References
- 1Axelsen TM, Vammen TL, Bak M, Pourhadi N, Stenør CM, Grønborg S. Case report: ‘AARS2 leukodystrophy’. Mol Genet Metab Rep. 2021 Jul 13; 28:
100782 . PMID: 34285876; PMCID: PMC8280508. DOI: 10.1016/j.ymgmr.2021.100782 - 2Della Sala S, Spinnler H, Venneri A. Walking difficulties in patients with Alzheimer’s disease might originate from gait apraxia. J Neurol Neurosurg Psychiatry. 2004 Feb; 75(2): 196–201. PMID: 14742586; PMCID: PMC1738895.
- 3Dale ML, Curtze C, Nutt JG. Apraxia of gait- or apraxia of postural transitions? Parkinsonism Relat Disord. 2018 May; 50: 19–22. Epub 2018 Feb 19. PMID: 29477458. DOI: 10.1016/j.parkreldis.2018.02.024
- 4Rajput A, Rajput A. Old age and Parkinson’s disease. In: Handbook of Clinical Neurology. 2007; 427–444. DOI: 10.1016/S0072-9752(07)84053-X
- 5Della Sala S, Francescani A, Spinnler H. Gait apraxia after bilateral supplementary motor area lesion. J Neurol Neurosurg Psychiatry. 2002 Jan; 72(1): 77–85. PMID: 11784830; PMCID: PMC1737704. DOI: 10.1136/jnnp.72.1.77
- 6Nadeau SE. Gait apraxia: further clues to localization. Eur Neurol. 2007; 58(3): 142–5. Epub 2007 Jun 29. PMID: 17622719. DOI: 10.1159/000104714
- 7Abou Zeid NE, Weinshenker BG, Keegan BM. Gait apraxia in multiple sclerosis. Can J Neurol Sci. 2009 Sep; 36(5): 562–5. PMID: 19831123. DOI: 10.1017/S0317167100008040
- 8Dallabona C, Diodato D, Kevelam SH, et al. Novel (ovario) leukodystrophy related to AARS2 mutations. Neurology. 2014; 82(23): 2063–2071. DOI: 10.1212/WNL.0000000000000497
- 9Zhang X, Li J, Zhang Y, Gao M, Peng T, Tian T. AARS2-Related Leukodystrophy: a Case Report and Literature Review. Cerebellum. 2022 Jan 27. DOI: 10.1007/s12311-022-01369-5
- 10Tang Y, Qin Q, Xing Y, Guo D, Di L, Jia J. AARS2 leukoencephalopathy: A new variant of mitochondrial encephalomyopathy. Mol Genet Genomic Med. 2019 Apr; 7(4):
e00582 . Epub 2019 Jan 31. PMID: 30706699; PMCID: PMC6465728. DOI: 10.1002/mgg3.582