2002 - Gene Therapy for Hereditary Cerebellar Ataxia
全件表示
論文 (165件):
Makito Hirano, Makoto Samukawa, Satoko Miyatake, Yuko Yamagishi, Chiharu Isono, Rino Yoshikawa, Kazumasa Saigoh, Atsushi Terayama, Yuji Higashimoto, Eriko Koshimizu, et al. Non-coding repeat analyses in patients with Parkinson’s disease. Frontiers in Neurology. 2025. 16
Ken-ichi Hirano, Satomi Okamura, Koichiro Sugimura, Hideyuki Miyauchi, Yusuke Nakano, Kotaro Nochioka, Chikako Hashimoto, Yoshitaka Iwanaga, Kenichi Nakajima, Satoshi Yamaguchi, et al. Long-term survival and durable recovery of heart failure in patients with triglyceride deposit cardiomyovasculopathy treated with tricaprin. Nature Cardiovascular Research. 2025
Daisuke Danno, Haruka Tada, Itsuki Oda, Norihito Kawashita, Makito Hirano, Shigekazu Kitamura, Shoji Kikui, Makoto Samukawa, Keisuke Yoshikawa, Yoshiyuki Mitsui, et al. Expanding the Genetic and Clinical Spectrum of SCN1A-Related Hemiplegic Migraine: Analysis of Mutations in Japanese. International Journal of Molecular Sciences. 2025. 26. 4. 1426-1426
Kensuke Daida, Hiroyo Yoshino, Laksh Malik, Breeana Baker, Mayu Ishiguro, Rylee Genner, Kimberly Paquette, Yuanzhe Li, Kenya Nishioka, Satoshi Masuzugawa, et al. The Utility of Long-Read Sequencing in Diagnosing Early Onset Parkinson's Disease. Annals of neurology. 2024
Tomohiko Ishihara, Masayoshi Tada, Yoshitomi Kanemitsu, Yuji Takahashi, Kinya Ishikawa, Kensuke Ikenaka, Makito Hirano, Takanori Yokota, Eiko N. Minakawa, Katsuhisa Saito, et al. L-arginine in patients with spinocerebellar ataxia type 6: a multicentre, randomised, double-blind, placebo-controlled, phase 2 trial. eClinicalMedicine. 2024. 78. 102952-102952
Analyses of the VCP gene in patients with sporadic amyotrophic lateral sclerosis, identify a novel mutation associated with increased susceptibility to oxidative stress.
(26th international symposium on ALS/MND, Orlando 2015)