-
1
-
-
0001633609
-
Basic reactions of muscle
-
Engel AG, Franzini-Armstrong C (eds) 2nd edn. McGraw-Hill, New York
-
Banker BQ, Engel AG (1994) Basic reactions of muscle. In: Engel AG, Franzini-Armstrong C (eds) Myology, 2nd edn. McGraw-Hill, New York, pp 832-888
-
(1994)
Myology
, pp. 832-888
-
-
Banker, B.Q.1
Engel, A.G.2
-
2
-
-
0026090209
-
Multiple defects of the mitochondrial respiretory chain in a mitochondrial encephalopathy (MERRF): A clinical, biochemical and molecular study
-
Bindoff LA, Desnuelle C, Birch-Machin MA, et al (1991) Multiple defects of the mitochondrial respiretory chain in a mitochondrial encephalopathy (MERRF): a clinical, biochemical and molecular study. J Neurol Sci 102:17-24
-
(1991)
J. Neurol. Sci.
, vol.102
, pp. 17-24
-
-
Bindoff, L.A.1
Desnuelle, C.2
Birch-Machin, M.A.3
-
3
-
-
0018776894
-
Hydroperoxide metabolism in mammalian organs
-
Chance B, Sies H, Boveris A (1979) Hydroperoxide metabolism in mammalian organs. Phys Rev 59: 527-605.
-
(1979)
Phys. Rev.
, vol.59
, pp. 527-605
-
-
Chance, B.1
Sies, H.2
Boveris, A.3
-
4
-
-
0026592966
-
8-Hydroxyguanosine, an abundant form of oxidative DNA damage, causes G→T and A→C substitutions
-
Cheng KC, Cahill DS, Kasai H, et al (1992) 8-Hydroxyguanosine, an abundant form of oxidative DNA damage, causes G→T and A→C substitutions. J Biol Chem 267:166-172
-
(1992)
J. Biol. Chem.
, vol.267
, pp. 166-172
-
-
Cheng, K.C.1
Cahill, D.S.2
Kasai, H.3
-
5
-
-
0026469073
-
Analyses of mitochondrial respiratory chain function and mitochondrial DNA deletion in human skeletal muscle: Effect of aging
-
Cooper JM, Mann VM, Schapira AH (1992) Analyses of mitochondrial respiratory chain function and mitochondrial DNA deletion in human skeletal muscle: effect of aging. J Neurol Sci 113:91-98
-
(1992)
J. Neurol. Sci.
, vol.113
, pp. 91-98
-
-
Cooper, J.M.1
Mann, V.M.2
Schapira, A.H.3
-
6
-
-
0027525492
-
Mitochondrial encephalomyopathies
-
DiMauro S, Moraes CT (1993) Mitochondrial encephalomyopathies. Arch Neurol 50:1197-1208
-
(1993)
Arch. Neurol.
, vol.50
, pp. 1197-1208
-
-
DiMauro, S.1
Moraes, C.T.2
-
7
-
-
0013967657
-
Electron microscopic observations in thyrotoxic and corticosteroid-induced myopathies
-
Engel AG (1966) Electron microscopic observations in thyrotoxic and corticosteroid-induced myopathies. Mayo Clin Proc 41:785-796
-
(1966)
Mayo Clin. Proc.
, vol.41
, pp. 785-796
-
-
Engel, A.G.1
-
8
-
-
0026542453
-
Polymyalgia rheumatica and mitochondrial myopathy: Clinicopathologic and biochemical studies in five cases
-
Harle J-R, Pellissier J-F, Desnuelle C, et al (1992) Polymyalgia rheumatica and mitochondrial myopathy: clinicopathologic and biochemical studies in five cases. Am J Med 92:167-172
-
(1992)
Am. J. Med.
, vol.92
, pp. 167-172
-
-
Harle, J.-R.1
Pellissier, J.-F.2
Desnuelle, C.3
-
9
-
-
0025948247
-
Age-associated accumulation of 8-hyroxydeoxyguanosine in mitochondrial DNA of human diaphragm
-
Hayakawa M, Torii K, Sugiyama S, et al (1991) Age-associated accumulation of 8-hyroxydeoxyguanosine in mitochondrial DNA of human diaphragm. Biochem Biophys Res Commun 179:1023-1029
-
(1991)
Biochem. Biophys. Res. Commun.
, vol.179
, pp. 1023-1029
-
-
Hayakawa, M.1
Torii, K.2
Sugiyama, S.3
-
10
-
-
0000523626
-
Endocrine myopathies (hyper-and hypofunction of adrenal, thyroid, pituitary, and parathyroid glands and introgenic corticosteroid myopathy
-
Engel AG, Franzini-Armstrong C (eds) 2nd edn. McGraw-Hill, New York
-
Kaminsky HJ, Ruff RF (1994) Endocrine myopathies (hyper-and hypofunction of adrenal, thyroid, pituitary, and parathyroid glands and introgenic corticosteroid myopathy. In: Engel AG, Franzini-Armstrong C (eds) Myology, 2nd edn. McGraw-Hill, New York, pp 1726-1753
-
(1994)
Myology
, pp. 1726-1753
-
-
Kaminsky, H.J.1
Ruff, R.F.2
-
11
-
-
0029010022
-
Mitochondrial encephalomyopathy with autosomal dominant inheritance: A clinical and genetic entity of mitochondrial diseases
-
Kawai H, Akaike M, Yokoi K, et al (1995) Mitochondrial encephalomyopathy with autosomal dominant inheritance: a clinical and genetic entity of mitochondrial diseases. Muscle Nerve 18:753-760
-
(1995)
Muscle Nerve
, vol.18
, pp. 753-760
-
-
Kawai, H.1
Akaike, M.2
Yokoi, K.3
-
12
-
-
0029094331
-
Adhalin gene mutations in patients with autosomal recessive childhood onset muscular dystrophy with adhalin deficiency
-
Kawai H, Akaike M, Endo T, et al (1995) Adhalin gene mutations in patients with autosomal recessive childhood onset muscular dystrophy with adhalin deficiency. J Clin Invest 96:1202-1207
-
(1995)
J. Clin. Invest.
, vol.96
, pp. 1202-1207
-
-
Kawai, H.1
Akaike, M.2
Endo, T.3
-
13
-
-
0023647116
-
Misreading of DNA templates containing 8-hydroxyoxyguanosine at the modified base and adjacent residues
-
Kuchino Y, Mori F, Kasai H, et al (1987) Misreading of DNA templates containing 8-hydroxyoxyguanosine at the modified base and adjacent residues. Nature 327:77-79
-
(1987)
Nature
, vol.327
, pp. 77-79
-
-
Kuchino, Y.1
Mori, F.2
Kasai, H.3
-
14
-
-
0030061079
-
Localization and amount of myoglobin and myoglobin mRNA in ragged-red fiber of patients with mitochondrial encephalomyopathy
-
Kunishige M, Mitsui T, Akaike M, et al (1996) Localization and amount of myoglobin and myoglobin mRNA in ragged-red fiber of patients with mitochondrial encephalomyopathy. Muscle Nerve 19:175-182
-
(1996)
Muscle Nerve
, vol.19
, pp. 175-182
-
-
Kunishige, M.1
Mitsui, T.2
Akaike, M.3
-
15
-
-
0025345775
-
Progressive increase of the mutated mitochondrial DNA fraction in Kearns-Sayre syndrome
-
Larsson NG, Holme B, Kristiansson B, Olfords A, Tulinius M (1990 Progressive increase of the mutated mitochondrial DNA fraction in Kearns-Sayre syndrome. Pediatr Res 28:131-136
-
(1990)
Pediatr. Res.
, vol.28
, pp. 131-136
-
-
Larsson, N.G.1
Holme, B.2
Kristiansson, B.3
Olfords, A.4
Tulinius, M.5
-
17
-
-
0029042420
-
Mitochondrial changes in steroid myopathy with respiratory failure and rapid fatal course: Report of a case
-
Mala?rini A, Scarpini C, Fabrizi GM, et al (1995) Mitochondrial changes in steroid myopathy with respiratory failure and rapid fatal course: report of a case. Eur Neurol 35:182-183
-
(1995)
Eur. Neurol.
, vol.35
, pp. 182-183
-
-
Malandrini, A.1
Scarpini, C.2
Fabrizi, G.M.3
-
18
-
-
34249922414
-
Steroid myopathy: Clinical and immunohistochemical study of a case
-
Marolda M, Palma V, Camporeale FS, et al (1991) Steroid myopathy: clinical and immunohistochemical study of a case. Ital J Neurol Sci 12:409-413
-
(1991)
Ital. J. Neurol. Sci.
, vol.12
, pp. 409-413
-
-
Marolda, M.1
Palma, V.2
Camporeale, F.S.3
-
19
-
-
0027391471
-
In vitro studies on the effects of dehydroepiandrosterone and corticosterone on hepatic steroid receptor binding and mitochondrial respiration
-
McIntosh MK, Pan J-S, Berdanier CD (1993) In vitro studies on the effects of dehydroepiandrosterone and corticosterone on hepatic steroid receptor binding and mitochondrial respiration. Comp Biochem Physiol Comp Physiol 104A:147-153
-
(1993)
Comp. Biochem. Physiol. Comp. Physiol.
, vol.104 A
, pp. 147-153
-
-
McIntosh, M.K.1
Pan, J.-S.2
Berdanier, C.D.3
-
20
-
-
0026698066
-
An update on the mitochondrial-DNA mutation hypothesis of cell aging
-
Miquel J (1992) An update on the mitochondrial-DNA mutation hypothesis of cell aging. Mutat Res 275:209-216
-
(1992)
Mutat. Res.
, vol.275
, pp. 209-216
-
-
Miquel, J.1
-
21
-
-
0027169692
-
In situ hybridization of myoglobin mRNA: Results on the skeletal muscles of normal subjects and patients with neuromuscular diseases
-
Mitsui T, Kawai H, Naruo T, Nishino H, Saito S (1993) In situ hybridization of myoglobin mRNA: results on the skeletal muscles of normal subjects and patients with neuromuscular diseases. Acta Neuropathol 86:313-318
-
(1993)
Acta Neuropathol.
, vol.86
, pp. 313-318
-
-
Mitsui, T.1
Kawai, H.2
Naruo, T.3
Nishino, H.4
Saito, S.5
-
22
-
-
0030601202
-
Induction of dystrophin-associated proteins together with nicotinic acetylcholine receptors by denervation in the absence of dystrophin in skeletal muscles of mdx mice
-
Mitsui T, Kawai H, Kawajiri M, Kunishige M, Aki K, Saito S. (1996) Induction of dystrophin-associated proteins together with nicotinic acetylcholine receptors by denervation in the absence of dystrophin in skeletal muscles of mdx mice. Biochem Biophys Res Commun 224:802-807
-
(1996)
Biochem. Biophys. Res. Commun.
, vol.224
, pp. 802-807
-
-
Mitsui, T.1
Kawai, H.2
Kawajiri, M.3
Kunishige, M.4
Aki, K.5
Saito, S.6
-
23
-
-
0030200795
-
Oxidative damage to skeletal muscle DNA from patients with mitochondrial encepahalomyopathies
-
Mitsui T, Kawai H, Nagasawa M, et al (1996) Oxidative damage to skeletal muscle DNA from patients with mitochondrial encepahalomyopathies. J Neurol Sci 136:111-116
-
(1996)
J. Neurol. Sci.
, vol.136
, pp. 111-116
-
-
Mitsui, T.1
Kawai, H.2
Nagasawa, M.3
-
24
-
-
0030641254
-
Preferential subsarcolemmal localization of dystrophin and β-dystroglycan mRNA in human skeletal muscles
-
Mitsui T, Kawai H, Shono M, Kawajiri M, Kunishige M, Saito S (1997) Preferential subsarcolemmal localization of dystrophin and β-dystroglycan mRNA in human skeletal muscles. J Neuropathol Exp Neurol 56:94-101
-
(1997)
J. Neuropathol. Exp. Neurol.
, vol.56
, pp. 94-101
-
-
Mitsui, T.1
Kawai, H.2
Shono, M.3
Kawajiri, M.4
Kunishige, M.5
Saito, S.6
-
25
-
-
0001765125
-
Mitochondrial diseases
-
Mastaglia FL, Walton JN (eds) 2nd edn. Churchill Livingstone, London
-
Morgan-Hughes JA (1992) Mitochondrial diseases. In: Mastaglia FL, Walton JN (eds) Skeletal muscle pathology, 2nd edn. Churchill Livingstone, London, pp 367-424
-
(1992)
Skeletal Muscle Pathology
, pp. 367-424
-
-
Morgan-Hughes, J.A.1
-
27
-
-
0030897739
-
Genetic and functional changes in mitochondria associated with aging
-
Ozawa T (1997) Genetic and functional changes in mitochondria associated with aging. Physiol Rev 77:425-464
-
(1997)
Physiol. Rev.
, vol.77
, pp. 425-464
-
-
Ozawa, T.1
-
28
-
-
0028936222
-
Ragged red fibers in normal aging and inflammatory myopathy
-
Rifai Z, Welle S, Kamp C, Thornton CA (1995) Ragged red fibers in normal aging and inflammatory myopathy. Ann Neurol 37:24-29
-
(1995)
Ann. Neurol.
, vol.37
, pp. 24-29
-
-
Rifai, Z.1
Welle, S.2
Kamp, C.3
Thornton, C.A.4
-
29
-
-
0025981359
-
Insertion of specific bases during DNA synthesis past the oxidation-damaged base 8-oxodG
-
Shibutani S, Takeshita M, Grollman AP (1991) Insertion of specific bases during DNA synthesis past the oxidation-damaged base 8-oxodG. Nature 349:431-434
-
(1991)
Nature
, vol.349
, pp. 431-434
-
-
Shibutani, S.1
Takeshita, M.2
Grollman, A.P.3
-
30
-
-
0026471872
-
Accumulation of deletions in human mitichondrial DNA during normal aging: Analysis by quantitative PCR
-
1180
-
Shimonetti S, Chen X, Dimauro S, Schon EA (1992) Accumulation of deletions in human mitichondrial DNA during normal aging: analysis by quantitative PCR. Biochim Biophys Acta 1180: 113-122
-
(1992)
Biochim. Biophys. Acta
, pp. 113-122
-
-
Shimonetti, S.1
Chen, X.2
Dimauro, S.3
Schon, E.A.4
-
31
-
-
0027534658
-
Mitochondrial DNA alterations as a source of human disorders
-
Tritshler H-J, Medori R (1993) Mitochondrial DNA alterations as a source of human disorders. Neurology 43:280-288
-
(1993)
Neurology
, vol.43
, pp. 280-288
-
-
Tritshler, H.-J.1
Medori, R.2
-
32
-
-
0036938845
-
Apoptosis-related changes in skeletal muscles of patients with mitochondrial diseases
-
Umaki Y, Mitsui T, Endo I, Akaike M, Matsumoto T (2002) Apoptosis-related changes in skeletal muscles of patients with mitochondrial diseases. Acta Neuropathol 103:163-170
-
(2002)
Acta Neuropathol.
, vol.103
, pp. 163-170
-
-
Umaki, Y.1
Mitsui, T.2
Endo, I.3
Akaike, M.4
Matsumoto, T.5
-
33
-
-
0015596693
-
Oxidative respiration of skeletal muscle in experimental corticosteroid myopathy
-
Vignos PJ, Greene R (1973) Oxidative respiration of skeletal muscle in experimental corticosteroid myopathy. J Lab Clin Med 81:365-378
-
(1973)
J. Lab. Clin. Med.
, vol.81
, pp. 365-378
-
-
Vignos, P.J.1
Greene, R.2
-
34
-
-
0026587335
-
Mitochondrial genetics: A paradigm for aging and degenerative diseases?
-
Wallace DC (1992) Mitochondrial genetics: a paradigm for aging and degenerative diseases? Science 256: 628-632
-
(1992)
Science
, vol.256
, pp. 628-632
-
-
Wallace, D.C.1
-
35
-
-
0024395481
-
Focal cytochrome c oxidase deficiency in various neuromuscular diseases
-
Yamamoto M, Koga Y, Ohtaki E, Nonaka I (1989) Focal cytochrome c oxidase deficiency in various neuromuscular diseases. J Neurol Sci 91:207-213
-
(1989)
J. Neurol. Sci.
, vol.91
, pp. 207-213
-
-
Yamamoto, M.1
Koga, Y.2
Ohtaki, E.3
Nonaka, I.4
|