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7. Human extraocular muscles in mitochondrial diseases: comparing chronic progressive external ophthalmoplegia with Leber's hereditary optic neuropathy. Carta A; Carelli V; D'Adda T; Ross-Cisneros FN; Sadun AA Br J Ophthalmol; 2005 Jul; 89(7):825-7. PubMed ID: 15965159 [TBL] [Abstract][Full Text] [Related]
8. [Chronic progressive external ophthalmoplegia (CPEO)--clinical features and histopathology of the extraocular muscles (author's transl)]. Mukuno K No Shinkei Geka; 1974; 2(7-8):529-35. PubMed ID: 4475372 [No Abstract] [Full Text] [Related]
10. Chronic progressive external ophthalmoplegia. Clinical, electrophysiological, histochemical and ultrastructural studies of 14 cases. Piccolo G; Cosi V; Poloni M; Moglia A; Marchetti C; Scelsi R Schweiz Arch Neurol Neurochir Psychiatr; 1982; 131(2):161-74. PubMed ID: 6298931 [TBL] [Abstract][Full Text] [Related]
11. "All-or-none" cytochrome c oxidase positivity in mitochondria in chronic progressive external ophthalmoplegia: an ultrastructural--cytochemical study. Matsuoka T; Goto Y; Nonaka I Muscle Nerve; 1993 Feb; 16(2):206-9. PubMed ID: 8381519 [TBL] [Abstract][Full Text] [Related]
12. [Partial deficiency of cytochrome c oxidase in skeletal muscles; two cousins presenting progressive external ophthalmoplegia and proximal weakness of the limbs]. Madarame H; Nomura T; Chiba K; Niitsu M; Sano M; Tohgi H Nihon Naika Gakkai Zasshi; 1987 Mar; 76(3):414-20. PubMed ID: 3039025 [No Abstract] [Full Text] [Related]
13. [A case of nemaline myopathy with ophthalmoplegia and mitochondrial abnormalities (author's transl)]. Fukunaga H; Osame M; Arimura Y; Igata A Rinsho Shinkeigaku; 1978 Jan; 18(1):35-43. PubMed ID: 630764 [No Abstract] [Full Text] [Related]
15. Multiple mitochondrial DNA deletions in a patient with mitochondrial myopathy and cardiomyopathy but no ophthalmoplegia. Takei Y; Ikeda S; Yanagisawa N; Takahashi W; Sekiguchi M; Hayashi T Muscle Nerve; 1995 Nov; 18(11):1321-5. PubMed ID: 7565930 [TBL] [Abstract][Full Text] [Related]
16. Myasthenia gravis presenting with unusual neurogenic muscle atrophy. Samuraki M; Furui E; Komai K; Takamori M; Yamada M Muscle Nerve; 2007 Sep; 36(3):394-9. PubMed ID: 17326121 [TBL] [Abstract][Full Text] [Related]
17. Mitochondrial encephalomyopathy with autosomal dominant inheritance: a clinical and genetic entity of mitochondrial diseases. Kawai H; Akaike M; Yokoi K; Nishida Y; Kunishige M; Mine H; Saito S Muscle Nerve; 1995 Jul; 18(7):753-60. PubMed ID: 7783765 [TBL] [Abstract][Full Text] [Related]
18. Minicore myopathy with ophthalmoplegia caused by mutations in the ryanodine receptor type 1 gene. Jungbluth H; Zhou H; Hartley L; Halliger-Keller B; Messina S; Longman C; Brockington M; Robb SA; Straub V; Voit T; Swash M; Ferreiro A; Bydder G; Sewry CA; Müller C; Muntoni F Neurology; 2005 Dec; 65(12):1930-5. PubMed ID: 16380615 [TBL] [Abstract][Full Text] [Related]