研究業績

1999

Papers (English)

 
Original papers


1. Itoh Y, Yamada M, Sodeyama N, Suematsu N, Matsushita M, Otomo E, Mizusawa H. Atherosclerosis is not implicated in association of apolipoprotein E 𝜀4 with Alzheimer's disease. Neurology 53:236-237, 1999

2. Komai K, Iwasa K, Takamori M. Calcium channel peptide can cause an autoimmune-mediated model of Lambert-Eaton myasthenic syndrome in rats. Journal of Neurological Sciences166:126-130, 1999

3. Sodeyama N, Yamada M, Itoh Y, Suematsu N, Matsushita Y, Otomo E, Mizusawa H. No association of paraoxonase gene polymorphism with atherosclerosis or Alzheimer's disease. Neurology 53:1146-1148, 1999

4. Sodeyama N, Yamada M, Itoh Y, Suematsu N, Matsushita M, Otomo E, Mizusawa H. Lack of genetic associations of α1-antichymotrypsin polymorphism with Alzheimer-type neuropathological changes or sporadic Alzheimer's disease. Dement Geriat Cog Disord 10:221-225, 1999

5. Sodeyama N, Yamada M, Itoh Y, Suematsu N, Matsushita M, Otomo E, Mizusawa H. Assocaition between butyrylcholinesterase K variant and the Alzheimer type neuropathological changes in the apolipoprotein E 𝜀4 carriers over 75 years. J Neurol Neurosurg Psychiatry 67:693-694, 1999

6. Sodeyama N, Ishida K, Jaeckle KA, Zhang L, Azuma A, Yamada M, Mizusawa H, Wada Y. Pattern of epitopic reactivity of the anti-Hu antibody on HuD with and without paraneoplastic syndrome. J Neurol Neurosurg Psychiatry 66:97-99, 1999

7. Taga H, Watanabe H, Yamaguchi Y, Ha A Hu Y, Motoo Y. A large duodenal tumor with positive K-ras mutation mimicking lateral spreading tumor of the colon: a case report. Digestive Endoscopy 11:70-75, 1999

8. Takamori M, Komai K, Iwasa K. Antibodies to calcium channel and synaptotagmin in Lambert-Eaton myasthenic syndrome. Am J Med Sci 319:204-208, 1999

9. Takamori M. An autoimmune channelopathy associated with cancer: Lambert-Eaton myasthenic syndrome. Intern Med 30:863-866, 1999

10. Tsunemi T, Yokota T, Kikyo H, Yamamoto M, Yamada M, Kobayashi T, Mizusawa H. Nonsystemic vasculitic neuropathy presenting with truncal segmental sensory disturbance and hyperhidrosis. Muscle Nerve 22:646-647, 1999

11. Toru S, Yokota T, Inaba A, Yamawaki M, Yamada M, Mizusawa H, Hayashi M. Autonomic dysfunction and orthostatic hypotention caused by vitamin B12 deficiency. J Neurol Neurosurg Psychiatry 66:804-805, 1999

12. Doi T, Iwasa K, Makifuchi T, Takamori M. White matter hyperintensities on MRI in a patient with corticobasal degeneration. Acta Neuro Scand 98:1-3, 1999

13. Furui E, Hanzawa K, Ohzeki H, Nakajima T, Fukuhara N. "Tail sign" associated with microembolic signals. Stroke 30:709-714,1999

14. Yamada M, Itoh Y, Inaba A, Wada Y, Takashima M, Satoh S, Kamata T, Okeda R, Kayano T, Suematsu N, Kitamoto T, Otomo E, Matsushita M, Mizusawa H. An inherited prion disease with a PrP P105L mutation: clinicopathologic and PrP heterogeneity. Neurology 53:181-188, 1999

15. Yamada M, Nonaka A, Kamata T, Furuya T, Mizusawa H. A sporadic case of late-onset familial amyloid polyneuropathy with Bence-Jones proteinuria. J Neurol 246:726-729, 1999

16. Yamada M, Sodeyama M, Itoh Y, Suematsu N, Otomo E, Matsushita M, Mizusawa H. A deletion polymorphism of α2-macroglobulin gene and cerebral amyloid angiopathy. Stroke 30:2277-2279, 1999

17. Yamada M, Tomimitsu H, Yokota T, Tomi H, Sunohara N, Mukoyama M, Itoh Y, Suematsu N, Otomo E, Okeda R, Matsushita M, Mizusawa H. Involvement of the spinal posterior horn in Gerstamann-Sträussler-Scheinker disease (PrP P102L). Neurology 52:260-265, 1999

18. Yasukawa Y, Yoshikawa H, Iwasa K, Takamori M. Diagnostic significance of thymic CT and 201Tl-SPECT in myasthenia gravis. Neuroradiology 41:600,1999

19. Yoshino M, Yoshimi Y, Taniguchi M, Nakamura S, Ikeda T. Syndrome of inappropriate secretion of antidiuretic hormone associated with idiopathic normal pressure hydrocepalus. Int Med 38:290-292, 1999
 
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