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Journal of Neurology|September 17, 2004
Quantitative evaluation of brainstem involvement in multiple system atrophy by diffusion-weighted MR imagingMasato Kanazawa, Takayoshi Shimohata, Kenshi Terajima, et al.Journal of the Neurological Sciences|July 24, 2012
Diffuse central hypomyelination presenting as 4H syndrome caused by compound heterozygous mutations in POLR3A encoding the catalytic subunit of polymerase IIIYasuo Terao, Hirotomo Saitsu, Masaya Segawa, et al.EMBO Molecular Medicine|October 12, 2013
Rescue of amyotrophic lateral sclerosis phenotype in a mouse model by intravenous AAV9-ADAR2 delivery to motor neuronsTakenari Yamashita, Hui Lin Chai, Sayaka Teramoto, et al.Journal of the Neurological Sciences|October 6, 2007
Attitude of outpatients with neuromuscular diseases in Japan to pain and use of analgesicsYoshiki Abe, Mitsunori Miyashita, Naomi Ito, et al.Journal of Human Genetics|May 12, 2017
SCA42 mutation analysis in a case series of Japanese patients with spinocerebellar ataxiaMari Kimura, Ichiro Yabe, Yuka Hama, et al.Gene|June 18, 1998
Molecular cloning, structural organization, sequence, chromosomal assignment, and expression of the mouse alpha-N-acetylgalactosaminidase geneT Herrmann, D Schindler, H Tabe, et al.Acta Paediatrica (Oslo, Norway : 1992)|June 30, 2019
High daily salt intake had a negative impact on how well nocturnal enuresis treatment worked on children aged 7-10 yearsShoji Tsuji, Tadashi Yamaguchi, Yuko Akagawa, et al.Neuroscience Research|October 18, 2005
Underediting of GluR2 mRNA, a neuronal death inducing molecular change in sporadic ALS, does not occur in motor neurons in ALS1 or SBMAYukio Kawahara, Hui Sun, Kyoko Ito, et al.Cerebellum (London, England)|May 18, 2005
Spinocerebellar ataxia type 15R J McKinlay Gardner, Melanie A Knight, Kenju Hara, et al.Clinical Nephrology|June 4, 2013
Different phenotypes of HNF1ß deletion mutants in familial multicystic dysplastic kidneysMasafumi Hasui, Kazunari Kaneko, Shoji Tsuji, et al.Pageof 53