Wen H, Deng H, Li B, Chen J, Zhu J, Zhang X
Signal Transduct Target Ther. 2025; 10(1):9.
PMID: 39788934
PMC: 11724432.
DOI: 10.1038/s41392-024-02044-3.
Saneto R
J Transl Genet Genom. 2021; 4:384-428.
PMID: 33426505
PMC: 7791531.
DOI: 10.20517/jtgg.2020.40.
Lv H, Qu Q, Liu H, Qian Q, Zheng X, Zhang Y
Exp Ther Med. 2020; 20(2):1770-1774.
PMID: 32742407
PMC: 7388235.
DOI: 10.3892/etm.2020.8822.
Cheung L, Manthey A, Lai J, Chiu K
Front Neurosci. 2017; 11:648.
PMID: 29213227
PMC: 5702640.
DOI: 10.3389/fnins.2017.00648.
Pavlakis S, Hirano M
Pediatr Neurol. 2016; 63:3-5.
PMID: 27460527
PMC: 8285080.
DOI: 10.1016/j.pediatrneurol.2016.05.014.
Mitochondrial DNA: impacting central and peripheral nervous systems.
Carelli V, Chan D
Neuron. 2014; 84(6):1126-42.
PMID: 25521375
PMC: 4271190.
DOI: 10.1016/j.neuron.2014.11.022.
The clinical maze of mitochondrial neurology.
DiMauro S, Schon E, Carelli V, Hirano M
Nat Rev Neurol. 2013; 9(8):429-44.
PMID: 23835535
PMC: 3959773.
DOI: 10.1038/nrneurol.2013.126.
Historical perspective on mitochondrial medicine.
DiMauro S, Garone C
Dev Disabil Res Rev. 2010; 16(2):106-13.
PMID: 20818724
PMC: 3839238.
DOI: 10.1002/ddrr.102.
A history of mitochondrial diseases.
DiMauro S
J Inherit Metab Dis. 2010; 34(2):261-76.
PMID: 20490929
DOI: 10.1007/s10545-010-9082-x.
Pathogenesis and treatment of mitochondrial disorders.
DiMauro S, Hirano M
Adv Exp Med Biol. 2010; 652:139-70.
PMID: 20225024
PMC: 10440730.
DOI: 10.1007/978-90-481-2813-6_10.
Mitochondrial disease: a historical, biochemical, and London perspective.
Land J, Morgan-Hughes J, Hargreaves I, Heales S
Neurochem Res. 2004; 29(3):483-91.
PMID: 15038596
DOI: 10.1023/b:nere.0000014819.53972.b0.
MELAS: a new disease associated mitochondrial DNA mutation and evidence for further genetic heterogeneity.
Hanna M, Nelson I, Morgan-Hughes J, Wood N
J Neurol Neurosurg Psychiatry. 1998; 65(4):512-7.
PMID: 9771776
PMC: 2170312.
DOI: 10.1136/jnnp.65.4.512.
Clinical, morphological, biochemical, and neuroradiological features of mitochondrial encephalomyopathies. Presentation of 19 patients.
Lindner A, Hofmann E, Naumann M, Becker G, Reichmann H
Mol Cell Biochem. 1997; 174(1-2):297-303.
PMID: 9309703
EEG and evoked potential findings in mitochondrial myopathies.
Smith S, Harding A
J Neurol. 1993; 240(6):367-72.
PMID: 8336178
DOI: 10.1007/BF00839969.
Mitochondrial myopathies. Clinical, morphological and biochemical aspects.
Sengers R, STADHOUDERS A, Trijbels J
Eur J Pediatr. 1984; 141(4):192-207.
PMID: 6329761
DOI: 10.1007/BF00572761.
Mitochondrial angiopathy in cerebral blood vessels of mitochondrial encephalomyopathy.
Ohama E, OHara S, Ikuta F, Tanaka K, Nishizawa M, Miyatake T
Acta Neuropathol. 1987; 74(3):226-33.
PMID: 3673514
DOI: 10.1007/BF00688185.
Computed tomography and angiography in MELAS (mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes); report of 3 cases.
Hasuo K, Tamura S, Yasumori K, Uchino A, Goda S, Ishimoto S
Neuroradiology. 1987; 29(4):393-7.
PMID: 3627423
DOI: 10.1007/BF00348922.
Involvement of choroid plexus in mitochondrial encephalomyopathy (MELAS).
Ohama E, Ikuta F
Acta Neuropathol. 1987; 75(1):1-7.
PMID: 3434208
DOI: 10.1007/BF00686785.
Mitochondrial encephalo-neuro-myopathy with myoclonus epilepsy, basal nuclei calcification and hyperlactacidemia.
Federico A, Cornelio F, Di Donato S, Ederli E, Fabrizi G, Manneschi L
Ital J Neurol Sci. 1988; 9(1):65-71.
PMID: 3356526
DOI: 10.1007/BF02334410.
Neuropathology of myoclonus epilepsy associated with ragged-red fibers (Fukuhara's disease).
Takeda S, Wakabayashi K, Ohama E, Ikuta F
Acta Neuropathol. 1988; 75(5):433-40.
PMID: 3132027
DOI: 10.1007/BF00687129.
