Danks DM - Search Results

1

Prevalence of K329E mutation in the medium-chain acyl-CoA dehydrogenase gene determined from Guthrie cards.

Matsubara Y, Narisawa K, Tada K, Ikeda H, Yeqi Y, Danks DM, Green A, McCabe ER. Matsubara Y, et al. Among authors: danks dm. Prog Clin Biol Res. 1992;375:453-62. Prog Clin Biol Res. 1992. PMID: 1359564 No abstract available.

2

Prevalence of K329E mutation in medium-chain acyl-CoA dehydrogenase gene determined from Guthrie cards.

Matsubara Y, Narisawa K, Tada K, Ikeda H, Yao YQ, Danks DM, Green A, McCabe ER. Matsubara Y, et al. Among authors: danks dm. Lancet. 1991 Aug 31;338(8766):552-3. doi: 10.1016/0140-6736(91)91110-g. Lancet. 1991. PMID: 1678810

3

Nonketotic hyperglycinemia: analyses of glycine cleavage system in typical and atypical cases.

Hayasaka K, Tada K, Fueki N, Nakamura Y, Nyhan WL, Schmidt K, Packman S, Seashore MR, Haan E, Danks DM, et al. Hayasaka K, et al. Among authors: danks dm. J Pediatr. 1987 Jun;110(6):873-7. doi: 10.1016/s0022-3476(87)80399-2. J Pediatr. 1987. PMID: 3585602 Free article.

4

Difficulties in assessing the effect of strychnine on the outcome of non-ketotic hyperglycinaemia. Observations on sisters with a mild T-protein defect.

Haan EA, Kirby DM, Tada K, Hayasaka K, Danks DM. Haan EA, et al. Among authors: danks dm. Eur J Pediatr. 1986 Sep;145(4):267-70. doi: 10.1007/BF00439398. Eur J Pediatr. 1986. PMID: 3769993

5

Identification of the mutations in the T-protein gene causing typical and atypical nonketotic hyperglycinemia.

Nanao K, Okamura-Ikeda K, Motokawa Y, Danks DM, Baumgartner ER, Takada G, Hayasaka K. Nanao K, et al. Among authors: danks dm. Hum Genet. 1994 Jun;93(6):655-8. doi: 10.1007/BF00201565. Hum Genet. 1994. PMID: 8005589

6

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

7

Biochemical basis of prolidase deficiency. Polypeptide and RNA phenotypes and the relation to clinical phenotypes.

Endo F, Tanoue A, Kitano A, Arata J, Danks DM, Lapière CM, Sei Y, Wadman SK, Matsuda I. Endo F, et al. Among authors: danks dm. J Clin Invest. 1990 Jan;85(1):162-9. doi: 10.1172/JCI114407. J Clin Invest. 1990. PMID: 1688567 Free PMC article.

8

Screening for cystic fibrosis: use of delta F508 mutation.

Bowling FG, McGill JJ, Shepherd RW, Danks DM. Bowling FG, et al. Among authors: danks dm. Lancet. 1990 Apr 14;335(8694):925-6. doi: 10.1016/0140-6736(90)90534-c. Lancet. 1990. PMID: 1970022 No abstract available.

9

"Cerebral" lactic acidosis: defects in pyruvate metabolism with profound brain damage and minimal systemic acidosis.

Brown GK, Haan EA, Kirby DM, Scholem RD, Wraith JE, Rogers JG, Danks DM. Brown GK, et al. Among authors: danks dm. Eur J Pediatr. 1988 Jan;147(1):10-4. doi: 10.1007/BF00442603. Eur J Pediatr. 1988. PMID: 3123240

10

Hereditary hyperammonaemic syndromes--a six year experience.

Haan EA, Danks DM, Hoogenraad NJ, Rogers JG. Haan EA, et al. Among authors: danks dm. Aust Paediatr J. 1979 Sep;15(3):142-6. doi: 10.1111/j.1440-1754.1979.tb01212.x. Aust Paediatr J. 1979. PMID: 518407 No abstract available.

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