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Rinsho Shinkeigaku = Clinical Neurology|September 24, 2004
[A case of chronic inflammatory demyelinating polyneuropathy presenting with acute pain and SIADH followed by weakness of all four limbs 2 month after the first symptoms]Jun Mitsui, Izumi Sugimoto, Satoko Kano, et al.The Laryngoscope|July 5, 2020
Esophageal Dysmotility is Common in Patients With Multiple System AtrophyRumi Ueha, Taku Sato, Takao Goto, et al.Journal of the Neurological Sciences|November 18, 2019
Rituximab improves not only back stiffness but also "stiff eyes" in stiff person syndrome: Implications for immune-mediated treatmentSatoshi Kodama, Shin-Ichi Tokushige, Yusuke Sugiyama, et al.Neuroradiology|February 23, 2010
Diffusion tensor tract-specific analysis of the uncinate fasciculus in patients with amyotrophic lateral sclerosisKanako Sato, Shigeki Aoki, Nobue K Iwata, et al.Movement Disorders : Official Journal of the Movement Disorder Society|January 2, 2009
A novel ferritin light chain gene mutation in a Japanese family with neuroferritinopathy: description of clinical features and implications for genotype-phenotype correlationsAkatsuki Kubota, Ayumi Hida, Yaeko Ichikawa, et al.Clinical Neurology and Neurosurgery|March 12, 2016
Exome sequencing reveals a novel missense mutation in the KIAA0196 gene in a Japanese patient with SPG8Yuta Ichinose, Kishin Koh, Megumi Fukumoto, et al.Journal of Stroke and Cerebrovascular Diseases : the Official Journal of National Stroke Association|March 27, 2017
Tacrolimus-Induced Reversible Cerebral Vasoconstriction Syndrome with Delayed Multi-Segmental VasoconstrictionSatoshi Kodama, Tatsuo Mano, Akihiro Masuzawa, et al.Journal of Human Genetics|February 26, 2016
Human genetic variation database, a reference database of genetic variations in the Japanese populationKoichiro Higasa, Noriko Miyake, Jun Yoshimura, et al.Brain : a Journal of Neurology|May 3, 2018
Mutations in COA7 cause spinocerebellar ataxia with axonal neuropathyYujiro Higuchi, Ryuta Okunushi, Taichi Hara, et al.Annals of Neurology|February 3, 2004
Aprataxin, the causative protein for EAOH is a nuclear protein with a potential role as a DNA repair proteinYasuteru Sano, Hidetoshi Date, Shuichi Igarashi, et al.Pageof 53