HUNTER'S SYNDROME AND COOLEY'S ANAEMIA IN THE SAME PATIENT = SYNDROME DE HUNTER ET ANEMIE DE COOLEY CHEZ LE MEME MALADEBARTSOCAS CS; PAPASOTIRIOU N; KARAGEORGA M et al.1973; ACTA PAEDIATR. SCAND.; SUEDE; DA. 1973; VOL. 62; NO 1; PP. 66-68; BIBL. 5 REF.Serial Issue

UN CAS DE MUCOPOLYSACCHARIDOSE II - SYNDROME DE HUNTERWALCZAK M; PAWLACZYK B; SIODA T et al.1976; PEDIATR. POLSKA; POLSKA; DA. 1976; VOL. 51; NO 1; PP. 77-80; BIBL. 20 REF.Article

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SEPARATION OF DERMATAN SULFATE FROM HEPARAN SULFATE IN MUCOPOLYSACCHARIDOSIS URINE BY CHROMATOGRAPHY ON SEPHADEX G-75HERD JK; FORREST T; TSCHIDA J et al.1976; CLIN. CHIM. ACTA; PAYS-BAS; DA. 1976; VOL. 68; NO 1; PP. 1-9; BIBL. 23 REF.Article

INEFFICACY OF FRESH FROZEN PLASMA THERAPY OF MUCOPOLYSACCHARIDOSIS II = INEFFICACITE DU TRAITEMENT DE LA MUCOPOLYSACCHARIDOSE II PAR LE PLASMA FRAIS CONGELEERICKSON RP; SANDMAN R; ROBERTSON WV et al.1972; PEDIATRICS; U.S.A.; DA. 1972; VOL. 50; NO 5; PP. 693-701; BIBL. 1P.Serial Issue

COMPARATIVE STRUCTURAL STUDIES OF URINARY GLYCOSAMINOGLYCANS IN THE HURLER AND HUNTER SYNDROMES.RAMAGE P; CUNNINGHAM WL.1975; BIOCHIM. BIOPHYS. ACTA; PAYS-BAS; DA. 1975; VOL. 411; NO 2; PP. 325-333; BIBL. 36 REF.Article

CLINICAL AND PROBABLE GENETIC HETEROGENEITY WITHIN MUCOPOLYSACCHARIDOSIS II. REPORT OF A FAMILY WITH A MILD FORM = HETEROGENEITE CLINIQUE ET PROBABLEMENT GENETIQUE DANS LES MUCOPOLYSACCHARIDOSES II. ETUDE D'UNE FAMILLE PRESENTANT UNE FORME BENIGNELICHTENSTEIN JR; BILBREY GL; MCKUSICK VA et al.1972; JOHNSHOPKINS MED. J.; U.S.A.; DA. 1972; VOL. 131; NO 6; PP. 425-435; BIBL. 1P.1/2Serial Issue

RELIABILITY OF THE BOOTH-NADLER TECHNIQUE FOR THE DETECTION OF HUNTER HETEROZYGOTES = FIABILITE DE LA TECHNIQUE DE BOOTH-NADLER POUR LA DETECTION DES HETEROZYGOTES DU HUNTERDONNELLY PV; DI FERRANTE N.1975; PEDIATRICS; U.S.A.; DA. 1975; VOL. 56; NO 3; PP. 429-433; BIBL. 7 REF.Article

MULTIPLE PERIPHERAL NERVE ENTRAPMENTS. AN UNUSUAL PHENOTYPICAL VARIANT OF THE HUNTER SYNDROME (MUCOPOLYSACCHARIDOSIS II) IN A FAMILY = COMPRESSIONS MULTIPLES DE NERFS PERIPHERIQUES. VARIANTE PHENOTYPIQUE RARE DU SYNDROME DE HUNTER FAMILIAL (MUCOPOLYSACCHARIDOSE DU TYPE II)KARPATI G; CARPENTER S; EISEN AA et al.1974; ARCH. NEUROL.; U.S.A.; DA. 1974; VOL. 31; NO 6; PP. 418-422; BIBL. 20REF.Article

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

THE HUNTER CORRECTIVE FACTOR: PURIFICATION AND PRELIMINARY CHARACTERIZATIONCANTZ M; CHRAMBACH A; BACH G et al.1972; J. BIOL. CHEM.; U.S.A.; DA. 1972; VOL. 247; NO 17; PP. 5456-5462; BIBL. 29REF.Serial Issue

LA MALADIE DE HUNTER. ( A PROPOS D'UNE OBSERVATION)FEMEL BURGAN SONIA.1980; ; FRA; DA. 1980; 24; 131-XVIII P.: ILL.; 30 CM; BIBL. 142 REF.; TH.: MED./ROUEN/1980Thesis

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COMMUNICATING HYDROCEPHALUS IN CHILDREN WITH GENETIC IN BORN ERRORS OF METABOLISM = HYDROCEPHALIE COMMUNICANTE CHEZ LES ENFANTS AVEC ERREURS INNEES DU METABOLISMEFOWLER GW; SUKOFF M; HAMILTON A et al.1975; CHILD'S BRAIN; SWITZ.; DA. 1975; VOL. 1; NO 4; PP. 251-254; BIBL. 10 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

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

GARGOYLISM IN A CHINESE BOY = GARGOILISME CHEZ UN GARCON CHINOISMING TSO TSUANG; HSIN YIH CHANG; ENG KUNG YEH et al.1970; J. MED. GENET.; G.B.; DA. 1970; VOL. 7; NO 4; PP. 422-425; BIBL. 5 REF.Serial Issue

Carrier detection in Hunter syndromeARCHER, I. M; YOUNG, I. D; REES, D. W et al.American journal of medical genetics. 1983, Vol 16, Num 1, pp 61-69, issn 0148-7299Article

MUCOPOLYSACCHARIDOSIS TYPE V (SCHEIE SYNDROME). A POSTMORTEM STUDY BY MULTIDISCIPLINARY TECHNIQUES WITH EMPHASIS ON THE BRAINDEKABAN AS; CONSTANTOPOULOS G; HERMAN MM et al.1976; ARCH. PATHOL. LAB. MED.; U.S.A.; DA. 1976; VOL. 100; NO 5; PP. 237-245; BIBL. 25 REF.Article

THE DIAGNOSIS OF MUCOPOLYSACCHARIDOSES BY ELECTRON MICROSCOPY OF SKIN BIOPSIESBIOULAC P; MERCIER M; BEYLOT C et al.1975; J. CUTAN. PATHOL.; DENM.; DA. 1975; VOL. 2; NO 4; PP. 179-190; BIBL. 1 P.Article

THE GENETIC MUCOPOLYSACCHARIDOSES (GMS) = LES MUCOPOLYSACCHARIDOSES GENETIQUES (GMS)HAUST MD.1973; INTERNATION. REV. EXPER. PATHOL.; U.S.A.; DA. 1973; VOL. 12; PP. 251-314; BIBL. 7P.1/2Serial Issue

AN IMPROVED ASSAY FOR IDURONATE 2-SULPHATE SULPHATASE IN SERUM AND ITS USE IN THE DETECTION OF CARRIERS OF THE HUNTER SYNDROMEARCHER IM; HARPER PS; WUSTEMAN FS et al.1981; CLIN. CHIM. ACTA; ISSN 0009-8981; NLD; DA. 1981; VOL. 112; NO 1; PP. 107-112; BIBL. 9 REF.Article

INCREASED BREAKDOWN OF GLYCOSAMINOGLYCANS AND APPEARANCE OF CORRECTIVE ENZYME AFTER SKIN TRANSPLANTS IN HUNTER SYNDROME = AUGMENTATION DE LA DEGRADATION DES GLYCOSAMINOGLYCANES ET APPARITION D'ENZYME CORRECTIVE APRES TRANSPLANTS DE PEAU DANS LE SYNDROME DE HUNTERDEAN MF; MUIR H; BENSON PF et al.1975; NATURE; G.B.; DA. 1975; VOL. 257; NO 5527; PP. 609-612; BIBL. 16 REF.Article

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