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Mitsuhiro Kato

Showing results (11-20 of 238) with videos related to

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Brain & Development|September 30, 2006
A case of acute cerebellitis accompanied by autoantibodies against glutamate receptor delta2Tomoyuki Shimokaze, Mitsuhiro Kato, Yozo Yoshimura, et al.
Child Neurology Open|May 16, 2017
A Mutation in the Tubulin-Encoding <i>TUBB3</i> Gene Causes Complex Cortical Malformations and Unilateral HypohidrosisShinobu Fukumura, Mitsuhiro Kato, Kentaro Kawamura, et al.
Brain & Development|August 29, 2013
Compound heterozygosity in GPR56 with bilateral frontoparietal polymicrogyriaYuji Fujii, Nobutsune Ishikawa, Yoshiyuki Kobayashi, et al.
Annals of Human Genetics|March 27, 2023
Identification of pathogenic deep intronic variant and exonic LINE-1 insertion in a patient with Meckel syndromeSachiko Miyamoto, Kazuyuki Nakamura, Mitsuhiro Kato, et al.
Journal of Child Neurology|September 24, 2011
Congenital dysplastic microcephaly and hypoplasia of the brainstem and cerebellum with diffuse intracranial calcificationKazuyuki Nakamura, Mitsuhiro Kato, Ayako Sasaki, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|September 26, 2012
Respiratory syncytial virus-associated encephalopathy complicated by congenital myopathyKazuyuki Nakamura, Mitsuhiro Kato, Ayako Sasaki, et al.
Brain & Development|December 3, 2023
Splicing variant of WDR37 in a case of Neurooculocardiogenitourinary syndromeMai Samejima, Mitsuko Nakashima, Jun Shibasaki, et al.
Brain & Development|October 20, 2006
Acute cerebellar ataxia and consecutive cerebellitis produced by glutamate receptor delta2 autoantibodyTakashi Shiihara, Mitsuhiro Kato, Akihiro Konno, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|July 9, 2026
Efficacy of fenfluramine in a pediatric epilepsy patient with a pathogenic SV2A variant: A case reportTakayuki Mori, Hiroshi Terashima, Yu Kakimoto, et al.
Journal of the Neurological Sciences|October 7, 2004
Asymptomatic hereditary Alexander's disease caused by a novel mutation in GFAPTakashi Shiihara, Yukio Sawaishi, Michito Adachi, et al.
Pageof 24

Showing results (11-20 of 238) with videos related to

Sort By:
Pageof 24
Brain & Development|September 30, 2006
A case of acute cerebellitis accompanied by autoantibodies against glutamate receptor delta2Tomoyuki Shimokaze, Mitsuhiro Kato, Yozo Yoshimura, et al.
Child Neurology Open|May 16, 2017
A Mutation in the Tubulin-Encoding <i>TUBB3</i> Gene Causes Complex Cortical Malformations and Unilateral HypohidrosisShinobu Fukumura, Mitsuhiro Kato, Kentaro Kawamura, et al.
Brain & Development|August 29, 2013
Compound heterozygosity in GPR56 with bilateral frontoparietal polymicrogyriaYuji Fujii, Nobutsune Ishikawa, Yoshiyuki Kobayashi, et al.
Annals of Human Genetics|March 27, 2023
Identification of pathogenic deep intronic variant and exonic LINE-1 insertion in a patient with Meckel syndromeSachiko Miyamoto, Kazuyuki Nakamura, Mitsuhiro Kato, et al.
Journal of Child Neurology|September 24, 2011
Congenital dysplastic microcephaly and hypoplasia of the brainstem and cerebellum with diffuse intracranial calcificationKazuyuki Nakamura, Mitsuhiro Kato, Ayako Sasaki, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|September 26, 2012
Respiratory syncytial virus-associated encephalopathy complicated by congenital myopathyKazuyuki Nakamura, Mitsuhiro Kato, Ayako Sasaki, et al.
Brain & Development|December 3, 2023
Splicing variant of WDR37 in a case of Neurooculocardiogenitourinary syndromeMai Samejima, Mitsuko Nakashima, Jun Shibasaki, et al.
Brain & Development|October 20, 2006
Acute cerebellar ataxia and consecutive cerebellitis produced by glutamate receptor delta2 autoantibodyTakashi Shiihara, Mitsuhiro Kato, Akihiro Konno, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|July 9, 2026
Efficacy of fenfluramine in a pediatric epilepsy patient with a pathogenic SV2A variant: A case reportTakayuki Mori, Hiroshi Terashima, Yu Kakimoto, et al.
Journal of the Neurological Sciences|October 7, 2004
Asymptomatic hereditary Alexander's disease caused by a novel mutation in GFAPTakashi Shiihara, Yukio Sawaishi, Michito Adachi, et al.
Pageof 24