Author:
Berra Bruno,De Gasperi Rita,Rapelli Silvana,Okada Shintaro,Li Su-Chen,Li Yu-Teh
Publisher
Springer Science and Business Media LLC
Subject
Neurology (clinical),Molecular Biology
Reference15 articles.
1. Berra B., Di Palma S., and Brunngraber E. G. (1974) Altered levels of tissue gangliosides and glycoproteins in the infantile form of GM1 gangliosidosis.Clin. Chim. Acta
57, 301–306.
2. Bhatti, T., Chambers, R. E., and Clamp, J. R. (1970) The gas chromatographic properties of biologically important N-acetylglucosamine derivatives, monosaccharides, disaccharides, trisaccharides, tetrasaccharides, and pentasaccharides.Biochim. Biophys. Acta
222, 339–347.
3. Di Palma S., Berra B., Li Y. T., and Li S. C., (1978) Storage of glycoproteins containing terminal galactose in brain of two patients with type I GM1 gangliosidosis, inPerspectives in Inherited Metabolic Diseases, vol. 1, pp. 155–164. Edi-Ermes, Milano.
4. Dubois M., Gilles K. A., Hamilton, J. K., Rebers, P. A., and Smith F. (1956) Colorimetric determination of sugars and related substances.Anal. Chem.
28, 350–356.
5. Harris G. and MacWilliam J. C. (1954) Dipping technique for revealing neutral sugars on paper chromatography.Chem. Ind. (London) pp. 249.