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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. Prenatal diagnosis of Maroteaux-Lamy syndrome. Van Dyke DL; Fluharty AL; Schafer IA; Shapiro LJ; Kihara H; Weiss L Am J Med Genet; 1981; 8(2):235-42. PubMed ID: 6792921 [TBL] [Abstract][Full Text] [Related]
5. 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]
6. 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]
7. 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]
8. 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]
9. Normal MPS excretion, but dermatan sulphaturia, combined with a mild Maroteaux-Lamy phenotype. Tønnesen T; Gregersen HN; Güttler F J Med Genet; 1991 Jul; 28(7):499-501. PubMed ID: 1832719 [TBL] [Abstract][Full Text] [Related]
10. 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]
11. Report of a mucopolysaccharidosis occurring in Australian aborigines. Taylor HR; Hollows FC; Hopwood JJ; Robertson EF J Med Genet; 1978 Dec; 15(6):455-61. PubMed ID: 106124 [TBL] [Abstract][Full Text] [Related]
12. Arylsulphatase B (Maroteaux-Lamy factor): a part of the enzyme system responsible for sulphate release from mucopolysaccharide fragment. Gniot-Szulzycka J; Donnelly PV FEBS Lett; 1976 May; 65(1):63-8. PubMed ID: 819304 [No Abstract] [Full Text] [Related]
13. 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]
14. [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]
15. 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]
16. [Mucopolysaccharidosis type VI (Maroteaux-Lamy syndrome)]. Sukegawa K; Tomatsu S; Kondo N; Orii T Ryoikibetsu Shokogun Shirizu; 1998; (19 Pt 2):446-8. PubMed ID: 9645105 [No Abstract] [Full Text] [Related]
18. Rapid method for measuring arylsulfatase A and B in leucocytes as a diagnosis for sulfatidosis, mucosulfatidosis and mucopolysaccharidosis VI. Humbel R Clin Chim Acta; 1976 May; 68(3):339-41. PubMed ID: 6172 [No Abstract] [Full Text] [Related]
19. Occurrence of multiple dentigerous cysts in a patient with the Maroteaux-Lamy syndrome (mucopolysaccharidosis, type VI). Roberts MW; Barton NW; Constantopoulos G; Butler DP; Donahue AH Oral Surg Oral Med Oral Pathol; 1984 Aug; 58(2):169-75. PubMed ID: 6435047 [TBL] [Abstract][Full Text] [Related]