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Journal of Inherited Metabolic Disease|January 1, 1992
X-linked pyruvate dehydrogenase E1 alpha subunit deficiency in heterozygous females: variable manifestation of the same mutationH H Dahl, L L Hansen, R M Brown, et al.European Journal of Pediatrics|January 1, 1988
"Cerebral" lactic acidosis: defects in pyruvate metabolism with profound brain damage and minimal systemic acidosisG K Brown, E A Haan, D M Kirby, et al.American Journal of Diseases of Children (1960)|November 1, 1975
The Opitz trigonocephaly syndrome. A case reportF Oberklaid, D M DanksJournal of Medical Genetics|August 1, 1983
Thoracic-pelvic dysostosis: a 'new' autosomal dominant formA Bankier, D M DanksJournal of Inherited Metabolic Disease|January 1, 1982
Normal hydroxylation of proline in collagen synthesized by skin fibroblasts from a patient with prolidase deficiencyP M Royce, D M DanksJournal of Paediatrics and Child Health|June 1, 1991
The natural history of untreated phenylketonuria over 20 yearsD B Pitt, D M DanksBiological Trace Element Research|April 1, 1991
A comparison of phenotype and copper distribution in blotchy and brindled mutant mice and in nutritionally copper deficient controlsM Phillips, J Camakaris, D M DanksThe Biochemical Journal|August 15, 1986
Comparisons of copper deficiency states in the murine mutants blotchy and brindled. Changes in copper-dependent enzyme activity in 13-day-old miceM Phillips, J Camakaris, D M DanksActa Paediatrica Scandinavica|March 1, 1975
A new form of prolonged transient tyrosinemia presenting with severe metabolic acidosisD M Danks, P Tippett, J RogersPageof 19