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Page 1
Leukocyte cytokine responses in adult patients with mitochondrial DNA defects.
J Mol Med (Berl). 2022 Jun;100(6):963-971. doi: 10.1007/s00109-022-02206-2. Epub 2022 May 30.
J Mol Med (Berl). 2022.
PMID: 35635577
Free PMC article.
Correction to: The evolution of the mitochondrial disease diagnostic odyssey.
Thompson JLP, Karaa A, Pham H, Yeske P, Krischer J, Xiao Y, Long Y, Kramer A, Dimmock D, Holbert A, Gorski C, Engelstad KM, Buchsbaum R, Rosales XQ, Hirano M.
Thompson JLP, et al. Among authors: engelstad km.
Orphanet J Rare Dis. 2023 Jul 20;18(1):194. doi: 10.1186/s13023-023-02832-0.
Orphanet J Rare Dis. 2023.
PMID: 37474973
Free PMC article.
No abstract available.
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The evolution of the mitochondrial disease diagnostic odyssey.
Thompson JLP, Karaa A, Pham H, Yeske P, Krischer J, Xiao Y, Long Y, Kramer A, Dimmock D, Holbert A, Gorski C, Engelstad KM, Buchsbaum R, Rosales XQ, Hirano M.
Thompson JLP, et al. Among authors: engelstad km.
Orphanet J Rare Dis. 2023 Jun 22;18(1):157. doi: 10.1186/s13023-023-02754-x.
Orphanet J Rare Dis. 2023.
PMID: 37349818
Free PMC article.
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Cerebral metabolic abnormalities in A3243G mitochondrial DNA mutation carriers.
Weiduschat N, Kaufmann P, Mao X, Engelstad KM, Hinton V, DiMauro S, De Vivo D, Shungu D.
Weiduschat N, et al.
Neurology. 2014 Mar 4;82(9):798-805. doi: 10.1212/WNL.0000000000000169. Epub 2014 Jan 29.
Neurology. 2014.
PMID: 24477106
Free PMC article.
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Brain microvasculature defects and Glut1 deficiency syndrome averted by early repletion of the glucose transporter-1 protein.
Tang M, Gao G, Rueda CB, Yu H, Thibodeaux DN, Awano T, Engelstad KM, Sanchez-Quintero MJ, Yang H, Li F, Li H, Su Q, Shetler KE, Jones L, Seo R, McConathy J, Hillman EM, Noebels JL, De Vivo DC, Monani UR.
Tang M, et al. Among authors: engelstad km.
Nat Commun. 2017 Jan 20;8:14152. doi: 10.1038/ncomms14152.
Nat Commun. 2017.
PMID: 28106060
Free PMC article.
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