Zobrazeno 1 - 10
of 270
pro vyhledávání: '"Haruki Koike"'
Autor:
Tomoyuki Kazuta, Ayuka Murakami, Seiya Noda, Satoko Hirano, Hiroshi Kito, Koyo Tsujikawa, Hirotaka Nakanishi, Seigo Kimura, Kentaro Sahashi, Haruki Koike, Masahisa Katsuno
Publikováno v:
Annals of Clinical and Translational Neurology, Vol 11, Iss 2, Pp 508-519 (2024)
Abstract Background and Objective Chronic graft versus host disease (GVHD)‐associated myositis targeting skeletal muscle is a relatively rare but potentially debilitating complication following allogeneic hematopoietic stem cell transplantation (HS
Externí odkaz:
https://doaj.org/article/32a56cbee4014ba8a83ba652c36a7fe6
Autor:
Yukio Ando, Marcia Waddington-Cruz, Yoshiki Sekijima, Haruki Koike, Mitsuharu Ueda, Hiroaki Konishi, Tomonori Ishii, Teresa Coelho
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 18, Iss 1, Pp 1-17 (2023)
Abstract Hereditary transthyretin (ATTRv) amyloidosis is a rare and autosomal dominant disorder associated with mutations in the transthyretin gene. Patients present with diverse symptoms related to sensory, motor, and autonomic neuropathy, as well a
Externí odkaz:
https://doaj.org/article/b4211bad5c5b4a2f92847c0a1e464bdc
Autor:
Laura Obici, Senda Ajroud-Driss, Kon-Ping Lin, John L. Berk, Julian D. Gillmore, Parag Kale, Haruki Koike, David Danese, Emre Aldinc, Chongshu Chen, John Vest, David Adams, the HELIOS-A Collaborators Study Group
Publikováno v:
Neurology and Therapy, Vol 12, Iss 5, Pp 1759-1775 (2023)
Abstract Introduction Hereditary transthyretin (ATTRv; v for variant) amyloidosis, also known as hATTR amyloidosis, is a progressive and fatal disease associated with rapid deterioration of physical function and patients' quality of life (QOL). Vutri
Externí odkaz:
https://doaj.org/article/731ded4c2340434890d8bbd61646c875
Publikováno v:
International Journal of Molecular Sciences, Vol 25, Iss 4, p 2296 (2024)
Autoimmune autonomic ganglionopathy (AAG) is a disease of autonomic failure caused by ganglionic acetylcholine receptor (gAChR) autoantibodies. Although the detection of autoantibodies is important for distinguishing the disease from other neuropathi
Externí odkaz:
https://doaj.org/article/019d8b6fe53c4849948c81a920014802
Autor:
Ayuka Murakami, Seiya Noda, Tomoyuki Kazuta, Satoko Hirano, Seigo Kimura, Hirotaka Nakanishi, Koji Matsuo, Koyo Tsujikawa, Madoka Iida, Haruki Koike, Kazuma Sakamoto, Yuichiro Hara, Satoshi Kuru, Kenji Kadomatsu, Teppei Shimamura, Tomoo Ogi, Masahisa Katsuno
Publikováno v:
Annals of Clinical and Translational Neurology, Vol 9, Iss 10, Pp 1602-1615 (2022)
Abstract Objective Sporadic inclusion body myositis (sIBM) is the most common acquired myopathy in patients older than 50 years of age. sIBM is hardly responds to any immunosuppressing theraphies, and its pathophysiology remains elusive. This study a
Externí odkaz:
https://doaj.org/article/3b07e9ffabbe43e98c89603134aaff9c
Autor:
Haruki Koike, Ryoji Nishi, Soma Furukawa, Naohiro Mouri, Yuki Fukami, Masahiro Iijima, Masahisa Katsuno
Publikováno v:
Allergology International, Vol 71, Iss 3, Pp 373-382 (2022)
Background: Although eosinophilic granulomatosis with polyangiitis (EGPA) has been considered as a single disease entity belonging to anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitis, several studies have suggested that in addition t
Externí odkaz:
https://doaj.org/article/ccab78674a7d4a7681e62a0f4a59e22d
Publikováno v:
EBioMedicine, Vol 90, Iss , Pp 104526- (2023)
Externí odkaz:
https://doaj.org/article/eb6bfd1dd3604e1ab4c2924dc8c65112
Autor:
Ryosuke Jozuka, Hiroki Kimura, Takashi Uematsu, Hidetsugu Fujigaki, Yasuko Yamamoto, Masato Kobayashi, Kazuya Kawabata, Haruki Koike, Toshiya Inada, Kuniaki Saito, Masahisa Katsuno, Norio Ozaki
Publikováno v:
Neuropsychopharmacology Reports, Vol 42, Iss 1, Pp 114-119 (2022)
Abstract Background Coronavirus disease 2019 (COVID‐19) is known to cause not only respiratory but also neuropsychiatric symptoms, which are assumed to be derived from a cytokine storm and its effects on the central nervous systems. Patients with C
Externí odkaz:
https://doaj.org/article/fb3f33b34975442384d232a755081e43
Autor:
Haruki Koike, Masahisa Katsuno
Publikováno v:
Neurology and Therapy, Vol 9, Iss 2, Pp 213-227 (2020)
Abstract Chronic inflammatory demyelinating polyneuropathy (CIDP) is classically defined as polyneuropathy with symmetric involvement of the proximal and distal portions of the limbs. In addition to this “typical CIDP”, the currently prevailing d
Externí odkaz:
https://doaj.org/article/d243a2efdb254818bd40c53c8cb1ce2f
Autor:
Hsueh-Wen Hsueh, Chi-Chao Chao, Koping Chang, Yung-Ming Jeng, Masahisa Katsuno, Haruki Koike, Sung-Tsang Hsieh
Publikováno v:
Frontiers in Aging Neuroscience, Vol 13 (2022)
ObjectiveHereditary transthyretin amyloidosis (ATTRv) encompasses different phenotypes among various genotypes. The analysis of the natural history and risk factors of faster progression in different genotypes would refine the treatment strategy.Meth
Externí odkaz:
https://doaj.org/article/ea2099255a0b40f696151f7b6459c026