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Journal Abstract Search
135 related items for PubMed ID: 224846
1. 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 [Abstract] [Full Text] [Related]
2. Mitochondrial oculoskeletal myopathy: case report. Colombo A, Merelli E, Sola P, Panzetti P, Quaglino D, Fornieri C. Ital J Neurol Sci; 1988 Aug; 9(4):385-9. PubMed ID: 2851565 [Abstract] [Full Text] [Related]
3. [Mitochondrial myopathy of progressive external ophthalmoplegia]. Guo YP. Zhonghua Bing Li Xue Za Zhi; 1992 Dec; 21(6):358-60. PubMed ID: 1299529 [Abstract] [Full Text] [Related]
4. 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]
5. Mitochondrial cytopathy. A multisystem disorder with ragged red fibres on muscle biopsy. Egger J, Lake BD, Wilson J. Arch Dis Child; 1981 Oct; 56(10):741-52. PubMed ID: 7305411 [Abstract] [Full Text] [Related]
20. Familial mitochondrial myopathy associated with peripheral neuropathy: partial deficiencies of complex I and complex IV. Mizusawa H, Watanabe M, Kanazawa I, Nakanishi T, Kobayashi M, Tanaka M, Suzuki H, Nishikimi M, Ozawa T. J Neurol Sci; 1988 Sep; 86(2-3):171-84. PubMed ID: 2851645 [Abstract] [Full Text] [Related] Page: [Next] [New Search]