ETHNIC STEREOTYPES: A CROSS-CULTURAL REPLICATION OF THEIR UNITARY DIMENSIONALITYGARDNER R. C; KIRBY D. M; ARBOLEDA A et al.JOURNAL (THE) OF SOCIAL PSYCHOLOGY. 1973, Vol 91, pp 189-195Article

Maternal tyrosinaemia II : management and successful outcomeFRANCIS, D. E. M; KIRBY, D. M; THOMPSON, G. N et al.European journal of pediatrics. 1992, Vol 151, Num 3, pp 196-199, issn 0340-6199Conference Paper

Respiratory chain complex in deficiency with pruritus : A novel vitamin responsive clinical featureMOWAT, D; KIRBY, D. M; KAMATH, K. R et al.The Journal of pediatrics. 1999, Vol 134, Num 3, pp 352-354, issn 0022-3476Article

Leigh syndrome : Clinical features and biochemical and DNA abnormalitiesRAHMAN, S; BLOK, R. B; DAHL, H.-H. M et al.Annals of neurology. 1996, Vol 39, Num 3, pp 343-351, issn 0364-5134Article

The importance of liver biopsy in the investigation of possible mitochondrial respiratory chain diseasePANETTA, J; GIBSON, K; KIRBY, D. M et al.Neuropediatrics. 2005, Vol 36, Num 4, pp 256-259, issn 0174-304X, 4 p.Article

Characterization of the mutations in three patients with pyruvate dehydrogenase E1α deficiencyHANSEN, L. L; BROWN, G. K; KIRBY, D. M et al.Journal of inherited metabolic disease. 1991, Vol 14, Num 2, pp 140-151, issn 0141-8955, 12 p.Article

Continuous venovenous hemofiltration in the management of acute decompensation in inborn errors of metabolismTHOMPSON, G. N; BUTT, W. W; SHANN, F. A et al.The Journal of pediatrics. 1991, Vol 118, Num 6, pp 879-884, issn 0022-3476Article

Leigh disease caused by the mitochondrial DNA G14459A mutation in unrelated familiesKIRBY, D. M; KAHLER, S. G; FRECKMANN, M.-L et al.Annals of neurology. 2000, Vol 48, Num 1, pp 102-104, issn 0364-5134Article

Respiratory chain complex I deficiency : An underdiagnosed energy generation disorderKIRBY, D. M; CRAWFORD, M; CLEARY, M. A et al.Neurology. 1999, Vol 52, Num 6, pp 1255-1264, issn 0028-3878Article

Pregnancy in phenylketonuria : dietary treatment aimed at normalising maternal plasma phenylalanine concentrationTHOMPSON, G. N; FRANCIS, D. E. M; KIRBY, D. M et al.Archives of disease in childhood. 1991, Vol 66, Num 11, pp 1346-1349, issn 0003-9888Article

Cerebral lactic acidosis: defects in pyruvate metabolism with profound braindamage and minimal systemic acidosisBROWN, G. K; HAAN, E. A; KIRBY, D. M et al.European journal of pediatrics. 1988, Vol 147, Num 1, pp 10-14, issn 0340-6199Article

Difficulties in assessing the effect of strychnine on the outcome of non-ketotic hyperglycinaemia: observations on sisters with a mild T-protein defectHAAN, E. A; KIRBY, D. M; TADA, K et al.European journal of pediatrics. 1986, Vol 145, Num 4, pp 267-270, issn 0340-6199Article

ETHNIC STEREOTYPES: AN ALTERNATIVE ASSESSMENT TECHNIQUE, THE STEREOTYPE DIFFERENTIALGARDNER R. C; KIRBY D. M; GOROSPE F. H et al.J. SOC. PSYCHOL. 1972, Vol 87, Num 2, pp 259-267Article