110 related articles for article (PubMed ID: 98112)
1. Characterization of a penta-and an octasaccharide from urine of a patient with juvenile GM1-gangliosidosis.
Lunblad A; Sjöblad S; Svensson S
Arch Biochem Biophys; 1978 May; 188(1):130-6. PubMed ID: 98112
[No Abstract] [Full Text] [Related]
2. Urinary oligosaccharides of GM1-gangliosidosis. Structures of oligosaccharides excreted in the urine of type 1 but not in the urine of type 2 patients.
Ohkura T; Yamashita K; Kobata A
J Biol Chem; 1981 Aug; 256(16):8485-90. PubMed ID: 6790542
[TBL] [Abstract][Full Text] [Related]
3. GM1 gangliosidosis: phenotypic variation in a single family.
Farrell DF; Ochs U
Ann Neurol; 1981 Mar; 9(3):225-31. PubMed ID: 6784662
[TBL] [Abstract][Full Text] [Related]
4. Urinary oligosaccharides of GM1-gangliosidosis. Different excretion patterns of oligosaccharides in the urine of type 1 and type 2 subgroups.
Yamashita K; Ohkura T; Okada S; Yabuuchi H; Kobata A
J Biol Chem; 1981 May; 256(10):4789-98. PubMed ID: 6785275
[TBL] [Abstract][Full Text] [Related]
5. GM1-gangliosidosis: accumulation of ganglioside GM1 in cultured skin fibroblasts and correlation with clinical types.
Suzuki Y; Nakamura N; Fukuoka K
Hum Genet; 1978 Aug; 43(2):127-31. PubMed ID: 99363
[TBL] [Abstract][Full Text] [Related]
6. Severity of GM1 gangliosidosis and urinary oligosaccharide excretion.
Takahashi Y; Orii T
Clin Chim Acta; 1989 Feb; 179(2):153-62. PubMed ID: 2493350
[TBL] [Abstract][Full Text] [Related]
7. Isolation and characterization of major urinary oligosaccharides excreted by a patient with type 3 GM1 gangliosidosis.
Tsuji S; Ariga T; Ando S; Tanaka Y; Kon K; Yahagi T; Ohta K; Miyatake T
J Biochem; 1991 May; 109(5):722-7. PubMed ID: 1917896
[TBL] [Abstract][Full Text] [Related]
8. Characterization of a novel type of chain-terminator Gal beta 1-6Gal beta 1-4)GlcNAc in an oligosaccharide related to N-glycosylated protein glycans isolated from GM1 the urine of patients with gangliosidosis.
Michalski JC; Lemoine J; Wieruszeski JM; Fournet B; Montreuil J; Strecker G
Eur J Biochem; 1991 Jun; 198(2):521-6. PubMed ID: 1904026
[TBL] [Abstract][Full Text] [Related]
9. GM1-Gangliosidosis: a molecular abnormality of acid beta-galactosidase in fibroblasts.
Furuya T; Suzuki Y
J Inherit Metab Dis; 1984; 7(3):145-6. PubMed ID: 6438402
[No Abstract] [Full Text] [Related]
10. Infantile GM1-gangliosidosis with marked manifestation of lungs.
Matsumoto T; Matsumori H; Taki T; Takagi T; Fukuda Y
Acta Pathol Jpn; 1979 Mar; 29(2):269-76. PubMed ID: 121907
[TBL] [Abstract][Full Text] [Related]
11. Application of a GM1 ganglioside beta-galactosidase microassay method to diagnosis of GM1 gangliosidosis.
Mutoh T; Kiuchi K; Sobue I; Naoi M
Clin Chim Acta; 1984 Jul; 140(3):223-30. PubMed ID: 6432371
[TBL] [Abstract][Full Text] [Related]
12. [Gangliosidosis GM1--type 1. Anatomo-clinical study of a case].
Barbosa-Coutinho LM; Assis-Brasil BM; Drachler Mde L; Rotta NT; Giuliani R
Arq Neuropsiquiatr; 1987 Mar; 45(1):60-6. PubMed ID: 3111451
[TBL] [Abstract][Full Text] [Related]
13. Characterization of neutral and acidic glycosphingolipids in brains of two patients with GM1 gangliosidosis type 1 and type 2.
Ishikawa Y; Makita A; Minami R
J Neurochem; 1985 Apr; 44(4):1100-6. PubMed ID: 3919156
[TBL] [Abstract][Full Text] [Related]
14. Neurophysiological investigations in GM1 and GM2 gangliosidoses.
Pampiglione G; Harden A
Neuropediatrics; 1984 Sep; 15 Suppl():74-84. PubMed ID: 6100798
[TBL] [Abstract][Full Text] [Related]
15. An explanation for variations in the clinical and biochemical symptoms of lysosomal-enzyme deficiency diseases such as GM1 gangliosidosis [proceedings].
Cheetham PS
Biochem Soc Trans; 1979 Oct; 7(5):980-2. PubMed ID: 116891
[No Abstract] [Full Text] [Related]
16. Neuronal-visceral GM1 gangliosidosis in a dog with beta-galactosidase deficiency.
Read DH; Harrington DD; Keenana TW; Hinsman EJ
Science; 1976 Oct; 194(4263):442-5. PubMed ID: 824730
[TBL] [Abstract][Full Text] [Related]
17. The simple detection of neuraminic acid-containing urinary oligosaccharides in patients with glycoprotein storage diseases.
Sewell AC
J Inherit Metab Dis; 1983; 6(4):153-7. PubMed ID: 6422155
[TBL] [Abstract][Full Text] [Related]
18. Gangliosidoses and the fetal retina.
Cogan DG; Kuwabara T; Kolodny E; Driscoll S
Ophthalmology; 1984 May; 91(5):508-12. PubMed ID: 6330639
[TBL] [Abstract][Full Text] [Related]
19. Diagnosis of GM1 gangliosidosis based on detection of urinary oligosaccharides with high performance liquid chromatography.
Warner TG; Robertson AD; O'Brien JS
Clin Chim Acta; 1983 Feb; 127(3):313-26. PubMed ID: 6404572
[TBL] [Abstract][Full Text] [Related]
20. Cerebral and visceral organ gangliosides and related glycolipids in gm1-gangliosidosis type 1, type 2 and chronic type.
Taketomi T; Hara A; Kasama T
Adv Exp Med Biol; 1984; 174():419-29. PubMed ID: 6430048
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]