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45. [Mucopolysaccharidosis without mucopolysacchariduria]. Marchal C; Grignon G; Humbel R; Vidailhet M; Fall M; Grignon M; Pierson M; Neimann N Ann Pediatr (Paris); 1968 Oct; 15(10):606-11. PubMed ID: 4237827 [No Abstract] [Full Text] [Related]
46. The enzymic defects in Morquio and Maroteaux-Lamy syndrome. Dorfman A; Arbogast B; Matalon R Adv Exp Med Biol; 1976; 68():261-76. PubMed ID: 820169 [No Abstract] [Full Text] [Related]
51. Mucolipidosis III (pseudo-Hurler polydystrophy): Clinical and laboratory studies in a series of 12 patients. Kelly TE; Thomas GH; Taylor HA; McKusick VA; Sly WS; Glaser JH; Robinow M; Luzzatti L; Espiritu C; Feingold M; Bull MJ; Ashenhurst EM; Ives EJ Johns Hopkins Med J; 1975 Oct; 137(4):156-75. PubMed ID: 810612 [TBL] [Abstract][Full Text] [Related]
52. [Sanfilippo's disease: clinico-genetic and biological study of 2 families]. Carlomagno S; Federico A; Vitiello F; Pinto L; Vertucci P; Marolda M; Balbi R; Guazzi GC Acta Neurol (Napoli); 1974; 29(3):231-51. PubMed ID: 4213902 [No Abstract] [Full Text] [Related]
53. Mannose metabolism. II. Herman RH Am J Clin Nutr; 1971 May; 24(5):556-61. PubMed ID: 4932830 [No Abstract] [Full Text] [Related]
54. The clinical spectrum of alpha-L-iduronidase deficiency. Roubicek M; Gehler J; Spranger J Am J Med Genet; 1985 Mar; 20(3):471-81. PubMed ID: 3922223 [TBL] [Abstract][Full Text] [Related]
55. Mannosidosis: isolation of oligosaccharide storage material from brain. Ockerman PA J Pediatr; 1969 Sep; 75(3):360-5. PubMed ID: 4979626 [No Abstract] [Full Text] [Related]
56. [Possibilities of serum heterozygote tests in genetic mucopolysaccharidoses]. Gehler J; Cantz M; Spranger J Monatsschr Kinderheilkd (1902); 1974 Jul; 122(7):578-9. PubMed ID: 4212748 [No Abstract] [Full Text] [Related]