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4. Scheie and Hurler syndromes: apparent identity of the biochemical defect. Wiesmann U; Neufeld EF Science; 1970 Jul; 169(3940):72-4. PubMed ID: 4246082 [TBL] [Abstract][Full Text] [Related]
5. 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]
6. The measurement of acid mucopolysaccharides (glycosaminoglycans) in amniotic fluid and urine. Duncan DM; Logan RW; Ferguson-Smith MA; Hall F Clin Chim Acta; 1973 Apr; 45(1):73-83. PubMed ID: 4123257 [No Abstract] [Full Text] [Related]
7. [Current possibilities of laboratory diagnosis in mucopolysaccharidoses]. Pinto L Pediatria (Napoli); 1967; 75(4):583-93. PubMed ID: 4231290 [No Abstract] [Full Text] [Related]
8. Cystic fibrosis: distribution of mucopolysaccharides in fibroblast cultures. Danes BS; Bearn AG Biochem Biophys Res Commun; 1969 Sep; 36(6):919-24. PubMed ID: 4186555 [No Abstract] [Full Text] [Related]
17. Tissue culture and study of cystic fibrosis and other inherited diseases. N Engl J Med; 1968 Sep; 279(10):547-8. PubMed ID: 4233593 [No Abstract] [Full Text] [Related]
18. [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]
19. Systemic hyalinosis or fibromatosis hyalinica multiplex juvenilis as a congenital syndrome. A new entity based on the inborn error of the acid mucopolysaccharide metabolism in connective tissue cells? Ishikawa H; Mori S Acta Derm Venereol; 1973; 53(3):185-91. PubMed ID: 4124008 [No Abstract] [Full Text] [Related]
20. Larsen's syndrome. Report of three cases in the one family, mother and two offspring. Trigueros AP; Vazquez V; De Miguel GF Acta Orthop Scand; 1978 Dec; 49(6):582-8. PubMed ID: 735785 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]