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Journal of the Neurological Sciences|October 7, 2008
A cross-sectional study for glucose intolerance of myotonic dystrophyTsuyoshi Matsumura, Hiromi Iwahashi, Tohru Funahashi, et al.Rinsho Shinkeigaku = Clinical Neurology|March 31, 2022
[Perspective on transition from pediatric to adult health care for patients with neurological disease: current situation and issues]Katsuhisa Ogata, Yoko Mochizuki, Toshio Saito, et al.The Kobe Journal of Medical Sciences|February 14, 2018
New, Improved Version of the mCOP-PCR Screening System for Detection of Spinal Muscular Atrophy Gene (SMN1) DeletionMasakazu Shinohara, Mawaddah Ar Rochmah, Kenta Nakanishi, et al.Neuromuscular Disorders : NMD|December 23, 2016
Study of Duchenne muscular dystrophy long-term survivors aged 40 years and older living in specialized institutions in JapanToshio Saito, Mitsuru Kawai, En Kimura, et al.Neurochemical Research|May 19, 2019
The Protective Effects of Levetiracetam on a Human iPSCs-Derived Spinal Muscular Atrophy ModelShiori Ando, Michinori Funato, Kazuki Ohuchi, et al.Eclinicalmedicine|February 5, 2024
Erythromycin for myotonic dystrophy type 1: a multicentre, randomised, double-blind, placebo-controlled, phase 2 trialMasayuki Nakamori, Daisaku Nakatani, Tomoharu Sato, et al.Pediatric Neurology|April 4, 2015
Two Japanese Patients With SMA Type 1 Suggest that Axonal-SMN May Not Modify the Disease SeverityHiroyuki Yamada, Yoshinobu Nishida, Toshiro Maihara, et al.Scientific Reports|March 8, 2019
Notch Signaling Mediates Astrocyte Abnormality in Spinal Muscular Atrophy Model SystemsKazuki Ohuchi, Michinori Funato, Yuta Yoshino, et al.Genes|February 25, 2022
Stability and Oligomerization of Mutated SMN Protein Determine Clinical Severity of Spinal Muscular AtrophyEmma Tabe Eko Niba, Hisahide Nishio, Yogik Onky Silvana Wijaya, et al.Brain & Development|October 10, 2020
Clinical phenotypes of spinal muscular atrophy patients with hybrid SMN geneEmma Tabe Eko Niba, Hisahide Nishio, Yogik Onky Silvana Wijaya, et al.Pageof 10