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

Year Number of Results
1993 8
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2000 1
2005 1
2007 1
2009 1
2010 1
2012 1
2013 2
2014 2
2015 2
2016 1
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2018 2
2020 3
2021 8
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2023 2
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2025 1

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Related Articles by Review for PMID: 28125198

29 results

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Page 1
Primary Coenzyme Q10 Deficiency Overview.
Salviati L, Trevisson E, Agosto C, Doimo M, Navas P. Salviati L, et al. 2017 Jan 26 [updated 2023 Jun 8]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2025. 2017 Jan 26 [updated 2023 Jun 8]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2025. PMID: 28125198 Free Books & Documents. Review.
Neuroimaging in Primary Coenzyme-Q10-Deficiency Disorders.
Münch J, Prasuhn J, Laugwitz L, Fung CW, Chung BH, Bellusci M, Mayatepek E, Klee D, Distelmaier F. Münch J, et al. Antioxidants (Basel). 2023 Mar 14;12(3):718. doi: 10.3390/antiox12030718. Antioxidants (Basel). 2023. PMID: 36978966 Free PMC article. Review.
Hereditary Ataxia Overview.
Perlman S. Perlman S. 1998 Oct 28 [updated 2025 Feb 20]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2025. 1998 Oct 28 [updated 2025 Feb 20]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2025. PMID: 20301317 Free Books & Documents. Review.
Mitochondrial Disease and the Kidney With a Special Focus on CoQ10 Deficiency.
Schijvens AM, van de Kar NC, Bootsma-Robroeks CM, Cornelissen EA, van den Heuvel LP, Schreuder MF. Schijvens AM, et al. Kidney Int Rep. 2020 Oct 10;5(12):2146-2159. doi: 10.1016/j.ekir.2020.09.044. eCollection 2020 Dec. Kidney Int Rep. 2020. PMID: 33305107 Free PMC article. Review.
29 results