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Brain & Development
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August 16, 2016
A case of Dravet syndrome with cortical myoclonus indicated by jerk-locked back-averaging of electroencephalogram data
Yoshinori Kobayashi, Yoshiyuki Hanaoka, Tomoyuki Akiayma, et al.
Brain & Development
|
January 1, 1981
Febrile convulsions and rolandic discharges
T Kajitani, K Ueoka, M Nakamura, et al.
Brain & Development
|
March 17, 2018
Clinical phenotype of hereditary spastic paraplegia due to KIF1C gene mutations across life span
Didem Yücel-Yılmaz, Emrah Yücesan, Dilek Yalnızoğlu, et al.
Brain & Development
|
March 20, 2018
Ambulatory capacity in Japanese patients with Duchenne muscular dystrophy
Hiroyuki Awano, Chieko Itoh, Yasuhiro Takeshima, et al.
Brain & Development
|
January 9, 2018
Scalp-recorded high-frequency oscillations in childhood epileptic encephalopathy with continuous spike-and-wave during sleep with different etiologies
Pan Gong, Jiao Xue, Ping Qian, et al.
Brain & Development
|
January 27, 2018
Quantitative microstructural cerebral changes in neurofibromatosis type 1
Eva Bültmann, Loukia M Spineli, Hans Hartmann, et al.
Brain & Development
|
March 31, 2018
Anti-N-methyl-d-aspartate receptor encephalitis in children: Incidence and experience in Hong Kong
Alvin Chi-Chung Ho, Sophelia Hoi-Shan Chan, Eric Chan, et al.
Brain & Development
|
March 5, 2018
Fazio-Londe syndrome in siblings from India with different phenotypes
Vykuntaraju K Gowda, Tamilarasan Udhayabanu, Perumal Varalakshmi, et al.
Brain & Development
|
March 6, 2018
A novel germline PIGA mutation causes early-onset epileptic encephalopathies in Chinese monozygotic twins
Ling-Ling Xie, Xiao-Jie Song, Tian-Yi Li, et al.
Brain & Development
|
January 1, 2018
l-Thyroxine-responsive drop attacks in childhood benign hereditary chorea: A case report
Tadashi Shiohama, Hirofumi Ohashi, Kenji Shimizu, et al.
Page
of 478
Search research articles
Search
Showing results (1261-1270 of 4,777) with videos related to
Sort By:
Page
of 478
Brain & Development
|
August 16, 2016
A case of Dravet syndrome with cortical myoclonus indicated by jerk-locked back-averaging of electroencephalogram data
Yoshinori Kobayashi, Yoshiyuki Hanaoka, Tomoyuki Akiayma, et al.
Brain & Development
|
January 1, 1981
Febrile convulsions and rolandic discharges
T Kajitani, K Ueoka, M Nakamura, et al.
Brain & Development
|
March 17, 2018
Clinical phenotype of hereditary spastic paraplegia due to KIF1C gene mutations across life span
Didem Yücel-Yılmaz, Emrah Yücesan, Dilek Yalnızoğlu, et al.
Brain & Development
|
March 20, 2018
Ambulatory capacity in Japanese patients with Duchenne muscular dystrophy
Hiroyuki Awano, Chieko Itoh, Yasuhiro Takeshima, et al.
Brain & Development
|
January 9, 2018
Scalp-recorded high-frequency oscillations in childhood epileptic encephalopathy with continuous spike-and-wave during sleep with different etiologies
Pan Gong, Jiao Xue, Ping Qian, et al.
Brain & Development
|
January 27, 2018
Quantitative microstructural cerebral changes in neurofibromatosis type 1
Eva Bültmann, Loukia M Spineli, Hans Hartmann, et al.
Brain & Development
|
March 31, 2018
Anti-N-methyl-d-aspartate receptor encephalitis in children: Incidence and experience in Hong Kong
Alvin Chi-Chung Ho, Sophelia Hoi-Shan Chan, Eric Chan, et al.
Brain & Development
|
March 5, 2018
Fazio-Londe syndrome in siblings from India with different phenotypes
Vykuntaraju K Gowda, Tamilarasan Udhayabanu, Perumal Varalakshmi, et al.
Brain & Development
|
March 6, 2018
A novel germline PIGA mutation causes early-onset epileptic encephalopathies in Chinese monozygotic twins
Ling-Ling Xie, Xiao-Jie Song, Tian-Yi Li, et al.
Brain & Development
|
January 1, 2018
l-Thyroxine-responsive drop attacks in childhood benign hereditary chorea: A case report
Tadashi Shiohama, Hirofumi Ohashi, Kenji Shimizu, et al.
Page
of 478