Green A - Search Results

1

Possible deleterious effect of L-carnitine supplementation in a patient with mild multiple acyl-CoA dehydrogenation deficiency (ethylmalonic-adipic aciduria).

Green A, Preece MA, de Sousa C, Pollitt RJ. Green A, et al. J Inherit Metab Dis. 1991;14(5):691-7. doi: 10.1007/BF01799937. J Inherit Metab Dis. 1991. PMID: 1779616

2

Riboflavin-responsive ethylmalonic-adipic aciduria.

Green A, Marshall TG, Bennett MJ, Gray RG, Pollitt RJ. Green A, et al. J Inherit Metab Dis. 1985;8(2):67-70. doi: 10.1007/BF01801667. J Inherit Metab Dis. 1985. PMID: 3939533

3

Population newborn screening for inherited metabolic disease: current UK perspectives.

Green A, Pollitt RJ. Green A, et al. J Inherit Metab Dis. 1999 Jun;22(4):572-9. doi: 10.1023/a:1005572710844. J Inherit Metab Dis. 1999. PMID: 10407789 Review.

4

Excessive excretion of beta-alanine and of 3-hydroxypropionic, R- and S-3-aminoisobutyric, R- and S-3-hydroxyisobutyric and S-2-(hydroxymethyl)butyric acids probably due to a defect in the metabolism of the corresponding malonic semialdehydes.

Pollitt RJ, Green A, Smith R. Pollitt RJ, et al. Among authors: green a. J Inherit Metab Dis. 1985;8(2):75-9. doi: 10.1007/BF01801669. J Inherit Metab Dis. 1985. PMID: 3939535

5

Population screening for the common G985 mutation causing medium-chain acyl-CoA dehydrogenase deficiency with Eu-labeled oligonucleotides and the DELFIA system.

Seddon HR, Gray G, Pollitt RJ, Iitiä A, Green A. Seddon HR, et al. Among authors: green a. Clin Chem. 1997 Mar;43(3):436-42. Clin Chem. 1997. PMID: 9068586

6

Biochemical monitoring of treatment for galactosaemia: biological variability in metabolite concentrations.

Hutchesson AC, Murdoch-Davis C, Green A, Preece MA, Allen J, Holton JB, Rylance G. Hutchesson AC, et al. Among authors: green a. J Inherit Metab Dis. 1999 Apr;22(2):139-48. doi: 10.1023/a:1005493701913. J Inherit Metab Dis. 1999. PMID: 10234609

7

Hyperinsulinism in tyrosinaemia type I.

Baumann U, Preece MA, Green A, Kelly DA, McKiernan PJ. Baumann U, et al. Among authors: green a. J Inherit Metab Dis. 2005;28(2):131-5. doi: 10.1007/s10545-005-5517-1. J Inherit Metab Dis. 2005. PMID: 15877201

8

Neonatal screening for dihydropteridine reductase deficiency.

Sahota A, Blair JA, Barford PA, Leeming RJ, Green A, Pollitt RJ. Sahota A, et al. Among authors: green a. J Inherit Metab Dis. 1985;8 Suppl 2:99-100. doi: 10.1007/BF01811477. J Inherit Metab Dis. 1985. PMID: 3930876 No abstract available.

9

Hypermethioninaemia and 3-hydroxyisobutyric aciduria in an apparently healthy baby.

Congdon PJ, Haigh D, Smith R, Green A, Pollitt RJ. Congdon PJ, et al. Among authors: green a. J Inherit Metab Dis. 1981;4(2):79-80. doi: 10.1007/BF02263600. J Inherit Metab Dis. 1981. PMID: 6790857

10

Regional variations in medium-chain acyl-CoA dehydrogenase deficiency.

Seddon HR, Green A, Gray RG, Leonard JV, Pollitt RJ. Seddon HR, et al. Among authors: green a. Lancet. 1995 Jan 14;345(8942):135-6. doi: 10.1016/s0140-6736(95)90105-1. Lancet. 1995. PMID: 7815879 No abstract available.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

6,732 results

Search Page