Carpenter K - Search Results

1

Genotype-phenotype correlations in CPT1A deficiency detected by newborn screening in Pacific populations.

Bernhardt I, Glamuzina E, Dowsett LK, Webster D, Knoll D, Carpenter K, Bennett MJ, Maeda M, Wilson C. Bernhardt I, et al. Among authors: carpenter k. JIMD Rep. 2022 Mar 26;63(4):322-329. doi: 10.1002/jmd2.12271. eCollection 2022 Jul. JIMD Rep. 2022. PMID: 35822099 Free PMC article.

2

Abnormal lysosomal cathepsin activities in leukocytes and cultured skin fibroblasts in late infantile, but not in juvenile neuronal ceroid-lipofuscinosis (Batten disease).

Bennett MJ, Chern L, Carpenter KH, Sladky JT. Bennett MJ, et al. Among authors: carpenter kh. Clin Chim Acta. 1992 Jun 15;208(1-2):111-7. doi: 10.1016/0009-8981(92)90028-o. Clin Chim Acta. 1992. PMID: 1638746 No abstract available.

3

Experience with a simple high-performance liquid chromatography method for the analysis of purine and pyrimidine nucleosides and bases in biological fluids.

Bennett MJ, Carpenter KH. Bennett MJ, et al. Among authors: carpenter kh. Ann Clin Biochem. 1984 Mar;21 ( Pt 2):131-6. doi: 10.1177/000456328402100210. Ann Clin Biochem. 1984. PMID: 6712144

4

Asymptomatic xanthinuria detected as a result of routine analysis of serum for urate.

Bennett MJ, Carpenter KH, Hill PG. Bennett MJ, et al. Among authors: carpenter kh. Clin Chem. 1985 Mar;31(3):492. Clin Chem. 1985. PMID: 3971577 No abstract available.

5

A pilot study of the effect of (e, e)-2, 4-undecadienal on the offensive odour of trimethylamine.

Garg P, Carpenter K, Chong S, Christodoulou J. Garg P, et al. Among authors: carpenter k. JIMD Rep. 2013;8:11-5. doi: 10.1007/8904_2012_149. Epub 2012 May 23. JIMD Rep. 2013. PMID: 23430514 Free PMC article.

6

Medium-chain acyl-CoA dehydrogenase deficiency: genotype-biochemical phenotype correlations.

Waddell L, Wiley V, Carpenter K, Bennetts B, Angel L, Andresen BS, Wilcken B. Waddell L, et al. Among authors: carpenter k. Mol Genet Metab. 2006 Jan;87(1):32-9. doi: 10.1016/j.ymgme.2005.09.020. Epub 2005 Nov 15. Mol Genet Metab. 2006. PMID: 16291504

7

Cyclosporin concentrations in whole blood and plasma.

Bennett MJ, Carpenter KH, Worthy E, Lilleyman JS. Bennett MJ, et al. Among authors: carpenter kh. Clin Chem. 1984 May;30(5):817. Clin Chem. 1984. PMID: 6713654 No abstract available.

8

Evaluation of newborn screening for medium chain acyl-CoA dehydrogenase deficiency in 275 000 babies.

Carpenter K, Wiley V, Sim KG, Heath D, Wilcken B. Carpenter K, et al. Arch Dis Child Fetal Neonatal Ed. 2001 Sep;85(2):F105-9. doi: 10.1136/fn.85.2.f105. Arch Dis Child Fetal Neonatal Ed. 2001. PMID: 11517203 Free PMC article.

9

Homocysteine measurement in dried blood spot for neonatal detection of homocystinurias.

Alodaib AN, Carpenter K, Wiley V, Wotton T, Christodoulou J, Wilcken B. Alodaib AN, et al. Among authors: carpenter k. JIMD Rep. 2012;5:1-6. doi: 10.1007/8904_2011_109. Epub 2011 Dec 13. JIMD Rep. 2012. PMID: 23430909 Free PMC article.

10

Expanded newborn screening in New South Wales: missed cases.

Estrella J, Wilcken B, Carpenter K, Bhattacharya K, Tchan M, Wiley V. Estrella J, et al. Among authors: carpenter k. J Inherit Metab Dis. 2014 Nov;37(6):881-7. doi: 10.1007/s10545-014-9727-2. Epub 2014 Jun 27. J Inherit Metab Dis. 2014. PMID: 24970580

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