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62. [Mucopolysaccharidoses. New therapeutic possibilities increase the need of early diagnosis]. Malm G; Bondeson ML; von Döbeln U; Månsson JE Lakartidningen; 2002 Apr; 99(16):1804-9. PubMed ID: 12043480 [TBL] [Abstract][Full Text] [Related]
63. Early manifestations of multiple sulfatase deficiency. Burk RD; Valle D; Thomas GH; Miller C; Moser A; Moser H; Rosenbaum KN J Pediatr; 1984 Apr; 104(4):574-8. PubMed ID: 6142938 [TBL] [Abstract][Full Text] [Related]
64. 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]
65. The genetic mucopolysaccharidoses and mucolipidoses: review and comment. Legum CP; Schorr S; Berman ER Adv Pediatr; 1976; 22():305-47. PubMed ID: 131478 [No Abstract] [Full Text] [Related]
66. Beta-glucuronidase deficiency in a girl with unusual clinical features. Pfeiffer RA; Kresse H; Bäumer N; Sattinger E Eur J Pediatr; 1977 Oct; 126(3):155-61. PubMed ID: 144057 [TBL] [Abstract][Full Text] [Related]
67. [Mucopolysaccharidoses. Apropos of 25 cases in 17 families]. Trabelsi M; Ben Dridi MF; Gharbi HA; Tabbane C; Ben Osman R Tunis Med; 1986 Jan; 64(1):49-56. PubMed ID: 3087042 [No Abstract] [Full Text] [Related]
68. Enzyme replacement therapy by transplantation of HLA-compatible fibroblasts in Sanfilippo A syndrome. Dean MF; Muir H; Benson PF; Button LR Pediatr Res; 1981 Jun; 15(6):959-63. PubMed ID: 6787549 [No Abstract] [Full Text] [Related]
69. Role of the pediatric otolaryngologist in diagnosis and management of children with mucopolysaccharidoses. Wold SM; Derkay CS; Darrow DH; Proud V Int J Pediatr Otorhinolaryngol; 2010 Jan; 74(1):27-31. PubMed ID: 19931921 [TBL] [Abstract][Full Text] [Related]
70. Mental retardation in mucopolysaccharidoses correlates with high molecular weight urinary heparan sulphate derived glucosamine. Coppa GV; Gabrielli O; Zampini L; Maccari F; Mantovani V; Galeazzi T; Santoro L; Padella L; Marchesiello RL; Galeotti F; Volpi N Metab Brain Dis; 2015 Dec; 30(6):1343-8. PubMed ID: 26016623 [TBL] [Abstract][Full Text] [Related]
71. Intrafamilial variability in lysosomal storage diseases. Zlotogora J Am J Med Genet; 1987 Jul; 27(3):633-8. PubMed ID: 3115101 [TBL] [Abstract][Full Text] [Related]
72. Functional capacity evaluation of patients with mucopolysaccharidosis. Guarany NR; Schwartz IV; Guarany FC; Giugliani R J Pediatr Rehabil Med; 2012; 5(1):37-46. PubMed ID: 22543891 [TBL] [Abstract][Full Text] [Related]
73. [Hereditary lysosomal diseases. I. Initial results of a diagnostic program in Mexico]. Zetina ME; González-Noriega A Rev Invest Clin; 1989; 41(4):319-26. PubMed ID: 2517151 [TBL] [Abstract][Full Text] [Related]
74. [Mucopolysaccharidoses--current aspects of diagnosis and therapy]. Fang-Kircher S Wien Klin Wochenschr; 1995; 107(22):698-701. PubMed ID: 8533432 [TBL] [Abstract][Full Text] [Related]
75. The mucopolysaccharidoses: a success of molecular medicine. Clarke LA Expert Rev Mol Med; 2008 Jan; 10():e1. PubMed ID: 18201392 [TBL] [Abstract][Full Text] [Related]
76. Determination of heterozygous carrier state from the urine of the parents of children suffering from mucopolysaccharidosis. Józsa L; Szabó L Acta Paediatr Acad Sci Hung; 1972; 13(1):39-50. PubMed ID: 4265710 [No Abstract] [Full Text] [Related]
77. New phenotype of adult alpha-L-iduronidase deficiency (mucopolysaccharidosis I) masquerading as Friedreich's ataxia with cardiopathy. Jellinger K; Paulus W; Grisold W; Paschke E Clin Neuropathol; 1990; 9(4):163-9. PubMed ID: 2121405 [TBL] [Abstract][Full Text] [Related]
78. Early presentation in the mucopolysaccharide disorders. Colville GA; Bax MA Child Care Health Dev; 1996 Jan; 22(1):31-6. PubMed ID: 8640962 [TBL] [Abstract][Full Text] [Related]
79. [Characteristics of intracellular and excretory glycosaminoglycans in hereditary mucopolysaccharidoses]. Odinokova ON; Bialik MA; Krasnopol'skaia KD; Iakovlev SA Vopr Med Khim; 1986; 32(1):87-92. PubMed ID: 3082072 [TBL] [Abstract][Full Text] [Related]
80. A straightforward, quantitative ultra-performance liquid chromatography-tandem mass spectrometric method for heparan sulfate, dermatan sulfate and chondroitin sulfate in urine: an improved clinical screening test for the mucopolysaccharidoses. Zhang H; Wood T; Young SP; Millington DS Mol Genet Metab; 2015 Feb; 114(2):123-8. PubMed ID: 25458519 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]