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27. A case of mitochondrial myopathy, encephalopathy and lactic acidosis due to cytochrome c oxidase deficiency with neurogenic muscular changes. Jinnai K, Yamada H, Kanda F, Masui Y, Tanaka M, Ozawa T, Fujita T. Eur Neurol; 1990; 30(1):56-60. PubMed ID: 2153548 [Abstract] [Full Text] [Related]
28. Mitochondrial encephalomyopathy (MELAS) with mental disorder. CT, MRI and SPECT findings. Suzuki T, Koizumi J, Shiraishi H, Ishikawa N, Ofuku K, Sasaki M, Hori T, Ohkoshi N, Anno I. Neuroradiology; 1990; 32(1):74-6. PubMed ID: 2333139 [Abstract] [Full Text] [Related]
29. Heterogeneous phenotypes of mitochondrial encephalomyopathy in a single kindred. Ishitsu T, Miike T, Kitano A, Haraguchi Y, Ohtani Y, Matsuda I, Shimoji A, Kimura H. Neurology; 1987 Dec; 37(12):1867-9. PubMed ID: 3683878 [Abstract] [Full Text] [Related]
30. [Mitochondrial encephalomyopathy]. Lin SH. Zhonghua Shen Jing Jing Shen Ke Za Zhi; 1987 Oct; 20(5):302-4. PubMed ID: 3450490 [No Abstract] [Full Text] [Related]
31. Mitochondrial encephalomyopathy. A variant with heart failure and liver steatosis. Oldfors A, Tulinius M, Holme E, Kalimo H, Kristiansson B, Eriksson BO. Acta Neuropathol; 1987 Oct; 74(3):287-93. PubMed ID: 3673521 [Abstract] [Full Text] [Related]
33. Myopathy, lactic acidosis, and sideroblastic anemia: a new syndrome. Inbal A, Avissar N, Shaklai M, Kuritzky A, Schejter A, Ben-David E, Shanske S, Garty BZ. Am J Med Genet; 1995 Jan 30; 55(3):372-8. PubMed ID: 7726239 [Abstract] [Full Text] [Related]
34. MELAS syndrome involving a mother and two children. Driscoll PF, Larsen PD, Gruber AB. Arch Neurol; 1987 Sep 30; 44(9):971-3. PubMed ID: 3619716 [Abstract] [Full Text] [Related]
40. [Pathology of mitochondrial encephalomyopathies]. Ohama E, Takeda S. No To Shinkei; 1990 Aug 30; 42(8):735-46. PubMed ID: 2171606 [No Abstract] [Full Text] [Related] Page: [Previous] [Next] [New Search]