Biomedical subjects
T Tsubaki
Publications and source records attributed to T Tsubaki.
[Roussy-Lévy syndrome].
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[A case of polyneuropathy due to dipterex associated with numerous tagetoids and cytoplasmic bodies in atrophic muscle fibres (author's transl)].
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[Amyotrophic lateral sclerosis on Guam Part 2 (author's transl)].
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Clinical and immunologic studies on multiple sclerosis.
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[Present status of clinical neurology in Japan. (2) Motor neuron disease].
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[Encephalitis (author's transl)].
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Fabry's disease on the mechanism of the peripheral nerve involvement.
A sural nerve biopsy of a patient with Fabry's disease showed depletion of larger myelinated fibres, but smaller myelinated and unmyelinated fibres were intact. Epineurial and to a lesser degree endoneurial vessels revealed abundant lamellar inclusions in the endothelial and perithelial cells. Larger myelinated nerve fibres contained glycogen granules in the vacuoles caused by splitting of the adaxonal membranes. A skin biopsy revealed abundant inclusions in the secretory cells and myoepithelial cells of the sweat glands. The lumen of the gland was packed with inclusions like those in the vessel walls. The pain and anhydrosis might be caused by accumulation of glycolipid in the vasa nervorum and sweat glands and not by autonomic nerve involvement.
Nationwide survey of multiple sclerosis in Japan. Clinical analysis of 1,084 cases.
Between October 1972 and October 1973, the first nationwide survey of the multiple sclerosis group of diseases in Japan was performed by the Multiple Sclerosis Research Committee of Japan, supported by the Japan Ministry of Health and Welfare. Reports on 1,084 patients with the multiple sclerosis group were collected: 509 patients with multiple sclerosis, 82 with Devic's disease, 357 with "multiple sclerosis possible," and 136 with "other or unclassified demyelinating diseases." The natural history in the present nationwide series of multiple sclerosis patients showed considerable similarity to that of patients in Western countries, suggesting that multiple sclerosis in Japan is essentially the same as that in the Western countries. However, the previously reported special characteristics of Japanese multiple sclerosis patients, namely, a higher rate of visual impairment at onset, a higher rate of optic nerve involvement during the course of illness, and a higher rate of Devic's disease, were reconfirmed in the present series.
[Therapeutic effects of Nicholin (CDP-choline): Parkinson's syndrome.--a double-blind study].
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[Increased vascular permeability in the peripheral nerves of rats intoxicated with methyl mercury].
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[Aetiological and clinical study on subacute myelo-optico-neuropathy (SMON) (author's transl)].
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Genetic and environmental factor in the pathogenesis of motor neuron disease; (1) Identification of the index cases.
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Genetic heterogeneity of Duchenne muscular dystrophy.
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[Myotonic dystrophy accompanying benign cutaneous tumor: with special reference to calcifying epithelioma].
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Rubella antibody in multiple sclerosis.
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Abortion programme in Duchenne muscular dystrophy in Japan.
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