Results 141 to 150 of about 3,736 (191)
Some of the next articles are maybe not open access.
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.
+4 more sources
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.
+4 more sources
Pediatric Clinics of North America, 1976
The disorders presented consist of those clinical entities in which a reasonably well defined lipid storage material accumulated within nervous tissue. Many other progressive, degenerative disorders are suspected of being storage disorders, but their chemical pathology remains unclear.
openaire +2 more sources
The disorders presented consist of those clinical entities in which a reasonably well defined lipid storage material accumulated within nervous tissue. Many other progressive, degenerative disorders are suspected of being storage disorders, but their chemical pathology remains unclear.
openaire +2 more sources
Journal of the American Oil Chemists' Society, 1967
AbstractFormal genetic analyses of family data in cases of errors of lipid metabolism are able to distin‐guish 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
openaire +2 more sources
AbstractFormal genetic analyses of family data in cases of errors of lipid metabolism are able to distin‐guish 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
openaire +2 more sources
Lipidoses: The Sphingolipidoses, Lysosomal Acid Lipase Deficiency, and Niemann-Pick Type C
Physician's Guide to the Diagnosis, Treatment, and Follow-Up of Inherited Metabolic Diseases, 2022C. Hollak
semanticscholar +1 more source
Lipidoses detected in Poland through 1993
Pediatric Neurology, 1994It is estimated that 70-100 children suffering from a lysosomal storage disease are born in Poland every year. From 1975 to 1993, the activity of various lysosomal enzymes was determined in the leukocytes, cultured skin fibroblasts, or hair roots from 5,594 patients, mainly children, in whom the diagnosis of a lipidosis was suspected.
B, Czartoryska +3 more
openaire +2 more sources
Serum protein electrophoresis pattern alterations on lipidoses patients
, 2020L. Frutos +9 more
semanticscholar +1 more source
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
openaire +1 more source
Neuronal and glial accumulation of α- and β-synucleins in human lipidoses
Acta Neuropathologica, 2007Kyoko Suzuki +12 more
semanticscholar +1 more source
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.
openaire +1 more source
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.
openaire +1 more source