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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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2001 | 1 |
2010 | 1 |
2011 | 1 |
2024 | 0 |
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Role of common gene variations in the molecular pathogenesis of short-chain acyl-CoA dehydrogenase deficiency.
Pediatr Res. 2001 Jan;49(1):18-23. doi: 10.1203/00006450-200101000-00008.
Pediatr Res. 2001.
PMID: 11134486
Fasting and fat-loading tests provide pathophysiological insight into short-chain acyl-coenzyme a dehydrogenase deficiency.
van Maldegem BT, Duran M, Wanders RJ, Waterham HR, de Koning TJ, Rubio E, Wijburg FA.
van Maldegem BT, et al.
J Pediatr. 2010 Jan;156(1):121-7. doi: 10.1016/j.jpeds.2009.07.008.
J Pediatr. 2010.
PMID: 19800078
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High prevalence of short-chain acyl-CoA dehydrogenase deficiency in the Netherlands, but no association with epilepsy of unknown origin in childhood.
van Maldegem BT, Kloosterman SF, Janssen WJ, Augustijn PB, van der Lee JH, Ijlst L, Waterham HR, Duran R, Wanders RJ, Wijburg FA.
van Maldegem BT, et al.
Neuropediatrics. 2011 Feb;42(1):13-7. doi: 10.1055/s-0031-1275342. Epub 2011 Apr 15.
Neuropediatrics. 2011.
PMID: 21500142
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