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Showing results (141-150 of 5,161) with videos related to
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Brain & Development
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August 30, 2008
Predicting executive function task scores with the Rey-Osterrieth Complex Figure
Tatsuya Ogino, Kiyoko Watanabe, Kousuke Nakano, et al.
Brain & Development
|
September 20, 2008
Hyperkinetic movement disorder in a child treated by globus pallidus stimulation
Ken Sato, Eiji Nakagawa, Yoshiaki Saito, et al.
Brain & Development
|
September 23, 2008
Abnormal fast activity in infancy with paroxysmal downwards gaze
Harumi Yoshinaga, Katsuhiro Kobayashi, Fumika Endo, et al.
Brain & Development
|
September 2, 2008
Hereditary neuropathy with liability to pressure palsy (HNPP) in childhood: a case study emphasizing the relevance of detailed electrophysiological examination for suspected HNPP in the first decade
Ayşe Oytun Bayrak, Esra Battaloglu, Hande Turker, et al.
Brain & Development
|
March 30, 2012
Pulmonary hypertension in a child with mitochondrial A3243G point mutation
Po-Cheng Hung, Huei-Shyong Wang, Hung-Tao Chung, et al.
Brain & Development
|
October 11, 2021
Ankle contractures and functional motor decline in Duchenne muscular dystrophy
Angelina L Woof, Kathryn Selby, Susan R Harris
Brain & Development
|
February 12, 2022
Retrocollis as the cardinal feature in a de novo ITRP1 variant
Athena Zachou, Danai Palaiologou, Emmanouil Kanavakis, et al.
Brain & Development
|
February 14, 2022
Differentiating early clinical features of Panayiotopoulos syndrome from acute encephalopathy
Saori Kawakami, Masaya Kubota, Hiroshi Terashima, et al.
Brain & Development
|
June 8, 2019
Genomic backgrounds of Japanese patients with undiagnosed neurodevelopmental disorders
Toshiyuki Yamamoto, Taichi Imaizumi, Keiko Yamamoto-Shimojima, et al.
Brain & Development
|
July 11, 2019
Single-fiber electromyography-based diagnosis of CACNA1A mutation in children: A potential role of the electrodiagnosis in the era of whole exome sequencing
Ayaka Hirasawa-Inoue, Akihiko Ishiyama, Eri Takeshita, et al.
Page
of 517
Search research articles
Search
Showing results (141-150 of 5,161) with videos related to
Sort By:
Page
of 517
Brain & Development
|
August 30, 2008
Predicting executive function task scores with the Rey-Osterrieth Complex Figure
Tatsuya Ogino, Kiyoko Watanabe, Kousuke Nakano, et al.
Brain & Development
|
September 20, 2008
Hyperkinetic movement disorder in a child treated by globus pallidus stimulation
Ken Sato, Eiji Nakagawa, Yoshiaki Saito, et al.
Brain & Development
|
September 23, 2008
Abnormal fast activity in infancy with paroxysmal downwards gaze
Harumi Yoshinaga, Katsuhiro Kobayashi, Fumika Endo, et al.
Brain & Development
|
September 2, 2008
Hereditary neuropathy with liability to pressure palsy (HNPP) in childhood: a case study emphasizing the relevance of detailed electrophysiological examination for suspected HNPP in the first decade
Ayşe Oytun Bayrak, Esra Battaloglu, Hande Turker, et al.
Brain & Development
|
March 30, 2012
Pulmonary hypertension in a child with mitochondrial A3243G point mutation
Po-Cheng Hung, Huei-Shyong Wang, Hung-Tao Chung, et al.
Brain & Development
|
October 11, 2021
Ankle contractures and functional motor decline in Duchenne muscular dystrophy
Angelina L Woof, Kathryn Selby, Susan R Harris
Brain & Development
|
February 12, 2022
Retrocollis as the cardinal feature in a de novo ITRP1 variant
Athena Zachou, Danai Palaiologou, Emmanouil Kanavakis, et al.
Brain & Development
|
February 14, 2022
Differentiating early clinical features of Panayiotopoulos syndrome from acute encephalopathy
Saori Kawakami, Masaya Kubota, Hiroshi Terashima, et al.
Brain & Development
|
June 8, 2019
Genomic backgrounds of Japanese patients with undiagnosed neurodevelopmental disorders
Toshiyuki Yamamoto, Taichi Imaizumi, Keiko Yamamoto-Shimojima, et al.
Brain & Development
|
July 11, 2019
Single-fiber electromyography-based diagnosis of CACNA1A mutation in children: A potential role of the electrodiagnosis in the era of whole exome sequencing
Ayaka Hirasawa-Inoue, Akihiko Ishiyama, Eri Takeshita, et al.
Page
of 517