Olpin SE[au] - Search Results

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

1

Pathophysiology of fatty acid oxidation disorders and resultant phenotypic variability.

Olpin SE. Olpin SE. J Inherit Metab Dis. 2013 Jul;36(4):645-58. doi: 10.1007/s10545-013-9611-5. Epub 2013 May 15. J Inherit Metab Dis. 2013. PMID: 23674167 Free PMC article. Review.

2

The metabolic investigation of sudden infant death.

Olpin SE. Olpin SE. Ann Clin Biochem. 2004 Jul;41(Pt 4):282-93. doi: 10.1258/0004563041201473. Ann Clin Biochem. 2004. PMID: 15298740 Review.

3

Implications of impaired ketogenesis in fatty acid oxidation disorders.

Olpin SE. Olpin SE. Prostaglandins Leukot Essent Fatty Acids. 2004 Mar;70(3):293-308. doi: 10.1016/j.plefa.2003.06.003. Prostaglandins Leukot Essent Fatty Acids. 2004. PMID: 14769488 Review.

4

Fatty acid oxidation defects as a cause of neuromyopathic disease in infants and adults.

Olpin SE. Olpin SE. Clin Lab. 2005;51(5-6):289-306. Clin Lab. 2005. PMID: 15991803 Review.

5

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

6

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.

7

Recurrent Ventricular Tachycardia in Medium-Chain Acyl-Coenzyme A Dehydrogenase Deficiency.

Bala P, Ferdinandusse S, Olpin SE, Chetcuti P, Morris AA. Bala P, et al. Among authors: olpin se. JIMD Rep. 2016;27:11-5. doi: 10.1007/8904_2015_463. Epub 2015 Sep 25. JIMD Rep. 2016. PMID: 26404458 Free PMC article.

8

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

9

Interstitial deletion of 1p22.2p31.1 and medium-chain acyl-CoA dehydrogenase deficiency in a patient with global developmental delay.

Maegawa GH, Poplawski NK, Andresen BS, Olpin SE, Nie G, Clarke JT, Teshima I. Maegawa GH, et al. Among authors: olpin se. Am J Med Genet A. 2008 Jun 15;146A(12):1581-6. doi: 10.1002/ajmg.a.32255. Am J Med Genet A. 2008. PMID: 18478588 Review.

10

Cholestatic Jaundice Associated with Carnitine Palmitoyltransferase IA Deficiency.

Morris AA, Olpin SE, Bennett MJ, Santani A, Stahlschmidt J, McClean P. Morris AA, et al. Among authors: olpin se. JIMD Rep. 2013;7:27-9. doi: 10.1007/8904_2012_135. Epub 2012 Mar 21. JIMD Rep. 2013. PMID: 23430491 Free PMC article.

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