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

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

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

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

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

Diagnosis of mucopolysaccharidoses using ¹H-n.m.r. spectroscopy of glycosaminoglycansSAVAGE, A. V; APPLEGARTH, D. A.Carbohydrate research. 1986, Vol 149, Num 2, pp 471-474, issn 0008-6215Conference Paper

Les mobilisations articulaires dans les mucopolysaccharidoses = Articular mobilization in mucopolysaccharidosisMULIER, C; GUFFON, N.Kinésithérapie scientifique. 1997, Num 367, pp 2-3, issn 0023-1576, 9 p.Article

Etude des mucopolysaccharidoses: à propos de 17 familles groupant 25 observations = A study of mucopolysaccharidosis concerning 17 families presenting 25 casesTRABELSI, M; BEN DRIDI, M. F; GHARBI, H. A et al.Tunisie médicale. 1986, Vol 64, Num 1, pp 49-56, issn 0041-4131Article

Hurler's syndrome. A case studyWORMINGTON, J.British orthoptic journal. 1986, Num 43, pp 76-79, issn 0068-2314Article

The suramin-treated rat as a model of mucopolysaccharidosis: variation in the reversibility of biochemical and morphological changes among different organsREES, S; CONSTANTOPOULOS, G; BRADY, R. O et al.Virchows Archiv. A, Pathological anatomy and histopathology. 1986, Vol 52, Num 3, pp 259-272, issn 0174-7398Article

Histopathological studies of the temporal bones in Hurler's disease [mucopolysaccharidosis (MPS) IH]FRIEDMANN, I; SPELLACY, E; CROW, J et al.Journal of laryngology and otology. 1985, Vol 99, Num 1, pp 29-41, issn 0022-2151Article

Multiple polymorphisms within the α-L-iduronidase gene (IDUA): implications for a role in modification of MPS-I disease phenotypeSCOTT, H. S; NELSON, P. V; LITJENS, T et al.Human molecular genetics (Print). 1993, Vol 2, Num 9, pp 1471-1473, issn 0964-6906Article

Children with mucopolysaccharidosis : perioperative care, morbility, mortality, and new findings. DiscussionBELANI, K. G; KRIVIT, W; WHITLEY, C. B et al.BELANI, K. G; Journal of pediatric surgery. 1993, Vol 28, Num 3, pp 403-410, issn 0022-3468Conference Paper