Clayton PT - Search Results

1

The monoamine neurotransmitter disorders: an expanding range of neurological syndromes.

Kurian MA, Gissen P, Smith M, Heales S Jr, Clayton PT. Kurian MA, et al. Among authors: clayton pt. Lancet Neurol. 2011 Aug;10(8):721-33. doi: 10.1016/S1474-4422(11)70141-7. Lancet Neurol. 2011. PMID: 21777827 Review.

2

Aromatic L-amino acid decarboxylase deficiency: clinical features, diagnosis, and treatment of a new inborn error of neurotransmitter amine synthesis.

Hyland K, Surtees RA, Rodeck C, Clayton PT. Hyland K, et al. Among authors: clayton pt. Neurology. 1992 Oct;42(10):1980-8. doi: 10.1212/wnl.42.10.1980. Neurology. 1992. PMID: 1357595

3

Neonatal presentation of coenzyme Q10 deficiency.

Rahman S, Hargreaves I, Clayton P, Heales S. Rahman S, et al. J Pediatr. 2001 Sep;139(3):456-8. doi: 10.1067/mpd.2001.117575. J Pediatr. 2001. PMID: 11562630

4

Neonatal epileptic encephalopathy.

Clayton PT, Surtees RA, DeVile C, Hyland K, Heales SJ. Clayton PT, et al. Lancet. 2003 May 10;361(9369):1614. doi: 10.1016/s0140-6736(03)13312-0. Lancet. 2003. PMID: 12747882 No abstract available.

5

Neonatal epileptic encephalopathy caused by mutations in the PNPO gene encoding pyridox(am)ine 5'-phosphate oxidase.

Mills PB, Surtees RA, Champion MP, Beesley CE, Dalton N, Scambler PJ, Heales SJ, Briddon A, Scheimberg I, Hoffmann GF, Zschocke J, Clayton PT. Mills PB, et al. Among authors: clayton pt. Hum Mol Genet. 2005 Apr 15;14(8):1077-86. doi: 10.1093/hmg/ddi120. Epub 2005 Mar 16. Hum Mol Genet. 2005. PMID: 15772097

6

Pyridoxal 5'-phosphate values in cerebrospinal fluid: reference values and diagnosis of PNPO deficiency in paediatric patients.

Ormazabal A, Oppenheim M, Serrano M, García-Cazorla A, Campistol J, Ribes A, Ruiz A, Moreno J, Hyland K, Clayton P, Heales S, Artuch R. Ormazabal A, et al. Mol Genet Metab. 2008 Jun;94(2):173-7. doi: 10.1016/j.ymgme.2008.01.004. Epub 2008 Feb 21. Mol Genet Metab. 2008. PMID: 18294893

7

Pyridoxal 5'-phosphate deficiency causes a loss of aromatic L-amino acid decarboxylase in patients and human neuroblastoma cells, implications for aromatic L-amino acid decarboxylase and vitamin B(6) deficiency states.

Allen GF, Neergheen V, Oppenheim M, Fitzgerald JC, Footitt E, Hyland K, Clayton PT, Land JM, Heales SJ. Allen GF, et al. Among authors: clayton pt. J Neurochem. 2010 Jul;114(1):87-96. doi: 10.1111/j.1471-4159.2010.06742.x. Epub 2010 Apr 9. J Neurochem. 2010. PMID: 20403077 Free article.

8

Pyridoxal 5'-phosphate in cerebrospinal fluid; factors affecting concentration.

Footitt EJ, Heales SJ, Mills PB, Allen GF, Oppenheim M, Clayton PT. Footitt EJ, et al. Among authors: clayton pt. J Inherit Metab Dis. 2011 Apr;34(2):529-38. doi: 10.1007/s10545-011-9279-7. Epub 2011 Feb 9. J Inherit Metab Dis. 2011. PMID: 21305354

9

Bile acid-CoA ligase deficiency--a new inborn error of bile acid metabolism.

Chong CP, Mills PB, McClean P, Gissen P, Bruce C, Stahlschmidt J, Knisely AS, Clayton PT. Chong CP, et al. Among authors: clayton pt. J Inherit Metab Dis. 2012 May;35(3):521-30. doi: 10.1007/s10545-011-9416-3. Epub 2011 Nov 17. J Inherit Metab Dis. 2012. PMID: 22089923

10

Measurement of plasma B6 vitamer profiles in children with inborn errors of vitamin B6 metabolism using an LC-MS/MS method.

Footitt EJ, Clayton PT, Mills K, Heales SJ, Neergheen V, Oppenheim M, Mills PB. Footitt EJ, et al. Among authors: clayton pt. J Inherit Metab Dis. 2013 Jan;36(1):139-45. doi: 10.1007/s10545-012-9493-y. Epub 2012 May 11. J Inherit Metab Dis. 2013. PMID: 22576361

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