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

Year Number of Results
1951 1
1993 2
1996 1
1997 1
1998 1
1999 2
2000 2
2001 2
2004 1
2005 2
2006 4
2007 1
2008 3
2009 1
2010 2
2011 3
2012 6
2013 1
2014 6
2015 4
2016 7
2017 11
2018 7
2019 6
2020 11
2021 10
2022 8
2023 7
2024 0

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PubMed for Bookshelf ID: 1474604

97 results

Results by year

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Page 1
Leigh Syndrome: Spectrum of Molecular Defects and Clinical Features in Russia.
Kistol D, Tsygankova P, Krylova T, Bychkov I, Itkis Y, Nikolaeva E, Mikhailova S, Sumina M, Pechatnikova N, Kurbatov S, Bostanova F, Migiaev O, Zakharova E. Kistol D, et al. Int J Mol Sci. 2023 Jan 13;24(2):1597. doi: 10.3390/ijms24021597. Int J Mol Sci. 2023. PMID: 36675121 Free PMC article.
Genetic testing for mitochondrial disease: the United Kingdom best practice guidelines.
Mavraki E, Labrum R, Sergeant K, Alston CL, Woodward C, Smith C, Knowles CVY, Patel Y, Hodsdon P, Baines JP, Blakely EL, Polke J, Taylor RW, Fratter C. Mavraki E, et al. Eur J Hum Genet. 2023 Feb;31(2):148-163. doi: 10.1038/s41431-022-01249-w. Epub 2022 Dec 13. Eur J Hum Genet. 2023. PMID: 36513735 Free PMC article.
Use of Whole-Genome Sequencing for Mitochondrial Disease Diagnosis.
Davis RL, Kumar KR, Puttick C, Liang C, Ahmad KE, Edema-Hildebrand F, Park JS, Minoche AE, Gayevskiy V, Mallawaarachchi AC, Christodoulou J, Schofield D, Dinger ME, Cowley MJ, Sue CM. Davis RL, et al. Neurology. 2022 Aug 16;99(7):e730-e742. doi: 10.1212/WNL.0000000000200745. Epub 2022 May 31. Neurology. 2022. PMID: 35641312 Free PMC article.
97 results