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No to Hattatsu = Brain and Development
|
November 12, 2013
[Epileptic encephalopathy associated with forced normalization after administration of levetiracetam]
Takahiro Kikuchi, Mitsuhiro Kato, Nobuya Takahashi, et al.
Journal of Human Genetics
|
August 18, 2019
A de novo variant in RAC3 causes severe global developmental delay and a middle interhemispheric variant of holoprosencephaly
Takuya Hiraide, Hikari Kaba Yasui, Mitsuhiro Kato, et al.
Brain & Development
|
August 5, 2023
Neurochemistry evaluated by magnetic resonance spectroscopy in a patient with FBXO28-related developmental and epileptic encephalopathy
Kentaro Sano, Fuyuki Miya, Mitsuhiro Kato, et al.
Journal of Child Neurology
|
May 25, 2002
Fluctuation of computed tomographic findings in white matter in Alexander's disease
Takashi Shiihara, Mitsuhiro Kato, Tomomi Honma, et al.
Pediatric Neurology
|
August 7, 2007
Megalencephaly and polymicrogyria with polydactyly syndrome
Jun Tohyama, Noriyuki Akasaka, Naka Saito, et al.
No to Hattatsu = Brain and Development
|
November 12, 2013
[A male case of subcortical band heterotopia with somatic mosaicism of DCX mutation]
Aiko Igarashi, Masao Kawatani, Genrei Ohta, et al.
No to Hattatsu = Brain and Development
|
December 18, 2012
[Questionnaire survey conducted on the parents of patients with spinal muscular atrophy type 1 in Japan regarding switch devices, language development, upper extremity function and QOL]
Shinya Sakai, Makoto Maki, Naoko Sakai, et al.
No to Hattatsu = Brain and Development
|
July 17, 2018
Combinatory use of central venous catheter and ethanol lock for a patient with X-linked lissencephaly with ambiguous genitalia (XLAG) syndrome
Hirotaka Motoi, Hiroyuki Shimizu, Yu Fujiwara, et al.
Journal of Child Neurology
|
April 16, 2003
Microcephaly, cerebellar atrophy, and focal segmental glomerulosclerosis in two brothers: a possible mild form of Galloway-Mowat syndrome
Takashi Shiihara, Mitsuhiro Kato, Toshiyuki Kimura, et al.
Brain & Development
|
October 10, 2008
Analysis of the hypothalamus in a case of X-linked lissencephaly with abnormal genitalia (XLAG)
Rie Miyata, Masaharu Hayashi, Kentaro Miyai, et al.
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of 24
Search research articles
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Showing results (21-30 of 238) with videos related to
Sort By:
Page
of 24
No to Hattatsu = Brain and Development
|
November 12, 2013
[Epileptic encephalopathy associated with forced normalization after administration of levetiracetam]
Takahiro Kikuchi, Mitsuhiro Kato, Nobuya Takahashi, et al.
Journal of Human Genetics
|
August 18, 2019
A de novo variant in RAC3 causes severe global developmental delay and a middle interhemispheric variant of holoprosencephaly
Takuya Hiraide, Hikari Kaba Yasui, Mitsuhiro Kato, et al.
Brain & Development
|
August 5, 2023
Neurochemistry evaluated by magnetic resonance spectroscopy in a patient with FBXO28-related developmental and epileptic encephalopathy
Kentaro Sano, Fuyuki Miya, Mitsuhiro Kato, et al.
Journal of Child Neurology
|
May 25, 2002
Fluctuation of computed tomographic findings in white matter in Alexander's disease
Takashi Shiihara, Mitsuhiro Kato, Tomomi Honma, et al.
Pediatric Neurology
|
August 7, 2007
Megalencephaly and polymicrogyria with polydactyly syndrome
Jun Tohyama, Noriyuki Akasaka, Naka Saito, et al.
No to Hattatsu = Brain and Development
|
November 12, 2013
[A male case of subcortical band heterotopia with somatic mosaicism of DCX mutation]
Aiko Igarashi, Masao Kawatani, Genrei Ohta, et al.
No to Hattatsu = Brain and Development
|
December 18, 2012
[Questionnaire survey conducted on the parents of patients with spinal muscular atrophy type 1 in Japan regarding switch devices, language development, upper extremity function and QOL]
Shinya Sakai, Makoto Maki, Naoko Sakai, et al.
No to Hattatsu = Brain and Development
|
July 17, 2018
Combinatory use of central venous catheter and ethanol lock for a patient with X-linked lissencephaly with ambiguous genitalia (XLAG) syndrome
Hirotaka Motoi, Hiroyuki Shimizu, Yu Fujiwara, et al.
Journal of Child Neurology
|
April 16, 2003
Microcephaly, cerebellar atrophy, and focal segmental glomerulosclerosis in two brothers: a possible mild form of Galloway-Mowat syndrome
Takashi Shiihara, Mitsuhiro Kato, Toshiyuki Kimura, et al.
Brain & Development
|
October 10, 2008
Analysis of the hypothalamus in a case of X-linked lissencephaly with abnormal genitalia (XLAG)
Rie Miyata, Masaharu Hayashi, Kentaro Miyai, et al.
Page
of 24