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

A CUTANEOUS MARKER IN THE HUNTER SYNDROME. A REPORT OF FOUR CASES.PRYSTOWSKY SD; MAUMENEE IH; FREEMAN RG et al.1977; ARCH. DERMATOL.; U.S.A.; DA. 1977; VOL. 113; NO 5; PP. 602-605; BIBL. 15 REF.Article

MUCOPOLYSACCHARIDOSIS II (HUNTER DISEASE) WITH CORNEAL OPACITIES: REPORT ON TWO PATIENTS AT THE EXTREMES OF A WIDE CLINICAL SPECTRUM.SPRANGER J; CANTZ M; GEHLER J et al.1978; EUROP. J. PEDIATR.; DEU; DA. 1978; VOL. 129; NO 1; PP. 11-16; BIBL. 17 REF.Article

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

DETECTION OF HUNTER HETEROZYGOTES BY ENZYMATIC ANALYSIS OF HAIR ROOTSNWOKORO N; NEUFELD EF.1979; AMER. J. HUM. GENET.; USA; DA. 1979; VOL. 31; NO 1; PP. 42-49; BIBL. 26 REF.Article

ENZYME REPLACEMENT THERAPY BY FIBROBLAST TRANSPLANTATION: LONG-TERM BIOCHEMICAL STUDY IN THREE CASES OF HUNTER'S SYNDROMEDEAN MF; STEVENS RL; MUIR H et al.1979; J. CLIN. INVEST.; USA; DA. 1979; VOL. 63; NO 1; PP. 138-146; BIBL. 44 REF.Article

IDORUNATE SULFATASE ANALYSIS OF HAIR ROOTS FOR IDENTIFICATION OF HUNTER SYNDROME HETEROZYGOTESYUTAKA T; FLUHARTY AL; STEVENS RL et al.1978; AMER. J. HUM. GENET.; USA; DA. 1978; VOL. 30; NO 6; PP. 575-582; BIBL. 20 REF.Article

X-LINKED HUNTER SYNDROME: THE HETEROZYGOUS PHENOTYPE IN CELL CULTURE.MIGEON BR; SPRENKLE JA; LIEBAERS I et al.1977; AMER. J. HUM. GENET.; U.S.A.; DA. 1977; VOL. 29; NO 5; PP. 448-454; BIBL. 17 REF.Article

CLINICAL HETEROGENEITY IN MUCOPOLYSACCHARIDOSIS. II. EVIDENCE FOR EPISTASIS.THURMON TF; DEFRAITES EB; ANDERSON EE et al.1974; BIRTH DEFECTS ORIGIN ARTICLE SER.; U.S.A.; DA. 1974; VOL. 10; NO 8; PP. 125-127; BIBL. 3 REF.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

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

PSYCHOSOCIAL PROBLEMS IN HUNTER'S SYNDROMEHOUNG LD; HARPER PS.1981; CHILD CARE HEALTH DEV.; ISSN 0305-1862; GBR; DA. 1981; VOL. 7; NO 4; PP. 201-209; BIBL. 7 REF.Article

LA DIAGNOSI DI MALATTIA DI HUNTER. STUDIO ENZIMATICO. = LE DIAGNOSTIC DE MALADIE DE HUNTER. ETUDE ENZYMATIQUESCHIAVULLI E; LOFFREDO L; VECCHIO L et al.1977; MINERVA PEDIATR.; ITAL.; DA. 1977; VOL. 29; NO 32; PP. 1937-1946; ABS. ANGL.; BIBL. 33 REF.Article

HYDROCEPHALUS IN HUNTER SYNDROMEVAN AERDE J; PLETS C; VAN DER HAUWAERT L et al.1981; ACTA PAEDIATR. BELG.; ISSN 0001-6535; BEL; DA. 1981; VOL. 34; NO 2; PP. 93-96; BIBL. 13 REF.Article

CYTOCHEMISTRY OF THE SKIN OF PATIENTS WITH MUCOPOLYSACCHARIDOSES.SPICER SS; GARVIN AJ; SIMSON JAV et al.1978; HISTOCHEM. J.; GBR; DA. 1978; VOL. 10; NO 2; PP. 137-150; BIBL. 1 P. 1/2Article

DIAGNOSIS OF HUNTER'S SYNDROME CARRIERS; RADIOACTIVE SULPHATE INCORPORATION INTO FIBROBLASTS IN THE PRESENCE OF FRUCTOSE 1-PHOSPHATETONNESEN T; LYKKELUND C; GUETTLER F et al.1982; HUM. GENET.; ISSN 0340-6717; DEU; DA. 1982; VOL. 60; NO 2; PP. 167-171; BIBL. 35 REF.Article

CHEMISTRY OF HEPARITIN SULFATE AND HEPARIN FROM NORMAL TISSUES AND FROM PATIENTS WITH HUNTER SYNDROMENADER HB; COHEN DM; DIETRICH CP et al.1979; BIOCHIM. BIOPHYS. ACTA; NLD; DA. 1979; VOL. 582; NO 1; PP. 33-43; BIBL. 21 REF.Article

A SUBSTRATE FOR DIRECT MEASUREMENT OF L-IDURONIC ACID 2-SULFATE SULFATASE.GINSBERG LC; DI FERRANTE DT; DI FERRANTE N et al.1978; CARBOHYD. RES.; NLD; DA. 1978; VOL. 64; PP. 225-235; BIBL. 13 REF.Article

DETECTION OF FEMALE CARRIERS OF HUNTER'S SYNDROME: COMPARISON OF SERUM AND HAIR-ROOT ANALYSISARCHER IM; REES DW; OLADIMEJI A et al.1982; J. INHERIT. METAB. DIS.; ISSN 0141-8955; GBR; DA. 1982; VOL. 5; SUPPL. 1; PP. 15-16; BIBL. 2 REF.Article

INCIDENCE OF HUNTER'S SYNDROMEYOUNG ID; HARPER PS.1982; HUM. GENET.; ISSN 0340-6717; DEU; DA. 1982; VOL. 60; NO 4; PP. 391-392; BIBL. 4 REF.Article

PROCEDERES DIAGNOSTICOS EN LAS MUCOPOLISACARIDOSIS = METHODES DIAGNOSTIQUES DES MUCOPOLYSACCHARIDOSESDOMENECH E; COLOMER J; MOYA M et al.1980; MED. ESP.; ESP; DA. 1980; VOL. 79; NO 465; PP. 105-115; ABS. ENG; BIBL. 18 REF.Article

PAPULOSE SOUS-SCAPULAIRE SYSTEMATISEE AVEC CORPS ANHISTES EN MICROSCOPIE ELECTRONIQUE: SIGNES CUTANES SPECIFIQUES DE LA MALADIE DE HUNTER.LARREGUE M; DEBRAY H; PERE C et al.1978; ANN. DERMATOL. VENEREOL.; FR.; DA. 1978; VOL. 105; NO 1; PP. 57-63; ABS. ANGL.; BIBL. 31 REF.Article

IDURONATE SULFATASE IN AMNIOTIC FLUID: AN AID IN THE PRENATAL DIAGNOSIS OF THE HUNTER SYNDROME.LIEBAERS I; DI NATALE P; NEUFELD EF et al.1977; J. PEDIATR.; U.S.A.; DA. 1977; VOL. 90; NO 3; PP. 423-425; BIBL. 10 REF.Article

PAPILLOEDEMA IN ASSOCIATION WITH HUNTER'S SYNDROMEBECK M.1983; BRITISH JOURNAL OF OPHTHALMOLOGY; ISSN 0007-1161; GBR; DA. 1983; VOL. 67; NO 3; PP. 174-177; BIBL. 13 REF.Article

GLYCOSAMINOGLYCAN IN THE SKIN AND URINE OF A HUNTER SYNDROME PATIENT WITH A SPECIFIC SKIN LESIONNAKAMURA T; NISHIDA K; MATSUDA K et al.1981; J. DERMATOL.; ISSN 0385-2407; JPN; DA. 1981; VOL. 8; NO 6; PP. 447-453; BIBL. 20 REF.Article