Bakhit Y, Tesson C, Ibrahim M, Eltom K, Eltazi I, Elsayed L
Ann Clin Transl Neurol. 2023; 10(6):983-989.
PMID: 37139542
PMC: 10270271.
DOI: 10.1002/acn3.51781.
Zou Y, Luo H, Yuan H, Xie K, Yang Y, Huang S
Front Neurol. 2022; 13:904027.
PMID: 35873758
PMC: 9298276.
DOI: 10.3389/fneur.2022.904027.
Tamim-Yecheskel B, Fraiberg M, Kokabi K, Freud S, Shatz O, Marvaldi L
Autophagy. 2020; 17(10):3082-3095.
PMID: 33218264
PMC: 8526015.
DOI: 10.1080/15548627.2020.1852724.
Onder H, Karli Oguz K, Soylemezoglu F, Varli K
Ann Indian Acad Neurol. 2020; 23(3):280-288.
PMID: 32606513
PMC: 7313596.
DOI: 10.4103/aian.AIAN_474_19.
Guo Y, Tang B, Guo J
Front Neurol. 2019; 9:1100.
PMID: 30619057
PMC: 6305538.
DOI: 10.3389/fneur.2018.01100.
Diversity of mitochondrial pathology in a mouse model of axonal degeneration in synucleinopathies.
Sekigawa A, Takamatsu Y, Sekiyama K, Takenouchi T, Sugama S, Waragai M
Oxid Med Cell Longev. 2013; 2013:817807.
PMID: 23577227
PMC: 3612494.
DOI: 10.1155/2013/817807.
A β-synuclein mutation linked to dementia produces neurodegeneration when expressed in mouse brain.
Fujita M, Sugama S, Sekiyama K, Sekigawa A, Tsukui T, Nakai M
Nat Commun. 2010; 1:110.
PMID: 21045828
PMC: 3060620.
DOI: 10.1038/ncomms1101.
Widespread Lewy body and tau accumulation in childhood and adult onset dystonia-parkinsonism cases with PLA2G6 mutations.
Paisan-Ruiz C, Li A, Schneider S, Holton J, Johnson R, Kidd D
Neurobiol Aging. 2010; 33(4):814-23.
PMID: 20619503
PMC: 3657696.
DOI: 10.1016/j.neurobiolaging.2010.05.009.
Adult onset leukodystrophy with neuroaxonal spheroids: clinical, neuroimaging and neuropathologic observations.
Freeman S, Hyman B, Sims K, Hedley-Whyte E, Vossough A, Frosch M
Brain Pathol. 2008; 19(1):39-47.
PMID: 18422757
PMC: 2757058.
DOI: 10.1111/j.1750-3639.2008.00163.x.
Effects of chronic vitamin E deficiency on the nervous system of the rat.
Towfighi J
Acta Neuropathol. 1981; 54(4):261-7.
PMID: 7270082
DOI: 10.1007/BF00696998.
Nasu-Hakola's disease (membranous lipodystrophy). A case report.
Matsushita M, OYANAGI S, Hanawa S, Shiraki H, Kosaka K
Acta Neuropathol. 1981; 54(2):89-93.
PMID: 7246060
DOI: 10.1007/BF00689400.
Spheroids and altered axons in the spinal gray matter of the normal cat. An electron-microscopic study.
Saito K
Acta Neuropathol. 1980; 52(3):213-22.
PMID: 7192470
DOI: 10.1007/BF00705809.
Mitochondrial accumulations in nerve fibres of human sympathetic ganglia.
Helen P, Zeitlin R, Hervonen A
Cell Tissue Res. 1980; 207(3):491-8.
PMID: 7190466
DOI: 10.1007/BF00224622.
Neuropathology of chronic vitamine E deficiency in fatal familial intrahepatic cholestasis.
Saito K, Yokoyama T, Okaniwa M, KAMOSHITA S
Acta Neuropathol. 1982; 58(3):187-92.
PMID: 7158298
DOI: 10.1007/BF00690800.
Onset and regression of neuroaxonal lesions in sheep with mannosidosis induced experimentally with swainsonine.
Huxtable C, Dorling P, Walkley S
Acta Neuropathol. 1982; 58(1):27-33.
PMID: 6814163
DOI: 10.1007/BF00692694.
[Neuro-muscular biopsy in the diagnosis of infantile neuroaxonal dystrophy. Ultrastructural study of 3 cases 2 of them familial].
Sengel A, Stoebner P
Acta Neuropathol. 1972; 21(2):109-16.
PMID: 5054695
DOI: 10.1007/BF00687565.
An analysis of the ultrastructural findings in infantile neuroaxonal dystrophy (Seitelberger's disease).
Liu H, Larson M, Mizuno Y
Acta Neuropathol. 1974; 27(3):201-13.
PMID: 4842105
DOI: 10.1007/BF00687630.
Neuroaxonal dystrophy in subacute dementia. Case report.
TORACK R, Hughes C
Acta Neuropathol. 1972; 22(3):264-8.
PMID: 4637008
DOI: 10.1007/BF00684529.
Infantile neuroaxonal dystrophy or Seitelberger's disease. IV. Autonomic nervous system involvement: electron microscopic study in two siblings.
BERARD-BADIER M, TOGA M, Gambarelli D, Hassoun J, Pellissier J, Pinsard N
Acta Neuropathol. 1974; 28(3):261-7.
PMID: 4372850
DOI: 10.1007/BF00719031.
[Ultrastructure of glial and axonal changes in the optic nerve of the rat induced by 6-aminonicotinamide (author's transl)].
Acta Neuropathol. 1973; 26(2):115-26.
PMID: 4271661
DOI: 10.1007/BF00697747.