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Mari Yoshida

Showing results (181-190 of 376) with videos related to

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Clinical Neuropathology|July 6, 2012
Nuclear factor κ B expression in patients with sporadic amyotrophic lateral sclerosis and hereditary amyotrophic lateral sclerosis with optineurin mutationsWataru Sako, Hidefumi Ito, Mari Yoshida, et al.
Neuropathology : Official Journal of the Japanese Society of Neuropathology|February 6, 2008
MM1-type sporadic Creutzfeldt-Jakob disease with unusually prolonged disease duration presenting with panencephalopathic-type pathologyAkira Hoshino, Yasushi Iwasaki, Masayuki Izumi, et al.
Neuroscience Letters|November 5, 2017
Immunohistochemical localization of exoribonucleases (DIS3L2 and XRN1) in intranuclear inclusion body diseaseFumiaki Mori, Kunikazu Tanji, Yasuo Miki, et al.
Journal of Neuropathology and Experimental Neurology|September 2, 2017
Pathologic Involvement of Glutamatergic Striatal Inputs From the Cortices in TAR DNA-Binding Protein 43 kDa-Related Frontotemporal Lobar Degeneration and Amyotrophic Lateral SclerosisYuichi Riku, Hirohisa Watanabe, Mari Yoshida, et al.
Rinsho Shinkeigaku = Clinical Neurology|July 1, 2016
Expanding concept of clinical conditions and symptoms in multiple system atrophyHirohisa Watanabe, Yuichi Riku, Tomohiko Nakamura, et al.
Acta Neuropathologica Communications|January 29, 2014
Dendritic retraction, but not atrophy, is consistent in amyotrophic lateral sclerosis-comparison between Onuf's neurons and other sacral motor neuronsTakahiro Takeda, Toshiki Uchihara, Yuki Nakayama, et al.
Neuropathology : Official Journal of the Japanese Society of Neuropathology|May 8, 2019
Autopsied case of sporadic Creutzfeldt-Jakob disease classified as MM1+2C-typeYasushi Iwasaki, Hiroko Kato, Tetsuo Ando, et al.
Journal of Neurology|May 3, 2011
Nationwide survey of Alexander disease in Japan and proposed new guidelines for diagnosisTomokatsu Yoshida, Masayuki Sasaki, Mari Yoshida, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|August 13, 2011
Brainstem and spinal cord motor neuron involvement with optineurin inclusions in proximal-dominant hereditary motor and sensory neuropathyKoji Fujita, Mari Yoshida, Wataru Sako, et al.
Neuropathology : Official Journal of the Japanese Society of Neuropathology|November 16, 2021
Unexpected postmortem diagnoses in cases of clinically diagnosed amyotrophic lateral sclerosisYuichi Riku, Mari Yoshida, Takuya Tamura, et al.
Pageof 38

Showing results (181-190 of 376) with videos related to

Sort By:
Pageof 38
Clinical Neuropathology|July 6, 2012
Nuclear factor κ B expression in patients with sporadic amyotrophic lateral sclerosis and hereditary amyotrophic lateral sclerosis with optineurin mutationsWataru Sako, Hidefumi Ito, Mari Yoshida, et al.
Neuropathology : Official Journal of the Japanese Society of Neuropathology|February 6, 2008
MM1-type sporadic Creutzfeldt-Jakob disease with unusually prolonged disease duration presenting with panencephalopathic-type pathologyAkira Hoshino, Yasushi Iwasaki, Masayuki Izumi, et al.
Neuroscience Letters|November 5, 2017
Immunohistochemical localization of exoribonucleases (DIS3L2 and XRN1) in intranuclear inclusion body diseaseFumiaki Mori, Kunikazu Tanji, Yasuo Miki, et al.
Journal of Neuropathology and Experimental Neurology|September 2, 2017
Pathologic Involvement of Glutamatergic Striatal Inputs From the Cortices in TAR DNA-Binding Protein 43 kDa-Related Frontotemporal Lobar Degeneration and Amyotrophic Lateral SclerosisYuichi Riku, Hirohisa Watanabe, Mari Yoshida, et al.
Rinsho Shinkeigaku = Clinical Neurology|July 1, 2016
Expanding concept of clinical conditions and symptoms in multiple system atrophyHirohisa Watanabe, Yuichi Riku, Tomohiko Nakamura, et al.
Acta Neuropathologica Communications|January 29, 2014
Dendritic retraction, but not atrophy, is consistent in amyotrophic lateral sclerosis-comparison between Onuf's neurons and other sacral motor neuronsTakahiro Takeda, Toshiki Uchihara, Yuki Nakayama, et al.
Neuropathology : Official Journal of the Japanese Society of Neuropathology|May 8, 2019
Autopsied case of sporadic Creutzfeldt-Jakob disease classified as MM1+2C-typeYasushi Iwasaki, Hiroko Kato, Tetsuo Ando, et al.
Journal of Neurology|May 3, 2011
Nationwide survey of Alexander disease in Japan and proposed new guidelines for diagnosisTomokatsu Yoshida, Masayuki Sasaki, Mari Yoshida, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|August 13, 2011
Brainstem and spinal cord motor neuron involvement with optineurin inclusions in proximal-dominant hereditary motor and sensory neuropathyKoji Fujita, Mari Yoshida, Wataru Sako, et al.
Neuropathology : Official Journal of the Japanese Society of Neuropathology|November 16, 2021
Unexpected postmortem diagnoses in cases of clinically diagnosed amyotrophic lateral sclerosisYuichi Riku, Mari Yoshida, Takuya Tamura, et al.
Pageof 38