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22. Ultrastructures of Reilly bodies (metachromatic granules) in the Maroteaux-Lamy syndrome (mucopolysaccharidosis VI). A histochemical study. Levy LA; Lewis JC; Sumner TE Am J Clin Pathol; 1980 Mar; 73(3):416-22. PubMed ID: 6767391 [TBL] [Abstract][Full Text] [Related]
23. Teaching NeuroImages: Mucopolysaccharidosis type VI (Maroteaux-Lamy syndrome) in a previously undiagnosed infant. Kwong Y; Jaspan T Neurology; 2012 Feb; 78(8):e53. PubMed ID: 22351802 [No Abstract] [Full Text] [Related]
24. [Mucopolysaccharidoses in 4 Sengalese children]. Fall M; Niang I; Kuakuvi N; Martin LS; Sanokho A Dakar Med; 1979; 24(4):341-55. PubMed ID: 120803 [No Abstract] [Full Text] [Related]
26. [Prenatal diagnosis of Sanfilippo A disease (mucopolysaccharidosis IIIA)]. Török O; Váradi V; Szondy M; Molnár M; Szabó M; Papp Z Orv Hetil; 1986 Sep; 127(39):2385-7. PubMed ID: 3095766 [No Abstract] [Full Text] [Related]
27. [Test for the characterization of hypermucopolysaccharidurias]. Rufini S; Ghebregzabher M; Lato M Minerva Pediatr; 1980 Dec; 32(24):1371-4. PubMed ID: 6454060 [No Abstract] [Full Text] [Related]
28. Histological and ultrastructural studies of the cornea in Maroteaux-Lamy syndrome. Süveges I Albrecht Von Graefes Arch Klin Exp Ophthalmol; 1979 Nov; 212(1):29-39. PubMed ID: 120117 [TBL] [Abstract][Full Text] [Related]
32. [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]
33. [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]
34. [Developmental skeletal anomalies in 2 children diagnosed as rheumatoid arthritis]. Berkan E Reumatologia; 1977; 15(1):83-9. PubMed ID: 142293 [No Abstract] [Full Text] [Related]
35. 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]
36. Compressive myelopathy associated with type VI mucopolysaccharidosis (Maroteaux-Lamy syndrome). Wald SL; Schmidek HH Neurosurgery; 1984 Jan; 14(1):83-8. PubMed ID: 6420724 [TBL] [Abstract][Full Text] [Related]
37. [Radiologic aspects of a severe form of Maroteaux-Lamy syndrome]. Riggio S; Felici L; Leone L; Freddara R; Coppa GV Radiol Med; 1984 Sep; 70(9):629-30. PubMed ID: 6443031 [No Abstract] [Full Text] [Related]
38. 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]