Luisa Grosse

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39, 712 (1963); 47, 278 (t967); Pearson, P.K., etal.: Astrophys. J. Lett. 184, L19 (1973); Arrington, C.A., Ogryzlo, E.A.:J. Chem. Phys. 63, 3670 (1975); Botschwina, P., Nachbaur, E., Rode, B.M. : Chem. Phys. Lett. 41, 486 (1976); Saykally, R.J., et al.: Astrophys. J. Lett. 204~ L 143 (1976); Blackman, G.L., et al.: Nature 261, 395 (1976); Brown, R.D., et(More)
Background Myotonic dystrophy type II (formerly denoted as proximal myotonic myopathy (PROMM)) is an autosomal dominantly inherited disease [1]. Sufferers are afflicted with skeletal muscle (SM) symptoms. Histopathologic changes of the SM include mild fibrosis and fatty degeneration[2]. The multisystemic disorder is also characterized by endocrine and(More)
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