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Adult (chronic) GM2 gangliosidosis. Atypical spinocerebellar degeneration in a Jewish sibship.
Arch Neurol. 1976 Feb;33(2):120-30
PMID: 175770
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A simple and novel method for tritium labeling of gangliosides and other sphingolipids.
Biochim Biophys Acta. 1978 Apr 28;529(1):106-14
PMID: 638174
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Probable metachromatic leukodystrophy/pseudodeficiency compound heterozygote at the arylsulfatase A locus with neurological and psychiatric symptomatology.
Am J Med Genet. 1988 Sep;31(1):169-75
PMID: 2906225
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Preparation of GM1 ganglioside molecular species having homogeneous fatty acid and long chain base moieties.
J Lipid Res. 1985 Feb;26(2):248-57
PMID: 3989384
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A simple chromogenic assay for arylsulfatase A.
Clin Chim Acta. 1987 Apr 30;164(2):171-80
PMID: 2885112
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Lysogangliosides: synthesis and use in preparing labeled gangliosides.
Methods Enzymol. 1987;138:319-41
PMID: 3600331
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Assay for cerebroside sulfate (sulfatide) sulfatase in cultured skin fibroblasts with the natural activator protein.
Clin Chim Acta. 1987 Sep 15;168(1):55-68
PMID: 2889546
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Incorporation and metabolism of ganglioside GM2 in skin fibroblasts from normal and GM2 gangliosidosis subjects.
Eur J Biochem. 1985 Jun 3;149(2):247-55
PMID: 3922757
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Hexosaminidase A deficiency in adults.
Am J Med Genet. 1986 May;24(1):179-96
PMID: 2939718
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Partial enzyme deficiencies: residual activities and the development of neurological disorders.
Dev Neurosci. 1983-1984;6(1):58-71
PMID: 6421563
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Impaired cerebroside sulfate hydrolysis in fibroblasts of sibs with "pseudo" arylsulfatase A deficiency without metachromatic leukodystrophy.
Pediatr Res. 1983 Sep;17(9):701-4
PMID: 6137805
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GM2-ganglioside metabolism in hexosaminidase A deficiency states: determination in situ using labeled GM2 added to fibroblast cultures.
Am J Hum Genet. 1985 Nov;37(6):1071-82
PMID: 2934978
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Morquio disease, type B: activation of GM1-beta-galactosidase by GM1-activator protein.
Biochem Biophys Res Commun. 1982 Nov 30;109(2):568-75
PMID: 6817758
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Specific radioactive labeling of terminal n-acetylgalactosamine of glycosphingolipids by the galactose oxidase-sodium borohydride method.
J Lipid Res. 1972 Sep;13(5):687-90
PMID: 5075513
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A correlation of intracellular cerebroside sulfatase activity in fibroblasts with latency in metachromatic leukodystrophy.
Biochem Biophys Res Commun. 1971 Aug 6;44(3):660-6
PMID: 5123204
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Glycosphingolipids in fetal Tay-Sachs disease brain and lung cultures.
J Neurochem. 1977 Sep;29(3):551-9
PMID: 894310
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Molecular basis of different forms of metachromatic leukodystrophy.
N Engl J Med. 1991 Jan 3;324(1):18-22
PMID: 1670590
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Prenatal diagnosis of metachromatic leukodystrophy in a family with pseudo arylsulfatase A deficiency by the cerebroside sulfate loading test.
Pediatr Res. 1980 Mar;14(3):224-7
PMID: 6104322
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Properties of N-acetyl-beta-D-hexosaminidase from isolated normal and I-cell lysosomes.
J Biol Chem. 1981 Sep 10;256(17):9352-62
PMID: 7263719
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Use of esters of N-hydroxysuccinimide in the synthesis of N-acylamino acids.
J Lipid Res. 1967 Mar;8(2):142-5
PMID: 14564721
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Activator proteins for lysosomal glycolipid hydrolysis.
Methods Enzymol. 1987;138:792-815
PMID: 2885714
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Genotype-phenotype relationship in various degrees of arylsulfatase A deficiency.
Hum Genet. 1991 Mar;86(5):463-70
PMID: 1673113
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Prenatal diagnosis of GM2 gangliosidosis with high residual hexosaminidase A activity (variant B1; pseudo AB variant).
Pediatr Res. 1985 Nov;19(11):1220-4
PMID: 2933632
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Pseudodeficiency of arylsulfatase A: a common genetic polymorphism with possible disease implications.
Hum Genet. 1989 Apr;82(1):45-8
PMID: 2565866
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A rapid method of total lipid extraction and purification.
Can J Biochem Physiol. 1959 Aug;37(8):911-7
PMID: 13671378
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Low arylsulphatase A activity and choreoathetotic syndrome in three siblings: differentiation of pseudodeficiency from metachromatic leukodystrophy.
Eur J Pediatr. 1991 Feb;150(4):287-90
PMID: 1674246
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Brain galactolipid content in a patient with pseudoarylsulfatase A deficiency and coincidental diffuse disseminated sclerosis, and in patients with metachromatic, adreno-, and other leukodystrophies.
J Neurochem. 1987 Jan;48(1):62-6
PMID: 2878976
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Lysosomal enzyme precursors in human fibroblasts. Activation of cathepsin D precursor in vitro and activity of beta-hexosaminidase A precursor towards ganglioside GM2.
Eur J Biochem. 1982 Jul;125(2):317-21
PMID: 6214395
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Activator proteins for lysosomal glycolipid hydrolysis.
Methods Biochem Anal. 1987;32:1-23
PMID: 3553853
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A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding.
Anal Biochem. 1976 May 7;72:248-54
PMID: 942051
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Enzyme-linked immunosorbent assay for the ganglioside GM2-activator protein. Screening of normal human tissues and body fluids, of tissues of GM2 gangliosidosis, and for its subcellular localization.
Hoppe Seylers Z Physiol Chem. 1984 Mar;365(3):347-56
PMID: 6724528
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Ganglioside GM2 N-acetyl-beta-D-galactosaminidase activity in cultured fibroblasts of late-infantile and adult GM2 gangliosidosis patients and of healthy probands with low hexosaminidase level.
Am J Hum Genet. 1983 Sep;35(5):900-13
PMID: 6614006
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Liberation of N-acetylglucosamine-6-sulfate by human beta-N-acetylhexosaminidase A.
J Biol Chem. 1981 Dec 25;256(24):12926-32
PMID: 6458607
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Variation in lysosomal enzyme activity during growth in culture of human fibroblasts and amniotic fluid cells.
Exp Cell Res. 1976 Feb;97(2):304-12
PMID: 1248521
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Purification and characterization of an activator protein for the degradation of glycolipids GM2 and GA2 by hexosaminidase A.
Hoppe Seylers Z Physiol Chem. 1979 Dec;360(12):1837-49
PMID: 527942