Results 141 to 150 of about 3,245 (185)
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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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Archives of Internal Medicine, 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.
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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.
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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
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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
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Lipidomics in diagnosis of lipidoses
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 J, Quinn
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Histochemical diagnosis of lipidoses.
Acta Universitatis Carolinae. Medica. Monographia, 1978Contemporary possibilities for the histochemical diagnosis of lipidoses are demonstrated in examples of phospholipidoses, Gaucher's disease, Fabry's disease, sulphatidosis, gangliosidosis and neuronal ceroid-lipofuscinoses.
M, Elleder, Z, Lojda
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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.
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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.
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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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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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