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42. [Treatment of mucopolysaccharidoses with perfusions of plasma or leukocytes]. Lambotte C; Winand R Acta Univ Carol Med Monogr; 1973; 56():191-5. PubMed ID: 4275463 [No Abstract] [Full Text] [Related]
43. [Increase of the serum activity of hyaluronidase, beta glucuronidase and beta acetylglucosaminidase in mucopolysaccharidoses]. Platt D; Koch F Klin Wochenschr; 1969 Aug; 47(16):888-9. PubMed ID: 4245626 [No Abstract] [Full Text] [Related]
44. [Mucopolysaccharidosis]. Maroteaux P; Hors-Cayla MC Ann Biol Clin (Paris); 1972; 30(5):451-8. PubMed ID: 4264383 [No Abstract] [Full Text] [Related]
45. Sanfilippo syndrome: profound deficiency of alpha-acetylglucosaminidase activity in organs and skin fibroblasts from type-B patients. O'Brien JS Proc Natl Acad Sci U S A; 1972 Jul; 69(7):1720-2. PubMed ID: 4261742 [TBL] [Abstract][Full Text] [Related]
46. [HS-mucopolysaccharidosis of Sanfilippo (polydystrophic oligophrenia). A report on 10 patients]. Spranger J; Teller W; Kosenow W; Murken J; Eckert-Husemann E Z Kinderheilkd; 1967; 101(1):71-84. PubMed ID: 4235306 [No Abstract] [Full Text] [Related]
47. The biochemistry of Hurler's syndrome. Harmel RP Enzymol Biol Clin (Basel); 1969; 10(6):534-48. PubMed ID: 4243200 [No Abstract] [Full Text] [Related]
48. The molecular basis of the mucopolysaccharidoses: current status of knowledge. Dorfman A Triangle; 1972; 11(2):43-50. PubMed ID: 4265869 [No Abstract] [Full Text] [Related]
49. Allelism, non-allelism, and genetic compounds among the mucopolysaccharidoses. McKusick VA; Howell RR; Hussels IE; Neufeld EF; Stevenson RE Lancet; 1972 May; 1(7758):993-6. PubMed ID: 4112371 [No Abstract] [Full Text] [Related]
50. [Mucopolysaccharidoses and disorders of glycoprotein metabolism]. Suzuki Y Tanpakushitsu Kakusan Koso; 1984 Dec; 29(14):1759-69. PubMed ID: 6241960 [No Abstract] [Full Text] [Related]
51. 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]
52. Hurler and Hunter syndromes: mutual correction of the defect in cultured fibroblasts. Fratantoni JC; Hall CW; Neufeld EF Science; 1968 Nov; 162(3853):570-2. PubMed ID: 4236721 [TBL] [Abstract][Full Text] [Related]
54. [The mucopolysaccharidoses in childhood. Clinical study]. De Angelis P Pediatria (Napoli); 1967; 75(4):561-82. PubMed ID: 4231289 [No Abstract] [Full Text] [Related]
55. Low beta-glucuronidase activity in a healthy member of a family with mucopolysaccharidosis VII. Chabas A; Giros ML; Guardiola A J Inherit Metab Dis; 1991; 14(6):908-14. PubMed ID: 1779649 [TBL] [Abstract][Full Text] [Related]
57. White blood cell cultures in genetic studies on the human mucopolysaccharidoses. Foley KM; Danes BS; Bearn AG Science; 1969 Apr; 164(3878):424-6. PubMed ID: 4180575 [TBL] [Abstract][Full Text] [Related]
58. Five year maintenance of corneal graft normality in systemic mucopolysaccharidosis. Rosen DA; Edmison DR; Robertson DM Can J Ophthalmol; 1972 Oct; 7(4):445-53. PubMed ID: 4265781 [No Abstract] [Full Text] [Related]
59. [Corneal and retinal disorders associated with mucopolysaccharidosis (8 cases)]. Thomas C; Raspiller A; Fall M Bull Soc Ophtalmol Fr; 1970; 70(9):933-41. PubMed ID: 4262237 [No Abstract] [Full Text] [Related]
60. Correction of murine mucopolysaccharidosis VII by a human beta-glucuronidase transgene. Kyle JW; Birkenmeier EH; Gwynn B; Vogler C; Hoppe PC; Hoffmann JW; Sly WS Proc Natl Acad Sci U S A; 1990 May; 87(10):3914-8. PubMed ID: 2111021 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]