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.
23. Use of isotopically radiolabelled GM3 ganglioside to study metabolic alterations in Salla disease. Chigorno V, Valsecchi M, Nicolini M, Sonnino S. Indian J Biochem Biophys; 1997; 34(1-2):150-6. PubMed ID: 9343943 [Abstract] [Full Text] [Related]
25. 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 15; 31(11):951-963. PubMed ID: 28370531 [Abstract] [Full Text] [Related]
26. Prenatal genetic diagnosis (second of three parts). Milunsky A, Littlefield JW, Kanfer JN, Kolodny EH, Shih VE, Atkins L. N Engl J Med; 1970 Dec 24; 283(26):1441-7. PubMed ID: 4098222 [No Abstract] [Full Text] [Related]
28. 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 Dec 24; 6(6):393-400. PubMed ID: 3809110 [Abstract] [Full Text] [Related]
35. 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 07; 127(3):313-26. PubMed ID: 6404572 [Abstract] [Full Text] [Related]
37. Infantile type of sialic acid storage disease with sialuria. Paschke E, Trinkl G, Erwa W, Pavelka M, Mutz I, Roscher A. Clin Genet; 1986 May 07; 29(5):417-24. PubMed ID: 3742847 [Abstract] [Full Text] [Related]
38. Prenatal detection of Salla disease based upon increased free sialic acid in amniocytes. Renlund M, Aula P. Am J Med Genet; 1987 Oct 07; 28(2):377-84. PubMed ID: 3425617 [Abstract] [Full Text] [Related]