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

Year Number of Results
1986 1
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1994 2
1995 2
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2003 2
2004 1
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2010 2
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Page 1
Genetic and Mitochondrial Metabolic Analyses of an Atypical Form of Leigh Syndrome.
Uittenbogaard M, Sen K, Whitehead M, Brantner CA, Wang Y, Wong LJ, Gropman A, Chiaramello A. Uittenbogaard M, et al. Among authors: chiaramello a. Front Cell Dev Biol. 2021 Dec 22;9:767407. doi: 10.3389/fcell.2021.767407. eCollection 2021. Front Cell Dev Biol. 2021. PMID: 35004675 Free PMC article.
Molecular genetic and mitochondrial metabolic analyses confirm the suspected mitochondrial etiology in a pediatric patient with an atypical form of alternating hemiplegia of childhood.
Gropman A, Uittenbogaard M, Brantner CA, Wang Y, Wong LJ, Chiaramello A. Gropman A, et al. Among authors: chiaramello a. Mol Genet Metab Rep. 2020 May 28;24:100609. doi: 10.1016/j.ymgmr.2020.100609. eCollection 2020 Sep. Mol Genet Metab Rep. 2020. PMID: 32489883 Free PMC article.
The m.11778 A > G variant associated with the coexistence of Leber's hereditary optic neuropathy and multiple sclerosis-like illness dysregulates the metabolic interplay between mitochondrial oxidative phosphorylation and glycolysis.
Uittenbogaard M, Brantner CA, Fang Z, Wong LJ, Gropman A, Chiaramello A. Uittenbogaard M, et al. Among authors: chiaramello a. Mitochondrion. 2019 May;46:187-194. doi: 10.1016/j.mito.2018.06.001. Epub 2018 Jun 8. Mitochondrion. 2019. PMID: 29890302 Free PMC article.
43 results