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

Year Number of Results
1979 1
1982 2
1988 1
1990 1
1992 1
1993 1
1994 3
1996 1
1997 3
1998 2
1999 3
2000 2
2001 2
2002 2
2003 1
2004 6
2005 3
2006 2
2007 3
2008 2
2009 2
2010 1
2012 3
2013 4
2014 1
2015 3
2016 1
2018 2
2019 1
2024 0

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55 results

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Page 1
The investigation and management of metabolic myopathies.
Olpin SE, Murphy E, Kirk RJ, Taylor RW, Quinlivan R. Olpin SE, et al. J Clin Pathol. 2015 Jun;68(6):410-7. doi: 10.1136/jclinpath-2014-202808. Epub 2015 Apr 15. J Clin Pathol. 2015. PMID: 25878327
Expanding the genetic and phenotypic spectrum of branched-chain amino acid transferase 2 deficiency.
Knerr I, Colombo R, Urquhart J, Morais A, Merinero B, Oyarzabal A, Pérez B, Jones SA, Perveen R, Preece MA, Rogers Y, Treacy EP, Mayne P, Zampino G, MacKinnon S, Wassmer E, Yue WW, Robinson I, Rodríguez-Pombo P, Olpin SE, Banka S. Knerr I, et al. Among authors: olpin se. J Inherit Metab Dis. 2019 Sep;42(5):809-817. doi: 10.1002/jimd.12135. Epub 2019 Aug 1. J Inherit Metab Dis. 2019. PMID: 31177572 Free article.
Carnitine-acylcarnitine translocase deficiency--a mild phenotype.
Olpin SE, Bonham JR, Downing M, Manning NJ, Pollitt RJ, Sharrard MJ, Tanner MS. Olpin SE, et al. J Inherit Metab Dis. 1997 Sep;20(5):714-5. doi: 10.1023/a:1005343013873. J Inherit Metab Dis. 1997. PMID: 9323572 No abstract available.
55 results