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8. Myopathy with mitochondrial inclusion bodies: histological and metabolic studies. Sulaiman WR; Doyle D; Johnson RH; Jennett S J Neurol Neurosurg Psychiatry; 1974 Nov; 37(11):1236-46. PubMed ID: 4376164 [TBL] [Abstract][Full Text] [Related]
9. [Delayed manifestation of mitochondrial myopathy--complex I and IV deficiency of the mitochondrial respiratory chain with progressive paresis]. Beyenburg S; von Wersebe O; Zierz S Nervenarzt; 1991 Aug; 62(8):506-11. PubMed ID: 1658669 [TBL] [Abstract][Full Text] [Related]
10. A familial mitochondrial myopathy with central defect in neural transmission. Barron SA; Heffner RR; Zwirecki R Arch Neurol; 1979 Sep; 36(9):553-6. PubMed ID: 224846 [TBL] [Abstract][Full Text] [Related]
11. Familial oculocranioskeletal neuromuscular disease with abnormal muscle mitochondria. Tamura K; Santa T; Kuroiwa Y Brain; 1974 Dec; 97(4):665-72. PubMed ID: 4154795 [No Abstract] [Full Text] [Related]
12. Progressive external ophthalmoplegia. Evidence for a generalised mitochondrial disease with a defect in pyruvate metabolism. Reske-Nielsen E; Lou HC; Lowes M Acta Ophthalmol (Copenh); 1976 Oct; 54(5):553-73. PubMed ID: 185877 [TBL] [Abstract][Full Text] [Related]
13. Neuropathy and mitochondrial myopathy. Peyronnard JM; Charron L; Bellavance A; Marchand L Ann Neurol; 1980 Mar; 7(3):262-8. PubMed ID: 6252825 [TBL] [Abstract][Full Text] [Related]
14. Neuromuscular disorders with abnormal muscle mitochondria. Kamieniecka Z; Schmalbruch H Int Rev Cytol; 1980; 65():321-57. PubMed ID: 6993406 [No Abstract] [Full Text] [Related]
15. Ophthalmoplegia plus: neuropathological and metabolic studies with a therapeutic trial in seven cases. Pellegrini G; Scarlato G; Moggio M Acta Neuropathol Suppl; 1981; 7():317-9. PubMed ID: 6939262 [TBL] [Abstract][Full Text] [Related]
16. [Morphological study of muscle fibers stained red by modified Gomori trichrome staining with special reference to smooth red fibers]. Yoshida K Hokkaido Igaku Zasshi; 1997 Mar; 72(2):163-80. PubMed ID: 9145310 [TBL] [Abstract][Full Text] [Related]
18. [Oculocraniosomatic neuromuscular disease, a multisystem disease with abnormal mitochondria demonstrated in skeletal muscle and liver (author's transl)]. Shima K; Hamada T; Tashiro K; Matsumoto H Nihon Naika Gakkai Zasshi; 1982 Mar; 71(3):357-63. PubMed ID: 7108326 [No Abstract] [Full Text] [Related]
19. Muscle fiber hypotrophy with intact neuromuscular junctions. A study of a patient with congenital neuromuscular disease and ophthalmoplegia. Bender AN; Bender MB Neurology; 1977 Mar; 27(3):206-12. PubMed ID: 557754 [TBL] [Abstract][Full Text] [Related]