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Ikuko Mizuta

Showing results (11-20 of 89) with videos related to

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Biomolecules|January 23, 2024
Progress to Clarify How <i>NOTCH3</i> Mutations Lead to CADASIL, a Hereditary Cerebral Small Vessel DiseaseIkuko Mizuta, Yumiko Nakao-Azuma, Hideki Yoshida, et al.
Rinsho Shinkeigaku = Clinical Neurology|April 3, 2018
[CADASIL with cysteine-sparing NOTCH3 mutation manifesting as dissociated progression between cognitive impairment and brain image findings in 3 years: A case report]Keisuke Tachiyama, Yuji Shiga, Yutaka Shimoe, et al.
Life Sciences|May 29, 2003
Effects of dopamine agonists bromocriptine, pergolide, cabergoline, and SKF-38393 on GDNF, NGF, and BDNF synthesis in cultured mouse astrocytesKiyoe Ohta, Sadako Kuno, Ikuko Mizuta, et al.
Journal of the Peripheral Nervous System : JPNS|June 28, 2012
A novel EGR2 mutation within a family with a mild demyelinating form of Charcot-Marie-Tooth diseaseKensuke Shiga, Yuichi Noto, Ikuko Mizuta, et al.
Rinsho Shinkeigaku = Clinical Neurology|December 1, 2017
[A case of hereditary sensory and autonomic neuropathy type 1E with frontal lobe dysfunction as an initial symptom]Masashi Watanabe, Yushi Matsumoto, Kensho Okamoto, et al.
Brain & Development|November 3, 2010
Serial MRI changes in a patient with infantile Alexander disease and prolonged survivalTakashi Shiihara, Toru Yoneda, Ikuko Mizuta, et al.
Experimental Neurology|February 25, 2025
CCL2/CCR2 signaling-mediated microglial migration leads to cerebral small vessel dysfunction in chronic hypertension model ratsTakashi Koizumi, Eline M Herckenrath, Katsutoshi Taguchi, et al.
Rinsho Shinkeigaku = Clinical Neurology|June 20, 2014
[Normokalemic periodic paralysis lasting for two weeks: a severe form of sodium channelopathy with M1592V mutation]Kensuke Shiga, Ikuko Mizuta, Yu-ichi Noto, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 31, 2003
Influence of monocyte chemoattractant protein 1 gene polymorphism on age at onset of sporadic Parkinson's diseaseMasataka Nishimura, Sadako Kuno, Ikuko Mizuta, et al.
Internal Medicine (Tokyo, Japan)|May 22, 2018
A Japanese Case of CADASIL with a Rare Mutation in Exon 24 of the NOTCH3 GeneYuka Ebihara, Hitoshi Mochizuki, Nobuyuki Ishii, et al.
Pageof 9

Showing results (11-20 of 89) with videos related to

Sort By:
Pageof 9
Biomolecules|January 23, 2024
Progress to Clarify How <i>NOTCH3</i> Mutations Lead to CADASIL, a Hereditary Cerebral Small Vessel DiseaseIkuko Mizuta, Yumiko Nakao-Azuma, Hideki Yoshida, et al.
Rinsho Shinkeigaku = Clinical Neurology|April 3, 2018
[CADASIL with cysteine-sparing NOTCH3 mutation manifesting as dissociated progression between cognitive impairment and brain image findings in 3 years: A case report]Keisuke Tachiyama, Yuji Shiga, Yutaka Shimoe, et al.
Life Sciences|May 29, 2003
Effects of dopamine agonists bromocriptine, pergolide, cabergoline, and SKF-38393 on GDNF, NGF, and BDNF synthesis in cultured mouse astrocytesKiyoe Ohta, Sadako Kuno, Ikuko Mizuta, et al.
Journal of the Peripheral Nervous System : JPNS|June 28, 2012
A novel EGR2 mutation within a family with a mild demyelinating form of Charcot-Marie-Tooth diseaseKensuke Shiga, Yuichi Noto, Ikuko Mizuta, et al.
Rinsho Shinkeigaku = Clinical Neurology|December 1, 2017
[A case of hereditary sensory and autonomic neuropathy type 1E with frontal lobe dysfunction as an initial symptom]Masashi Watanabe, Yushi Matsumoto, Kensho Okamoto, et al.
Brain & Development|November 3, 2010
Serial MRI changes in a patient with infantile Alexander disease and prolonged survivalTakashi Shiihara, Toru Yoneda, Ikuko Mizuta, et al.
Experimental Neurology|February 25, 2025
CCL2/CCR2 signaling-mediated microglial migration leads to cerebral small vessel dysfunction in chronic hypertension model ratsTakashi Koizumi, Eline M Herckenrath, Katsutoshi Taguchi, et al.
Rinsho Shinkeigaku = Clinical Neurology|June 20, 2014
[Normokalemic periodic paralysis lasting for two weeks: a severe form of sodium channelopathy with M1592V mutation]Kensuke Shiga, Ikuko Mizuta, Yu-ichi Noto, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 31, 2003
Influence of monocyte chemoattractant protein 1 gene polymorphism on age at onset of sporadic Parkinson's diseaseMasataka Nishimura, Sadako Kuno, Ikuko Mizuta, et al.
Internal Medicine (Tokyo, Japan)|May 22, 2018
A Japanese Case of CADASIL with a Rare Mutation in Exon 24 of the NOTCH3 GeneYuka Ebihara, Hitoshi Mochizuki, Nobuyuki Ishii, et al.
Pageof 9