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

Year Number of Results
1999 4
2004 1
2005 1
2006 1
2007 2
2008 1
2009 2
2010 3
2011 1
2012 1
2014 1
2015 2
2016 1
2017 4
2019 7
2021 1
2022 0
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30 results
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Page 1
The relationship between d-beta-hydroxybutyrate blood concentrations and seizure control in children treated with the ketogenic diet for medically intractable epilepsy.
Buchhalter JR, D'Alfonso S, Connolly M, Fung E, Michoulas A, Sinasac D, Singer R, Smith J, Singh N, Rho JM. Buchhalter JR, et al. Among authors: sinasac d. Epilepsia Open. 2017 May 19;2(3):317-321. doi: 10.1002/epi4.12058. eCollection 2017 Sep. Epilepsia Open. 2017. PMID: 29588960 Free PMC article.
Analyzing complex traits with congenic strains.
Shao H, Sinasac DS, Burrage LC, Hodges CA, Supelak PJ, Palmert MR, Moreno C, Cowley AW Jr, Jacob HJ, Nadeau JH. Shao H, et al. Among authors: sinasac ds. Mamm Genome. 2010 Jun;21(5-6):276-86. doi: 10.1007/s00335-010-9267-5. Epub 2010 Jun 4. Mamm Genome. 2010. PMID: 20524000 Free PMC article.
SS-31 Peptide Reverses the Mitochondrial Fragmentation Present in Fibroblasts From Patients With DCMA, a Mitochondrial Cardiomyopathy.
Machiraju P, Wang X, Sabouny R, Huang J, Zhao T, Iqbal F, King M, Prasher D, Lodha A, Jimenez-Tellez N, Ravandi A, Argiropoulos B, Sinasac D, Khan A, Shutt TE, Greenway SC. Machiraju P, et al. Among authors: sinasac d. Front Cardiovasc Med. 2019 Nov 15;6:167. doi: 10.3389/fcvm.2019.00167. eCollection 2019. Front Cardiovasc Med. 2019. PMID: 31803760 Free PMC article.
Characterization of the C584R variant in the mtDNA depletion syndrome gene FBXL4, reveals a novel role for FBXL4 as a regulator of mitochondrial fusion.
Sabouny R, Wong R, Lee-Glover L, Greenway SC, Sinasac DS; Care4Rare Canada, Khan A, Shutt TE. Sabouny R, et al. Among authors: sinasac ds. Biochim Biophys Acta Mol Basis Dis. 2019 Nov 1;1865(11):165536. doi: 10.1016/j.bbadis.2019.165536. Epub 2019 Aug 20. Biochim Biophys Acta Mol Basis Dis. 2019. PMID: 31442532 Free article.
PISD is a mitochondrial disease gene causing skeletal dysplasia, cataracts, and white matter changes.
Zhao T, Goedhart CM, Sam PN, Sabouny R, Lingrell S, Cornish AJ, Lamont RE, Bernier FP, Sinasac D, Parboosingh JS; Care4Rare Canada Consortium, Vance JE, Claypool SM, Innes AM, Shutt TE. Zhao T, et al. Among authors: sinasac d. Life Sci Alliance. 2019 Mar 11;2(2):e201900353. doi: 10.26508/lsa.201900353. Print 2019 Apr. Life Sci Alliance. 2019. PMID: 30858161 Free PMC article.
Pivotal role of inter-organ aspartate metabolism for treatment of mitochondrial aspartate-glutamate carrier 2 (citrin) deficiency, based on the mouse model.
Saheki T, Moriyama M, Kuroda E, Funahashi A, Yasuda I, Setogawa Y, Gao Q, Ushikai M, Furuie S, Yamamura KI, Takano K, Nakamura Y, Eto K, Kadowaki T, Sinasac DS, Furukawa T, Horiuchi M, Tai YH. Saheki T, et al. Among authors: sinasac ds. Sci Rep. 2019 Mar 12;9(1):4179. doi: 10.1038/s41598-019-39627-y. Sci Rep. 2019. PMID: 30862943 Free PMC article.
30 results