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DIAGNOSIS OF VARIANTS OF HYPERPHENYLALANIMEMIA BY DETERMINATION OF PTERINS IN URINEDHONDT JL; LARGILLIERE C; ARDOUIN P et al.1981; CLIN. CHIM. ACTA; ISSN 0009-8981; NLD; DA. 1981; VOL. 110; NO 2-3; PP. 205-214; BIBL. 24 REF.Article

CHRONIC HYPERPHENYLALANINEMIA PRODUCES CEREBRAL HYPERGLYCINEMIA IN IMMATURE RATSDIENEL GA.1981; J. NEUROCHEM.; ISSN 0022-3042; GBR; DA. 1981; VOL. 36; NO 1; PP. 34-43; BIBL. 2 P.Article

A CLINICAL EPIDEMIOLOGIC STUDY OF HYPERPHENYLALANINEMIAWRONA RM.1979; AMER. J. PUBLIC HEALTH; USA; DA. 1979; VOL. 69; NO 7; PP. 673-679; BIBL. 29 REF.Article

A PROPOS DU DEPISTAGE NEONATAL DES HYPERPHENYLALANINEMIES ET DES HYPERTYROSINEMIES.DHONDT JL; FARRIAUX JP.1977; ARCH. FR. PEDIATR.; FR.; DA. 1977; VOL. 34; NO 5; PP. 474-475; BIBL. 8 REF.Article

HYPERPHENYLALANINEMIE INDUITE PAR LA PYRIMETHAMINE.COSTIL J; RICHARDET JM; AYMARD P et al.1976; NOUV. PRESSE MED.; FR.; DA. 1976; VOL. 5; NO 26; PP. 1646-1647; BIBL. 2 REF.Article

INHIBITION OF CEREBRAL PROTEIN KINASE ACTIVITY AND CYCLIC AMP-DEPENDENT RIBOSOMAL-PROTEIN PHOSPHORYLATION IN EXPERIMENTAL HYPERPHENYLALANINAEMIAROBERTS S; MORELOS BS.1982; BIOCHEM. J. (LOND.); ISSN 0006-2936; GBR; DA. 1982; VOL. 202; NO 2; PP. 343-351; BIBL. 44 REF.Article

HYPERPHENYLALANINAEMIA DUE TO DIHYDROPTERIDINE REDUCTASE DEFICIENCYGROBE H; BARTHOLOME K; MILSTIEN S et al.1978; EUROP. J. PEDIATR.; DEU; DA. 1978; VOL. 129; NO 2; PP. 93-98; BIBL. 18 REF.Article

ON INDICATIONS FOR TREATMENT OF THE HYPERPHENYLALANINEMIC NEONATE.GUTTLER F; WAMBERG E.1977; ACTA PAEDIATR. SCAND.; SUEDE; DA. 1977; VOL. 66; NO 3; PP. 339-344; BIBL. 20 REF.Article

Maternal phenylketonuria with increased tyrosine supplementsSHEIL, O; DUIGNAN, N; SAUL, I. P et al.Journal of inherited metabolic disease. 1986, Vol 9, pp 231-233, issn 0141-8955, suppl. 2Conference Paper

TETRAHYDROFOLATE AND HYDROXOCOBALAMIN IN THE MANAGEMENT OF DIHYDROPTERIDINE REDUCTASE DEFICIENCYLEEMING RJ; HARPEY JP; BROWN SM et al.1982; J. MENT. DEFIC. RES.; ISSN 0022-264X; GBR; DA. 1982; VOL. 26; NO 1; PP. 21-25; BIBL. 14 REF.Article

EFFECT OF LEAD ON TETRAHYDROBIOPTERIN SYNTHESIS AND SALVAGE: A CAUSE OF NEUROLOGICAL DYSFUNCTIONPURDY SE; BLAIR JA; LEEMING RJ et al.1981; INT. J. ENVIRON. STUD.; ISSN 0020-7233; GBR; DA. 1981; VOL. 17; NO 2; PP. 141-145; BIBL. 35 REF.Article

THE ASSAY ON A DEFINED MEDIUM OF THE EFFECTS OF BETA -2-THIENYLALANINE ON THE GROWTH OF ANAEROBIC BACTERIAL ISOLATES FROM PHENYLKETONURIC PATIENTSBROWN KJ; VESEY BV; TANNOCK GW et al.1980; MED. MICROBIOL. IMMUNOL.; DEU; DA. 1980; VOL. 168; NO 1; PP. 11-24; BIBL. 40 REF.Article

A PROPOS D'UNE OBSERVATION D'HYPERPHENYLALANINEMIE SANS PHENYLCETONURIE.FESSARD C; AMAR R; DAILLY R et al.1977; OUEST MED.; FR.; DA. 1977; VOL. 30; NO 6; PP. 371-372Article

PTERIN METABOLISM IN NORMAL SUBJECTS AND HYPERPHENYLALANINAEMIC PATIENTSDHONDT JL; FARRIAUX JP; LARGILLIERE C et al.1981; J. INHERIT. METAB. DIS.; ISSN 0141-8955; GBR; DA. 1981; VOL. 4; NO 2; PP. 47-48; BIBL. 11 REF.Article

LA PHENYCETONURIE "TRANSITOIRE"REY F; LEEMING RJ; CURTIUS HC et al.1979; ARCH. FR. PEDIATR.; FRA; DA. 1979 PUBL. 1980; VOL. 36; SUPPL. 1; PP. XLVIII-LV; ABS. ENG; BIBL. 28 REF.Article

L'IPERFENILALANINEMIA MATERNA COME CAUSA DI EMBRIOFETOPATIA: RASSEGNA DELLA LETTERATURA E CONTRIBUTO CLINICO = L'HYPERPHENYLALANINEMIE MATERNELLE EN TANT QUE CAUSE D'EMBRYO-FOETOPATHIE: REVUE DE LA LITTERATURE ET CONTRIBUTION CLINIQUEGIOVANNINI M; RIVA E; MAGNONI D et al.1979; MINERVA PEDIATR.; ITA; DA. 1979; VOL. 31; NO 8; PP. 615-624; ABS. ENG; BIBL. 2 P.Article

Incidence of phenylketonuria and hyperphenylalaninaemia in a sample of the Turkish newborn populationOZALP, I; COSKUN, T; CEYHAN, M et al.Journal of inherited metabolic disease. 1986, Vol 9, pp 237-239, issn 0141-8955, suppl. 2Conference Paper

LA TETRAHYDROBIOPTERINE. METABOLISME PHYSIOLOGIQUE ET PATHOLOGIQUE DES PTERIDINES NON CONJUGUEESDHONDT JL; FARRIAUX JP.1980; PATHOL. BIOL.; FRA; DA. 1980; VOL. 28; NO 6; PP. 397-405; ABS. ENG; BIBL. 77 REF.Article

SERUM TYROSINE WITHIN THE FIRST HOUR AFTER AN ORAL LOAD OF PHENYLALANINE.GUTTLER F; HANSEN G.1977; SCAND. J. CLIN. LAB. INVEST.; NORWAY; DA. 1977; VOL. 37; NO 8; PP. 717-722; BIBL. 25 REF.Article

DIHYDROPTERIDINE REDUCTASE DEFICIENCY: DIAGNOSIS BY LEUKOCYTE ENZYME ASSAYNARISAWA K; ARAI N; ISHIZAWA S et al.1980; CLIN. CHIM. ACTA; NLD; DA. 1980; VOL. 105; NO 3; PP. 335-342; BIBL. 37 REF.Article

LA DIFFERENZIAZIONE DELLE IPERFENILALANINEMIE MEDIANTE DIETA DA CARICO. = LA DIFFERENCIATION DES HYPERPHENYLALANINEMIES AU MOYEN DU REGIME DE CHARGEZAMMARCHI E; BARDINI MR; DE NIGRIS L et al.1978; MINERVA PEDIATR.; ITA; DA. 1978; VOL. 30; NO 9; PP. 713-726; ABS. ANGL.; BIBL. 13 REF.Article

LE DEPISTAGE SYSTEMATIQUE EN PICARDIE DE L'HYPOTHYROIDIE CONGENITALE ET DE L'HYPERPHENYLALAMINEMIEBOUDAILLIEZ B; LENAERTS C; PIUSSAN C et al.1982; REVUE MEDICALE DE PICARDIE; ISSN 0301-116X; FRA; DA. 1982; VOL. 10; NO 9; PP. 354-356; BIBL. 5 REF.Article

AUSSCHEIDUNG VON TRANSAMINIERUNGSPRODUKTEN BEI HYPERPHENYLALANINAEMIEN = EXCRETION DES PRODUITS TRANSAMINES DANS L'HYPERPHENYLALANINEMIEOLEK K; WARDENBACH P; BYRD D et al.1980; KLIN. WSCHR.; DEU; DA. 1980; VOL. 58; NO 3; PP. 135-140; ABS. ENG; BIBL. 24 REF.Article

LES HYPERPHENYLALANINEMIES NEO-NATALES EN 1980DHONDT JL; FARRIAUX JP.1980; MED. INFANT.; FRA; DA. 1980; VOL. 87; NO 2; PP. 225-232; BIBL. 32 REF.Article

ZWOELF JAHRE OESTERREICHISCHES PROGRAMM ZUR FRUEHERFASSUNG ANGEBORENER STOFFWECHSELANOMALIEN. ERGEBNISSE UNTER BESONDERER BERUECKSICHTIGUNG VON PHENYLKETONURIE, HYPERPHENYLALANINAEMIE UND HISTIDINAEMIE = LE PROGRAMME AUTRICHIEN DE 12 ANNEES POUR LE DEPISTAGE PRECOCE DES ANOMALIES METABOLIQUES CONGENITALES. LES RESULTATS EN TENANT COMPTE EN PARTICULIER DE LA PHENYLCETONURIE, DE L'HYPERPHENYLALANINEMIE ET DE L'HISTIDINEMIETHALHAMMER O; SCHEIBENREITER S; KNOLL E et al.1980; KLIN. PAEDIATR.; ISSN 0300-8630; DEU; DA. 1980; VOL. 192; NO 6; PP. 589-598; ABS. ENG; BIBL. 25 REF.Article

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