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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
2022 0
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Article attribute
Article type
Publication date

Search Results

55 results
Results by year
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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
Response to Finsterer: CPT-II deficiency needs to be detected in army personnel.
Balasubramanian M, Jenkins TM, Kirk RJ, Nesbitt IM, Olpin SE, Hill M, Gillett GT. Balasubramanian M, et al. Among authors: olpin se. Mol Genet Metab Rep. 2018 Jun 8;16:12. doi: 10.1016/j.ymgmr.2018.06.002. eCollection 2018 Sep. Mol Genet Metab Rep. 2018. PMID: 29992091 Free PMC article. No abstract available.
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
55 results