ASPECTS RADIOLOGIQUES DE LA MALADIE DE HURLERBOUDOU A; COTONI P; PLEYBER JY et al.1973; J. RADIOL. ELECTROL. MED. NUCL.; FR.; DA. 1973; VOL. 54; NO 4; PP. 349Serial Issue

PLASMA INFUSIONS IN AN INFANT WITH HURLER'S SYNDROME = PERFUSIONS DE PLASMA CHEZ UN NOURRISSON ATTEINT D'UN SYNDROME DE HURLERBOOTH CW; NADLER HL.1973; J. PEDIATR.; U.S.A.; DA. 1973; VOL. 82; NO 2; PP. 273-278; BIBL. 18REF.Serial Issue

ASPECTS RADIOLOGIQUES DE LA MALADIE DE HURLERBOUDOU A; COTONI P; PLEYBER JY et al.sdJ. RADIOL. ELECTROL. MED. NUCL.; FR.; DA. 197; VOL. 54; NO 4; PP. 349Serial Issue

THE HURLER SYNDROME: A STUDY OF CULTURED LYMPHOID CELL LINES = LE SYNDROME DE HURLER: UNE ETUDE DE LIGNEES DE CELLULES LYMPHOIDES CULTIVEESDANES BS; HUETTEROTH TH; CLEVE H et al.1972; J. EXPER. MED.; U.S.A.; DA. 1972; VOL. 136; NO 3; PP. 644-649; BIBL. 1P.Serial Issue

AN ULTRASTRUCTURAL COMPARISON OF NORMAL AND HURLER SYNDROME DERMAL FIBROBLATS = UNE COMPARAISON D'ULTRASTRUCTURE DES FIBROBLASTES DERMIQUES NORMAUX ET DU SYNDROME DE HURLERCONRAD GW; SHERMAN D; DORFMAN A et al.1972; PEDIATR. RES.; SWITZ.; DA. 1972; VOL. 6; NO 6; PP. 563-575; BIBL. 1P.Serial Issue

MUCOPOLYSACCHARIDOSES. RELATION OF ELEVATED CEREBRAL SPINAL FLUID TO MENTAL RETARDATION = MUCOPOLYSACCHARIDOSES: RELATION ENTRE TAUX ELEVES DANS LE LCR ET RETARD MENTALDEKABAN AS; CONSTANTOPOULOS G.1973; ARCH. NEUROL.; U.S.A.; DA. 1973; VOL. 28; NO 6; PP. 385-388; BIBL. 25 REF.Article

IN VITRO CORRECTION OF HURLER FIBROBLASTS WITH BOVINE TESTICULAR HYALURONIDASEHERD JK; HAYHOME BA; TSCHIDA J et al.1976; PROC. SOC. EXPER. BIOL. MED.; U.S.A.; DA. 1976; VOL. 151; NO 4; PP. 642-649; BIBL. 21 REF.Article

ALPHA -L-IDURONIDASE-AKTIVITAET IN FIBROBLASTEN VON PATIENTEN MIT HURLER-SYNDROM. = L'ACTIVITE DE LA ALPHA -U6-IDURONIDASE DANS LES FIBROBLASTES DE MALADES AYANT UN SYNDROME DE HURLERSTAREPRAWO G; GRIMM U; MACHILL G et al.1975; ACTA BIOL. MED. GERM.; ALLEM.; DA. 1975; VOL. 34; NO 6; PP. 1079-1082; BIBL. 9 REF.Article

ULTRASTRUCTURE OF METACHROMATIC FIROBLASTS = ULTRASTRUCTURE DES FIBROBLASTES METACHROMATIQUESTENCONI R; BACCICHETTI C; SARTOURI E et al.1972; AMER. J. DIS. CHILD.; U.S.A.; DA. 1972; VOL. 124; NO 2; PP. 296-297; BIBL. 4 REF.Serial Issue

THE USE OF ALPHA -L-IDURONIDASE ACTIVITY DETERMINATIONS IN LEUCOCYTES FOR THE DETECTION OF HURLER AND SCHEIE SYNDROMES = UTILISATION DU DOSAGE DE L'ACTIVITE ALPHA -L-IDURONIDASIQUE DES LEUCOCYTES POUR LA DETECTION DES SYNDROMES DE HURLER ET DE SCHEIELIEM KO; HOOGHWINKEL GJM.1975; CLIN. CHIM. ACTA; U.S.A.; DA. 1975; VOL. 60; NO 2; PP. 259-262; BIBL. 12REF.Article

THE HURLER SYNDROME: TREATMENT OF CULTURED HURLER FIBROBLASTS WITH NORMAL HUMAN SERUM. = SYNDROME DE HURLER: TRAITEMENT DES FIBROBLASTES DE HURLER CULTIVES PAR DU SERUM HUMAIN NORMALHERD JK; HAYHOME B; TSCHIDA J et al.1975; PROC. SOC. EXPER. BIOL. MED.; U.S.A.; DA. 1975; VOL. 150; NO 1; PP. 194-201; BIBL. 27 REF.Article

ACCUMULATION OF SULFATE-CONTAINING ACID MUCOPOLYSACCHARIDES IN I-CELL FIBROBLASTS. = ACCUMULATION DE MUCOPOLYSACCHARIDES ACIDES SULFATES DANS LES CELLULES FIBROBLASTIQUES ISCHMICKEL RD; DISTLER JJ; JOURDIAN GW et al.1975; J. LAB. CLIN. MED.; U.S.A.; DA. 1975; VOL. 86; NO 4; PP. 672-682; BIBL. 31 REF.Article

THE ULTRASTRUCTURE OF THE SKIN IN PATIENTS WITH MUCOPOLYSACCHARIDOSES = L'ULTRASTRUCTURE DE LA PEAU DES SUJETS ATTEINTS DE MUCOPOLYSACCHARIDOSESSPICER SS; GARVIN AJ; WOHLTMANN HJ et al.1974; LAB. INVEST.; U.S.A.; DA. 1974; VOL. 31; NO 5; PP. 488-501; BIBL. 42REF.Article

BIOCHEMICAL STUDIES ON THE SULPHATED GLUCOSAMINOGLYCAN FRACTION OF SKIN FIBROBLASTS CULTURED FROM A PATIENT WITH THE HURLER SYNDROMEGERMINARIO RJ; KAHLENBERG A; PINSKY L et al.1973; BIOCHEM. J.; G.B.; DA. 1973; VOL. 132; NO 3; PP. 395-402; BIBL. 34 REF.Serial Issue

EFFECTS OF FRESH PLASMA OR WHOLE BLOOD TRANSFIONS ON PATIENTS WITH VARIOUS TYPES OF MUCOPOLYSACCHARIDOSIS = EFFETS DES TRANSFUSIONS DE PLASMA FRAIS OU DE SANG TOTAL SUR LES MALADES ATTEINTS DE DIVERS TYPES DE MUCOPOLYSACCHARIDOSEDEKABAN AS; HOLDEN KR; CONSTANTOPOULOS G et al.1972; PEDIATRICS; U.S.A.; DA. 1972; VOL. 50; NO 5; PP. 688-692; BIBL. 12REF.Serial Issue

SIMPLIFIED ASSAY METHOD OF ALPHA -L-IDURONIDASE ACTIVITY IN LEUCOCYTES FOR DETECTION OF HURLER SYNDROME AND ITS CORRIERS.MOMOI T; SUDO M; TANIOKA K et al.1977; CLIN. CHIM. ACTA; PAYS-BAS; DA. 1977; VOL. 81; NO 3; PP. 311-313; BIBL. 10 REF.Article

THE IDURONIDASE-DEFICIENT MUCOPOLYSACCHARIDOSES: CLINICAL AND ROENTGENOGRAPHIC FEATURESSTEVENSON RE; HOWELL RR; MCKUSICK VA et al.1976; PEDIATRICS; U.S.A.; DA. 1976; VOL. 57; NO 1; PP. 111-122; BIBL. 10 REF.Article

MOLECULAR SIZE DIFFERENCE OF URINARY HEPARAN SULFATES FROM NORMAL INDIVIDUALS AND GENETIC MUCOPOLY-SACCHARIDOSES. = DIFFERENCE DE DIAMETRE MOLECULAIRE DES SULFATES D'HEPARANE URINAIRES DES SUJETS NORMAUX ET DES MUCOPOLYSACCHARIDOSES GENETIQUESTANIGUCHI N; MIYAWAKI T; MORIYA N et al.1975; CLIN. CHIM. ACTA; PAYS-BAS; DA. 1975; VOL. 60; NO 3; PP. 363-369; BIBL. 23 REF.Article

DEUX CAS DE MALADIE DE HURLER AVEC GLAUCOME CONGENITALSTERGAR S.1974; AN. KLIN. BOLNICE DR M. STOJANOVIC; JUGOSL.; DA. 1974; VOL. 13; NO 1-2; PP. 122-125; ABS. ANGL.; BIBL. 11REF.Article

SU DI UN CASO DI MUCOPOLISACCARIDOSI CLINICAMENTE ATIPICA, EPATO-SPLENOMEGALICA CON GRAVE PATIMENTO EMATOLOGICO, AD INSORGENZA IN ETA NEONATALE = SUR UN CAS DE MICROPOLYSACCHARIDOSE CLINIQUEMENT ATYPIQUE, AVEC HEPATO-SPLENOMEGALIE, AVEC ATTEINTE HEMATOLOGIQUE GRAVE, APPARUE CHEZ UN NOUVEAU-NEDEGLI ESPOSTI A; FAVERO A.1972; CLIN. PEDIATR.; ITAL.; DA. 1972; VOL. 54; NO 1; PP. 3-26; ABS. FR. ANGL. ALLEM. ESP.; BIBL. 1P.1/2Serial Issue

REVERSAL OF CLINICAL FEATURES OF HURLER'S DISEASE AND BIOCHEMICAL IMPROVEMENT AFTER TREATMENT BY BONE MARROW TRANSPLANTATIONHOBBS JR; JONES KH; BARRETT AJ et al.1982; J. INHERIT. METAB. DIS.; ISSN 0141-8955; GBR; DA. 1982; VOL. 5; SUPPL. 1; PP. 59-60; BIBL. 10 REF.Article

ACUTE MYELOGENOUS LEUKAEMIA IN HURLER' SYNDROME.CHEN KTK; MCKENNA RW; DESNICK RJ et al.1978; J. MED. GENET.; GBR; DA. 1978; VOL. 15; NO 3; PP. 239-242; BIBL. 13 REF.Article

TREATMENT OF MUCOPOLYSACCHARIDOSESHUSSELS IE; EIKMAN EA; KENYON KR et al.1974; BIRTH DEFECTS ORIGIN. ARTICLE SER.; U.S.A.; DA. 1974; VOL. 10; NO 12; PP. 212-225; BIBL. 17 REF.Article

SERUM DEPENDENCY OF CELLULAR PHENOTYPE IN MUCOPOLYSACCHARIDOSES: THE INFLUENCE OF AUTOLOGOUS SERUM ON METACHROMASIA = DEPENDANCE VIS-A-VIS DU SERUM DU PHENOTYPE CELLULAIRE DES MUCOPOLYSACCHARIDOSES: INFLUENCE DU SERUM AUTOLOGUE SUR LA METACHROMASIETEN KATE LP; ANDERS GJPA; DE GROOT CJ et al.1973; HUMANGENETIK; DTSCH.; DA. 1973; VOL. 18; NO 1; PP. 95-98; ABS. ALLEM.; BIBL. 10 REF.Serial Issue

THE DISORDER OF HYALURONIC ACID METABOLISM IN CULTURED SKIN FIBROBLASTS DERIVED FROM A PATIENT WITH THE HURLER SYNDROMEGERMINARIO RJ; KAHLENBERG A; PINSKY L et al.1973; BIOCHEM. J.; G.B.; DA. 1973; VOL. 132; NO 3; PP. 403-408; BIBL. 15REF.Serial Issue