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au.\*:("WADMAN SK")

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LANTHIONINE DETECTED IN HUMAN URINE.WADMAN SK; DE BREE PK; KAMERLING JP et al.1978; CLIN. CHIM. ACTA; PAYS-BAS; DA. 1978; VOL. 82; NO 3; PP. 281-284; BIBL. 13 REF.Article

EXCRETION OF CIS- AND TRANS-HYDROXYCYCLOHEXYLACETIC ACID IN ADDITION TO HAWKINSIN IN A FAMILY WITH A POSTULATED DEFECT OF 4-HYDROXYPHENYLPYRUVATE DIOXYGENASENIEDERWIESER A; WADMAN SK; DANKS DM et al.1978; CLIN. CHIM. ACTA; NLD; DA. 1978; VOL. 90; NO 2; PP. 195-200; BIBL. 8 REF.Article

CLINICAL AND BIOCHEMICAL OBSERVATIONS ON A CHILD WITH A DEFICIENCY OF 3-HYDROXY-3-METHYLGLUTARYL COENZYME A LYASEKETEL A; KET JL; SCHUTGENS RBH et al.1980; J. INHERIT. METAB. DIS.; GBR; DA. 1980; VOL. 3; NO 3; PP. 89-90; BIBL. 5 REF.Article

METHYLMALONATE EXCRETION IN A PREGNANCY AT RISK FOR METHYLMALONIC ACIDAEMIA.BAKKER HD; VAN GENNIP AH; DURAN M et al.1978; CLIN. CHIM. ACTA; NLD; DA. 1978; VOL. 86; NO 3; PP. 349-352; BIBL. 7 REF.Article

LINEAR RELATIONSHIP BETWEEN THE R- AND S-ENANTIOMERS OF BETA -AMINOISOBUTYRIC ACID IN HUMAN URINEVAN GENNIP AH; KAMERLING JP; DE BREE PK et al.1981; CLIN. CHIM. ACTA; ISSN 0009-8981; NLD; DA. 1981; VOL. 116; NO 3; PP. 261-267; BIBL. 13 REF.Article

D-LACTIC ACIDURIA, AN INBORN ERROR OF METABOLISM.DURAN M; VAN BIERVLIET JPGM; KAMERLING JP et al.1977; CLIN. CHIM. ACTA; PAYS-BAS; DA. 1977; VOL. 74; NO 53; PP. 297-300; BIBL. 7 REF.Article

TWO-DIMENSIONAL THIN-LAYER CHROMATOGRAPHY FOR THE SCREENING OF DISORDERS OF PURINE AND PYRIMIDINE METABOLISM.VANGENNIP AH; VAN NOORDENBURG HUISTRA DY; DE BREE PK et al.1978; CLIN. CHIM. ACTA; NLD; DA. 1978; VOL. 86; NO 1; PP. 7-20; BIBL. 35 REF.Article

EFFECTS OF THIAMINE IN A PATIENT WITH A VARIANT FORM OF BRANCHED-CHAIN KETOACIDURIA.DURAN M; TIELENS AGM; WADMAN SK et al.1978; ACTA PAEDIATR. SCAND.; SUEDE; DA. 1978; VOL. 67; NO 3; PP. 367-372; BIBL. 16 REF.Article

A NEW PATIENT WITH 4-HYDROXYBUTYRIC ACIDURIA, A POSSIBLE DEFECT OF 4-AMINOBUTYRATE METABOLISMDIVRY P; BALTASSAT P; ROLLAND MO et al.1983; CLINICA CHIMICA ACTA; ISSN 0009-8981; NLD; DA. 1983; VOL. 129; NO 3; PP. 303-309; BIBL. 14 REF.Article

CHROMATOGRAPHIC DETERMINATION AND MASS SPECTROMETRIC IDENTIFICATION OF GAMMA -GLUTAMYLPHENYLALANINE, A URINARY CONSTITUENT IN PHENYLKETONURIAKAMERLING JP; AARSEN GJ; DURAN M et al.1980; CLIN. CHIM. ACTA; NLD; DA. 1980; VOL. 102; NO 2-3; PP. 137-145; BIBL. 21 REF.Article

ORGANIC ACID EXCRETION IN A PATIENT WITH 3-HYDROXY-3-METHYLGLUTARYL-COA LYASE DEFICIENCY: FACTS AND ARTEFACTSDURAN M; KETTING D; WADMAN SK et al.1978; CLIN. CHIM. ACTA; NLD; DA. 1978; VOL. 90; NO 2; PP. 187-193; BIBL. 16 REF.Article

ANALYSE D'E.E.G. PAR CALCULATEUR POUR DEFINIR L'ARRET DU TRAITEMENT DIETETIQUE DES PHENYLCETONURIES.DONKER DNJ; REITS D; VAN LEEUWEN WS et al.1978; REV. ELECTROENCEPHALOGR. NEUROPHYSIOL. CLIN.; FR.; DA. 1978; VOL. 8; NO 1; PP. 55-60; ABS. ANGL.; BIBL. 8 REF.Article

UN CAS DE MALADIE DE MAROTEAUX-LAMY DECOUVERT PRECOCEMENT. CONFIRMATION DU DEFICIT EN ARYLSULFATASE B.VAN BIERVLIET JPGM; VAN LEEUWEN EF; ABELING NGGM et al.1977; ARCH. FR. PEDIATR.; FR.; DA. 1977; VOL. 34; NO 4; PP. 362-370; ABS. ANGL.; BIBL. 22 REF.Article

PERMANENT CHEMICAL PHENYLKETONURIA AND A NORMAL PHENYLALANINE TOLERANCE IN TWO SISTERS WITH A NORMAL MENTAL DEVELOPMENT. = PHENYLCETONURIE CHIMIQUE PERMANENTE ET TOLERANCE A LA PHENYLALANINE NORMALE CHEZ DEUX SOEURS AVEC UN DEVELOPPEMENT MENTAL NORMALWADMAN SK; KETTING D; DE BREE PK et al.1975; CLIN. CHIM. ACTA; PAYS-BAS; DA. 1975; VOL. 65; NO 2; PP. 197-204; BIBL. 14 REF.Article

5-OXOPROLINURIA DUE TO HEREDITARY 5-OXOPROLINASE DEFICIENCY IN TWO BROTHERS - A NEW INBORN ERROR OF THE GAMMA -GLUTAMYL CYCLELARSSON A; MATTSSON B; WAUTERS EAK et al.1981; ACTA PAEDIATR. SCAND.; ISSN 0001-656X; SWE; DA. 1981; VOL. 70; NO 3; PP. 301-308; BIBL. 29 REF.Article

ATTEMPTED DIETARY TREATMENT OF A BOY WITH HYPERAMMONEMIA DUE TO ORNITHINE TRANSFERASE DEFICIENCYVANDERHEIDEN C; BAKKER HD; DESPLANQUE J et al.1978; EUROP. J. PEDIATR.; DEU; DA. 1978; VOL. 128; NO 4; PP. 261-272; BIBL. 43 REF.Article

URINARY PURINES AND PYRIMIDINES IN PATIENTS WITH HYPERAMMONEMIA OF VARIOUS ORIGINSVAN GENNIP AH; VAN BREE BLOM EJ; GRIFT J et al.1980; CLIN. CHIM. ACTA; NLD; DA. 1980; VOL. 104; NO 2; PP. 227-239; BIBL. 52 REF.Article

SIMULTANEOUS OCCURRENCE OF XANTHINE OXIDASE AND SULFITE OXIDASE DEFICIENCY. A MOLYBDENUM DEPENDENT INBORN ERROR OF METABOLISMVAN DER HEIDEN C; BEEMER FA; BRINK W et al.1979; CLIN. BIOCHEM.; CAN; DA. 1979; VOL. 12; NO 6; PP. 206-208; BIBL. 18 REF.Article

THE BEHAVIOUR OF LDH-3 IN PATIENTS WITH MALIGNANT DISEASES DURING THERAPY WITH CYTOSTATIC DRUGS AND PREDNISONE, STUDIED BY LDH-ISOENZYME ELECTROPHORESIS ON CELLULOSE ACETATE = ETUDE PAR L'ELECTROPHORESE DES ISOZYMES DE LA LDH SUR ACETATE DE CELLULOSE DU COMPORTEMENT DE LA LDH-3 CHEZ LES MALADES ATTEINTS D'AFFECTIONS MALIGNES AU COURS DU TRAITEMENT PAR LES CYTOSTATIQUES ET LA PREDNISONEVAN GENNIP AH; TABAK VAN GORCUM JA; TAMINIAU JAJM et al.1975; CLIN. CHIM. ACTA; PAYS-BAS; DA. 1975; VOL. 58; NO 1; PP. 85-94; BIBL. 22REF.Article

CHEMICAL PARAMETERS IN DIAGNOSIS AND PROGNOSIS OF NEUROBLASTOMA = PARAMETRES CHIMIQUES DANS LE DIAGNOSTIC ET LES PRONOSTICS DU NEUROBLASTOMEWADMAN SK; KETTING D; DE BREE PK et al.1974; MAANDSCHR. KINDERGENEESKDE; NEDERL.; DA. 1974; VOL. 42; NO 11-12; PP. 439-448; H.T. 1; BIBL. 9REF.Article

ISOLATED BIOTIN-RESISTANT 3-METHYLCROTONYL-COA CARBOXYLASE DEFICIENCY IN TWO SIBSBEEMER FA; BARTLETT K; DURAN M et al.1982; EUR. J. PEDIATR.; ISSN 0340-6199; DEU; DA. 1982; VOL. 138; NO 4; PP. 351-354; BIBL. 18 REF.Article

THE IDENTIFICATION OF (E)-2-METHYLGLUTACONIC ACID, A NEW ISOLEUCINE METABOLITE, IN THE URINE OF PATIENTS WITH BETA -KETOTHIOLASE DEFICIENCY, PROPIONIC ACIDAEMIA AND METHYLMALONIC ACIDAEMIADURAN M; BRUINVIS L; KETTING D et al.1982; BIOMED. MASS SPECTROM.; ISSN 0306-042X; GBR; DA. 1982; VOL. 9; NO 1; PP. 1-5; BIBL. 17 REF.Article

1-2-HYDROXYGLUTARIC ACIDURIA: AN INBORN ERROR OF METABOLISM.DURAN M; KAMERLING JP; BAKKER HD et al.1980; J. INHERIT. METAB. DIS.; ISSN 0141-8955; GBR; DA. 1980; VOL. 3; NO 4; PP. 109-112; BIBL. 15 REF.Article

LETHAL HYPOGLYCEMIA IN A CHILD WITH A DEFICIENCY OF 3-HYDROXY-3-METHYLGLUTARYLCOENZYME A LYASESCHUTGENS RBH; HEYMANS H; KETEL A et al.1979; J. PEDIATR.; USA; DA. 1979; VOL. 94; NO 1; PP. 89-91; BIBL. 9 REF.Article

URINARY EXCRETION OF OROTIC ACID, OROTIDINE AND OTHER PYRIMIDINES IN A PATIENT WITH PURINE NUCLEOSIDE PHOSPHORYLASE DEFICIENCYVAN GENNIP AH; GRIFT J; DE BREE PK et al.1979; CLIN. CHIM. ACTA; NLD; DA. 1979; VOL. 93; NO 3; PP. 419-428; BIBL. 30 REF.Article

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