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25. [Anatomo-pathology and study of lipids in Hurler's and Sanfilippo's mucopolysaccharidosis]. Dekaban AS; Patton VM Nouv Presse Med; 1973 Feb; 2(7):415-7. PubMed ID: 4265855 [No Abstract] [Full Text] [Related]
26. Cellular metachromasia, a genetic marker for studying the mucopolysaccharidoses. Danes BS; Bearn AG Lancet; 1967 Feb; 1(7484):241-3. PubMed ID: 4163146 [No Abstract] [Full Text] [Related]
27. Mucopolysaccharide storage diseases and lysosomal hydrolases in cultured fibroblasts. den Tandt WR; Schaberg A Pathol Eur; 1973; 8(1):3-11. PubMed ID: 4269628 [No Abstract] [Full Text] [Related]
28. Marchesani's syndrome: (case report). Sarma CM J All India Ophthalmol Soc; 1969 Aug; 17(4):158-9. PubMed ID: 5381761 [No Abstract] [Full Text] [Related]
32. I-cell disease, mucolipidosis II. Pathological, histochemical, ultrastructural and biochemical observations in four cases. Gilbert EF; Dawson G; zu Rhein GM; Opitz JM; Spranger Z Kinderheilkd; 1973; 114(4):259-92. PubMed ID: 4353613 [No Abstract] [Full Text] [Related]
33. Weill-Marchesani syndrome. Growth hormone, thyroid and chromosome studies. Götz M; Schenk E Z Kinderheilkd; 1973 Dec; 116(1):43-9. PubMed ID: 4203835 [No Abstract] [Full Text] [Related]
34. [Biochemical heterogeneity of Sanfilippos' disease (mucopolysaccharidosis 3). Purification and enzymatic activity of one of the missing proteins]. Kresse H Hoppe Seylers Z Physiol Chem; 1972 May; 353(5):728-9. PubMed ID: 4262625 [No Abstract] [Full Text] [Related]