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Showing results (1421-1430 of 4,777) with videos related to
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Brain & Development
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December 10, 2014
Nationwide survey of glucose transporter-1 deficiency syndrome (GLUT-1DS) in Japan
Yasushi Ito, Satoru Takahashi, Kuriko Kagitani-Shimono, et al.
Brain & Development
|
December 11, 2014
Identification and functional study of novel PLP1 mutations in Chinese patients with Pelizaeus-Merzbacher disease
Han Xie, Hongchun Feng, Jinhua Ji, et al.
Brain & Development
|
October 31, 2015
MRI and MRS findings in fucosidosis; a rare lysosomal storage disease
Suna Sahin Ediz, Ayse Aralasmak, Temel Fatih Yilmaz, et al.
Brain & Development
|
November 19, 2015
Bilateral ophthalmoplegia in a child with migraine
Rachana Dubey, Biswaroop Chakrabarty, Lokesh Saini, et al.
Brain & Development
|
March 1, 2016
A novel PIGA mutation in a family with X-linked, early-onset epileptic encephalopathy
Young Ok Kim, Jae Hyuk Yang, Chungoo Park, et al.
Brain & Development
|
February 13, 2016
Focal seizures and epileptic spasms in a child with Down syndrome from a family with a PRRT2 mutation
Ayuko Igarashi, Akihisa Okumura, Keiko Shimojima, et al.
Brain & Development
|
March 17, 2016
Refractory and severe status epilepticus in a patient with ring chromosome 20 syndrome
Yoshiko Hirano, Hirokazu Oguni, Satoru Nagata
Brain & Development
|
April 14, 2016
Trends in the prevalence of cerebral palsy in children born between 1988 and 2007 in Okinawa, Japan
Mayumi Touyama, Jun Touyama, Satoshi Toyokawa, et al.
Brain & Development
|
December 3, 2014
A Japanese girl with an early-infantile onset vanishing white matter disease resembling Cree leukoencephalopathy
Kyoko Takano, Yu Tsuyusaki, Mutsumi Sato, et al.
Brain & Development
|
December 3, 2014
A unilateral optic perineuritis in a teenager - A case report
Ahmad Ameilia, Ismail Shatriah, Wan Hazabbah Wan-Hitam, et al.
Page
of 478
Search research articles
Search
Showing results (1421-1430 of 4,777) with videos related to
Sort By:
Page
of 478
Brain & Development
|
December 10, 2014
Nationwide survey of glucose transporter-1 deficiency syndrome (GLUT-1DS) in Japan
Yasushi Ito, Satoru Takahashi, Kuriko Kagitani-Shimono, et al.
Brain & Development
|
December 11, 2014
Identification and functional study of novel PLP1 mutations in Chinese patients with Pelizaeus-Merzbacher disease
Han Xie, Hongchun Feng, Jinhua Ji, et al.
Brain & Development
|
October 31, 2015
MRI and MRS findings in fucosidosis; a rare lysosomal storage disease
Suna Sahin Ediz, Ayse Aralasmak, Temel Fatih Yilmaz, et al.
Brain & Development
|
November 19, 2015
Bilateral ophthalmoplegia in a child with migraine
Rachana Dubey, Biswaroop Chakrabarty, Lokesh Saini, et al.
Brain & Development
|
March 1, 2016
A novel PIGA mutation in a family with X-linked, early-onset epileptic encephalopathy
Young Ok Kim, Jae Hyuk Yang, Chungoo Park, et al.
Brain & Development
|
February 13, 2016
Focal seizures and epileptic spasms in a child with Down syndrome from a family with a PRRT2 mutation
Ayuko Igarashi, Akihisa Okumura, Keiko Shimojima, et al.
Brain & Development
|
March 17, 2016
Refractory and severe status epilepticus in a patient with ring chromosome 20 syndrome
Yoshiko Hirano, Hirokazu Oguni, Satoru Nagata
Brain & Development
|
April 14, 2016
Trends in the prevalence of cerebral palsy in children born between 1988 and 2007 in Okinawa, Japan
Mayumi Touyama, Jun Touyama, Satoshi Toyokawa, et al.
Brain & Development
|
December 3, 2014
A Japanese girl with an early-infantile onset vanishing white matter disease resembling Cree leukoencephalopathy
Kyoko Takano, Yu Tsuyusaki, Mutsumi Sato, et al.
Brain & Development
|
December 3, 2014
A unilateral optic perineuritis in a teenager - A case report
Ahmad Ameilia, Ismail Shatriah, Wan Hazabbah Wan-Hitam, et al.
Page
of 478