Gray RG - Search Results

1

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: gray rg. Lancet. 1995 Jan 14;345(8942):135-6. doi: 10.1016/s0140-6736(95)90105-1. Lancet. 1995. PMID: 7815879 No abstract available.

2

Prenatal diagnosis of medium-chain acyl-CoA dehydrogenase deficiency in family with sudden infant death.

Bennett MJ, Allison F, Pollitt RJ, Manning NJ, Gray RG, Green A, Hale DE, Coates PM. Bennett MJ, et al. Among authors: gray rg. Lancet. 1987 Feb 21;1(8530):440-1. doi: 10.1016/s0140-6736(87)90135-8. Lancet. 1987. PMID: 2880228 No abstract available.

3

Prenatal diagnosis of medium-chain acyl-coenzyme A dehydrogenase deficiency.

Bennett MJ, Allison F, Lowther GW, Gray RG, Johnston DI, Fitzsimmons JS, Manning NJ, Pollitt RJ. Bennett MJ, et al. Among authors: gray rg. Prenat Diagn. 1987 Feb;7(2):135-41. doi: 10.1002/pd.1970070210. Prenat Diagn. 1987. PMID: 3575262

4

Molecular characterization of methylmalonate semialdehyde dehydrogenase deficiency.

Chambliss KL, Gray RG, Rylance G, Pollitt RJ, Gibson KM. Chambliss KL, et al. Among authors: gray rg. J Inherit Metab Dis. 2000 Jul;23(5):497-504. doi: 10.1023/a:1005616315087. J Inherit Metab Dis. 2000. PMID: 10947204

5

Methylmalonic semialdehyde dehydrogenase deficiency: demonstration of defective valine and beta-alanine metabolism and reduced malonic semialdehyde dehydrogenase activity in cultured fibroblasts.

Gray RG, Pollitt RJ, Webley J. Gray RG, et al. Biochem Med Metab Biol. 1987 Aug;38(1):121-4. doi: 10.1016/0885-4505(87)90069-7. Biochem Med Metab Biol. 1987. PMID: 3117077

6

Diagnosis and management of non-immune hydrops in the newborn.

Gray RG, Green A. Gray RG, et al. Arch Dis Child Fetal Neonatal Ed. 1994 Sep;71(2):F148-9. doi: 10.1136/fn.71.2.f148-b. Arch Dis Child Fetal Neonatal Ed. 1994. PMID: 7979476 Free PMC article. No abstract available.

7

Enzyme studies on a new case of ornithine carbamoyl transferase deficiency: remaining problems and a method of diagnosis based on plasma enzyme ratios.

Pollitt RJ, Black JA, Gray RG, Lyons VH. Pollitt RJ, et al. Among authors: gray rg. Ann Clin Biochem. 1977 May;14(3):139. doi: 10.1177/000456327701400129. Ann Clin Biochem. 1977. PMID: 17346 No abstract available.

8

Ornithine transcarbamylase deficiency: enzyme studies on a further case and a method of diagnosis using plasma enzyme ratios.

Gray RG, Black JA, Lyons VH, Pollitt RJ. Gray RG, et al. Pediatr Res. 1976 Nov;10(11):918-23. doi: 10.1203/00006450-197611000-00003. Pediatr Res. 1976. PMID: 980551

9

The diagnosis and biochemical investigation of a patient with a short chain fatty acid oxidation defect.

Bennett MJ, Gray RG, Isherwood DM, Murphy N, Pollitt RJ. Bennett MJ, et al. Among authors: gray rg. J Inherit Metab Dis. 1985;8 Suppl 2:135-6. doi: 10.1007/BF01811496. J Inherit Metab Dis. 1985. PMID: 3930866 No abstract available.

10

Riboflavin-responsive ethylmalonic-adipic aciduria.

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

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