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28. [Clinico-pathological study of 10 cases with ocular myopathy - with special reference to mitochondrial abnormalities]. Santa T; Hosokawa S; Tamura K; Kuroiwa Y; Okamura K Rinsho Shinkeigaku; 1975 Oct; 15(10):683-93. PubMed ID: 1241341 [No Abstract] [Full Text] [Related]
30. [Disorders of mitochondrial energy metabolism in patients with the Kearns-Sayre syndrome]. Capková M; Tesarová M; Wenchich L; Cerná L; Hansíková H; Hůlková H; Hrubá E; Elleder M; Zeman J Cas Lek Cesk; 2002 Feb; 141(2):51-4. PubMed ID: 11925663 [TBL] [Abstract][Full Text] [Related]
32. [Neuromuscular mitochondriopathy. A morphological expression of disorders of the energy metabolism (author's transl)]. Walter GF Veroff Pathol; 1981; 117():1-111. PubMed ID: 6210998 [No Abstract] [Full Text] [Related]
33. 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]
34. Early mitochondrial changes in chronic progressive ocular myopathy. Aasly J; Lindal S; Torbergsen T; Borud O; Mellgren SI Eur Neurol; 1990; 30(6):314-8. PubMed ID: 1963142 [TBL] [Abstract][Full Text] [Related]
35. Metabolic effects of pyridoxine alpha-ketoglutarate in ophthalmoplegia plus. Scarlato G; Pellegrini G; Moggio M; Ferini Strambi L Acta Neurol (Napoli); 1982 Apr; 4(2):92-7. PubMed ID: 7113779 [No Abstract] [Full Text] [Related]
36. Morphological methods in the diagnosis of mitochondrial encephalomyopathies: the role of electron microscopy. Kyriacou K; Hadjisavvas A; Zenios A; Papacharalambous R; Kyriakides T Ultrastruct Pathol; 2005; 29(3-4):169-74. PubMed ID: 16036873 [TBL] [Abstract][Full Text] [Related]
37. [Adult onset mitochondrial myopathy without ophthalmoplegia. Four cases attributable to complex III and IV deficits in the respiratory chain]. Bautista J; Muñoz-Málaga A; Chinchón I; Segura D; Salazar JA; Bescansa E; Campos Y; Arenas J Neurologia; 1995 Oct; 10(8):319-23. PubMed ID: 8554781 [TBL] [Abstract][Full Text] [Related]
38. 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]
39. 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]
40. [Clinical characteristics and ultra-structural features of skeletal muscle in mitochondrial cytopathies]. Zhang ZQ; Sun YL; Niu ST; Liang XH; Wang YJ Zhonghua Yi Xue Za Zhi; 2009 May; 89(17):1185-8. PubMed ID: 19595083 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]