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Epilepsia|August 22, 2009
Congenital long QT syndrome presenting with a history of epilepsy: misdiagnosis or relationship between channelopathies of the heart and brain?Chikaya Omichi, Yoshio Momose, Shigemi KitaharaJournal of Pharmaceutical Health Care and Sciences|January 25, 2017
Impact of Pharmacists' audit on improving the quality of prescription of dabigatran etexilate methanesulfonate: a retrospective studyTeppei Shimizu, Yoshio Momose, Ryuichi Ogawa, et al.Journal of Neurology|October 28, 2003
Toward identification of susceptibility genes for sporadic Parkinson's diseaseTatsushi Toda, Yoshio Momose, Miho Murata, et al.Rinsho Shinkeigaku = Clinical Neurology|April 8, 2009
[Alien hand sign observed at the initial stage of a case of Creutzfeldt-Jakob disease]Meiko Hashimoto, Jun Shimizu, Yuichiro Shirota, et al.Annals of Neurology|January 10, 2002
Association studies of multiple candidate genes for Parkinson's disease using single nucleotide polymorphismsYoshio Momose, Miho Murata, Kazuhiro Kobayashi, 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.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.Journal of Neurology, Neurosurgery, and Psychiatry|October 21, 2011
Neurovascular changes in prolonged migraine aura in FHM with a novel ATP1A2 gene mutationTakahiro Iizuka, Yuji Takahashi, Mayumi Sato, et al.Archives of Neurology|April 11, 2007
Multiplex families with multiple system atrophyKenju Hara, Yoshio Momose, Susumu Tokiguchi, et al.Journal of Human Genetics|August 13, 2008
Appropriate data cleaning methods for genome-wide association studyTaku Miyagawa, Nao Nishida, Jun Ohashi, et al.Pageof 2