Hepatic fibrosis in the mucopolysaccharidosesPARFREY, N. A; HUTCHINS, G. M.The American journal of medicine. 1986, Vol 81, Num 5, pp 825-829, issn 0002-9343Article

Further evidence localising the gene for Hunter's syndrome to the distal region of the X-chromosome long armROBERTS, S. H; UPADHYAYA, M; SARFARAZI, M et al.Journal of medical genetics. 1989, Vol 26, Num 5, pp 309-313, issn 0022-2593, 5 p.Article

First international congress on mucopolysaccharidosis and related diseases ― 70 years of research, University of Minnesota, Minneapolis, May 20-23, 1988WHITLEY, C. B.American journal of medical genetics. 1989, Vol 32, Num 2, pp 277-278, issn 0148-7299Article

Focal dendritic swellings in Purkinje cells in mucopolysaccharidoses types I, II and III. A Golgi and ultrastructural studyFERRER, I; CUSI, V; PINEDA, M et al.Neuropathology and applied neurobiology (Print). 1988, Vol 14, Num 4, pp 315-323, issn 0305-1846Article

Transplantation of fetal fibroblasts and correction of enzymatic deficiencies in patients with Hunter's or Hurler's disordersADINOLFI, M; MCCOLL, I; FENSOM, A. H et al.Transplantation. 1986, Vol 42, Num 3, pp 271-274, issn 0041-1337Article

Electroretinographic findings in the mucopolysaccharidosesCARUSO, R. C; KAISER-KUPFER, M. I; MUENZER, J et al.Ophthalmology (Rochester, MN). 1986, Vol 93, Num 12, pp 1612-1616, issn 0161-6420Article

Airway changes in children with mucopolysaccharidoses: CT evaluationSHIH, S.-L; LEE, Y.-J; LIN, S.-P et al.Acta radiologica (1987). 2002, Vol 43, Num 1, pp 40-43, issn 0284-1851Article

Bone marrow transplantation in canine mucopolysaccharidosis I. Effects within the central nervous systemSHULL, R. M; HASTINGS, N. E; SELCER, R. R et al.The Journal of clinical investigation. 1987, Vol 79, Num 2, pp 435-443, issn 0021-9738Article

Measuring urinary glycosaminoglycans in the presence of protein : an improved screening procedure for mucopolysaccharidoses based on dimethylmethylene blueDE JONG, J. G. N; WEVERS, R. A; LIEBRAND-VAN SAMBEEK, R et al.Clinical chemistry (Baltimore, Md.). 1992, Vol 38, Num 6, pp 803-807, issn 0009-9147Article

Atypical radiological features of β-glucuronidase deficiency (mucopolysaccharidosis VII) occurring in an elderly patient from an inbred kindredCHAPMAN, S; GRAY, R. G. F; CONSTABLE, T. J et al.British journal of radiology. 1989, Vol 62, Num 737, pp 491-494, issn 0007-1285, 4 p.Article

The mucopolysaccharidoses: a study of 48 casesKAGALWALA, T. Y; BHARUCHA, B. A; KUMTA, N. B et al.Indian journal of pediatrics. 1988, Vol 55, Num 6, pp 919-925, issn 0019-5456Article

The mucopolysaccharidoses and related conditionsEGGLI, K. D; DORSI, J. P.Seminars in roentgenology. 1986, Vol 21, Num 4, pp 275-294, issn 0037-198XArticle

Amniotic tissue transplantation as a trial of treatment in some lysosomal storage diseasesTYLKI-SZYMANSKA, A; MACIEJKO, D; KIDAWA, M et al.Journal of inherited metabolic disease. 1985, Vol 8, Num 3, pp 101-104, issn 0141-8955Article

A case of genetic abnormality, Hunter syndromeUMA SHANKAR PRASAD.Indian Medical Journal. 1991, Vol 85, Num 1, issn 0019-5871, p. 13Article

Ocular symptoms and histopathology in mucopolysaccharidosesSUVEGES, I.Bulletin de la Société belge d'ophtalmologie. 1987, Vol 224, pp 23-25, issn 0081-0746Article

Hunter syndrome (mucopolysaccharidosis II)FINLAYSON, L. A.Pediatric dermatology. 1990, Vol 7, Num 2, pp 150-152, issn 0736-8046, 3 p.Article

Enzyme Replacement Therapy in an Attenuated Case of Mucopolysaccharidosis Type I (Scheie Syndrome): A 6.5-Year Detailed Follow-UpJURECKA, Agnieszka; MARUCHA, Jolanta; JURKIEWICZ, Elżbieta et al.Pediatric neurology. 2012, Vol 47, Num 6, pp 461-465, issn 0887-8994, 5 p.Article

Mucopolysaccharides type I subtypes: presence of immunologically cross-reactive material and in vitro enhancement of the residual α-L-iduronidase activitiesSCHUCHMAN, E. H; DESNICK, R. J.The Journal of clinical investigation. 1988, Vol 81, Num 1, pp 98-105, issn 0021-9738Article

Airway obstruction and sleep apnea in Hurler and Hunter syndromesSHAPIRO, J; STROME, M; CROCKER, A. C et al.The Annals of otology, rhinology & laryngology. 1985, Vol 94, Num 5, pp 458-461, issn 0003-4894Article

Sub-pleural bullous changes in two adults with Mucopolysaccharidosis type I (Hurler-Scheie)TCHAN, Michel C; GRAF, Nicole; SILLENCE, David O et al.Journal of inherited metabolic disease. 2011, Vol 34, Num 2, pp 547-548, issn 0141-8955, 2 p.Article

Intrafamilial variability in Hurler syndrome and Sanfilippo syndrome type A : implications for evaluation of new therapiesMCDOWELL, G. A; COWAN, T. M; BLITZER, M. G et al.American journal of medical genetics. 1993, Vol 47, Num 7, pp 1092-1095, issn 0148-7299Article

Hurler-Scheie phenotype associated with consanguinityDAVIES, D. L; DUTTON, G. N; FARQUHARSON, J et al.Journal of inherited metabolic disease. 1989, Vol 12, pp 365-368, issn 0141-8955, suppl. 2Article

MR Imaging of cavity lesions in the brain with Hurler/ScheieRAUCH, R. A; FRILOUX, L. A. III; LOTT, I. T et al.American journal of neuroradiology. 1989, Vol 10, Num 5, pp S1-S3, issn 0195-6108, supplArticle

Sanfilippo disease in GreeceBERATIS, N. G; SKLOWER, S. L; WILBUR, L et al.Clinical genetics. 1986, Vol 29, Num 2, pp 129-132, issn 0009-9163Article

An unusually mild variant of Hunter's syndrome in a 14-year-old boy: normal growth and developmentTSUZAKI, S; MATSUO, N; NAGAI, T et al.Acta paediatrica scandinavica. 1987, Vol 76, Num 5, pp 844-846, issn 0001-656XArticle