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.
143 related articles for article (PubMed ID: 4260081)
1. A form of mucopolysaccharidosis with visceral storage and excessive urinary excretion of chondroitin sulphate. Benson PF; Dean MF; Muir H Dev Med Child Neurol; 1972 Feb; 14(1):69-74. PubMed ID: 4260081 [No Abstract] [Full Text] [Related]
2. Pattern of urinary acid mucopolysaccharide excretion in five patients with genetic mucopolysaccharidoses. Orii T; Minami R; Takase A; Nakao T Tohoku J Exp Med; 1973 May; 110(1):41-8. PubMed ID: 4269662 [No Abstract] [Full Text] [Related]
3. Thin layer chromatography of urinary acid glycosaminoglycans as screening procedure for mucopolysaccharidoses. Teller WM; Ziemann A Horm Metab Res; 1969 Jan; 1(1):32-5. PubMed ID: 4258873 [No Abstract] [Full Text] [Related]
4. A mucopolysaccharidosis with increased urinary excretion of chondroitin-4 sulfate. Thompson GR; Nelson NA; Castor CW; Grobelny SL Ann Intern Med; 1971 Sep; 75(3):421-6. PubMed ID: 4254954 [No Abstract] [Full Text] [Related]
5. Enzymatic studies of urinary chondroitin sulfates in normal and systemic connective tissue disease states. Murata K; Ishikawa T; Oshima Y Clin Chim Acta; 1970 Apr; 28(1):213-22. PubMed ID: 4245391 [No Abstract] [Full Text] [Related]
6. [Mucopolysaccharidosis--synthesis and prospects]. Bulgarelli R; Romano C Minerva Pediatr; 1972 Oct; 24(35):1703-5. PubMed ID: 4264768 [No Abstract] [Full Text] [Related]
7. The systemic mucopolysaccharidoses. Spranger J Ergeb Inn Med Kinderheilkd; 1972; 32():165-265. PubMed ID: 4261654 [No Abstract] [Full Text] [Related]
8. Heterogeneity of disorders in patients with corneal clouding, normal intellect, and mucopolysaccharidosis. Constantopoulos G; Dekabian AS; Scheie HG Am J Ophthalmol; 1971 Dec; 72(6):1106-17. PubMed ID: 4256845 [No Abstract] [Full Text] [Related]
9. [Ultrastructural study of the perisinusoidal cells of the liver in 3 cases of mucopolysaccharidosis]. Lafon J; Berard-Badier M; Chamlian A; Mariani R; Casanova P; Adechy-Benkoel L Pathol Biol (Paris); 1972 Jan; 20(1):15-21. PubMed ID: 4335125 [No Abstract] [Full Text] [Related]
10. Chondroitin-4-sulphate mucopolysaccharidosis--a new variant of Hurler's syndrome. Philippart M; Sugarman GI Lancet; 1969 Oct; 2(7625):854. PubMed ID: 4186316 [No Abstract] [Full Text] [Related]
11. [Clinical picture of mucopolysaccharidoses in childhood]. Cáp J; Némethová V Cesk Pediatr; 1973; 28(5):240-2. PubMed ID: 4267985 [No Abstract] [Full Text] [Related]
12. Arylsulfatase B deficiency in Maroteaux-Lamy syndrome cultured fibroblasts. Fluharty AL; Stevens RL; Sanders DL; Kihara H Biochem Biophys Res Commun; 1974 Jul; 59(2):455-61. PubMed ID: 4277366 [No Abstract] [Full Text] [Related]
16. Electron microscopy of intestinal suction-biopsy specimens as an aid in the diagnosis of mucopolysaccharidoses and other lysosomal storage diseases. Van Gemund JJ; Daems WT; Vio PA; Giesberts MA Maandschr Kindergeneeskd; 1971 Oct; 39(7):211-7. PubMed ID: 4258610 [No Abstract] [Full Text] [Related]