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• A comparative study of sialyloligosaccharides isolated from sialidosis and galactosialidosis urine.

  Van Pelt J, Kamerling JP, Bakker HD, Vliegenthart JF. Van Pelt J, et al. J Inherit Metab Dis. 1991;14(5):730-40. doi: 10.1007/BF01799942. J Inherit Metab Dis. 1991. PMID: 1779619
• A case of neuraminidase deficiency associated with a partial beta-galactosidase defect. Clinical, biochemical and radiological studies.

  Okada S, Yutaka T, Kato T, Ikehara C, Yabuuchi H, Okawa M, Inui M, Chiyo H. Okada S, et al. Eur J Pediatr. 1979 Apr 3;130(4):239-49. doi: 10.1007/BF00441360. Eur J Pediatr. 1979. PMID: 436849
• Exploration of the Sialic Acid World.

  Schauer R, Kamerling JP. Schauer R, et al. Adv Carbohydr Chem Biochem. 2018;75:1-213. doi: 10.1016/bs.accb.2018.09.001. Epub 2018 Nov 28. Adv Carbohydr Chem Biochem. 2018. PMID: 30509400 Free PMC article. Review.
• Loss of kidney function due to proteinuria, common problem with a rare cause: Answer.

  Steinke J, Gessner M, Frauenfeld L, Fischer AK, Solass W. Steinke J, et al. Pediatr Nephrol. 2020 Sep;35(9):1627-1629. doi: 10.1007/s00467-020-04505-7. Epub 2020 Mar 11. Pediatr Nephrol. 2020. PMID: 32162101 Free PMC article. No abstract available.
• Purification and characterization of sialic acid containing materials accumulated in cultured skin fibroblasts from a patient with type II sialidosis.

  Scocca JR, Thomas GH, Miller C, Reynolds L. Scocca JR, et al. J Inherit Metab Dis. 1987;10(1):33-47. doi: 10.1007/BF01799486. J Inherit Metab Dis. 1987. PMID: 3106715