論文・総説 - 石川　欽也

21. Kubota Tomoya, Hama Manami, Sugiura Yoshihiro, Takahashi Yuji, Ishikawa Kinya, Mizusawa Hidehiro, Takahashi Masanori P.. 日本における発作性運動失調症の全国調査(A nationwide survey of episodic ataxia in Japan) Neurology and Clinical Neuroscience. 2021.11; 9 (6): 443-451. ( 医中誌 )

22. Ozaki K, Irioka T, Uchihara T, Yamada A, Nakamura A, Majima T, Igarashi S, Shintaku H, Yakeishi M, Tsuura Y, Okazaki Y, Ishikawa K, Yokota T. Neuropathology of SCA34 showing widespread oligodendroglial pathology with vacuolar white matter degeneration: a case study. Acta neuropathologica communications. 2021.10; 9 (1): 172. ( PubMed, DOI )

23. Shibata T, Nagano K, Ueyama M, Ninomiya K, Hirose T, Nagai Y, Ishikawa K, Kawai G, Nakatani K. Small molecule targeting r(UGGAA)(n) disrupts RNA foci and alleviates disease phenotype in Drosophila model. Nature communications. 2021.01; 12 (1): 236. ( PubMed, DOI )

24. Ishikawa, K. Molecular Pathogenesis in Spinocerebellar Ataxia Type 31 (SCA31) CEREBELLUM AS A CNS HUB. 2021; 507-516. ( DOI )

25. Ishiguro T, Nagai Y, Ishikawa K. Insight Into Spinocerebellar Ataxia Type 31 (SCA31) From Drosophila Model. Frontiers in neuroscience. 2021; 15 648133. ( PubMed, DOI )

26. Toru S, Ishida S, Uchihara T, Hirokawa K, Kitagawa M, Ishikawa K. Comorbid argyrophilic grain disease in an 87-year-old male with spinocerebellar ataxia type 31 with dementia: a case report. BMC neurology. 2020.04; 20 (1): 136. ( PubMed, DOI )

27. Ishikawa K, Nagai Y. Molecular Mechanisms and Future Therapeutics for Spinocerebellar Ataxia Type 31 (SCA31). Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics. 2019.11; 16 (4): 1106-1114. ( PubMed, DOI )

28. Hashiguchi Shunta, Doi Hiroshi, Kunii Misako, Nakamura Yukihiro, Shimuta Misa, Suzuki Etsuko, Koyano Shigeru, Okubo Masaki, Kishida Hitaru, Shiina Masaaki, Ogata Kazuhiro, Hirashima Fumiko, Inoue Yukichi, Kubota Shun, Hayashi Noriko, Nakamura Haruko, Takahashi Keita, Katsumoto Atsuko, Tada Mikiko, Tanaka Kenichi, Sasaoka Toshikuni, Miyatake Satoko, Miyake Noriko, Saitsu Hirotomo, Sato Nozomu, Ozaki Kokoro, Ohta Kiyobumi, Yokota Takanori, Mizusawa Hidehiro, Mitsui Jun, Ishiura Hiroyuki, Yoshimura Jun, Morishita Shinichi, Tsuji Shoji, Takeuchi Hideyuki, Ishikawa Kinya, Matsumoto Naomichi, Ishikawa Taro, Tanaka Fumiaki. Ataxic phenotype with altered Ca(v)3.1 channel property in a mouse model for spinocerebellar ataxia 42 NEUROBIOLOGY OF DISEASE. 2019.10; 130 104516. ( PubMed, DOI )

29. Ozaki Kokoro, Ansai Ayaka, Nobuhara Kouji, Araki Toshihiko, Kubodera Takayuki, Ishii Takashi, Higashi Miwa, Sato Nozomu, Soga Kazumasa, Mizusawa Hidehiro, Ishikawa Kinya, Yokota Takanori. Prevalence and clinicoradiological features of spinocerebellar ataxia type 34 in a Japanese ataxia cohort PARKINSONISM & RELATED DISORDERS. 2019.08; 65 238-242. ( PubMed, DOI )

30. Guo Long, Bertola Debora Romeo, Takanohashi Asako, Saito Asuka, Segawa Yuko, Yokota Takanori, Ishibashi Satoru, Nishida Yoichiro, Yamamoto Guilherme Lopes, da Silva Franco Jose Francisco, Honjo Rachel Sayuri, Kim Chong Ae, Musso Camila Manso, Timmons Margaret, Pizzino Amy, Taft Ryan J., Lajoie Bryan, Knight Melanie A., Fischbeck Kenneth H., Singleton Andrew B., Ferreira Carlos R., Wang Zheng, Yan Li, Garbern James Y., Simsek-Kiper Pelin O., Ohashi Hirofumi, Robey Pamela G., Boyde Alan, Matsumoto Naomichi, Miyake Noriko, Spranger Juergen, Schiffmann Raphael, Vanderver Adeline, Nishimura Gen, dos Santos Passos-Bueno Maria Rita, Simons Cas, Ishikawa Kinya, Ikegawa Shiro. Bi-allelic CSF1R Mutations Cause Skeletal Dysplasia of Dysosteosclerosis-Pyle Disease Spectrum and Degenerative Encephalopathy with Brain Malformation AMERICAN JOURNAL OF HUMAN GENETICS. 2019.05; 104 (5): 925-935. ( PubMed, DOI )

31. Ishikawa Kinya. Calcium channel protein aggregations and role of lysozomes in SCA6 BRAIN PATHOLOGY. 2019.02; 29 8.

32. Furukawa Fumiko, Ishikawa Kinya, Yokota Takanori, Sanjo Nobuo. Cross-Sectional Area Analysis of the Head of the Caudate Nucleus in Huntington's Disease EUROPEAN NEUROLOGY. 2019; 81 (1-2): 13-18. ( PubMed, DOI )

33. Bando K, Honda T, Ishikawa K, Takahashi Y, Mizusawa H, Hanakawa T. Impaired Adaptive Motor Learning Is Correlated With Cerebellar Hemispheric Gray Matter Atrophy in Spinocerebellar Ataxia Patients: A Voxel-Based Morphometry Study. Frontiers in neurology. 2019; 10 1183. ( PubMed, DOI )

34. Ishikawa Kinya, Ishiguro Taro, Nagai Yoshitaka. 神経疾患の克服を目指して　SCA31　分子病態とRNAシャペロンの役割(SCA31: molecular pathogenesis and role of RNA chaperone) 臨床神経学. 2018.12; 58 (Suppl.): S28. ( 医中誌 )

35. Honda Takeru, Nagao Soichi, Hashimoto Yuji, Ishikawa Kinya, Yokota Takanori, Mizusawa Hidehiro, Ito Masao. Tandem internal models execute motor learning in the cerebellum PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA. 2018.07; 115 (28): 7428-7433. ( PubMed, DOI )

36. Itaya Sakiko, Kobayashi Zen, Ozaki Kokoro, Sato Nozomu, Numasawa Yoshiyuki, Ishikawa Kinya, Yokota Takanori, Matsuda Hiroshi, Shintani Shuzo. 眼瞼痙攣を伴う脊髄小脳失調症31型(Spinocerebellar Ataxia Type 31 with Blepharospasm) Internal Medicine. 2018.06; 57 (11): 1651-1654. ( 医中誌 )

37. Higashi Miwa, Ozaki Kokoro, Hattori Takaaki, Ishii Takashi, Soga Kazumasa, Sato Nozomu, Tomita Makoto, Mizusawa Hidehiro, Ishikawa Kinya, Yokota Takanori. A diagnostic decision tree for adult cerebellar ataxia based on pontine magnetic resonance imaging JOURNAL OF THE NEUROLOGICAL SCIENCES. 2018.04; 387 187-195. ( PubMed, DOI )

38. Itaya Sakiko, Kobayashi Zen, Ozaki Kokoro, Sato Nozomu, Numasawa Yoshiyuki, Ishikawa Kinya, Yokota Takanori, Matsuda Hiroshi, Shintani Shuzo. Spinocerebellar Ataxia Type 31 with Blepharospasm INTERNAL MEDICINE. 2018; 57 (11): 1651-1654. ( PubMed, DOI )

39. Hu Yajun, Hashimoto Yuji, Ishii Takashi, Rayle Mamut, Soga Kazumasa, Sato Nozomu, Okita Michi, Higashi Miwa, Ozaki Kokoro, Mizusawa Hidehiro, Ishikawa Kinya, Yokota Takanori. Sequence configuration of spinocerebellar ataxia type 8 repeat expansions in a Japanese cohort of 797 ataxia subjects JOURNAL OF THE NEUROLOGICAL SCIENCES. 2017.11; 382 87-90.

40. Hu Y, Hashimoto Y, Ishii T, Rayle M, Soga K, Sato N, Okita M, Higashi M, Ozaki K, Mizusawa H, Ishikawa K, Yokota T. Sequence configuration of spinocerebellar ataxia type 8 repeat expansions in a Japanese cohort of 797 ataxia subjects. Journal of the neurological sciences. 2017.11; 382 87-90. ( PubMed, DOI )