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Brain & Development
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December 24, 2010
A novel proteolipid protein 1 gene mutation causing classical type Pelizaeus-Merzbacher disease
Shinobu 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 syndrome
Rumiko Takayama, Shinobu Fukumura, Kimio Minagawa, et al.
Pediatric Neurology
|
December 3, 2014
Paroxysmal tonic upward gaze complicating Angelman syndrome
Shinobu 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 Complex
Shinobu 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 stimulation
Sachiko 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 syndrome
Kazuyuki 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 Hypohidrosis
Shinobu 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 penetrance
Takuya 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 child
Kosuke Tsuchida, Shinobu Fukumura, Akiyo Yamamoto, et al.
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of 4
Search research articles
Search
Showing results (1-10 of 36) with videos related to
Sort By:
Page
of 4
Brain & Development
|
December 24, 2010
A novel proteolipid protein 1 gene mutation causing classical type Pelizaeus-Merzbacher disease
Shinobu 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 syndrome
Rumiko Takayama, Shinobu Fukumura, Kimio Minagawa, et al.
Pediatric Neurology
|
December 3, 2014
Paroxysmal tonic upward gaze complicating Angelman syndrome
Shinobu 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 Complex
Shinobu 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 stimulation
Sachiko 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 syndrome
Kazuyuki 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 Hypohidrosis
Shinobu 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 penetrance
Takuya 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 child
Kosuke Tsuchida, Shinobu Fukumura, Akiyo Yamamoto, et al.
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of 4