Showing results (1-10 of 9) with videos related to
Sort By:
Pageof 1
Journal of Human Genetics|April 27, 2001
A linkage disequilibrium at the candidate gene locus for 16q-linked autosomal dominant cerebellar ataxia type III in JapanM Takashima, K Ishikawa, U Nagaoka, et al.Rinsho Shinkeigaku = Clinical Neurology|July 7, 1999
[Diffusion images on brain MRI in Creutzfeldt-Jakob disease]U Nagaoka, K Kurita, T Hosoya, et al.Histochemistry and Cell Biology|February 24, 2001
Dual enhancement of double immunofluorescent signals by CARD: participation of ubiquitin during formation of neurofibrillary tanglesT Uchihara, A Nakamura, U Nagaoka, et al.Thrombosis and Haemostasis|April 8, 1998
Novel deletion and insertion mutations cause splicing defects, leading to severe reduction in mRNA levels of the A subunit in severe factor XIII deficiencyT Izumi, U Nagaoka, T Saito, et al.Neuroscience Letters|November 8, 1996
Localization of the gustatory pathway in the human midbrainY Shikama, T Kato, U Nagaoka, et al.Journal of Neurology, Neurosurgery, and Psychiatry|April 18, 2003
Attenuated nuclear shrinkage in neurones with nuclear inclusions of SCA1 brainsU Nagaoka, T Uchihara, K Iwabuchi, et al.Radiation Medicine|December 23, 1998
Abducens nerve enhancement in acute ophthalmoparesisA Shibata, T Hosoya, T Kato, et al.Neurology|May 24, 2000
A gene on SCA4 locus causes dominantly inherited pure cerebellar ataxiaU Nagaoka, M Takashima, K Ishikawa, et al.Journal of the Neurological Sciences|July 13, 1999
Regional differences in genetic subgroup frequency in hereditary cerebellar ataxia, and a morphometrical study of brain MR images in SCA1, MJD and SCA6U Nagaoka, Y Suzuki, T Kawanami, et al.Pageof 1