phosphatase in Lipidoses
Archives of Pediatrics & Adolescent Medicine, 1959 Long before the scientific age in which we live, mankind has striven to evade or to neutralize the mysterious dangers, lurking on all sides, by giving them names through which they may be recognized and identified. This propensity has been rationalized in modern times and one has consciously and proudly pointed to the contributions made by systematic ...
H, SOBOTKA, G, GOLDSTEIN, S, WEISSBARTH
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, 2019 Abstract Chapter 83 discusses lipidoses. The lipidoses are genetic diseases caused by enzyme deficiencies, which result in the cellular accumulation of lipids. These abnormal cells infiltrate tissues, including bone marrow, resulting in their dysfunction.
Kevin B. Hoover
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Journal of the American Oil Chemists' Society, 1967 AbstractFormal genetic analyses of family data in cases of errors of lipid metabolism are able to distinâguish monogenic vs. multigenic and nongenetic disorders. These data, together with population data, provide criteria for the homogeneity of cases which can be useful in the interpretation of biochemical findings. The peculiarly elevated incidence of
Alfred G. Knudson
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