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22. Variation in the phenotypic expression of beta-glucuronidase deficiency. Beaudet AL; DiFerrante NM; Ferry GD; Nichols BL; Mullins CE J Pediatr; 1975 Mar; 86(3):388-94. PubMed ID: 803560 [TBL] [Abstract][Full Text] [Related]
23. 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]
24. Biochemical heterogeneity of the Sanfilippo syndrome: preliminary characterization of two deficient factors. Kresse H; Wiesmann U; Cantz M; Hall CW; Neufeld EF Biochem Biophys Res Commun; 1971 Mar; 42(5):892-8. PubMed ID: 4252428 [No Abstract] [Full Text] [Related]
25. Mucopolysaccharidosis type VI (Maroteaux-Lamy syndrome). I. Sulfatase B deficiency in tissues. Stumpf DA; Austin JH; Crocker AC; LaFrance M Am J Dis Child; 1973 Dec; 126(6):747-55. PubMed ID: 4271367 [No Abstract] [Full Text] [Related]
26. Acid hydrolases in the serum and liver in mucopolysaccharidoses types I and 3. Gordon BA; Feleki V Clin Biochem; 1970 Sep; 3(3):193-202. PubMed ID: 4258597 [No Abstract] [Full Text] [Related]
28. The nosology of the mucopolysaccharidoses. McKusick VA Am J Med; 1969 Nov; 47(5):730-47. PubMed ID: 4242813 [No Abstract] [Full Text] [Related]
29. [Biochemical diagnosis of mucopolysaccharidoses in cell culture (author's transl)]. Wendel U; Rüdiger HW; Passarge E Monatsschr Kinderheilkd (1902); 1974 Jan; 122(1):23-30. PubMed ID: 4274396 [No Abstract] [Full Text] [Related]
30. [Significance and value of metachromic granule in in vitro cultured fibroblasts durng mucopolysaccharidosis]. Hartung M Pathol Biol (Paris); 1972 Sep; 20(15):649-54. PubMed ID: 4116648 [No Abstract] [Full Text] [Related]
32. A recognition marker required for uptake of a lysosomal enzyme by cultured fibroblasts. Hickman S; Shapiro LJ; Neufeld EF Biochem Biophys Res Commun; 1974 Mar; 57(1):55-61. PubMed ID: 4364008 [No Abstract] [Full Text] [Related]
33. [A new method for the study of metachromatic granuli of peripheral leukocytes and its importance in the diagnosis of mucopolysaccharidosis]. Szabó L; László A; Puljer I; Halász K Orv Hetil; 1973 Apr; 114(17):988-90. PubMed ID: 4121398 [No Abstract] [Full Text] [Related]
34. 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]
35. Chondroitin-6-sulfate mucopolysaccharidosis in conjuntion withlymphopenia, defective cellular immunity and the nephrotic syndrome. Danes BS; Degnan M Birth Defects Orig Artic Ser; 1974; 10(12):251-7. PubMed ID: 4282259 [No Abstract] [Full Text] [Related]
37. [Mucopolysaccharidoses in clinical practice]. Szabó L Orv Hetil; 1972 May; 113(19):1095-102. PubMed ID: 4260087 [No Abstract] [Full Text] [Related]
38. [Mucopolysaccharidosis type 3 (Sanfilippo's syndrome). A cause of progressive mental retardation]. Börjeson M; Heinegård D; Ockerman PA Nord Med; 1969 May; 81(18):567-9. PubMed ID: 4238726 [No Abstract] [Full Text] [Related]
39. Mucopolysaccharidosis 3 A (Sanfilippo A disease): deficiency of a heparin sulfamidase in skin fibroblasts and leucocytes. Kresse H Biochem Biophys Res Commun; 1973 Oct; 54(3):1111-8. PubMed ID: 4201808 [No Abstract] [Full Text] [Related]