Leonard JV - Search Results

1

The measurement of carnitine and acyl-carnitines: application to the investigation of patients with suspected inherited disorders of mitochondrial fatty acid oxidation.

Bhuiyan AK, Jackson S, Turnbull DM, Aynsley-Green A, Leonard JV, Bartlett K. Bhuiyan AK, et al. Among authors: leonard jv. Clin Chim Acta. 1992 May 15;207(3):185-204. doi: 10.1016/0009-8981(92)90118-a. Clin Chim Acta. 1992. PMID: 1327583

2

Measurement of propionate turnover in vivo using sodium [2H5]propionate and sodium [13C]propionate.

Walter JH, Thompson GN, Leonard JV, Heatherington CS, Bartlett K. Walter JH, et al. Among authors: leonard jv. Clin Chim Acta. 1989 Jun 30;182(2):141-50. doi: 10.1016/0009-8981(89)90073-9. Clin Chim Acta. 1989. PMID: 2776349

3

Ultrastructure of liver in inherited disorders of fat oxidation.

Lake BD, Clayton PT, Leonard JV, Bhuiyan AK, Bartlett K, Green AA. Lake BD, et al. Among authors: leonard jv. Lancet. 1987 Feb 14;1(8529):382-3. doi: 10.1016/s0140-6736(87)91752-1. Lancet. 1987. PMID: 2880182 No abstract available.

4

A new simple screening method for the diagnosis of medium chain acyl-CoA dehydrogenase deficiency.

Bhuiyan AK, Watmough NJ, Turnbull DM, Aynsley-Green A, Leonard JV, Bartlett K. Bhuiyan AK, et al. Among authors: leonard jv. Clin Chim Acta. 1987 May 29;165(1):39-44. doi: 10.1016/0009-8981(87)90216-6. Clin Chim Acta. 1987. PMID: 3608187

5

Impaired ketogenesis in fructose-1,6-bisphosphatase deficiency: a pitfall in the investigation of hypoglycaemia.

Morris AA, Deshphande S, Ward-Platt MP, Whitfield AE, Aynsley-Green A, Leonard JV, Pourfarzam M, Bartlett K. Morris AA, et al. Among authors: leonard jv. J Inherit Metab Dis. 1995;18(1):28-32. doi: 10.1007/BF00711369. J Inherit Metab Dis. 1995. PMID: 7623439

6

Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency.

Jackson S, Bartlett K, Land J, Moxon ER, Pollitt RJ, Leonard JV, Turnbull DM. Jackson S, et al. Among authors: leonard jv. Pediatr Res. 1991 Apr;29(4 Pt 1):406-11. doi: 10.1203/00006450-199104000-00016. Pediatr Res. 1991. PMID: 1830138 Free article.

7

A combined defect of three mitochondrial carboxylases presenting as biotin-responsive 3-methylcrotonyl glycinuria and 3-hydroxyisovaleric aciduria.

Bartlett K, Ng H, Leonard JV. Bartlett K, et al. Among authors: leonard jv. Clin Chim Acta. 1980 Jan 15;100(2):183-6. doi: 10.1016/0009-8981(80)90081-9. Clin Chim Acta. 1980. PMID: 6766095

8

A patient with carnitine-acylcarnitine translocase deficiency with a mild phenotype.

Morris AA, Olpin SE, Brivet M, Turnbull DM, Jones RA, Leonard JV. Morris AA, et al. Among authors: leonard jv. J Pediatr. 1998 Mar;132(3 Pt 1):514-6. doi: 10.1016/s0022-3476(98)70030-7. J Pediatr. 1998. PMID: 9544911

9

Glucose production rates in type 1 glycogen storage disease.

Collins JE, Bartlett K, Leonard JV, Aynsley-Green A. Collins JE, et al. Among authors: leonard jv. J Inherit Metab Dis. 1990;13(2):195-206. doi: 10.1007/BF01799686. J Inherit Metab Dis. 1990. PMID: 2116551

10

The effect of ethanol on glucose production in phosphorylase b kinase deficiency.

Collins JE, Bartlett K, Leonard JV, Aynsley-Green A. Collins JE, et al. Among authors: leonard jv. J Inherit Metab Dis. 1989;12(3):317-22. doi: 10.1007/BF01799224. J Inherit Metab Dis. 1989. PMID: 2515373

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