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Cowden Syndrome with a Novel PTEN Mutation Presenting with Partial Epilepsy Related to Focal CorticalDysplasia , Adachi Tadashi, Takigawa Hiroshi, , Nomura Takashi, Watanabe Yasuhiro, Kowa Hisanori , Intern Med , vol.16 , 2017 , The Multiple Authorship , English
Gene expression analysis of the murine model of amyotrophic lateral sclerosis: studies of the Leu126delTT mutation in SOD1 , Fukada, Y., Yasui, K., Kitayama, M., Doi, K., Nakano, T., Watanabe, Y., and Nakashima, K. , Brain Res , vol.1160 (0) (p.1 - 10) , 2007 , There is Review , The Multiple Authorship , English
Olfactory ensheathing cell transplantation in ALS model mice , Watanabe, Y., Morita, E., Ishimoto, M., Kitayama, M., Yasui, K., Fukada, Y., Doi, K., Nakano, T., Murrell, WG, Mackay-Sim, A., and Nakashima, K. , 17th International Symposium on ALS/MND (Yokohama) , vol.7 (0) (p.119) , 2006 , The Multiple Authorship , English
Towards gene therapy using genetically engineered cells and stem cells in a mouse model of ALS , Karunarantne, A., Watanabe, Y., Cameron, N., Mackay-Sim, A., and Murrell W. , 17th International Symposium on ALS/MND (Yokohama) , vol.7 (0) (p.119 - 129) , 2006 , The Multiple Authorship , English
Mouse motor neuron disease caused by truncated Cu/Zn superoxide dismutase , Watanabe, Y., Yasui, K., Nakano, T., Kitayama, M., Doi, K., Fukada, Y., Morita, E., and Nakashima, K. , 16th International Symposium on ALS/MND (Dublin) , vol.6 (0) (p.93 - 94) , 2005 , The Multiple Authorship , English
Mouse motor neuron disease caused by truncated SOD1 with or without C-terminal modification , Watanabe, Y., Yasui, K., Nakano, T., Doi, K., Fukada, Y., Kitayama, M., Ishimoto, M., Kurihara, S., Kawashima, M., Fukuda, H., Adachi, Y., Inoue, T. and Nakashima, K. , Brain Res Mol Brain Res , vol.135 (0) (p.12 - 20) , 2005 , There is Review , The Multiple Authorship , English
Tetanus toxin fragment C and Bcl-2 fusion protein prevents death of serum- and NGF-withdrawn PC12 cells , Watanabe, Y., Matsuba, T., Nakano, T., Michio, K., Yasui1, K., Fukada1, Y., Doi, K., Tanaka, Y., and Nakashima, K. , 16th International Symposium on ALS/MND (Dublin) , vol.6 (0) (p.109) , 2005 , The Multiple Authorship , English
Steroid-responsive limbic encephalitis , Watanabe, Y. Shimizu, Y. Ooi, S. et al. , Intern Med , vol.42 (5) (p.428 - 432) , 2003 , There is Review , The Multiple Authorship , English
Vertical ophthalmoplegia in a demented patient with striatopallidodentate calcification , Watanabe, Y. Shimizu, Y. Urakami, K. et al. , Psychiatry Clin Neurosci , vol.57 (4) (p.447 - 450) , 2003 , There is Review , The Multiple Authorship , English
Japanese familial amyotrophic lateral sclerosis family with a two-base deletion in the superoxide dismutase-1 gene , Watanabe, Y. Adachi, Y. Nakashima, K. , Neuropathology , vol.21 (1) (p.61 - 66) , 2001 , There is Review , The Multiple Authorship , English
Extraosseous epidural IgD myeloma presenting with compression myelopathy , Watanabe, Y. Endou, A. Ooi, S. , Psychiatry Clin Neurosci , vol.54 (6) (p.665 - 667) , 2000 , There is Review , The Multiple Authorship , English
Frameshift, nonsense and non amino acid altering mutations in SOD1 in familial ALS: report of a Japanese pedigree and literature review , Watanabe, Y. Kato, S. Adachi, Y. et al. , Amyotroph Lateral Scler Other Motor Neuron Disord , vol.1 (4) (p.251 - 258) , 2000 , There is Review , The Multiple Authorship , English
Analysis of the CAG repeat number in a patient with Huntington's disease , Kono, Y. Agawa, Y. Watanabe, Y. et al. , Intern Med , vol.38 (5) (p.407 - 411) , 1999 , There is Review , The Multiple Authorship , English
Tc 99m ECD-SPECT during migraine aura without headache , Wakutani, Y. Shimizu, Y. Matsushima, E. Watanabe, Y. et al. , Headache , vol.39 (6) (p.446 - 448) , 1999 , There is Review , The Multiple Authorship , English
NPC1 gene mutations in Japanese patients with Niemann-Pick disease type C , Yamamoto, T. Nanba, E. Watanabe, Y. et al. , Hum Genet , vol.105 (1) (p.10 - 16) , 1999 , There is Review , The Multiple Authorship , English
Increased levels of GM2 ganglioside in fibroblasts from a patient with juvenile Niemann-Pick disease type C , Watanabe, Y. Akaboshi, S. Ishida, G. et al. , Brain Dev , vol.20 (2) (p.95 - 97) , 1998 , There is Review , The Multiple Authorship , English
Absence of the mutant SOD1 in familial amyotrophic lateral sclerosis (FALS) with two base pair deletion in the SOD1 gene , Watanabe, Y. Kono, Y. Kono, Y. et al. , Acta Neurol Scand , vol.95 (3) (p.167 - 172) , 1997 , There is Review , The Multiple Authorship , English
Instability of expressed Cu/Zn superoxide dismutase with 2 bp deletion found in familial amyotrophic lateral sclerosis , Watanabe, Y. Kono, Y. Nanba, E. et al. , FEBS Lett , vol.400 (1) (p.108 - 112) , 1997 , There is Review , The Multiple Authorship , English
Epidemiological and genetic studies of Huntington's disease in the San-in area of Japan , Nakashima, K. Watanabe, Y. Kusumi, M. et al. , Neuroepidemiology , vol.15 (3) (p.126 - 131) , 1996 , There is Review , The Multiple Authorship , English
Familial amyotrophic lateral sclerosis with a two base pair deletion in superoxide dismutase 1: gene multisystem degeneration with intracytoplasmic hyaline inclusions in astrocytes , Kato, S. Shimoda, M. Watanabe, Y. et al. , J Neuropathol Exp Neurol , vol.55 (10) (p.1089 - 1101) , 1996 , There is Review , The Multiple Authorship , English
Abnormality of Cu/Zn superoxide dismutase (SOD1) activity in Japanese familial amyotrophic lateral sclerosis with two base pair deletion in the SOD1 gene , Nakashima, K. Watanabe, Y. Kuno, N. et al. , Neurology , vol.45 (5) (p.1019 - 1020) , 1995 , There is Review , The Multiple Authorship , English
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