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Trimethylaminuria: an under-recognised and socially debilitating metabolic disorder.
Christodoulou J. Christodoulou J. J Paediatr Child Health. 2012 Mar;48(3):E153-5. doi: 10.1111/j.1440-1754.2010.01978.x. Epub 2011 Jan 31. J Paediatr Child Health. 2012. PMID: 21276117 Review.
Retrospective diagnosis of medium chain acyl-CoA dehydrogenase deficiency.
Christodoulou J, Clarke JT, Rupar CA, Gordon BA, Kelly DP. Christodoulou J, et al. J Paediatr Child Health. 1993 Jun;29(3):237-8. doi: 10.1111/j.1440-1754.1993.tb00496.x. J Paediatr Child Health. 1993. PMID: 8518011
Pregnancy and argininosuccinic aciduria.
Worthington S, Christodoulou J, Wilcken B, Peat B. Worthington S, et al. Among authors: christodoulou j. J Inherit Metab Dis. 1996;19(5):621-3. doi: 10.1007/BF01799836. J Inherit Metab Dis. 1996. PMID: 8892017
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. 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
Progressive myoclonic epilepsies: recent genetic advances.
Ellaway CJ, Elliott EJ, Christodoulou J. Ellaway CJ, et al. Among authors: christodoulou j. J Paediatr Child Health. 1997 Apr;33(2):91-5. doi: 10.1111/j.1440-1754.1997.tb01006.x. J Paediatr Child Health. 1997. PMID: 9145347 Review.
Rett syndrome: significant clinical overlap with Angelman syndrome but not with methylation status.
Ellaway C, Buchholz T, Smith A, Leonard H, Christodoulou J. Ellaway C, et al. Among authors: christodoulou j. J Child Neurol. 1998 Sep;13(9):448-51. doi: 10.1177/088307389801300907. J Child Neurol. 1998. PMID: 9733292
Respiratory chain complex III [correction of complex] in deficiency with pruritus: a novel vitamin responsive clinical feature.
Mowat D, Kirby DM, Kamath KR, Kan A, Thorburn DR, Christodoulou J. Mowat D, et al. Among authors: christodoulou j. J Pediatr. 1999 Mar;134(3):352-4. doi: 10.1016/s0022-3476(99)70463-4. J Pediatr. 1999. PMID: 10064675 Review.
Rett syndrome: randomized controlled trial of L-carnitine.
Ellaway C, Williams K, Leonard H, Higgins G, Wilcken B, Christodoulou J. Ellaway C, et al. Among authors: christodoulou j. J Child Neurol. 1999 Mar;14(3):162-7. doi: 10.1177/088307389901400306. J Child Neurol. 1999. PMID: 10190267 Clinical Trial.
Surfactant protein B deficiency: clinical, histological and molecular evaluation.
Williams GD, Christodoulou J, Stack J, Symons P, Wert SE, Murrell MJ, Nogee LM. Williams GD, et al. Among authors: christodoulou j. J Paediatr Child Health. 1999 Apr;35(2):214-20. doi: 10.1046/j.1440-1754.1999.00307.x. J Paediatr Child Health. 1999. PMID: 10365365
Flow cytometric evaluation of defects of the mitochondrial respiratory chain.
Williams AJ, Coakley JC, Christodoulou J. Williams AJ, et al. Among authors: christodoulou j. J Child Neurol. 1999 Aug;14(8):518-23. doi: 10.1177/088307389901400807. J Child Neurol. 1999. PMID: 10456762
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