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GM₁ gangliosidosis: clinical and laboratory findings in eight familiesGIUGLIANI, R; COELHO DUTRA, J; SARAIVA PEREIRA, M. L et al.Human genetics. 1985, Vol 70, Num 4, pp 347-354, issn 0340-6717Article

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Failure of plasma membranes of astrocytes in primary culture to insert exogenous ganglioside GM1ASOU, H; BRUNNGRABER, E. G.Neuroscience letters. 1984, Vol 46, Num 1, pp 115-118, issn 0304-3940Article

GM₁ GANGLIOSIDOSIS: PHENOTYPIC VARIATION IN A SINGLE FAMILYFARRELL DF; OCHS U.1981; ANN. NEUROL.; ISSN 0364-5134; USA; DA. 1981; VOL. 9; NO 3; PP. 225-231; BIBL. 36 REF.Article

ATYPICAL EXPRESSION OF BETA -GALACTOSIDASE DEFICIENCY IN A CHILD WITH HURLER-LIKE FEATURES BUT WITHOUT NEUROLOGICAL ABNORMALITIES.ANDRIA G; DEL GIUDICE E; REUSER AJJ et al.1978; CLIN. GENET.; DNK; DA. 1978; VOL. 14; NO 1; PP. 16-23; BIBL. 2 P.Article

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Antibodies to gangliosides in Guillain-Barré syndrome : specificity and relationship to clinical featuresGREGSON, N. A; KOBLAR, S; HUGHES, R. A. C et al.Quarterly journal of medicine. 1993, Vol 86, Num 2, pp 111-117, issn 0033-5622Article

Canine G_M1-gangliosidosis. A clinical, morphologic, histochemical, and biochemical comparison of two different modelsALROY, J; ORGAD, U; DEGASPERI, R et al.The American journal of pathology. 1992, Vol 140, Num 3, pp 675-689, issn 0002-9440Article

Ovine GM-1 gangliosidosisPRIEUR, D. J; AHERN-RINDELL, A. J; MURNANE, R. D et al.The American journal of pathology. 1991, Vol 139, Num 6, pp 1511-1513, issn 0002-9440Article

Presence of glycoproteins containing the polylactosamine structure in brain and liver of G_M1 gangliosidosis patients: comparative study between clinical types I and II, using endo-β-galactosidase enzymeBERRA, B; DE GASPERI, R; RAPELLI, S et al.Neurochemical pathology. 1986, Vol 4, Num 2, pp 107-117, issn 0734-600XArticle

Severity of GM1 gangliosidosis and urinary oligosaccharide excretionTAKAHASHI, Y; ORII, T.Clinica chimica acta. 1989, Vol 179, Num 2, pp 153-162, issn 0009-8981Article

Tunicamycin inhibits ganglioside biosynthesis in rat liver Golgi apparatus by blocking sugar nucleotide transport across the membrane vesiclesYUSUF, H. K; POHLENTZ, G; SANDHOFF, K et al.Proceedings of the National Academy of Sciences of the United States of America. Biological sciences. 1983, Vol 80, Num 23, pp 7075-7079, issn 0273-1134Article

A severe infantile sialidosis (β-galactosidase-α-neuraminidase deficiency) mimicking GM₁-gangliosidosis type 1OKADA, S; SUGINO, H; KATO, T et al.European journal of pediatrics. 1983, Vol 140, Num 4, pp 295-298, issn 0340-6199Article

Improved GM1-enzyme-linked immunosorbent assay for detection of Escherichia coli heat-labile enterotoxinRISTAINO, P. A; LEVINE, M. M; YOUNG, C. R et al.Journal of clinical microbiology (Print). 1983, Vol 18, Num 4, pp 808-815, issn 0095-1137Article

Morquio B syndrome: a primary defect in β-galactosidaseVAN DER HORST, G. T. J; KLEIJER, W. J; HOOGEVEEN, A. T et al.American journal of medical genetics. 1983, Vol 16, Num 2, pp 261-275, issn 0148-7299Article