[Glycosphingolipids as tumor markers].

Cardiocyte storage and hypertrophy as a sole manifestation of Fabry's disease. Report on a case simulating hypertrophic non-obstructive cardiomyopathy. Virchows Arch A Pathol Anat Histopathol (1990) 1.62

Niemann-Pick disease type C. Study on the nature of the cerebral storage process. Acta Neuropathol (1985) 1.06

A novel mutation in the coding region of the prosaposin gene leads to a complete deficiency of prosaposin and saposins, and is associated with a complex sphingolipidosis dominated by lactosylceramide accumulation. Hum Mol Genet (2001) 1.02

Lex glycosphingolipids-mediated cell aggregation. Glycobiology (1998) 0.95

Prosaposin deficiency: further characterization of the sphingolipid activator protein-deficient sibs. Multiple glycolipid elevations (including lactosylceramidosis), partial enzyme deficiencies and ultrastructure of the skin in this generalized sphingolipid storage disease. Hum Genet (1993) 0.90

Niemann-Pick disease. Analysis of liver tissue in sphingomyelinase-deficient patients. Virchows Arch A Pathol Anat Histol (1980) 0.83

Histochemical detection of GM1 ganglioside using cholera toxin-B subunit. Evaluation of critical factors optimal for in situ detection with special emphasis to acetone pre-extraction. Eur J Histochem (2010) 0.82

Niemann-Pick disease type C with enhanced glycolipid storage. Report on further case of so-called lactosylceramidosis. Virchows Arch A Pathol Anat Histopathol (1984) 0.82

Lipidosis with a predominant storage of phosphoglycerides (phospholipidosis type II--Baar, Wiedemann). Virchows Arch A Pathol Anat Histol (1975) 0.79

Peripheral nervous system affection in experimental lipidosis induced by 4,4'-diethylaminoethoxyhexesterol. Virchows Arch B Cell Pathol (1977) 0.79

Degradation of blood group A glycolipid A-6-2 by normal and mutant human skin fibroblasts. J Lipid Res (1998) 0.78

Mutagenicity of glycerol chlorohydrines and of their esters with higher fatty acids present in protein hydrolysates. Mutat Res (1982) 0.77

Niemann-Pick disease (Crocker's type C): A histological study of the distribution and qualitative differences fo the storage process. Acta Neuropathol (1975) 0.77

Lysosomal non-lipid component of Gaucher's cells. Virchows Arch B Cell Pathol (1977) 0.77

Liver findings in Niemann-Pick disease type C. Histochem J (1984) 0.77

Carcinoembryonic antigen-related cell adhesion molecule 1 is the 85-kilodalton pronase-resistant biliary glycoprotein in the cholesterol crystallization promoting low density protein-lipid complex. Hepatology (2001) 0.77

The effect of heme oxygenase on ganglioside redistribution within hepatocytes in experimental estrogen-induced cholestasis. Physiol Res (2014) 0.76

Immunoaffinity isolation of CEACAM1 on hydrazide-derivatized cellulose with immobilized monoclonal anti-CEA antibody. Biomed Chromatogr (2001) 0.75

Biochemistry of sphingolipids. XXIV. Long-chain base vriations in gangliosides of developing human brain. Brain Res (1968) 0.75

[Vesicular and pronuclear glycoproteins in the pathogenesis of cholesterol lithiasis]. Cas Lek Cesk (1998) 0.75

Remarks on the cis-aconitic anhydride method. Histochemie (1968) 0.75

Rapid ion-exchange separation of human brain gangliosides. J Chromatogr (1986) 0.75

[Present trends and methodological basis for the cognitive process in pathology]. Cas Lek Cesk (1983) 0.75

[Pronuclear and antinuclear factors in the pathogenesis of cholesterol cholelithiasis]. Cas Lek Cesk (2000) 0.75

Studies in lipid histochemistry. V. Remarks on histochromatography. Histochemie (1971) 0.75

An unusual case of phospholipidosis. Virchows Arch A Pathol Anat Histol (1978) 0.75

Possible relationship between tumour malignancy and the pattern of glycolipids as an important glycocalyx component. Folia Biol (Praha) (1979) 0.75

Biochemistry of sphingolipids. 23. Paper chromatography of human brain gangliosides. J Chromatogr (1968) 0.75

Multiple sulphatase deficiency in homozygotic twins. J Inherit Metab Dis (1984) 0.75

Fine specificity of anti-Le(X) monoclonal antibody TEC-01. Folia Biol (Praha) (1998) 0.75

Adrenal changes in Niemann-Pick disease: differences between sphingomyelinase deficiency and type C. Acta Histochem (1985) 0.75

Factors influencing the activity of cellular alkaline phosphatase during growth and sporulation of Bacillus cereus. Folia Microbiol (Praha) (1987) 0.75

[Infantile form of S.C. neuronal ceroid - lipofuscinosis (author's transl)]. Sb Lek (1976) 0.75

A densitometric method for the determination of gangliosides after their separation by thin-layer chromatography and detection with resorcinol reagent. J Chromatogr (1973) 0.75