Hammond J - Search Results

1

Mitochondrial electron transport chain defect presenting as hypoglycemia.

Freckmann ML, Thorburn DR, Kirby DM, Kamath KR, Hammond J, Dennett X, Christodoulou J. Freckmann ML, et al. Among authors: hammond j. J Pediatr. 1997 Mar;130(3):431-6. doi: 10.1016/s0022-3476(97)70206-3. J Pediatr. 1997. PMID: 9063420

2

Neonatal onset of medium-chain acyl-coenzyme A dehydrogenase deficiency with confusing biochemical features.

Christodoulou J, Hoare J, Hammond J, Ip WC, Wilcken B. Christodoulou J, et al. Among authors: hammond j. J Pediatr. 1995 Jan;126(1):65-8. doi: 10.1016/s0022-3476(95)70504-x. J Pediatr. 1995. PMID: 7815228

3

Acylcarnitine profiles in fibroblasts from patients with respiratory chain defects can resemble those from patients with mitochondrial fatty acid beta-oxidation disorders.

Sim KG, Carpenter K, Hammond J, Christodoulou J, Wilcken B. Sim KG, et al. Among authors: hammond j. Metabolism. 2002 Mar;51(3):366-71. doi: 10.1053/meta.2002.30521. Metabolism. 2002. PMID: 11887175

4

Quantitative fibroblast acylcarnitine profiles in mitochondrial fatty acid beta-oxidation defects: phenotype/metabolite correlations.

Giak Sim K, Carpenter K, Hammond J, Christodoulou J, Wilcken B. Giak Sim K, et al. Among authors: hammond j. Mol Genet Metab. 2002 Aug;76(4):327-34. doi: 10.1016/s1096-7192(02)00112-9. Mol Genet Metab. 2002. PMID: 12208138

5

First prenatal diagnosis of the carnitine transporter defect.

Christodoulou J, Teo SH, Hammond J, Sim KG, Hsu BY, Stanley CA, Watson B, Lau KC, Wilcken B. Christodoulou J, et al. Among authors: hammond j. Am J Med Genet. 1996 Dec 2;66(1):21-4. doi: 10.1002/(SICI)1096-8628(19961202)66:1<21::AID-AJMG5>3.0.CO;2-Z. Am J Med Genet. 1996. PMID: 8957505

6

A fatal neonatal case of medium-chain acyl-coenzyme A dehydrogenase deficiency with homozygous A-->G985 transition.

Leung KC, Hammond JW, Chabra S, Carpenter KH, Potter M, Wilcken B. Leung KC, et al. Among authors: hammond jw. J Pediatr. 1992 Dec;121(6):965-8. doi: 10.1016/s0022-3476(05)80353-1. J Pediatr. 1992. PMID: 1447668 Review.

7

Strategies for the diagnosis of mitochondrial fatty acid beta-oxidation disorders.

Sim KG, Hammond J, Wilcken B. Sim KG, et al. Among authors: hammond j. Clin Chim Acta. 2002 Sep;323(1-2):37-58. doi: 10.1016/s0009-8981(02)00182-1. Clin Chim Acta. 2002. PMID: 12135806 Review.

8

Neonatal symptoms in medium chain acyl coenzyme A dehydrogenase deficiency.

Wilcken B, Carpenter KH, Hammond J. Wilcken B, et al. Among authors: hammond j. Arch Dis Child. 1993 Sep;69(3 Spec No):292-4. doi: 10.1136/adc.69.3_spec_no.292. Arch Dis Child. 1993. PMID: 8215568 Free PMC article.

9

Neonatal multiple acyl-CoA dehydrogenase deficiency: essentially absent fatty acid oxidation activity in proband but normal activity in parental cultured skin fibroblasts.

Ip WC, Hammond JW, Wilcken B. Ip WC, et al. Among authors: hammond jw. J Inherit Metab Dis. 1996;19(3):379-80. doi: 10.1007/BF01799277. J Inherit Metab Dis. 1996. PMID: 8803790 No abstract available.

10

Morbidity and mortality in medium chain acyl coenzyme A dehydrogenase deficiency.

Wilcken B, Hammond J, Silink M. Wilcken B, et al. Among authors: hammond j. Arch Dis Child. 1994 May;70(5):410-2. doi: 10.1136/adc.70.5.410. Arch Dis Child. 1994. PMID: 8017963 Free PMC article.

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