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Biochemical and Biophysical Research Communications|February 11, 2014
Endogenous and exogenous hydrogen sulfide facilitates T-type calcium channel currents in Cav3.2-expressing HEK293 cellsFumiko Sekiguchi, Yosuke Miyamoto, Daiki Kanaoka, et al.
Brain & Development|October 17, 2021
Involuntary movements as a prognostic factor for acute encephalopathy with biphasic seizures and late reduced diffusionYosuke Miyamoto, Tohru Okanishi, Masanori Maeda, et al.
Frontiers in Neurology|November 18, 2021
Predicting the Onset of Acute Encephalopathy With Biphasic Seizures and Late Reduced Diffusion by Using Early Laboratory DataMasanori Maeda, Tohru Okanishi, Yosuke Miyamoto, et al.
Kyobu Geka. the Japanese Journal of Thoracic Surgery|November 9, 2016
[Delayed Diagnosis of Aortic Dissection Following Thrombolytic Therapy in a Patient with Acute Ischemic Stroke;Report of a Case]Yosuke Miyamoto, Zenichi Masuda, Yasuhiro Kotani, et al.
Respiratory Medicine Case Reports|January 9, 2016
Foreign body granuloma mimicking recurrence of malignant pleural mesotheliomaTakamasa Nakasuka, Nobukazu Fujimoto, Naofumi Hara, et al.
General Thoracic and Cardiovascular Surgery|December 23, 2019
Acute mitral valve endocarditis at the 24th gestational weekZenichi Masuda, Yosuke Miyamoto, Dai Une, et al.
Human Genome Variation|June 6, 2022
Thyroid hypogenesis is associated with a novel AKT3 germline variant that causes megalencephaly and cortical malformationJun Mori, Tatsuji Hasegawa, Yosuke Miyamoto, et al.
Journal for Immunotherapy of Cancer|October 29, 2021
JME-001 phase II trial of first-line combination chemotherapy with cisplatin, pemetrexed, and nivolumab for unresectable malignant pleural mesotheliomaYosuke Miyamoto, Toshiyuki Kozuki, Keisuke Aoe, et al.
Respiratory Medicine Case Reports|January 9, 2016
Lymphoproliferative disorder in pleural effusion in a subject with past asbestos exposureNaofumi Hara, Nobukazu Fujimoto, Yosuke Miyamoto, et al.
Journal of Human Genetics|March 8, 2025
Functional verification and allele-specific silencing of a novel AKT3 variant that causes megalencephaly, polymicrogyria and intractable epilepsyYosuke Miyamoto, Takenori Tozawa, Eisuke Ichise, et al.
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