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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

Anaesthetic implications of the mucopolysaccharidoses: a fifteen-year experience in a children's hospitalBAINES, D; KENEALLY, J.Anaesthesia and intensive care. 1983, Vol 11, Num 3, pp 198-202, issn 0310-057XArticle

Mucopolysaccharidosis VI (Maroteaux-Lamy syndrome)THOMAS, S; MENON, P. S. N; KHURANA, A et al.Indian pediatrics. 1983, Vol 20, Num 5, pp 378-380, issn 0019-6061Article

Decreased ganglioside neuraminidase activity in fibroblasts from Mucopolysaccharidosis patients: inhibition of the activity in vitro by sulfated glycosaminoglycans and other compoundsBAUMKÖTTER, J; CANTZ, M.Biochimica et biophysica acta. 1983, Vol 761, Num 2, pp 163-170, issn 0006-3002Article

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

Suramin-induced storage disease: MucopolysaccharidosisCONSTANTOPOULOS, G; REES, S; BARRANGER, J. A et al.The American journal of pathology. 1983, Vol 113, Num 2, pp 266-268, issn 0002-9440Article

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

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

FELINE MUCOPOLYSACCHARIDOSIS. VI: PURIFICATION AND CHARACTERIZATION OF THE RESIDUAL ARYLSULFATASE B ACTIVITYVINE DT; MCGOVERN MM; HASKINS ME et al.1981; AM. J. HUM. GENET.; ISSN 0002-9297; USA; DA. 1981; VOL. 33; NO 6; PP. 916-927; BIBL. 26 REF.Article

Apparent allelism of the Hurler, Scheie, and Hurler/Scheie syndromesMUELLER, O. T; SHOWS, T. B; OPITZ, J. M et al.American journal of medical genetics. 1984, Vol 18, Num 3, pp 547-556, issn 0148-7299Article

LES MUCOPOLYSACCHARIDOSES.GAJDOS A.1977; NOUV. PRESSE MED.; FR.; DA. 1977; VOL. 6; NO 20; PP. 1745-1752 (4P.); BIBL. 10 REF.Article

Feline mucopolysaccharidosis. VI: General ocular and pigment epithelial pathologyAGUIRRE, G; STRAMM, L; HASKINS, M et al.Investigative ophthalmology & visual science. 1983, Vol 24, Num 8, pp 991-1007, issn 0146-0404Article

HISTOCHEMICAL INVESTIGATION OF ACID MUCOPOLYSACCHARIDES IN AMYLOID, COLLOID AND HYALINESASAI Y; NAGATA M; INOKUCHI K et al.1978; ACTA HISTOCHEM.; DDR; DA. 1978; VOL. 62; NO 2; PP. 223-236; BIBL. 27 REF.Article

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

THE MUCOPOLYSACCHARIDOSES: CLINICAL AND BIOCHEMICAL CORRELATIONSMORWITZ AL.1979; AMER. J. MENTAL DEFIC.; USA; DA. 1979; VOL. 84; NO 2; PP. 113-123; BIBL. 3 P.Article

Animal models for mucopolysaccharidosis disorders and their clinical relevance. CommentaryBECK, Michael; WRAITH, Ed; HASKINS, Mark E et al.Acta paediatrica. Supplement. 2007, Vol 96, Num 455, issn 0803-5326, 55,56-77 [23 p.]Article

PHAENOTYP BEI HETEROGLYKANOSEN UND SPHINGOLIPIDOSEN = PHENOTYPES DES MUCOPOLYOSIDOSES HETEROGENES ET SPHINGOLIPIDOSESGEHLER J.1981; MONATSSCHR. KINDERHEILKD.; ISSN 0026-9298; DEU; DA. 1981; VOL. 129; NO 11; PP. 610-620; ABS. ENG; BIBL. 45 REF.Article

CORNEAL MANIFESTATIONS OF THE SYSTEMIC MUCOPOLYSACCHARIDOSESSUGAR J.1979; ANN. OPHTHALMOL.; USA; DA. 1979; VOL. 11; NO 4; PP. 531-535; BIBL. 13 REF.Article

MUKOPOLYSACCHARIDOSE. V. MORBUS ULLRICH-SCHEIE = MUCOPOLYSACCHARIDOSE. V. MALADIE DE MORBUS ULLRICH SCHEIEKOVARIK J; VORMITTAG W; GEBHART W et al.1978; WIEN. KLIN. WSCHR.; AUT; DA. 1978; VOL. 90; NO 23; PP. 839-844; ABS. ENG; BIBL. 21 REF.Article

THE MUCOPOLYSACCHARIDOSES.PENNOCK CA; BARNES IC.1976; J. MED. GENET.; G.B.; DA. 1976; VOL. 13; NO 3; PP. 169-181; BIBL. 3 P.Article

MUCOPOLYSACCHARIDOSIS WITH SPECIAL REFERENCE TO SCHEIE SYNDROME.HORIUCHI R; ISHIKAWA H; ISHII Y et al.1976; J. DERMATOL.; JAP.; DA. 1976; VOL. 3; NO 4; PP. 171-178; BIBL. 19 REF.Article

STUDIO ELETTRORETINOGRAFICO IN PAZIENTI AFFETTI DA MUCOPOLISACCARIDOSI. = ETUDE ELECTRORETINOGRAPHIQUE CHEZ DES MALADES ATTEINTS DE MUCOPOLYSACCHARIDOSEFUSCO G; ROMANO A; APPONI BATTINI G et al.1976; BOLL. OCULIST.; ITAL.; DA. 1976; VOL. 55; NO 7-8; PP. 195-203; ABS. FR. ANGL. ALLEM.; BIBL. 18 REF.Article

OBSERVATIONS ON HAIR SHAFT MORPHOLOGY IN MUCOPOLYSACCHARIDOSESTESCHLER NICOLA M; KILLIAN W.1982; J. MENT. DEFIC. RES.; ISSN 0022-264X; GBR; DA. 1982; VOL. 26; NO 3; PP. 193-202; BIBL. 16 REF.Article

PRESENT STATUS OF TREATMENT OF THE MUCOPOLYSACCHARIDOSES.CROCKER AC.1974; BIRTH DEFECTS ORIGIN ARTICLE SER.; U.S.A.; DA. 1974; VOL. 10; NO 8; PP. 113-124; BIBL. 1 P. 1/2Article

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