Olpin S[au] - Search Results

Year	Number of Results
1979	1
1982	2
1988	1
1990	1
1992	1
1993	2
1994	3
1996	1
1997	3
1998	2
1999	5
2000	3
2001	2
2002	3
2003	2
2004	7
2005	7
2006	5
2007	6
2008	5
2009	2
2010	3
2011	1
2012	4
2013	6
2014	2
2015	6
2016	2
2018	2
2019	2
2020	1
2021	1
2022	1
2024	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

MCAD deficiency in Denmark.

Andresen BS, Lund AM, Hougaard DM, Christensen E, Gahrn B, Christensen M, Bross P, Vested A, Simonsen H, Skogstrand K, Olpin S, Brandt NJ, Skovby F, Nørgaard-Pedersen B, Gregersen N. Andresen BS, et al. Among authors: olpin s. Mol Genet Metab. 2012 Jun;106(2):175-88. doi: 10.1016/j.ymgme.2012.03.018. Epub 2012 Apr 4. Mol Genet Metab. 2012. PMID: 22542437

3

Thermo-sensitive mitochondrial trifunctional protein deficiency presenting with episodic myopathy.

Schwantje M, Ebberink MS, Doolaard M, Ruiter JPN, Fuchs SA, Darin N, Hedberg-Oldfors C, Régal L, Donker Kaat L, Huidekoper HH, Olpin S, Cole D, Moat SJ, Visser G, Ferdinandusse S. Schwantje M, et al. Among authors: olpin s. J Inherit Metab Dis. 2022 Jul;45(4):819-831. doi: 10.1002/jimd.12503. Epub 2022 May 5. J Inherit Metab Dis. 2022. PMID: 35403730 Free PMC article.

4

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.

5

Fumarate hydratase mutations and predisposition to cutaneous leiomyomas, uterine leiomyomas and renal cancer.

Alam NA, Olpin S, Leigh IM. Alam NA, et al. Among authors: olpin s. Br J Dermatol. 2005 Jul;153(1):11-7. doi: 10.1111/j.1365-2133.2005.06678.x. Br J Dermatol. 2005. PMID: 16029320 Review.

6

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.

7

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

8

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.

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

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.

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