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Kinya Ishikawa

Showing results (1-10 of 99) with videos related to

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Journal of Human Genetics|November 2, 2022
Spinocerebellar ataxia type 31 (SCA31)Kinya Ishikawa
Journal of Human Genetics|November 16, 2012
A commentary on confirmation and refinement of an autosomal dominant congenital motor nystagmus locus in chromosome 1q31.3-q32.1Kinya Ishikawa
Neurology|October 19, 2023
How Certain Are You When Making the Diagnosis of Multiple System Atrophy?Kinya Ishikawa
Neuropathology : Official Journal of the Japanese Society of Neuropathology|July 30, 2010
The chromosome 16q-linked autosomal dominant cerebellar ataxia (16q-ADCA): A newly identified degenerative ataxia in Japan showing peculiar morphological changes of the Purkinje cell: The 50th Anniversary of Japanese Society of NeuropathologyKinya Ishikawa, Hidehiro Mizusawa
Neuropathology : Official Journal of the Japanese Society of Neuropathology|September 12, 2006
On autosomal dominant cerebellar ataxia (ADCA) other than polyglutamine diseases, with special reference to chromosome 16q22.1-linked ADCAKinya Ishikawa, Hidehiro Mizusawa
Neurotherapeutics : the Journal of the American Society for Experimental Neurotherapeutics|November 23, 2019
Molecular Mechanisms and Future Therapeutics for Spinocerebellar Ataxia Type 31 (SCA31)Kinya Ishikawa, Yoshitaka Nagai
Rinsho Shinkeigaku = Clinical Neurology|September 17, 2011
[SCA6: From gene identification to recent progress on pathogenesis]Kei Watase, Kinya Ishikawa, Hidehiro Mizusawa
Frontiers in Neuroscience|June 11, 2021
Insight Into Spinocerebellar Ataxia Type 31 (SCA31) From <i>Drosophila</i> ModelTaro Ishiguro, Yoshitaka Nagai, Kinya Ishikawa
European Neurology|April 24, 2019
Cross-Sectional Area Analysis of the Head of the Caudate Nucleus in Huntington's DiseaseFumiko Furukawa, Kinya Ishikawa, Takanori Yokota, et al.
Neuroscience Letters|October 7, 2008
Cell-type-specific alternative splicing in spinocerebellar ataxia type 6Taiji Tsunemi, Kinya Ishikawa, Honglian Jin, et al.
Pageof 10

Showing results (1-10 of 99) with videos related to

Sort By:
Pageof 10
Journal of Human Genetics|November 2, 2022
Spinocerebellar ataxia type 31 (SCA31)Kinya Ishikawa
Journal of Human Genetics|November 16, 2012
A commentary on confirmation and refinement of an autosomal dominant congenital motor nystagmus locus in chromosome 1q31.3-q32.1Kinya Ishikawa
Neurology|October 19, 2023
How Certain Are You When Making the Diagnosis of Multiple System Atrophy?Kinya Ishikawa
Neuropathology : Official Journal of the Japanese Society of Neuropathology|July 30, 2010
The chromosome 16q-linked autosomal dominant cerebellar ataxia (16q-ADCA): A newly identified degenerative ataxia in Japan showing peculiar morphological changes of the Purkinje cell: The 50th Anniversary of Japanese Society of NeuropathologyKinya Ishikawa, Hidehiro Mizusawa
Neuropathology : Official Journal of the Japanese Society of Neuropathology|September 12, 2006
On autosomal dominant cerebellar ataxia (ADCA) other than polyglutamine diseases, with special reference to chromosome 16q22.1-linked ADCAKinya Ishikawa, Hidehiro Mizusawa
Neurotherapeutics : the Journal of the American Society for Experimental Neurotherapeutics|November 23, 2019
Molecular Mechanisms and Future Therapeutics for Spinocerebellar Ataxia Type 31 (SCA31)Kinya Ishikawa, Yoshitaka Nagai
Rinsho Shinkeigaku = Clinical Neurology|September 17, 2011
[SCA6: From gene identification to recent progress on pathogenesis]Kei Watase, Kinya Ishikawa, Hidehiro Mizusawa
Frontiers in Neuroscience|June 11, 2021
Insight Into Spinocerebellar Ataxia Type 31 (SCA31) From <i>Drosophila</i> ModelTaro Ishiguro, Yoshitaka Nagai, Kinya Ishikawa
European Neurology|April 24, 2019
Cross-Sectional Area Analysis of the Head of the Caudate Nucleus in Huntington's DiseaseFumiko Furukawa, Kinya Ishikawa, Takanori Yokota, et al.
Neuroscience Letters|October 7, 2008
Cell-type-specific alternative splicing in spinocerebellar ataxia type 6Taiji Tsunemi, Kinya Ishikawa, Honglian Jin, et al.
Pageof 10