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Translational Pediatrics|December 10, 2025
Safety and efficacy of vibegron in pediatric patients with treatment-resistant nocturnal enuresis: a multicenter retrospective studyHirokazu Ikeda, Yoshitaka Watanabe, Yoshiyuki Ohtomo, et al.Neurobiology of Aging|February 6, 2018
Frequency and characteristics of the TBK1 gene variants in Japanese patients with sporadic amyotrophic lateral sclerosisGenki Tohnai, Ryoichi Nakamura, Jun Sone, et al.Eclinicalmedicine|May 31, 2023
High-dose ubiquinol supplementation in multiple-system atrophy: a multicentre, randomised, double-blinded, placebo-controlled phase 2 trialJun Mitsui, Takashi Matsukawa, Yukari Uemura, et al.Brain : a Journal of Neurology|April 5, 2007
Novel locus for benign hereditary chorea with adult onset maps to chromosome 8q21.3 q23.3Takayoshi Shimohata, Kenju Hara, Kazuhiro Sanpei, et al.Journal of Neurology, Neurosurgery, and Psychiatry|February 14, 2014
Autosomal-recessive complicated spastic paraplegia with a novel lysosomal trafficking regulator gene mutationHaruo Shimazaki, Junko Honda, Tametou Naoi, et al.Archives of Neurology|February 22, 2012
Mutational origin of Machado-Joseph disease in the Australian Aboriginal communities of Groote Eylandt and YirrkalaSandra Martins, Bing-Wen Soong, Virginia C N Wong, et al.Journal of Human Genetics|January 24, 2014
Molecular epidemiology and clinical spectrum of hereditary spastic paraplegia in the Japanese population based on comprehensive mutational analysesHiroyuki Ishiura, Yuji Takahashi, Toshihiro Hayashi, et al.Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|May 13, 2010
Two distinct mechanisms of augmented antitumor activity by modulation of immunostimulatory/inhibitory signalsJun Mitsui, Hiroyoshi Nishikawa, Daisuke Muraoka, et al.Archives of Neurology|April 11, 2007
Multiplex families with multiple system atrophyKenju Hara, Yoshio Momose, Susumu Tokiguchi, et al.Brain : a Journal of Neurology|April 14, 2011
Genotype-phenotype correlations in early onset ataxia with ocular motor apraxia and hypoalbuminaemiaAkio Yokoseki, Tomohiko Ishihara, Akihide Koyama, et al.Pageof 53