Familial Creutzfeldt-Jakob disease with D178N-129M mutation of PRNP presenting as cerebellar ataxia without insomnia

Y. Taniwaki; H. Hara; K. Doh-Ura; I. Murakami; H. Tashiro; T. Yamasaki; H. Shigeto; K. Arakawa; E. Araki; T. Yamada; T. Iwaki; J. Kira

doi:10.1136/jnnp.68.3.388

Familial Creutzfeldt-Jakob disease with D178N-129M mutation of PRNP presenting as cerebellar ataxia without insomnia

Y. Taniwaki, H. Hara, K. Doh-Ura, I. Murakami, H. Tashiro, T. Yamasaki, H. Shigeto, K. Arakawa, E. Araki, T. Yamada, T. Iwaki, J. Kira

Research output: Contribution to journal › Letter › peer-review

32 Citations (Scopus)

Original language	English
Pages (from-to)	388
Number of pages	1
Journal	Journal of Neurology Neurosurgery and Psychiatry
Volume	68
Issue number	3
DOIs	https://doi.org/10.1136/jnnp.68.3.388
Publication status	Published - 2000

All Science Journal Classification (ASJC) codes

Surgery
Clinical Neurology
Psychiatry and Mental health

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10.1136/jnnp.68.3.388

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Taniwaki, Y., Hara, H., Doh-Ura, K., Murakami, I., Tashiro, H., Yamasaki, T., Shigeto, H., Arakawa, K., Araki, E., Yamada, T., Iwaki, T., & Kira, J. (2000). Familial Creutzfeldt-Jakob disease with D178N-129M mutation of PRNP presenting as cerebellar ataxia without insomnia. Journal of Neurology Neurosurgery and Psychiatry, 68(3), 388. https://doi.org/10.1136/jnnp.68.3.388

Taniwaki, Y, Hara, H, Doh-Ura, K, Murakami, I, Tashiro, H, Yamasaki, T, Shigeto, H, Arakawa, K, Araki, E, Yamada, T, Iwaki, T & Kira, J 2000, 'Familial Creutzfeldt-Jakob disease with D178N-129M mutation of PRNP presenting as cerebellar ataxia without insomnia', Journal of Neurology Neurosurgery and Psychiatry, vol. 68, no. 3, pp. 388. https://doi.org/10.1136/jnnp.68.3.388

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author = "Y. Taniwaki and H. Hara and K. Doh-Ura and I. Murakami and H. Tashiro and T. Yamasaki and H. Shigeto and K. Arakawa and E. Araki and T. Yamada and T. Iwaki and J. Kira",

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AU - Taniwaki, Y.

AU - Hara, H.

AU - Doh-Ura, K.

AU - Murakami, I.

AU - Tashiro, H.

AU - Yamasaki, T.

AU - Shigeto, H.

AU - Arakawa, K.

AU - Araki, E.

AU - Yamada, T.

AU - Iwaki, T.

AU - Kira, J.

PY - 2000

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Familial Creutzfeldt-Jakob disease with D178N-129M mutation of PRNP presenting as cerebellar ataxia without insomnia

All Science Journal Classification (ASJC) codes

UN SDGs

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