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DIAGNOSIS OF TRACE METAL DEFICIENCY-WITH EMPHASIS ON COPPER AND ZINCDANKS DM.1981; AM. J. CLIN. NUTR.; ISSN 0002-9165; USA; DA. 1981; VOL. 34; NO 2; PP. 278-280; BIBL. 6 REF.Article

COPPER TRANSPORT AND UTILISATION IN MENKES' SYNDROME AND IN MOTTLED MICE.DANKS DM.1977; INORG. PERSPECT. BIOL. MED.; NETHERL.; DA. 1977; VOL. 1; NO 2; PP. 73-100; BIBL. 2 P.Article

PROSPECTS FOR THE PREVENTION OF GENETIC DISEASE = PERSPECTIVES DANS LA PREVENTION DES MALADIES GENETIQUESDANKS DM.1973; MED. J. AUSTRAL.; AUSTRAL.; DA. 1973; VOL. 1; NO 12; PP. 573-577; BIBL. 11REF.Serial Issue

MANAGEMENT OF NEWBORN BABIES IN WHOM SERIOUS METABOLIC ILLNESS IS ANTICIPATED = CONDUITE A TENIR VIS-A-VIS DES NOUVEAU-NES SUSPECTS D'UNE MALADIE METABOLIQUE GRAVEDANKS DM.1974; ARCH. DIS. CHILDH.; G.B.; DA. 1974; VOL. 49; NO 7; PP. 576-578; BIBL. 2REF.Article

EARLY DIAGNOSIS OF HYPERPHENYLALANINEMIA DUE TO TETRAHYDROBIOPTERIN DEFICIENCY (MALIGNANT HYPERPHENYLALANINEMIA)DANKS DM; COTTON RGH.1980; J. PEDIATR.; USA; DA. 1980; VOL. 96; NO 5; PP. 854-856; BIBL. 17 REF.Article

HYPOTHESES REGARDING MYELINATION DERIVED FROM COMPARISONS OF MYELIN SUBFRACTIONSDANKS DM; MATHIEU JM.1979; LIFE SCI.; GBR; DA. 1979; VOL. 24; NO 16; PP. 1425-1440; BIBL. 32 REF.Article

PURIFICATION OF INACTIVE PHENYLALANINE HYDROXYLASE PROTEIN FROM LIVER IN CLASSICAL PHENYLKETONURIACOTTON RGH; DANKS DM.1976; NATURE; G.B.; DA. 1976; VOL. 260; NO 5546; PP. 63-64; BIBL. 8 REF.Article

THE OPITZ TRIGONOCEPHALY SYNDROME. A CASE REPORT = LE SYNDROME DE TRIGONOCEPHALIE D'OPITZ. OBSERVATION D'UN CASOBERKLAID F; DANKS DM.1975; AMER. J. DIS. CHILD.; U.S.A.; DA. 1975; VOL. 129; NO 11; PP. 1348-1349; BIBL. 2 REF.Article

CONGENITAL HYPOTHYROIDISM AND NEONATAL JAUNDICE = HYPOTHYROIDIE CONGENITALE ET ICTERE NEONATALWELDON AP; DANKS DM.1972; ARCH. DIS. CHILDH.; G.B.; DA. 1972; VOL. 47; NO 253; PP. 469-471; BIBL. 2REF.Article

FRONTOMETAPHYSEAL DYSPLASIA : A PROGRESSIVE DISEASE OF BONE AND CONNECTIVE TISSUE = DYSPLASIE FRONTOMETAPHYSAIRE: UNE MALADIE PROGRESSIVE DE L'OS ET DU TISSU CONJONCTIFDANKS DM; MAYNE V.1974; BIRTH DEFECTS ORIGIN. ARTICLE SER.; U.S.A.; DA. 1974; VOL. 10; NO 12; PP. 57-60; BIBL. 2REF.Article

NORMAL HYDROXYLATION OF PROLINE IN COLLAGEN SYNTHESIZED BY SKIN FIBROBLASTS FROM A PATIENT WITH PROLIDASE DEFICIENCYROYCE PM; DANKS DM.1982; J. INHERIT. METAB. DIS.; ISSN 0141-8955; GBR; DA. 1982; VOL. 5; NO 2; PP. 111-113; BIBL. 24 REF.Article

SECONDARY COPPER ACCUMULATION WITH NEUROLOGICAL DAMAGE IN CHILD WITH CHRONIC LIVER DISEASESMITH AL; DANKS DM.1978; BRIT. MED. J.; GBR; DA. 1978; NO 6149; PP. 1400-1401; BIBL. 5 REF.Article

THE CLINICAL AND BIOCHEMICAL FINDINGS IN THREE CASES OF HYPERSARSOCINEMIA AND ONE CASE OF TRANSIENT HYPERSARCOSINURIA ASSOCIATED WITH FOLIC ACID DEFICIENCY = LES DONNEES CLINIQUES ET BIOCHIMIQUES DANS 3CAS D'HYPERSARCOSINEMIE ET DANS UN CAS D'HYPERSARCOSINEMIE TRANSITOIRE ASSOCIEE A UN DEFICIT EN ACIDE FOLIQUETIPPETT P; DANKS DM.1974; HELV. PAEDIATR. ACTA; SUISSE; DA. 1974; VOL. 29; NO 3; PP. 261-267; ABS. ALLEM.; BIBL. 16 REF.Article

CLINICAL VARIABILITY IN OSTEOGENESIS IMPERFECTA-VARIABLE EXPRESSIVITY OR GENETIC HETEROGENEITYSILLENCE DO; RIMOIN DL; DANKS DM et al.1979; BIRTH DEFECTS ORIGIN. ARTICLE SER.; USA; DA. 1979; VOL. 15; NO 5B; PP. 113-129; BIBL. 66 REF.Article

GENETIC HETEROGENEITY IN OSTEOGENESIS IMPERFECTASILLENCE DO; SENN A; DANKS DM et al.1979; J. MED. GENET.; GBR; DA. 1979; VOL. 16; NO 2; PP. 101-116; BIBL. 2 P.Article

ABNORMAL COPPER METABOLISM IN CULTURED FIBROBLASTS FROM PATIENTS WITH WILSON'S DISEASECAMAKARIS J; ACKLAND L; DANKS DM et al.1980; J. INHERIT. METAB. DIS.; ISSN 0141-8955; GBR; DA. 1980; VOL. 3; NO 4; PP. 155-157; BIBL. 5 REF.Article

PHENYLALANINE HYDROXYLATION AND TYROSINE REQUIREMENT OF CULTURED CELLS. EVIDENCE OF PHENYLALANINE HYDROXYLATION IN MASTOCYTOMA CELLS IN CULTURE.CHOO KH; COTTON RGH; DANKS DM et al.1976; EXPER. CELL RES.; U.S.A.; DA. 1976; VOL. 101; NO 2; PP. 370-382; BIBL. 40 REF.Article

SEVERE-NEONATAL CITRULLINAEMIA = CITRULLINEMIE NEONATALE GRAVEDANKS DM; TIPPETT P; ZENTNER G et al.1974; ARCH. DIS. CHILDH.; G.B.; DA. 1974; VOL. 49; NO 7; PP. 579-581; BIBL. 6REF.Article

DIFFICULTY IN SHOWING MOSAICISM IN THE MOTHER OF THREE MONGOLS = DIFFICULTES DE MISE EN EVIDENCE D'UN MOSAISME CHEZ LA MERE DE TROISMONGOLIENSSUTHERLAND GR; FITZGERALD G; DANKS DM et al.1972; ARCH. DIS. CHOLDH.; G.B.; DA. 1972; VOL. 47; NO 256; PP. 970-971; BIBL. 1REF.Serial Issue

DIHYDROPTERIDINE REDUCTASE DEFICIENCY DIAGNOSIS BY ASSAYS ON PERIPHERAL BLOOD-CELLSFIRGAIRA FA; COTTON RGH; DANKS DM et al.1979; LANCET; GBR; DA. 1979; NO 8155; PP. 1260-1263; BIBL. 18 REF.Article

HUMAN COPPER DEFICIENCY. ULTRASTRUCTURAL STUDIES OF THE AORTA AND SKIN IN A CHILD WITH MENKES' SYNDROME.OAKES BW; DANKS DM; CAMPBELL PE et al.1976; EXPER. MOLEC. PATHOL.; U.S.A.; DA. 1976; VOL. 25; NO 1; PP. 82-98; BIBL. 2 P. 1/2Article

COMMENTS UPON THE CLASSIFICATION OF INFANTILE POLYCYSTIC DISEASES OF THE LIVER AND KIDNEY, BASED UPON THREE-DIMENSIONAL RECONSTRUCTION OF THE LIVER = REFLEXIONS SUR LA CLASSIFICATION DES MALADIES POLYKYSTIQUES INFANTILES DU FOIE ET DES REINS BASEE SUR LA RECONSTITUTION TRIDIMENSIONNELLE DU FOIEADAMS CM; DANKS DM; CAMPBELL PE et al.1974; J. MED. GENET.; G.B.; DA. 1974; VOL. 11; NO 3; PP. 234-243; BIBL. 8REF.Article

COPPER METABOLISM IN MOTTLED MOUSE MUTANTS. COPPER CONCENTRATIONS IN TISSUES DURING DEVELOPMENTCAMAKARIS J; MANN JR; DANKS DM et al.1979; BIOCHEM. J.; GBR; DA. 1979; VOL. 180; NO 3; PP. 597-604; BIBL. 29 REF.Article

COPPER METABOLISM IN MOTTLED MOUSE MUTANTS. DISTRIBUTION OF 64CU IN BRINDLED (MOBR) MICEMANN JR; CAMAKARIS J; DANKS DM et al.1979; BIOCHEM. J.; GBR; DA. 1979; VOL. 180; NO 3; PP. 613-619; BIBL. 16 REF.Article

HUMAN DIHYDROPTERIDINE REDUCTASE. A METHOD FOR THE MEASUREMENT OF ACTIVITY IN CULTURED CELLS, AND ITS APPLICATION TO MALIGNANT HYPERPHENYLALANINEMIAFIRGAIRA FA; COTTON RGH; DANKS DM et al.1979; CLIN. CHIM. ACTA; NLD; DA. 1979; VOL. 95; NO 1; PP. 47-59; BIBL. 22 REF.Article

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