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Cerebral Circulation - Cognition and Behavior
|
November 3, 2022
Perfusion abnormality in neuronal intranuclear inclusion disease with stroke-like episode: A case report
Fumiya Kutsuna, Yohei Tateishi, Kairi Yamashita, et al.
Eneurologicalsci
|
June 12, 2025
A case of fragile X-associated tremor/ataxia syndrome with superior cerebellar peduncle lesions
Kunihiko Ishizawa, Kentaro Hashimoto, Hironori Oka, et al.
Neurology. Genetics
|
June 16, 2021
Case of Neuronal Intranuclear Inclusion Disease With Dynamic Perfusion Changes Lacking Typical Signs on Diffusion-Weighted Imaging
Mai Kikumoto, Tomohisa Nezu, Yuji Shiga, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
September 17, 2013
Neuronal intranuclear inclusion disease cases with leukoencephalopathy diagnosed via skin biopsy
Jun Sone, Naoyuki Kitagawa, Eriko Sugawara, et al.
Medicine
|
May 12, 2023
NOTCH2NLC mutation-positive neuronal intranuclear inclusion disease with retinal dystrophy: A case report and literature review
Takayuki Katayama, Kae Takahashi, Osamu Yahara, et al.
Journal of Human Genetics
|
March 26, 2026
Clinical and imaging characteristics of NOTCH3-negative CADASIL-suspected patients with NOTCH2NLC GGC repeat expansions
Hiraku Matsuura, Daiki Fukunaga, Ikuko Mizuta, et al.
The Journal of Biological Chemistry
|
June 19, 2009
TDP-43 depletion induces neuronal cell damage through dysregulation of Rho family GTPases
Yohei Iguchi, Masahisa Katsuno, Jun-Ichi Niwa, et al.
Brain : a Journal of Neurology
|
March 11, 2022
Motor neuron TDP-43 proteinopathy in progressive supranuclear palsy and corticobasal degeneration
Yuichi Riku, Yasushi Iwasaki, Shinsuke Ishigaki, et al.
Brain Pathology (Zurich, Switzerland)
|
August 3, 2023
Neuropathological hallmarks in autopsied cases with mitochondrial diseases caused by the mitochondrial 3243A>G mutation
Hiroaki Miyahara, Chisato Tamai, Masanori Inoue, et al.
Annals of Neurology
|
June 17, 2020
Reply to "GGC Repeat Expansion of NOTCH2NLC is Rare in European Leukoencephalopathy"
Hiroshi Doi, Masaki Okubo, Ryoko Fukai, et al.
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of 9
Search research articles
Search
Showing results (61-70 of 84) with videos related to
Sort By:
Page
of 9
Cerebral Circulation - Cognition and Behavior
|
November 3, 2022
Perfusion abnormality in neuronal intranuclear inclusion disease with stroke-like episode: A case report
Fumiya Kutsuna, Yohei Tateishi, Kairi Yamashita, et al.
Eneurologicalsci
|
June 12, 2025
A case of fragile X-associated tremor/ataxia syndrome with superior cerebellar peduncle lesions
Kunihiko Ishizawa, Kentaro Hashimoto, Hironori Oka, et al.
Neurology. Genetics
|
June 16, 2021
Case of Neuronal Intranuclear Inclusion Disease With Dynamic Perfusion Changes Lacking Typical Signs on Diffusion-Weighted Imaging
Mai Kikumoto, Tomohisa Nezu, Yuji Shiga, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
September 17, 2013
Neuronal intranuclear inclusion disease cases with leukoencephalopathy diagnosed via skin biopsy
Jun Sone, Naoyuki Kitagawa, Eriko Sugawara, et al.
Medicine
|
May 12, 2023
NOTCH2NLC mutation-positive neuronal intranuclear inclusion disease with retinal dystrophy: A case report and literature review
Takayuki Katayama, Kae Takahashi, Osamu Yahara, et al.
Journal of Human Genetics
|
March 26, 2026
Clinical and imaging characteristics of NOTCH3-negative CADASIL-suspected patients with NOTCH2NLC GGC repeat expansions
Hiraku Matsuura, Daiki Fukunaga, Ikuko Mizuta, et al.
The Journal of Biological Chemistry
|
June 19, 2009
TDP-43 depletion induces neuronal cell damage through dysregulation of Rho family GTPases
Yohei Iguchi, Masahisa Katsuno, Jun-Ichi Niwa, et al.
Brain : a Journal of Neurology
|
March 11, 2022
Motor neuron TDP-43 proteinopathy in progressive supranuclear palsy and corticobasal degeneration
Yuichi Riku, Yasushi Iwasaki, Shinsuke Ishigaki, et al.
Brain Pathology (Zurich, Switzerland)
|
August 3, 2023
Neuropathological hallmarks in autopsied cases with mitochondrial diseases caused by the mitochondrial 3243A>G mutation
Hiroaki Miyahara, Chisato Tamai, Masanori Inoue, et al.
Annals of Neurology
|
June 17, 2020
Reply to "GGC Repeat Expansion of NOTCH2NLC is Rare in European Leukoencephalopathy"
Hiroshi Doi, Masaki Okubo, Ryoko Fukai, et al.
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of 9