These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
126 related articles for article (PubMed ID: 6412544)
1. Prenatal diagnosis of GM1 gangliosidosis by detection of galactosyl-oligosaccharides in amniotic fluid with high-performance liquid chromatography. Warner TG; Robertson AD; Mock AK; Johnson WG; O'Brien JS Am J Hum Genet; 1983 Sep; 35(5):1034-41. PubMed ID: 6412544 [TBL] [Abstract][Full Text] [Related]
2. Prenatal diagnosis of infantile GM 2 gangliosidosis type II (Sandhoff disease) by detection of N-acetylglucosaminyl-oligosaccharides in amniotic fluid with high-performance liquid chromatography. Warner TG; Turner MW; Toone JR; Applegarth D Prenat Diagn; 1986; 6(6):393-400. PubMed ID: 3809110 [TBL] [Abstract][Full Text] [Related]
3. 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]
4. Congenital ascites as a presenting sign of lysosomal storage disease. Gillan JE; Lowden JA; Gaskin K; Cutz E J Pediatr; 1984 Feb; 104(2):225-31. PubMed ID: 6420531 [TBL] [Abstract][Full Text] [Related]
5. 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]
7. [The use of loading tests with labeled GM1-ganglioside for differential diagnosis of GM1-gangliosidosis]. Akhunov VS; Krasnopol'skaia KD; Mirenburg TV Vopr Med Khim; 1989; 35(5):119-22. PubMed ID: 2515652 [TBL] [Abstract][Full Text] [Related]
8. Diagnosis of subtypes of GM1 gangliosidosis in vitro and in vivo--using urinary oligosaccharides as substrates. Takahashi Y; Orii T Clin Chim Acta; 1989 Feb; 179(3):219-27. PubMed ID: 2496942 [TBL] [Abstract][Full Text] [Related]
9. 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]
10. Structure analysis of the major oligosaccharides accumulating in canine GM1 gangliosidosis liver. Warner TG; O'Brien JS J Biol Chem; 1982 Jan; 257(1):224-32. PubMed ID: 6796586 [TBL] [Abstract][Full Text] [Related]
11. Use of microtechniques for the detection of lysosomal enzyme disorders: Tay-Sachs disease, Gm1-gangliosidosis and Fabry disease. Bladon MT; Milunsky A Clin Genet; 1978 Dec; 14(6):359-66. PubMed ID: 215359 [TBL] [Abstract][Full Text] [Related]
12. N-Acetyl-beta-hexosaminidase isoenzymes of amniotic fluid and maternal serum. Their relevance to prenatal diagnosis of the GM2 gangliosidoses. Potier M; Boire G; Dallaire L; Melancon SB Clin Chim Acta; 1977 May; 76(3):309-15. PubMed ID: 404100 [TBL] [Abstract][Full Text] [Related]
13. Development of a new tandem mass spectrometry method for urine and amniotic fluid screening of oligosaccharidoses. Piraud M; Pettazzoni M; Menegaut L; Caillaud C; Nadjar Y; Vianey-Saban C; Froissart R Rapid Commun Mass Spectrom; 2017 Jun; 31(11):951-963. PubMed ID: 28370531 [TBL] [Abstract][Full Text] [Related]
14. Infantile sialidosis: a phenocopy of type 1 GM1 gangliosidosis distinguished by genetic complementation and urinary oligosaccharides. Gravel RA; Lowden JA; Callahan JW; Wolfe LS; Ng Yin Kin NM Am J Hum Genet; 1979 Nov; 31(6):669-79. PubMed ID: 117700 [TBL] [Abstract][Full Text] [Related]
15. Rapid prenatal diagnosis of GM1-gangliosidosis using microchemical methods. Kleijer WJ; Van der Veer E; Niermeijer MF Hum Genet; 1976 Aug; 33(3):299-305. PubMed ID: 823094 [TBL] [Abstract][Full Text] [Related]
16. A case of type 2 Gm1-gangliosidosis with long survival. Kikuchi K; Minami R; Kudoh T; Nakao T; Tsugawa S Brain Dev; 1982; 4(2):153-6. PubMed ID: 6807121 [TBL] [Abstract][Full Text] [Related]
17. [Fetal ascites as a manifestation of infantile sialidosis. Significance of a study of oligosaccharides in amniotic fluid]. Guibaud P; Cottin X; Maire I; Boyer S; Guibaud S; Coicaud C; Bellon-Azzouzi C; Duvernois JP J Genet Hum; 1985 Sep; 33(3-4):317-24. PubMed ID: 2414397 [TBL] [Abstract][Full Text] [Related]
18. Increased concentration of GM1-ganglioside in cerebrospinal fluid in dogs with GM1- and GM2-gangliosidoses and its clinical application for diagnosis. Satoh H; Yamato O; Asano T; Yamasaki M; Maede Y J Vet Diagn Invest; 2004 May; 16(3):223-6. PubMed ID: 15152837 [TBL] [Abstract][Full Text] [Related]
19. Variability of acid hydrolase activities in cultured skin fibroblasts and amniotic fluid cells. Young E; Willcox P; Whitfield AE; Patrick AD J Med Genet; 1975 Sep; 12(3):224-9. PubMed ID: 809585 [TBL] [Abstract][Full Text] [Related]
20. Manifestation of infantile GM1 gangliosidosis in the fetal eye. An electron microscopic study. Schmitt-Gräff A Graefes Arch Clin Exp Ophthalmol; 1988; 226(1):84-8. PubMed ID: 3125087 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]