ABOVE-NORMAL URINARY EXCRETION OF URINARY CERAMIDES IN FARBER'S DISEASE, AND CHARACTERIZATION OF THEIR COMPONENTS BY HIGH-PERFORMANCE LIQUID CHROMATOGRAPHY = EXCRETION URINAIRE SUPERIEURE A LA NORMALE DE CERAMIDES URINAIRES DANS LA MALADIE DE FARBER ET CARACTERISATION DE LEURS COMPOSANTES PAR CHROMATOGRAPHIE DE PHASE LIQUIDE DE RESOLUTION ELEVEEIWAMORI M; MOSER HW.1975; CLIN. CHEM.; U.S.A.; DA. 1975; VOL. 21; NO 6; PP. 725-729; BIBL. 23REF.Article

ANALYSIS AND QUANTITATION OF FREE CERAMIDE CONTAINING NONHYDROXY AND 2-HYDROXY FATTY ACIDS, AND PHYTOSPHINGOSINE BY HIGH-PERFORMANCE LIQUID CHROMATOGRAPHYIWAMORI M; COSTELLO C; MOSER HW et al.1979; J. LIPID RES.; USA; DA. 1979; VOL. 20; NO 1; PP. 86-96; BIBL. 32 REF.Article

SOLUBILIZATION AND PARTIAL PURIFICATION OF STEROID SULFATASE FROM RAT LIVER: CHARACTERIZATION OF ESTRONE SULFATASE.IWAMORI M; MOSER HW; KISHIMOTO Y et al.1976; ARCH. BIOCHEM. BIOPHYS.; U.S.A.; DA. 1976; VOL. 174; NO 1; PP. 199-208; BIBL. 25 REF.Article

FAMILIAL X-LINKED ADDISON DISEASE AS AN EXPRESSION OF ADRENOLEUKODYSTROPHY (ALD): ELEVATED C₂₆ FATTY ACID IN CULTURED SKIN FIBROBLASTSO'NEILL BP; MOSER HW; SAYENA KM et al.1982; NEUROLOGY; ISSN 0028-3878; USA; DA. 1982; VOL. 32; NO 5; PP. 543-547; BIBL. 17 REF.Article

STEROID SULFATASE IN BRAIN: COMPARISON OF SULFOHYDROLASE ACTIVITIES FOR VARIOUS STEROID SULFATES IN NORMAL AND PATHOLOGICAL BRAINS, INCLUDING THE VARIOUS FORMS OF METACHROMATIC LEUKODYSTROPHY.IWAMORI M; MOSER HW; KISHIMOTO Y et al.1976; J. NEUROCHEM.; G.B.; DA. 1976; VOL. 27; NO 6; PP. 1389-1395; BIBL. 16 REF.Article

ADRENOLEUKODYSTROPHY: ELEVATED C₂₆ FATTY ACID IN CULTURED SKIN FIBROBLASTS AND CORRELATION WITH DISEASE EXPRESSION IN THREE GENERATIONS OF A KINDREDO'NEILL BP; MOSER HW; MARMION LC et al.1982; NEUROLOGY; ISSN 0028-3878; USA; DA. 1982; VOL. 32; NO 5; PP. 540-542; BIBL. 19 REF.Article

VERY LONG CHAIN FATTY ACID OXIDATION IN RAT LIVERKAWAMURA N; MOSER HW; KISHIMOTO Y et al.1981; BIOCHEM. BIOPHYS. RES. COMMUN.; ISSN 0006-291X; USA; DA. 1981; VOL. 99; NO 4; PP. 1216-1225; BIBL. 13 REF.Article

DETECTION OF THE CARRIER STATE OF HURLER'S SYNDROME BY ASSAY OF ALPHA -L-IDURONIDASE IN LEUKOCYTES.DULANEY JT; MILUNSKY A; MOSER HW et al.1976; CLIN. CHIM. ACTA; PAYS-BAS; DA. 1976; VOL. 69; NO 2; PP. 305-310; BIBL. 16 REF.Article

SPECIFIC TRITIUM LABELING OF CEREBROSIDES AT THE 3-POSITIONS OF ERYTHRO-SPHINGOSINE AND THREO-SPHINGOSINE.IWAMORI M; MOSER HW; KISHIMOTO Y et al.1975; J. LIPID RES.; U.S.A.; DA. 1975; VOL. 16; NO 4; PP. 332-336; BIBL. 27 REF.Article

CERAMIDASE DEFICIENCY IN FARBER'S DISEASE (LIPOGRANULOMATOSIS) = DEFICIENCE EN CERAMIDASE DANS LA MALADIE DE FARBER (LIPOGRANULOMATOSE)SUGITA M; DULANEY JT; MOSER HW et al.1972; SCIENCE; U.S.A.; DA. 1972; VOL. 178; NO 4065; PP. 1100-1102; BIBL. 19REF.Serial Issue

CHOLESTEROL SULFATE IN RAT TISSUES. TISSUE DISTRIBUTION DEVELOPMENTAL CHANGE AND BRAIN SUBCELLULAR LOCALIZATION.IWAMORI M; MOSER HW; KISHIMOTO Y et al.1976; BIOCHIM. BIOPHYS. ACTA; PAYS-BAS; DA. 1976; VOL. 441; NO 2; PP. 268-279; BIBL. 41 REF.Article

DIRECT QUANTITATION OF GLYCOSAMINOGLYCANS IN 2 ML OF URINE FROM PATIENTS WITH MUCOPOLYSACCHARIDOSESBURLINGAME RW; THOMAS GH; STEVENS RL et al.1981; CLIN. CHEM.; ISSN 0009-9147; USA; DA. 1981; VOL. 27; NO 1; PP. 124-128; BIBL. 19 REF.Article

DIAGNOSIS OF LIPOGRANULOMATOSIS (FARBER DISEASE) BY USE OF CULTURED FIBROBLASTS. = DIAGNOSTIC DE LA LIPOGRANULOMATOSE OU MALADIE DE FARBER GRACE AUX CULTURES DE FIBROBLASTESDULANEY JT; MILUNSKY A; SIDBURY JB et al.1976; J. PEDIATR.; U.S.A.; DA. 1976; VOL. 89; NO 1; PP. 59-61; BIBL. 15 REF.Article

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

NEONATAL ADRENOLENKODYSTROPHY: CLINICAL, PATHOLOGIC, AND BIOCHEMICAL DELINEATION OF A SYNDROME AFFECTING BOTH MALES AND FEMALESJAFFE R; CRUMRINE P; HASHIDA Y et al.1982; AMERICAN JOURNAL OF PATHOLOGY (THE); ISSN 0002-9440; USA; DA. 1982; VOL. 108; NO 1; PP. 100-111; BIBL. 24 REF.Article

REVERSE PHASE HIGH-PERFORMANCE LIQUID CHROMATOGRAPHY OF CEREBROSIDES, SULFATIDES, AND CERAMIDES: MICROANALYSIS OF HOMOLOG COMPOSITION WITHOUT HYDROLYSIS AND APPLICATION TO CEREBROSIDE ANALYSIS IN PERIPHERAL NERVES OF ADRENOLEUKODYSTROPHY PATIENTSYAHARA S; MOSER HW; KOLODNY EH et al.1980; J. NEUROCHEM.; GBR; DA. 1980; VOL. 34; NO 3; PP. 694-699; BIBL. 17 REF.Article

APPARENT BIOCHEMICAL HOMOZYGOSITY IN TWO OBLIGATORY HETEROZYGOTES FOR METACHROMATIC LEUKODYSTROPHY.LOTT IT; DULANEY JT; MILUNSKY A et al.1976; J. PEDIATR.; U.S.A.; DA. 1976; VOL. 89; NO 3; PP. 438-440; BIBL. 10 REF.Article

CERAMIDASE AND CERAMIDE SYNTHESIS IN HUMAN KIDNEY AND CEREBELLUM. DESCRIPTION OF A NEW ALKALINE CERAMIDASE.SUGITA M; WILLIAMS M; DULANEY JT et al.1975; BIOCHIM. BIOPHYS. ACTA; PAYS-BAS; DA. 1975; VOL. 398; NO 1; PP. 125-131; BIBL. 18 REF.Article

VALUE OF C26: O FATTY ACID DETERMINATION FOR THE DIAGNOSIS OF ATYPICAL ADRENOLEUKODYSTROPHYPHILIPPART M; NUWER MR; MORTIER W et al.1982; ANN. NEUROL.; ISSN 0364-5134; USA; DA. 1982; VOL. 11; NO 1; PP. 105; BIBL. 3 REF.Article

3-KETOSPHINGOLIPIDS: APPLICATION TO THE DETERMINATION OF SPHINGOLIPIDS WHICH CONTAIN 4-SPHINGENINEIWAMORI M; MOSER HW; MCCLUER RH et al.1975; BIOCHIM. BIOPHYS. ACTA; PAYS-BAS; DA. 1975; VOL. 380; NO 2; PP. 308-319; BIBL. 30REF.Article

CATAPLEXY IN VARIANT FORMS OF NIEMANN-PICK DISEASEKANDR RS; EMERSON RG; SINGER HS et al.1982; ANN. NEUROL.; ISSN 0364-5134; USA; DA. 1982; VOL. 12; NO 3; PP. 285-288; BIBL. 26 REF.Article

FETAL ADRENOLEUKODYSTROPHY: THE SIGNIFICANCE OF PATHOLOGIC LESIONS IN ADRENAL GLAND AND TESTISPOWERS JM; MOSER HW; MOSER AB et al.1982; HUMAN PATHOLOGY; ISSN 0046-8177; USA; DA. 1982; VOL. 13; NO 11; PP. 1013-1019; BIBL. 39 REF.Article

ADRENOLEUKODYSTROPHY: IMPAIRED OXIDATION OF LONG CHAIN FATTY ACIDS IN CULTURED SKIN FIBROBLASTS AND ADRENAL CORTEXSINGH I; MOSER HW; MOSER AB et al.1981; BIOCHEM. BIOPHYS. RES. COMMUN.; ISSN 0006-291X; USA; DA. 1981; VOL. 102; NO 4; PP. 1223-1229; BIBL. 19 REF.Article

PLASMA EXCHANGE REMOVES GLYCOSPHINGOLIPID IN FABRY DISEASEPYERITZ RE; ULLMAN MD; MOSER AB et al.1980; AMER. J. MED. GENET.; USA; DA. 1980; VOL. 7; NO 3; PP. 301-307; BIBL. 16 REF.Article

IMPROVED THIN-LAYER CHROMATOGRAPHIC METHOD IN THE DIAGNOSIS OF MANNOSIDOSISFRIEDMANN RB; WILLIAMS MA; MOSER HW et al.1978; CLIN. CHEM.; USA; DA. 1978; VOL. 24; NO 9; PP. 1576-1577; BIBL. 9 REF.Article