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2. Apparent allelism of the Hurler, Scheie, and Hurler/Scheie syndromes. Mueller OT, Shows TB, Opitz JM. Am J Med Genet; 1984 Jul; 18(3):547-56. PubMed ID: 6433708 [Abstract] [Full Text] [Related]
3. The iduronidase-deficient mucopolysaccharidoses: clinical and roentgenorgraphic features. Stevenson RE, Howell RR, McKusick VA, Suskind R, Hanson JW, Elliott DE, Neufeld EF. Pediatrics; 1976 Jan; 57(1):111-22. PubMed ID: 813180 [Abstract] [Full Text] [Related]
7. [Mucopolysaccharidoses. New therapeutic possibilities increase the need of early diagnosis]. Malm G, Bondeson ML, von Döbeln U, Månsson JE. Lakartidningen; 2002 Apr 18; 99(16):1804-9. PubMed ID: 12043480 [Abstract] [Full Text] [Related]
8. [Hereditary diseases caused by disorders in glycoconjugate metabolism]. Rozenfel'd EL. Vopr Med Khim; 1977 Apr 18; (1):3-12. PubMed ID: 404759 [No Abstract] [Full Text] [Related]
14. [Mucopolysaccharidosis. Nosology--clinical aspects--therapeutic approaches]. Beck M. Monatsschr Kinderheilkd; 1991 Mar 08; 139(3):120-7. PubMed ID: 1829136 [Abstract] [Full Text] [Related]
15. The clinical spectrum of alpha-L-iduronidase deficiency. Roubicek M, Gehler J, Spranger J. Am J Med Genet; 1985 Mar 08; 20(3):471-81. PubMed ID: 3922223 [Abstract] [Full Text] [Related]