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Shinobu Fukumura

Showing results (1-10 of 36) with videos related to

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Brain & Development|December 24, 2010
A novel proteolipid protein 1 gene mutation causing classical type Pelizaeus-Merzbacher diseaseShinobu Fukumura, Noriaki Adachi, Masayoshi Nagao, et al.
No to Hattatsu = Brain and Development|July 17, 2018
Short-term efficacy and safety of rufinamide for Lennox-Gastaut syndromeRumiko Takayama, Shinobu Fukumura, Kimio Minagawa, et al.
Pediatric Neurology|December 3, 2014
Paroxysmal tonic upward gaze complicating Angelman syndromeShinobu Fukumura, Toshihide Watanabe, Rumiko Takayama, et al.
No to Hattatsu = Brain and Development|November 19, 2014
[Importance of measuring blood level of lamotrigine for optimum dosing schedule]Kimio Minagawa, Toshihide Watanabe, Reiki Oyanagi, et al.
Journal of Child Neurology|August 22, 2014
Everolimus Treatment for an Early Infantile Subependymal Giant Cell Astrocytoma With Tuberous Sclerosis ComplexShinobu Fukumura, Toshihide Watanabe, Rumiko Takayama, et al.
Neurogenetics|February 11, 2022
An intronic GNAO1 variant leading to in-frame insertion cause movement disorder controlled by deep brain stimulationSachiko Miyamoto, Mitsuko Nakashima, Shinobu Fukumura, et al.
Brain & Development|April 11, 2022
A new case of concurrent existence of PRRT2-associated paroxysmal movement disorders with c.649dup variant and 16p11.2 microdeletion syndromeKazuyuki Komatsu, Shinobu Fukumura, Kimio Minagawa, et al.
Child Neurology Open|May 16, 2017
A Mutation in the Tubulin-Encoding <i>TUBB3</i> Gene Causes Complex Cortical Malformations and Unilateral HypohidrosisShinobu Fukumura, Mitsuhiro Kato, Kentaro Kawamura, et al.
Brain & Development|November 17, 2020
Familial periodic paralysis associated with a rare KCNJ5 variant that supposed to have incomplete penetranceTakuya Hiraide, Shinobu Fukumura, Akiyo Yamamoto, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|May 7, 2018
Rapidly progressive fatal idiopathic hypertrophic pachymeningitis with brainstem involvement in a childKosuke Tsuchida, Shinobu Fukumura, Akiyo Yamamoto, et al.
Pageof 4

Showing results (1-10 of 36) with videos related to

Sort By:
Pageof 4
Brain & Development|December 24, 2010
A novel proteolipid protein 1 gene mutation causing classical type Pelizaeus-Merzbacher diseaseShinobu Fukumura, Noriaki Adachi, Masayoshi Nagao, et al.
No to Hattatsu = Brain and Development|July 17, 2018
Short-term efficacy and safety of rufinamide for Lennox-Gastaut syndromeRumiko Takayama, Shinobu Fukumura, Kimio Minagawa, et al.
Pediatric Neurology|December 3, 2014
Paroxysmal tonic upward gaze complicating Angelman syndromeShinobu Fukumura, Toshihide Watanabe, Rumiko Takayama, et al.
No to Hattatsu = Brain and Development|November 19, 2014
[Importance of measuring blood level of lamotrigine for optimum dosing schedule]Kimio Minagawa, Toshihide Watanabe, Reiki Oyanagi, et al.
Journal of Child Neurology|August 22, 2014
Everolimus Treatment for an Early Infantile Subependymal Giant Cell Astrocytoma With Tuberous Sclerosis ComplexShinobu Fukumura, Toshihide Watanabe, Rumiko Takayama, et al.
Neurogenetics|February 11, 2022
An intronic GNAO1 variant leading to in-frame insertion cause movement disorder controlled by deep brain stimulationSachiko Miyamoto, Mitsuko Nakashima, Shinobu Fukumura, et al.
Brain & Development|April 11, 2022
A new case of concurrent existence of PRRT2-associated paroxysmal movement disorders with c.649dup variant and 16p11.2 microdeletion syndromeKazuyuki Komatsu, Shinobu Fukumura, Kimio Minagawa, et al.
Child Neurology Open|May 16, 2017
A Mutation in the Tubulin-Encoding <i>TUBB3</i> Gene Causes Complex Cortical Malformations and Unilateral HypohidrosisShinobu Fukumura, Mitsuhiro Kato, Kentaro Kawamura, et al.
Brain & Development|November 17, 2020
Familial periodic paralysis associated with a rare KCNJ5 variant that supposed to have incomplete penetranceTakuya Hiraide, Shinobu Fukumura, Akiyo Yamamoto, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|May 7, 2018
Rapidly progressive fatal idiopathic hypertrophic pachymeningitis with brainstem involvement in a childKosuke Tsuchida, Shinobu Fukumura, Akiyo Yamamoto, et al.
Pageof 4