Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Kazutake Mori"'
Autor:
Mitsuko Nagasawa, Joann Bodurtha, Masahiko Koike, Tadayasu Hiraoka, Kichiko Koike, Ryuji Hazama, Tooru Hoshino, Kazutake Mori
Publikováno v:
The Tohoku Journal of Experimental Medicine. 136:373-377
BODURTHA, J., HIRAOKA, T., KOIKE, K., KOIKE, M., MORI, K., HAZAMA, R., HOSHINO, T. and NAGASAWA, M. The Density and Distribution of IntramembraneParticles in Erythrocytes from Persons with Muscular Dystrophies. Tohoku J. exp. Med., 1982, 136 (4), 373
Publikováno v:
Pathology International. 27:231-238
An autopsy case of Creutzfeldt-Jakob disease with Kuru-like neuropathological changes which revealed clinically extrapyramidal, pyramidal and psychic symptoms is presented in this report. On microscopic examination, status spongiosus, neuronal degene
Autor:
Noritoshi Shibuya, Kazutake Mori, Masataka Mori, Masaharu Takamori, Mitsuhiro Tsujihata, Ryuji Hazama
Publikováno v:
Journal of the Neurological Sciences. 51:69-79
Ambenonium chloride was administered orally in a dosage of 6 mg/kg/day to rats for 14–360 days. Motor end-plate fine structure and junctional AChR were quantitatively analyzed in red (soleus) and white (EDL) muscle fibers. In treated animals, degen
Neuromuscular transmission block due to an injury of the peripheral nerve appears in the early stages of reinnervation. In microelectrode methods, miniature end-plate potentials (MEPPs) were of normal amplitude but of decreased frequency. The quantum
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8e63719a072c2db0caa51f3285eb9552
https://doi.org/10.1016/b978-0-444-80079-4.50042-9
https://doi.org/10.1016/b978-0-444-80079-4.50042-9
Publikováno v:
Neurology. 29:1486-1486
Clinical and genetic studies were made on progressive muscular dystrophy in six young girls. No chromosome abnormality was observed in these patients. The pedigree of one case implied a sex-linked recessive trait, and clinical features were identical
Publikováno v:
Neurology. 28:804-804
We studied the effects of normal and myasthenic sera on the miniature endplate potential (MEPP) and resting membrane potential (RP) of rat muscle in vitro by conventional intracellular microelectrode techniques. Normal sera had little or no effect on