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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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2012 | 1 |
2016 | 1 |
2019 | 2 |
2025 | 0 |
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Ann Neurol. 2016 Aug;80(2):314. doi: 10.1002/ana.24722. Epub 2016 Jul 25.
Ann Neurol. 2016.
PMID: 27393207
No abstract available.
NAD(P)HX dehydratase (NAXD) deficiency: a novel neurodegenerative disorder exacerbated by febrile illnesses.
Van Bergen NJ, Guo Y, Rankin J, Paczia N, Becker-Kettern J, Kremer LS, Pyle A, Conrotte JF, Ellaway C, Procopis P, Prelog K, Homfray T, Baptista J, Baple E, Wakeling M, Massey S, Kay DP, Shukla A, Girisha KM, Lewis LES, Santra S, Power R, Daubeney P, Montoya J, Ruiz-Pesini E, Kovacs-Nagy R, Pritsch M, Ahting U, Thorburn DR, Prokisch H, Taylor RW, Christodoulou J, Linster CL, Ellard S, Hakonarson H.
Van Bergen NJ, et al.
Brain. 2019 Jan 1;142(1):50-58. doi: 10.1093/brain/awy310.
Brain. 2019.
PMID: 30576410
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Instability of the mitochondrial alanyl-tRNA synthetase underlies fatal infantile-onset cardiomyopathy.
Sommerville EW, Zhou XL, Oláhová M, Jenkins J, Euro L, Konovalova S, Hilander T, Pyle A, He L, Habeebu S, Saunders C, Kelsey A, Morris AAM, McFarland R, Suomalainen A, Gorman GS, Wang ED, Thiffault I, Tyynismaa H, Taylor RW.
Sommerville EW, et al.
Hum Mol Genet. 2019 Jan 15;28(2):258-268. doi: 10.1093/hmg/ddy294.
Hum Mol Genet. 2019.
PMID: 30285085
Free PMC article.
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Single deletions in mitochondrial DNA--molecular mechanisms and disease phenotypes in clinical practice.
Pitceathly RD, Rahman S, Hanna MG.
Pitceathly RD, et al.
Neuromuscul Disord. 2012 Jul;22(7):577-86. doi: 10.1016/j.nmd.2012.03.009. Epub 2012 May 9.
Neuromuscul Disord. 2012.
PMID: 22578526
Free article.
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