Results 131 to 140 of about 3,736 (191)
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Musculoskeletal Imaging Volume 2, 2019
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. Gaucher
K. Hoover
semanticscholar +2 more sources
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. Gaucher
K. Hoover
semanticscholar +2 more sources
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, G. Schmidt
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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, G. Schmidt
semanticscholar +3 more sources
Lipidomics in diagnosis of lipidoses.
Sub-cellular biochemistry, 2008A 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.
C. Wolf, P. Quinn
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Lipidoses, Histiocytoses, and Hyperlipoproteinemias
, 2005D. Resnick, M. Kransdorf
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Suggested use of rectal biopsy in the diagnosis of neural lipidoses.
Pediatrics, 1960The histochemical properties of nerve cells of the myenteric plexus in five forms of neural lipidosis (Tay-Sachs infantile amaurotic idiocy, Hurler's disease, Niemann-Pick disease, Jansky-Bielschowsky early juvenile amaurotic idiocy, and Spielmeyer-Vogt ...
Hisayo Nakai, Benjamin H. Landing
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Serum Phosphatase in Lipidoses
Archives of Pediatrics & Adolescent Medicine, 1959Long 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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