Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Mika Dozono"'
Autor:
Satoshi Nozuma, Akiko Yoshimura, Shun-Chung Pai, Hung-Jen Chen, Eiji Matsuura, Masakazu Tanaka, Daisuke Kodama, Mika Dozono, Toshio Matsuzaki, Hiroshi Takashima, Ya-Chien Yang, Ryuji Kubota
Publikováno v:
PLoS Neglected Tropical Diseases, Vol 18, Iss 2, p e0011928 (2024)
BackgroundAlthough Japan is a major endemic area for human T-lymphotropic virus type 1 (HTLV-1) and the virus has been well-studied in this region, there is limited research on HTLV-1 in surrounding regions. In this study, we determined the complete
Externí odkaz:
https://doaj.org/article/2ce83ec0c5634d589081b6943a0c0900
Autor:
Eiji Matsuura, Satoshi Nozuma, Ayano Shigehisa, Mika Dozono, Tomonori Nakamura, Masakazu Tanaka, Ryuji Kubota, Akihiro Hashiguchi, Hiroshi Takashima
Publikováno v:
BMC Musculoskeletal Disorders, Vol 24, Iss 1, Pp 1-6 (2023)
Abstract Background Sporadic late onset nemaline myopathy (SLONM) is a muscle disorder characterized by the presence of nemaline rods in muscle fibers. SLONM has no known genetic cause but has been associated with monoclonal gammopathy of undetermine
Externí odkaz:
https://doaj.org/article/2ee8ec70d7044e4a8e032fcf931c3e95
Autor:
Ryusei Nagata, Eiji Matsuura, Satoshi Nozuma, Mika Dozono, Yutaka Noguchi, Masahiro Ando, Yu Hiramatsu, Daisuke Kodama, Masakazu Tanaka, Ryuji Kubota, Munekazu Yamakuchi, Yujiro Higuchi, Yusuke Sakiyama, Hitoshi Arata, Keiko Higashi, Teruto Hashiguchi, Shunya Nakane, Hiroshi Takashima
Publikováno v:
Frontiers in Neurology, Vol 14 (2023)
ObjectiveAutoimmune autonomic ganglionopathy (AAG) is a rare disorder characterized by autonomic failure associated with the presence of anti-ganglionic acetylcholine receptor (gAChR) antibodies; however, several studies have reported that individual
Externí odkaz:
https://doaj.org/article/399277845a9f4c39bab17fb72b5506a5
Autor:
Eiji Matsuura, Satoshi Nozuma, Mika Dozono, Daisuke Kodama, Masakazu Tanaka, Ryuji Kubota, Hiroshi Takashima
Publikováno v:
Pathogens, Vol 12, Iss 4, p 592 (2023)
Human T-cell leukemia virus-1 (HTLV-1)-associated myelopathy/tropical spastic paraparesis (HAM/TSP) is a slowly progressive neurological disease that arises from HTLV-1 infection. Pathologically, the condition is characterized by diffuse myelitis, wh
Externí odkaz:
https://doaj.org/article/08f6406651d84d779f33a6c16b2ff4f0
Autor:
Masahiro Ando, Yujiro Higuchi, Jun-Hui Yuan, Akiko Yoshimura, Mika Dozono, Takahiro Hobara, Fumikazu Kojima, Yutaka Noguchi, Mika Takeuchi, Jun Takei, Yu Hiramatsu, Satoshi Nozuma, Tomonori Nakamura, Yusuke Sakiyama, Akihiro Hashiguchi, Eiji Matsuura, Yuji Okamoto, Jun Sone, Hiroshi Takashima
Publikováno v:
Journal of Neurology, Neurosurgery & Psychiatry; Aug2023, Vol. 94 Issue 8, p622-630, 9p
Autor:
Ryusei Nagata, Eiji Matsuura, Satoshi Nozuma, Mika Dozono, Yutaka Noguchi, Masahiro Ando, Yu Hiramatsu, Daisuke Kodama, Masakazu Tanaka, Ryuji Kubota, Munekazu Yamakuchi, Yujiro Higuchi, Yusuke Sakiyama, Hitoshi Arata, Keiko Higashi, Teruto Hashiguchi, Shunya Nakane, Hiroshi Takashima
BackgroundAutoimmune autonomic ganglionopathy (AAG) is a rare disorder characterized by autonomic failure associated with the presence of anti-ganglionic acetylcholine receptor (gAChR) antibodies; however, several studies have reported that individua
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2047f084a5a5b6062ece81595c66a4b1
https://doi.org/10.1101/2022.10.08.22280876
https://doi.org/10.1101/2022.10.08.22280876
Autor:
Mika Dozono, Ayano Shigehisa, Takaki Taniguchi, Satoshi Nozuma, Yuichi Tashiro, Tomonori Nakamura, Akihiro Hashiguchi, Ryuichi Okubo, Hiroshi Takashima
Publikováno v:
Nihon Naika Gakkai Zasshi. 110:598-604
Autor:
Masahiro Ando, Yujiro Higuchi, Jun-Hui Yuan, Akiko Yoshimura, Mika Dozono, Takahiro Hobara, Fumikazu Kojima, Yutaka Noguchi, Mika Takeuchi, Jun Takei, Yu Hiramatsu, Satoshi Nozuma, Tomonori Nakamura, Yusuke Sakiyama, Akihiro Hashiguchi, Eiji Matsuura, Yuji Okamoto, Jun Sone, Hiroshi Takashima
Publikováno v:
Journal of Neurology, Neurosurgery & Psychiatry. :jnnp-2022
BackgroundNOTCH2NLCGGC repeat expansions have been associated with various neurogenerative disorders, including neuronal intranuclear inclusion disease and inherited peripheral neuropathies (IPNs). However, only a fewNOTCH2NLC-related disease studies
Autor:
Ayano Shigehisa, Keiko Higashi, Satoshi Nozuma, Yukitoshi Takahashi, Hiroshi Takashima, Eiji Matsuura, Mika Dozono, Tomonori Nakamura, Yusuke Sakiyama, Yuki Hamada, Akihiro Hashiguchi
Publikováno v:
Internal Medicine
We herein report a 50-year-old man with alcoholic cirrhosis who developed loss of consciousness and tremor of the upper limbs. Magnetic resonance imaging findings were suggestive of limbic encephalitis with bilateral hippocampal damage, and a cerebro