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.
Phadke R
J Clin Med. 2017; 6(7).
PMID: 28677615
PMC: 5532572.
DOI: 10.3390/jcm6070064.
Pavlakis S, Hirano M
Pediatr Neurol. 2016; 63:3-5.
PMID: 27460527
PMC: 8285080.
DOI: 10.1016/j.pediatrneurol.2016.05.014.
Rios P, Kalra A, Wilson J, Tanji K, Akman H, Area Gomez E
Arch Neurol. 2012; 69(5):657-61.
PMID: 22782513
PMC: 8276349.
DOI: 10.1001/archneurol.2011.2333.
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.
Mitochondria.
Chinnery P, Schon E
J Neurol Neurosurg Psychiatry. 2003; 74(9):1188-99.
PMID: 12933917
PMC: 1738655.
DOI: 10.1136/jnnp.74.9.1188.
Megamitochondria formation - physiology and pathology.
Wakabayashi T
J Cell Mol Med. 2003; 6(4):497-538.
PMID: 12611638
PMC: 6741312.
DOI: 10.1111/j.1582-4934.2002.tb00452.x.
Mitochondrial megaconia and pleioconia in the rat brain as possible adaptive reactions in conditions of lethal radiation and radiomodified lesions.
ZABOLOTSKII N, Onishchenko L, Galeev I
Neurosci Behav Physiol. 2000; 30(5):497-501.
PMID: 11037138
DOI: 10.1007/BF02462605.
Congenital type II fibre deficient myopathy.
Dinn J, ODoherty N
Ir J Med Sci. 1980; 149(2):53-8.
PMID: 7372448
DOI: 10.1007/BF02939111.
Ophthalmoplegia-plus.
Godel V, Nemet P, Messer G, Lazar M
Doc Ophthalmol. 1981; 51(4):373-82.
PMID: 7307870
DOI: 10.1007/BF00143339.
Mitochondrial cytopathy. A multisystem disorder with ragged red fibres on muscle biopsy.
Egger J, Lake B, Wilson J
Arch Dis Child. 1981; 56(10):741-52.
PMID: 7305411
PMC: 1627326.
DOI: 10.1136/adc.56.10.741.
Ultrastructural study of the childhood mitochondrial myopathic syndrome associated with lactic acidosis.
Kobayashi Y, Miyabayashi S, Takada G, Narisawa K, Tada K, Yamamoto T
Eur J Pediatr. 1982; 139(1):25-30.
PMID: 7173254
DOI: 10.1007/BF00442074.
"Mitochondrial myopathy" or mitochondrial disease? EEG, ERG, VEP studies in 13 children.
Harden A, Pampiglione G, Battaglia A
J Neurol Neurosurg Psychiatry. 1982; 45(7):627-32.
PMID: 7119830
PMC: 491478.
DOI: 10.1136/jnnp.45.7.627.
Ca2+-uptake properties of two populations of mitochondria from normal and denervated rat soleus muscle.
Joffe M, Savage N, Isaacs H
Biochem J. 1981; 200(3):671-7.
PMID: 7044369
PMC: 1163590.
DOI: 10.1042/bj2000671.
Familial megaconial myopathy: a real nosologic entity. Clinical and histopathologic studies in two siblings.
Pellegrini G, Moggio M, Cheldi A, Scarlato G, PISTONE F, Picco P
Acta Neuropathol. 1983; 59(1):70-4.
PMID: 6837270
DOI: 10.1007/BF00690319.
[Diagnostic significance of muscle biopsies in metabolic myopathies. I. Myopathology].
Pongratz D, Hubner G, Deufel T, Paetzke I, Wieland O
Klin Wochenschr. 1984; 62(13):603-12.
PMID: 6592394
DOI: 10.1007/BF01721915.
A clinico-pathological study of chronic hereditary motor neuropathy.
Matsubara S, Tanabe H
Acta Neuropathol. 1983; 61(1):43-51.
PMID: 6312725
DOI: 10.1007/BF00688385.
Teaching monograph: pathology of skeletal muscle diseases.
DeGirolami U, Smith T
Am J Pathol. 1982; 107(2):231-76.
PMID: 6282129
PMC: 1916001.