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

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

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

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

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

HEREDITARY MITOCHONDRIAL MYOPATHY WITH LACTIC ACIDEMIA, A DETONI-FANCONI-DEBRE SYNDROME, AND A DEFECTIVE RESPIRATORY CHAIN IN VOLUNTARY STRIATED MUSCLES.VAN BIERVLIET JPGM; BRUINVIS L; KETTING D et al.1977; PEDIATR. RES.; U.S.A.; DA. 1977; VOL. 11; NO 10 PART. 2; PP. 1088-1093; BIBL. 38 REF.Article

D-GLYCERIC ACIDEMIA IN A PATIENT WITH CHRONIC METABOLIC ACIDOSIS.WADMAN SK; DURAN M; KETTING D et al.1976; CLIN. CHIM. ACTA; PAYS-BAS; DA. 1976; VOL. 71; NO 3; PP. 477-484; BIBL. 13 REF.Article

The identification of acylcarnitines by desorption chemical ionization mass spectrometryDURAN, M; KETTING, D; DORLAND, L et al.Journal of inherited metabolic disease. 1985, Vol 8, pp 143-144, issn 0141-8955, suppl. 2Article

The occurrence of lactyl lactate and succinyl lactate in the urine of patients screened for inherited metabolic diseaseKETTING, D; WADMAN, S. K; BRUINWIS, L et al.Clinica chimica acta. 1985, Vol 146, Num 1, pp 29-35, issn 0009-8981Article

1,6-Anhydro-β-D-glucopyranose (β-glucosan), a constituent of human urineDORLAND, L; WADMAN, S. K; DE JONGE, H. F et al.Clinica chimica acta. 1986, Vol 159, Num 1, pp 11-16, issn 0009-8981Article

D-glyceric acidemia: an inborn error associated with fructose metabolismDURAN, M; BEEMER, F. A; BRUINVIS, L et al.Pediatric research. 1987, Vol 21, Num 5, pp 502-506, issn 0031-3998Article

Urinary D-4-hydroxyphenyllactate, D-phenyllactate and D-2-hydroxyisocaproate, abnormalities of bacterial originSPAAPEN, L. J. M; KETTING, D; WADMAN, S. K et al.Journal of inherited metabolic disease. 1987, Vol 10, Num 4, pp 383-390, issn 0141-8955Article

Cis-4-decenoic acid in plasma: a characteristic metabolite in medium-chain acyl-CoA dehydrogenase deficiencyDURAN, M; BRUINVIS, L; KETTING, D et al.Clinical chemistry (Baltimore, Md.). 1988, Vol 34, Num 3, pp 548-551, issn 0009-9147Article

Direct identification of propionylcarnitine in propionic acidaemia: biochemical and clinical results of oral carnitine supplementationDURAN, M; KETTING, D; BECKENINGH, T. E et al.Journal of inherited metabolic disease. 1986, Vol 9, Num 2, pp 202-207, issn 0141-8955Article

The differential diagnosis of dicarboxylic aciduriaDURAN, M; DE KLERK, J. B. C; WADMAN, S. K et al.Journal of inherited metabolic disease. 1984, Vol 7, pp 48-51, issn 0141-8955, suppl. 1Article

Octaglucuronide excretion in patients with a defective oxidation of medium-chain fatty acidsDURAN, M; KETTING, D; VAN VOSSEN, R et al.Clinica chimica acta. 1985, Vol 152, Num 3, pp 253-260, issn 0009-8981Article

A patient with mevalonic aciduria presenting with hepatosplenomegaly, congenital anaemia, thrombocytopenia and leukocytosisDE KLERK, J. B. C; DURAN, M; DORLAND, L et al.Journal of inherited metabolic disease. 1988, Vol 11, pp 233-236, issn 0141-8955, suppl. 2Article

Identification of the stereoisomeric configurations of methylcitric acid produced by si-citrate synthase and methylcitrate synthase using capillary gas chromatography-mass spectrometryVAN ROOYEN, J. P. G; MIENIE, L. J; ERASMUS, E et al.Journal of inherited metabolic disease. 1994, Vol 17, Num 6, pp 738-747, issn 0141-8955Article

Urinary excretion of 2-methyl-2,3-butanediol and 2,3-pentanediol in patients with disorders of propionate and methylmalonate metabolismDURAN, M; KETTING, D; BRUINVIS, L et al.Clinica chimica acta. 1987, Vol 165, Num 2-3, pp 197-204, issn 0009-8981Article

3-hydroxydicarboxylic aciduria due to long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency associated with sudden neonatal death : protective effect of medium-chain triglyceride treatmentDURAN, M; WANDERS, R. J. A; DE JAGER, J. P et al.European journal of pediatrics. 1991, Vol 150, Num 3, pp 190-195, issn 0340-6199Article