HOMOCYSTINURIA. REDUCED FOLATE LEVELS DURING PYRIDOXINE TREATMENT = HOMOCYSTINURIE. REDUCTION DES TAUX DE FOLATE AU COURS DU TRAITEMENT PAR LA PYRIDOXINEWILCKEN B; TURNER B.1973; ARCH. DIS. CHILDH.; G.B.; DA. 1973; VOL. 48; NO 1; PP. 58-62; BIBL. 22REF.Serial Issue

PREVALENCE OF UNSUSPECTED URINARY BACTERIAL CONTAMINATION: EFFECTS OF SCREENING TESTS FOR DETECTION OF INBORN ERRORS OF METABOLISM.VIDLER J; WILCKEN B.1978; CLIN. CHIM. ACTA; PAYS-BAS; DA. 1978; VOL. 82; NO 1-2; PP. 173-178; BIBL. 9 REF.Article

Recent advances in newborn screening : Science Oriented Congress and PatnershipWILCKEN, B.Journal of inherited metabolic disease. 2007, Vol 30, Num 2, pp 129-133, issn 0141-8955, 5 p.Conference Paper

URINE SCREENING FOR AMINOACIDOPATHIES: IS-IT BENEFICIAL. RESULTS OF A LONG-TERM FOLLOW-UP OF CASES DETECTED BY SCREENING ONE MILLION BABIESWILCKEN B; SMITH A; BROWN DA et al.1980; J. PEDIATR.; ISSN 0022-3476; USA; DA. 1980; VOL. 97; NO 3; PP. 492-497; BIBL. 31 REF.Article

DETECTION OF ABNORMAL SULPHUR-CONTAINING AMINO ACID EXCRETION IN A MASS URINE-SCREENING PROGRAMME = DETECTION DE L'EXCRETION ANORMALE D'UN AMINO-ACIDE SULFURE PAR UN PROGRAMME D'ANALYSE D'URINE DE MASSEWILCKEN B; TURNER B; BROWN DA et al.1972; MED. J. AUSTRAL.; AUSTRAL.; DA. 1972; VOL. 59; NO 23; PP. 1193-1195; BIBL. 19 REF.Serial Issue

METHYLMALONIC ACIDURIA: A VARIANT FORM OF METHYLMALONYL COENZYME A APOMUTASE DEFICIENCY.WILCKEN B; KILHAM HA; FAULL K et al.1977; J. PEDIATR.; U.S.A.; DA. 1977; VOL. 91; NO 3; PP. 428-430; BIBL. 11 REF.Article

SCREENING FOR CYSTIC FIBROSIS BY A STOOL TRYPSIN METHODFORREST DC; WILCKEN B; TURNER G et al.1981; ARCT. DIS. CHILD.; ISSN 0003-9888; GBR; DA. 1981; VOL. 56; NO 2; PP. 151-153; BIBL. 4 REF.Article

CYSTIC FIBROSIS SCREENING BY DRIED BLOOD SPOT TRYPSIN ASSAY: RESULTS IN 75000 NEWBORN INFANTSWILCKEN B; BROWN ARD; URWIN R et al.1983; JOURNAL OF PEDIATRICS; ISSN 0022-3476; USA; DA. 1983; VOL. 102; NO 3; PP. 383-387; BIBL. 18 REF.Article

Rare diseases and the assessment of intervention : What sorts of clinical trials can we use?WILCKEN, B.Journal of inherited metabolic disease. 2001, Vol 24, Num 2, pp 291-298, issn 0141-8955Conference Paper

Homozygous cystinuria in New South Wales: a study of 110 individuals with cystinuria ascertained by methods other than neonatal screeningSMITH, A; WILCKEN, B.Medical journal of Australia. 1984, Vol 141, Num 8, pp 500-502, issn 0025-729XArticle

Neonatal diagnosis of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency and implications for newborn screening by tandem mass spectrometryCARPENTER, K. H; WILCKEN, B.Journal of inherited metabolic disease. 1999, Vol 22, Num 7, pp 840-841, issn 0141-8955Article

STUDIES ON A CHILD SUSPECTED OF HAVING A DEFICIENCY IN 3-HYDROXY-3-METHYLGLUTARYL-COA LYASETRUSCOTT RJW; HALPERN B; WYSOCKI SJ et al.1979; CLIN. CHIM. ACTA; NLD; DA. 1979; VOL. 95; NO 1; PP. 11-16; BIBL. 11 REF.Article

Sialuria : a follow-up reportDON, N. A; WILCKEN, B.Journal of inherited metabolic disease. 1991, Vol 14, Num 6, issn 0141-8955, p. 942Article

3-Hydroxy-3-methylglutaric, 3-methylglutaconic and 3-methylglutaric acids can be non-specific indicators of metabolic diseaseHAMMOND, J; WILCKEN, B.Journal of inherited metabolic disease. 1984, Vol 7, Num 2, pp 117-118, issn 0141-8955, supplArticle

Clinical approach to inborn errors of metabolism presenting in the newborn periodELLAWAY, C. J; WILCKEN, B; CHRISTODOULOU, J et al.Journal of paediatrics and child health. 2002, Vol 38, Num 5, pp 511-517, issn 1034-4810, 7 p.Article

The long-term evolution of a case of 3-hydroxy-3-methylglutaryl-coenzyme A lyase deficiency associated with deafness and retinitis pigmentosaJONES, K. J; WILCKEN, B; KILHAM, H et al.Journal of inherited metabolic disease. 1997, Vol 20, Num 6, pp 833-834, issn 0141-8955Article

Neonatal multiple acyl-CoA dehyrogenase deficiency : essentially absent fatty acid oxidation activity in proband but normal activity in parental cultured skin fibroblastsIP, W. C; HAMMOND, J. W; WILCKEN, B et al.Journal of inherited metabolic disease. 1996, Vol 19, Num 3, pp 379-380, issn 0141-8955Article

Pregnancy and argininosuccinic aciduriaWORTHINGTON, S; CHRISTODOULOU, J; WILCKEN, B et al.Journal of inherited metabolic disease. 1996, Vol 19, Num 5, pp 621-623, issn 0141-8955Article

PRECISE LOCATION OF THE CROSSOVER REGION IN THE LAMBDA ATTACHMENT SEQUENCE.SCHREIER PH; DAVIES RW; BUCHELL DE et al.1977; NATURE; G.B.; DA. 1977; VOL. 267; NO 5611; PP. 555-557; BIBL. 26 REF.Article

3-Hydroxyglutarate excretion is increased in ketotic patients: Implications for glutaryl-CoA dehydrogenase deficiency testingPITT, J; CARPENTER, K; WILCKEN, B et al.Journal of inherited metabolic disease. 2002, Vol 25, Num 2, pp 83-88, issn 0141-8955Article

Morbidity and mortality in medium chain acyl coenzyme A dehydrogenase deficiencyWILCKEN, B; HAMMOND, J; SILINK, M et al.Archives of disease in childhood. 1994, Vol 70, Num 5, pp 410-412, issn 0003-9888Article

HAWKINSINURIA: A DOMINANTLY INHERITED DEFECT OF TYROSINE METABOLISM WITH SEVERE EFFECTS IN INFANCYWILCKEN B; HAMMOND JW; HOWARD N et al.1981; N. ENGL. J. MED.; ISSN 0028-4793; USA; DA. 1981; VOL. 305; NO 15; PP. 865-869; BIBL. 17 REF.Article

Neonatal screening for cystic fibrosis : a comparison of two strategies for case detection in 1.2 million babiesWILCKEN, B; WILEY, V; SHERRY, G et al.The Journal of pediatrics. 1995, Vol 127, Num 6, pp 965-970, issn 0022-3476Article

Neonatal symptoms in medium chain acyl coenzyme A dehydrogenase deficiencyWILCKEN, B; CARPENTER, K. H; HAMMOND, J et al.Archives of disease in childhood. 1993, Vol 69, Num 3, pp 292-294, issn 0003-9888, SUPArticle

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