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3. [The early diagnosis of Maroteaux-Lamy syndrome with confirmation of arylsulphatase deficiency]. Van Biervliet JP; Van Leeuwen EF; Abeling NG; De Jonge HF; Liem KO; Wadman SK Arch Fr Pediatr; 1977 Apr; 34(4):362-70. PubMed ID: 142458 [TBL] [Abstract][Full Text] [Related]
4. Deficiency of arylsulfatase B in 2 brothers aged 40 and 38 years (Maroteaux-Lamy syndrome, type B). Pilz H; von Figura K; Goebel HH Ann Neurol; 1979 Oct; 6(4):315-25. PubMed ID: 122048 [TBL] [Abstract][Full Text] [Related]
5. Maroteaux-Lamy syndrome in a large consanguineous kindred: biochemical and immunological studies. Black SH; Pelias MZ; Miller JB; Blitzer MG; Shapira E Am J Med Genet; 1986 Oct; 25(2):273-9. PubMed ID: 3096137 [TBL] [Abstract][Full Text] [Related]
6. Arylsulphatase B studies in skin fibroblasts from patients with Maroteaux--Lamy syndrome with special reference to electrophoretic mobility and prenatal diagnosis. Schwartz M; Brandt NJ; Christensen E; Pedersen C J Inherit Metab Dis; 1980; 3(3):99-100. PubMed ID: 6775150 [No Abstract] [Full Text] [Related]
7. Mucopolysaccharidosis in a cat with arylsulfatase B deficiency: a model of Maroteaux-Lamy syndrome. Jezyk PF; Haskins ME; Patterson DF; Mellman WJ; Greenstein M Science; 1977 Nov; 198(4319):834-6. PubMed ID: 144321 [TBL] [Abstract][Full Text] [Related]
8. Quantification of arylsulfatase B activity and diagnosis of Maroteaux-Lamy syndrome. Hwu WL; Wang TR Zhonghua Min Guo Xiao Er Ke Yi Xue Hui Za Zhi; 1991; 32(5):280-5. PubMed ID: 1776456 [TBL] [Abstract][Full Text] [Related]
9. Arylsulfatases A and B in metachromatic leukodystrophy and Maroteaux-Lamy syndrome: studies with 4-methylumelliferyl sulfate. Kolodny EH; Mumford RA Adv Exp Med Biol; 1976; 68():239-51. PubMed ID: 7105 [TBL] [Abstract][Full Text] [Related]
10. [Maroteaux-Lamy syndrome: a case report]. Mtar A; Charfeddine B; Braham I; Ben Abdallah J; Neffati S; Smach MA; Bourfifa Z; Ksouri M; Dridi H; Limem K Ann Biol Clin (Paris); 2011; 69(6):693-7. PubMed ID: 22123570 [TBL] [Abstract][Full Text] [Related]
11. Mental retardation in a patient with Maroteaux-Lamy. Vestermark S; Tønnesen T; Andersen MS; Güttler F Clin Genet; 1987 Feb; 31(2):114-7. PubMed ID: 3103957 [TBL] [Abstract][Full Text] [Related]
12. Diagnosis of Maroteaux-Lamy syndrome by the use of radiolabelled oligosaccharides as substrates for the determination of arylsulphatase B activity. Hopwood JJ; Elliott H; Muller VJ; Saccone GT Biochem J; 1986 Mar; 234(3):507-14. PubMed ID: 3087346 [TBL] [Abstract][Full Text] [Related]
13. Reclassification of previously reported cases of mucopolysaccharidosis type IS to mucopolysaccharidosis type VI. Constantopoulos G; Stowens DW; Barranger JA Clin Chim Acta; 1982 Sep; 124(1):137-9. PubMed ID: 6812996 [No Abstract] [Full Text] [Related]
14. Diagnosis of the mucopolysaccharidoses using cultured skin fibroblasts and amniotic fluid cells. Butterworth J J Inherit Metab Dis; 1978; 1(1):25-8. PubMed ID: 117232 [TBL] [Abstract][Full Text] [Related]
16. Arylsulfatase B deficiency in Maroteaux-Lamy syndrome: Cellular studies and carrier identification. Beratis NG; Turner BM; Weiss R; Hirschhorn K Pediatr Res; 1975 May; 9(5):475-80. PubMed ID: 806052 [TBL] [Abstract][Full Text] [Related]
17. Mucopolysaccharidosis VI (Maroteaux-Lamy syndrome). Thomas S; Menon PS; Khurana A; Irshad M; Khan MA Indian Pediatr; 1983 May; 20(5):378-80. PubMed ID: 6414952 [No Abstract] [Full Text] [Related]
18. Proceedings: The defect in Maroteaux-Lamy disease (mucopolysaccharidosis VI, subtype A): deficiency of N-acetylgalactosamine-4-sulfatase. O'Brien JF; Spranger J; Cantz M Hoppe Seylers Z Physiol Chem; 1974 Oct; 355(10):1235. PubMed ID: 4218834 [No Abstract] [Full Text] [Related]
19. Arylsulfatases A and B in EBV-transformed lymphoid cell lines: studies on their molecular forms in cells from patients with inborn sulfatase deficiencies. Comparative diagnostic value of enzymatic assays. Tempesta MC; Levade T; Salvayre R Clin Chim Acta; 1991 Oct; 202(3):149-65. PubMed ID: 1687673 [TBL] [Abstract][Full Text] [Related]