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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2002 2
2003 3
2004 7
2005 3
2006 3
2007 6
2008 6
2009 4
2010 5
2011 4
2012 4
2013 7
2014 7
2015 9
2016 8
2017 13
2018 1
2019 6
2020 4
2021 5
2022 7
2023 3
2024 2

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101 results

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Page 1
Hereditary diseases of coenzyme A thioester metabolism.
Yang H, Zhao C, Wang Y, Wang SP, Mitchell GA. Yang H, et al. Among authors: mitchell ga. Biochem Soc Trans. 2019 Feb 28;47(1):149-155. doi: 10.1042/BST20180423. Epub 2019 Jan 9. Biochem Soc Trans. 2019. PMID: 30626707 Review.
The Québec NTBC Study.
Québec NTBC Study Group; Alvarez F, Atkinson S, Bouchard M, Brunel-Guitton C, Buhas D, Bussières JF, Dubois J, Fenyves D, Goodyer P, Gosselin M, Halac U, Labbé P, Laframboise R, Maranda B, Melançon S, Merouani A, Mitchell GA, Mitchell J, Parizeault G, Pelletier L, Phan V, Turcotte JF. Québec NTBC Study Group, et al. Among authors: mitchell ga. Adv Exp Med Biol. 2017;959:187-195. doi: 10.1007/978-3-319-55780-9_17. Adv Exp Med Biol. 2017. PMID: 28755196 Review.
Reply.
Ghaddhab C, Morin C, Brunel-Guitton C, Mitchell GA, Van Vliet G, Huot C. Ghaddhab C, et al. Among authors: mitchell ga. J Pediatr. 2017 Aug;187:334-335. doi: 10.1016/j.jpeds.2017.04.067. Epub 2017 May 24. J Pediatr. 2017. PMID: 28550952 No abstract available.
Inborn errors of cytoplasmic triglyceride metabolism.
Wu JW, Yang H, Wang SP, Soni KG, Brunel-Guitton C, Mitchell GA. Wu JW, et al. Among authors: mitchell ga. J Inherit Metab Dis. 2015 Jan;38(1):85-98. doi: 10.1007/s10545-014-9767-7. Epub 2014 Oct 10. J Inherit Metab Dis. 2015. PMID: 25300978 Review.
Disorders of mitochondrial function.
Debray FG, Lambert M, Mitchell GA. Debray FG, et al. Among authors: mitchell ga. Curr Opin Pediatr. 2008 Aug;20(4):471-82. doi: 10.1097/MOP.0b013e328306ebb6. Curr Opin Pediatr. 2008. PMID: 18622207 Free article. Review.
101 results