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23. Mass screening newborns for mucopolysaccharidoses. Sabater J; Villalba M; Maya A Clin Genet; 1973; 4(3):260-3. PubMed ID: 4203061 [No Abstract] [Full Text] [Related]
24. Biochemical and histopathological studies on patients with mucopolysaccharidoses, two of whom had been treated by fibroblast transplantation. Crow J; Gibbs DA; Cozens W; Spellacy E; Watts RW J Clin Pathol; 1983 Apr; 36(4):415-30. PubMed ID: 6403596 [TBL] [Abstract][Full Text] [Related]
25. Deficiency of beta-galactosidase and alpha-mannosidase--primary enzyme defects in gargoylism and a new generalized disease? Ockerman PA Acta Paediatr Scand; 1967; ():Suppl 177:35-6. PubMed ID: 4967547 [No Abstract] [Full Text] [Related]
26. 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]
27. Lysosomes and mucopolysaccharidoses. Hers HG; van Hoof F Biochem J; 1969 Dec; 115(5):34P-36P. PubMed ID: 4243352 [No Abstract] [Full Text] [Related]
28. Mucopolysaccharidosis by absence of alpha-fucosidase. Van Hoof F; Hers HG Lancet; 1968 Jun; 1(7553):1198. PubMed ID: 4172303 [No Abstract] [Full Text] [Related]
29. The mucopolysaccaridoses: clinical and biochemical correlations. Horwitz AL Am J Ment Defic; 1979 Sep; 84(2):113-23. PubMed ID: 115315 [TBL] [Abstract][Full Text] [Related]
30. Clinical ultrastructural and tissue culture studies in a possible compound Hurler-Scheie case. Tondeur M; Vamos-Hurwitz E; Cantz M; Cremer N; Libert J; Pardou A Acta Paediatr Belg; 1976; 29(2):109-15. PubMed ID: 826105 [No Abstract] [Full Text] [Related]
31. [Biochemical characteristics and diagnosis of lysosomal diseases related to hereditary glycosidase deficiency]. Vidershaĭn GIa Vestn Akad Med Nauk SSSR; 1982; (6):42-7. PubMed ID: 6810572 [No Abstract] [Full Text] [Related]
32. Early initiation of enzyme replacement therapy for the mucopolysaccharidoses. Muenzer J Mol Genet Metab; 2014 Feb; 111(2):63-72. PubMed ID: 24388732 [TBL] [Abstract][Full Text] [Related]
33. [Possible genetic nature of phenotypical differences of mucopolysaccharidosis 1]. Kobrinskiĭ BA Vopr Med Khim; 1982; 28(3):55-7. PubMed ID: 6808766 [No Abstract] [Full Text] [Related]
34. [Enzymatic disorders in mucopolysac charidosis]. Gadowska M Przegl Lek; 1976; 33(8):737-42. PubMed ID: 136012 [No Abstract] [Full Text] [Related]
35. 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]