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130 related items for PubMed ID: 2721536
1. Lipid peroxidation and superoxide dismutase activity in muscle and erythrocytes in adult muscular dystrophies and neurogenic atrophies. Diószeghy P, Imre S, Mechler F. Eur Arch Psychiatry Neurol Sci; 1989; 238(3):175-7. PubMed ID: 2721536 [Abstract] [Full Text] [Related]
2. Lipid peroxidation and superoxide dismutase activity in muscle and erythrocytes in Duchenne muscular dystrophy. Mechler F, Imre S, Dioszeghy P. J Neurol Sci; 1984 Mar; 63(3):279-83. PubMed ID: 6726273 [Abstract] [Full Text] [Related]
3. [A study of superoxide dismutase in erythrocytes in Duchenne muscular dystrophy]. Shen DG. Zhonghua Shen Jing Jing Shen Ke Za Zhi; 1989 Aug; 22(4):208-10, 253. PubMed ID: 2620589 [Abstract] [Full Text] [Related]
4. Possible neurogenic factor in muscular dystrophy: its similarity to denervation atrophy. Dastur DK, Razzak ZA. J Neurol Neurosurg Psychiatry; 1973 Jun; 36(3):399-410. PubMed ID: 4714102 [Abstract] [Full Text] [Related]
5. Superoxide dismutase, glutathione peroxidase and thiobarbituric acid-reactive compounds in erythrocytes in Duchenne muscular dystrophy. Hunter MI, Brzeski MS, de Vane PJ. Clin Chim Acta; 1981 Jun; 115(1):93-8. PubMed ID: 7261410 [Abstract] [Full Text] [Related]
10. Blood levels of superoxide dismutase and glutathione peroxidase in Duchenne muscular dystrophy. Burri BJ, Chan SG, Berry AJ, Yarnell SK. Clin Chim Acta; 1980 Aug 04; 105(2):249-55. PubMed ID: 7398093 [Abstract] [Full Text] [Related]
11. Focal cytochrome c oxidase deficiency in various neuromuscular diseases. Yamamoto M, Koga Y, Ohtaki E, Nonaka I. J Neurol Sci; 1989 Jun 04; 91(1-2):207-13. PubMed ID: 2545831 [Abstract] [Full Text] [Related]
12. Serum manganese-superoxide dismutase in patients with neuromuscular disorders as judged by an ELISA. Yahara O, Hashimoto K, Taniguchi N, Ishikawa M, Sato Y, Yamashita H, Ohno H. Res Commun Chem Pathol Pharmacol; 1991 Jun 04; 72(3):315-26. PubMed ID: 1947435 [Abstract] [Full Text] [Related]
13. Elevated serum levels of manganese superoxide dismutase in polymyositis and dermatomyositis. Mokuno K, Kiyosawa K, Honda H, Hirose Y, Murayama T, Yoneyama S, Kato K. Neurology; 1996 May 04; 46(5):1445-7. PubMed ID: 8628497 [Abstract] [Full Text] [Related]
15. Creatine phosphokinase isozymes in muscles. Human fetus and patients. Goto I, Nagamine M, Katsuki S. Arch Neurol; 1969 Apr 04; 20(4):422-9. PubMed ID: 5816040 [No Abstract] [Full Text] [Related]
16. Glyoxalase enzyme system in human muscular dystrophy. Kar NC, Pearson CM. Clin Chim Acta; 1975 Nov 15; 65(1):153-5. PubMed ID: 1192606 [Abstract] [Full Text] [Related]
17. Abnormal expression of a serine protease in human dystrophic muscle. Katunuma N, Yasogawa N, Kito K, Sanada Y, Kawai H, Miyoshi K. J Biochem; 1978 Feb 15; 83(2):625-8. PubMed ID: 632237 [Abstract] [Full Text] [Related]
18. The significance of the detection of alkaline phosphatase in the diagnosis of neuromuscular diseases. Schmidt A. Biomed Biochim Acta; 1986 Feb 15; 45(1-2):S115-7. PubMed ID: 3964233 [Abstract] [Full Text] [Related]
19. A comparative study of superoxide dismutase, catalase and lipid peroxidation in red blood cells from muscular dystrophy patients and normal controls. Matkovics B, László A, Szabó L. Clin Chim Acta; 1982 Feb 05; 118(2-3):289-92. PubMed ID: 7055986 [No Abstract] [Full Text] [Related]
20. CT muscle imaging and the clinical assessment of neuromuscular disease. Swash M, Brown MM, Thakkar C. Muscle Nerve; 1995 Jul 05; 18(7):708-14. PubMed ID: 7783760 [Abstract] [Full Text] [Related] Page: [Next] [New Search]