Danks DM - Search Results

1

Trimethylaminuria, fish odour syndrome: a new method of detection and response to treatment with metronidazole.

Treacy E, Johnson D, Pitt JJ, Danks DM. Treacy E, et al. Among authors: danks dm. J Inherit Metab Dis. 1995;18(3):306-12. doi: 10.1007/BF00710420. J Inherit Metab Dis. 1995. PMID: 7474897

2

Mutations of the flavin-containing monooxygenase gene (FMO3) cause trimethylaminuria, a defect in detoxication.

Treacy EP, Akerman BR, Chow LM, Youil R, Bibeau C, Lin J, Bruce AG, Knight M, Danks DM, Cashman JR, Forrest SM. Treacy EP, et al. Among authors: danks dm. Hum Mol Genet. 1998 May;7(5):839-45. doi: 10.1093/hmg/7.5.839. Hum Mol Genet. 1998. PMID: 9536088

3

Striatal degeneration in glutaric acidaemia type II.

Chow CW, Frerman FE, Goodman SI, Brown GK, Pitt JJ, Danks DM. Chow CW, et al. Among authors: danks dm. Acta Neuropathol. 1989;77(5):554-6. doi: 10.1007/BF00687259. Acta Neuropathol. 1989. PMID: 2718749

4

Ketotic hypoglycaemia presenting as a life-threatening situation in a child with amelia.

Treacy E, Danks DM. Treacy E, et al. Among authors: danks dm. Eur J Pediatr. 1994 Jan;153(1):53. doi: 10.1007/BF02000790. Eur J Pediatr. 1994. PMID: 8313927 No abstract available.

5

Deoxyribose-5-phosphate aldolase deficiency--a harmless inborn error of metabolism.

Chappel A, Scholem RD, Brown GK, Truscott RM, Cotton RG, Haan EA, Danks DM. Chappel A, et al. Among authors: danks dm. J Inherit Metab Dis. 1983;6(3):105-7. doi: 10.1007/BF01800736. J Inherit Metab Dis. 1983. PMID: 6422138

6

Cytochrome c oxidase deficiency in subacute necrotizing encephalopathy (Leigh syndrome).

Hayasaka K, Brown GK, Danks DM, Droste M, Kadenbach B. Hayasaka K, et al. Among authors: danks dm. J Inherit Metab Dis. 1989;12(3):247-56. doi: 10.1007/BF01799214. J Inherit Metab Dis. 1989. PMID: 2559245

7

Liver enzyme activities in hyperphenylalaninaemia due to a defective synthesis of tetrahydrobiopterin.

Dhondt JL, Cotton RG, Danks DM. Dhondt JL, et al. Among authors: danks dm. J Inherit Metab Dis. 1985;8(2):47-8. doi: 10.1007/BF01801660. J Inherit Metab Dis. 1985. PMID: 3939528

8

X-linked pyruvate dehydrogenase E1 alpha subunit deficiency in heterozygous females: variable manifestation of the same mutation.

Dahl HH, Hansen LL, Brown RM, Danks DM, Rogers JG, Brown GK. Dahl HH, et al. Among authors: danks dm. J Inherit Metab Dis. 1992;15(6):835-47. doi: 10.1007/BF01800219. J Inherit Metab Dis. 1992. PMID: 1293379

9

Malonyl coenzyme A decarboxylase deficiency.

Brown GK, Scholem RD, Bankier A, Danks DM. Brown GK, et al. Among authors: danks dm. J Inherit Metab Dis. 1984;7(1):21-6. doi: 10.1007/BF01805615. J Inherit Metab Dis. 1984. PMID: 6145813

10

Malignant hyperphenylalaninaemia--current status (June 1977).

Danks DM, Bartholomé K, Clayton BE, Curtius H, Gröbe H, Kaufman S, Leeming R, Pfleiderer W, Rembold H, Rey F. Danks DM, et al. J Inherit Metab Dis. 1978;1(2):49-53. doi: 10.1007/BF01801843. J Inherit Metab Dis. 1978. PMID: 117241 No abstract available.

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