相似文献
1
[Mitochondrial encephalomyopathy].
Recenti Prog Med. 1989 Dec;80(12):665-72.
2
Mitochondrial DNA deletions in progressive external ophthalmoplegia and Kearns-Sayre syndrome.
N Engl J Med. 1989 May 18;320(20):1293-9. doi: 10.1056/NEJM198905183202001.
3
Mitochondrial myopathies: divergences of genetic deletions, biochemical defects and the clinical syndromes.
J Neurol. 1990 Feb;237(1):5-10. doi: 10.1007/BF00319660.
4
Mitochondrial myopathies: clinical and biochemical features of 30 patients with major deletions of muscle mitochondrial DNA.
Ann Neurol. 1989 Dec;26(6):699-708. doi: 10.1002/ana.410260603.
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Mitochondrial encephalomyopathies.
Acta Neurol (Napoli). 1989 Oct;11(5):322-9.
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[Familial cases of mitochondrial cytopathy].
Rinsho Shinkeigaku. 1987 Aug;27(8):983-9.
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[Mitochondrial encephalomyopathy].
Tanpakushitsu Kakusan Koso. 1990 May;35(7 Suppl):1236-45.
8
Histological, enzymatic and mitochondrial DNA studies in patients with Kearns-Sayre syndrome and chronic progressive external ophthalmoplegia.
Eur Neurol. 1991;31(2):108-13. doi: 10.1159/000116656.
9
[Kearns-Sayre syndrome: mitochondrial encephalomyopathy caused by deficiency of the respiratory chain].
Rev Neurol (Paris). 1989;145(12):842-50.
10
[Biochemistry of mitochondrial encephalomyopathy].
No To Shinkei. 1990 Aug;42(8):707-17.
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