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GAS CHROMATOGRAPHIC DETERMINATION OF URINARY VANILGLYCOL, VANILACETIC ACID AND VANILLACTIC ACID-CHEMICAL PARAMETERS FOR THE DIAGNOSIS OF NEUROGENIC TUMOURS AND THE EVALUATION OF THEIR TREATMENT.WADMAN SK; KETTING D; VOUTE PA et al.1976; CLIN. CHIM. ACTA; PAYS-BAS; DA. 1976; VOL. 72; NO 1; PP. 49-68; BIBL. 30 REF.Article

THE VARIABILITY OF METABOLITE EXCRETION IN PROPIONICACIDAEMIA.DURAN M; GOMPERTZ D; BRUINVIS L et al.1978; CLIN. CHIM. ACTA; PAYS-BAS; DA. 1978; VOL. 82; NO 1-2; PP. 93-99; BIBL. 19 REF.Article

THE ABSOLUTE CONFIGURATION OF URINARY 2-HYDROXYBUTYRIC ACID IN PATIENTS WITH KETOSIS AND LACTIC ACIDOSISKAMERLING JP; GERWIG GJ; DURAN M et al.1978; CLIN. CHIM. ACTA; NLD; DA. 1978; VOL. 88; NO 1; PP. 183-188; BIBL. 12 REF.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

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

A CASE OF FORMIMINOGLUTAMIC ACIDURIA. CLINICAL AND BIOCHEMICAL STUDIESDURAN M; KETTING D; DE BREE PK et al.1981; EUR. J. PEDIATR.; ISSN 0340-6199; DEU; DA. 1981; VOL. 136; NO 3; PP. 319-323; BIBL. 10 REF.Article

3-METHYL-3-BUTENOIC ACID: AN ARTEFACT IN THE URINARY METABOLIC PATTERN OF PATIENTS WITH 3-HYDROXY-3-METHYL-GLUTARYL-COA LYASE DEFICIENCYJAKOBS C; BOJASCH M; DURAN M et al.1980; CLIN. CHIM. ACTA; NLD; DA. 1980; VOL. 106; NO 1; PP. 85-89; BIBL. 12 REF.Article

TWO SISTERS WITH ISOVALERIC ACIDAEMIA, MULTIPLE ATTACKS OF KETOACIDOSIS AND NORMAL DEVELOPMENTDURAN M; VAN SPRANG FJ; DREWES JG et al.1979; EUROP. J. PEDIATR.; DEU; DA. 1979; VOL. 131; NO 3; PP. 205-211; BIBL. 16 REF.Article

TYROSINEMIA AND TYROSYLURIA IN HEALTHY PREMATURES: TIME COURSES NOT VITAMIN C-DEPENDENT = LA TYROSINEMIE ET LA TYROSYLURIE CHEZ LES PREMATURES NORMAUX. EVOLUTION DANS LE TEMPS INDEPENDANTE DE LA VITAMINE CBAKKER HD; WADMAN SK; VAN SPRANG FJ et al.1975; CLIN. CHIM. ACTA; PAYS-BAS; DA. 1975; VOL. 61; NO 1; PP. 73-90; BIBL. 43REF.Article

FRUCTOSE-1,6-DIPHOSPHATASE DEFICIENCY: ANOTHER ENZYME DEFECT WICH CAN PRESENT ITSELF WITH THE CLINICAL FEATURES OF TYROSINOSISBAKKER HD; DE BREE PK; KETTING D et al.1974; CLIN: CHIM. ACTA; PAYS-BAS; DA. 1974; VOL. 55; NO 1; PP. 41-47; BIBL. 28 REF.Article

ISOVALERIC ACIDAEMIA PRESENTING WITH DWARFISM, CATARACT AND CONGENITAL ABNORMALITIESDURAN M; BRUINVIS L; KETTING D et al.1982; J. INHERIT. METAB. DIS.; ISSN 0141-8955; GBR; DA. 1982; VOL. 5; NO 2; PP. 125-127; BIBL. 11 REF.Article

THE ABSOLUTE CONFIGURATION OF URINARY 5-HYDROXYHEXANOIC ACID - A PRODUCT OF FATTY ACID (CO-1)-OXIDATION - IN PATIENTS WITH NON-KETOTIC DICARBOXYLIC ACIDURIAKAMERLING JP; DURAN M; BRUINVIS L et al.1982; CLIN. CHIM. ACTA; ISSN 0009-8981; NLD; DA. 1982; VOL. 125; NO 3; PP. 247-254; BIBL. 22 REF.Article

DEFICIENCY OF FUMARYLACETOACETATE IN A PATIENT WITH HEREDITARY TYROSINEMIABERGER R; SMIT GPA; STOKER DE VRIES SA et al.1981; CLIN. CHIM. ACTA; ISSN 0009-8981; NLD; DA. 1981; VOL. 114; NO 1; PP. 37-44; BIBL. 17 REF.Article

URINARY EXCRETION OF METHYLATED PURINES IN MAN AND IN THE RAT AFTER THE ADMINISTRATION OF THEOPHYLLINEVAN GENNIP AH; GRIFT J; VAN BREE BLOM EJ et al.1979; J. CHROMATOGR.; NLD; DA. 1979; VOL. 163; NO 4; PP. 351-362; BIBL. 16 REF.Article

DETERMINATION OF THE CONFIGURATIONS OF LACTIC AND GLYCERIC ACID FROM HUMAN SERUM AND URINE BY CAPILLARY GAS-LIQUID CHROMATOGRAPHY.KAMERLING JP; GERWIG GJ; VLIEGENTHART JFG et al.1977; J. CHROMATOGR.; NETHERL.; DA. 1977; VOL. 143; NO 2; PP. 117-123; BIBL. 14 REF.Article

(2-ETHOXYETHOXY) ACETIC ACID: AN UNUSUAL COMPOUND FOUND IN THE GAS CHROMATOGRAPHIC ANALYSIS OF URINARY ORGANIC ACIDS.KAMERLING JP; DURAN M; BRUINVIS L et al.1977; CLIN. CHIM. ACTA; PAYS-BAS; DA. 1977; VOL. 77; NO 3; PP. 397-405; BIBL. 11 REF.Article

GLUTARIC ACIDURIA TYPE II: REPORT ON A PREVIOUSLY UNDESCRIBED METABOLIC DISORDER.PRZYREMBEL H; WENDEL U; BECKER K et al.1976; CLIN. CHIM. ACTA; PAYS-BAS; DA. 1976; VOL. 66; NO 2; PP. 227-239; BIBL. 49 REF.Article

REPORT OF A PATIENT WITH SEVERE, CHRONIC LACTIC ACIDAEMIA AND PYRUVATE CARBOXYLASE DEFICIENCY.VAN BIERVLIET JPGM; BRUINVIS L; VAN DER HEIDEN C et al.1977; DEVELOP. MED. CHILD NEUROL.; G.B.; DA. 1977; VOL. 19; NO 3; PP. 392-401; ABS. FR. ALLEM. ESP.; BIBL. 1 P.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

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