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Mayumi Matsufuji

Showing results (1-10 of 14) with videos related to

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Brain & Development|May 22, 2017
Neuroimaging and neuropathological characteristics of cerebellar injury in extremely low birth weight infantsMayumi Matsufuji, Nozomi Sano, Hisashi Tsuru, et al.
Journal of Clinical Neurophysiology : Official Publication of the American Electroencephalographic Society|October 21, 2016
Evaluation of Cognitive Function When Hearing One's Own Name in Patients With Brain Injuries in Early Developmental StagesKaori Tamura, Takaaki Mizuba, Tsuyoshi Okamoto, et al.
Brain & Development|December 23, 2014
Phase-locked theta activity evoked in patients with severe motor and intellectual disabilities upon hearing own namesKaori Tamura, Chihiro Karube, Takaaki Mizuba, et al.
Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE Engineering in Medicine and Biology Society. Annual International Conference|October 11, 2013
Measurement of brain activity responded by subjects'own name using EEGKaori Tamura, Chihiro Karube, Takaaki Mizuba, et al.
Pediatric Neurology|October 8, 2013
Partial PLP1 deletion causing X-linked dominant spastic paraplegia type 2Mayumi Matsufuji, Hitoshi Osaka, Leo Gotoh, et al.
Brain & Development|January 9, 2017
Aspartylglucosaminuria caused by a novel homozygous mutation in the AGA gene was identified by an exome-first approach in a patient from JapanToshiyuki Yamamoto, Keiko Shimojima, Mayumi Matsufuji, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|August 4, 2011
Magnetic resonance imaging volumetry and clinical analysis of epilepsy patients with unilateral hippocampal abnormalityMayumi Matsufuji, Hidetsuna Utsunomiya, Takahito Inoue, et al.
Brain & Development|May 12, 2010
A long-term survival case of arginase deficiency with severe multicystic white matter and compound mutationsYoshie Segawa, Mayumi Matsufuji, Naoya Itokazu, et al.
Brain & Development|October 13, 2019
Sodium phenylbutyrate improved the clinical state in an adult patient with arginase 1 deficiencyMayumi Matsufuji, Eiko Takeshita, Masayuki Nakashima, et al.
European Journal of Medical Genetics|November 7, 2016
Concurrent occurrence of an inherited 16p13.11 microduplication and a de novo 19p13.3 microdeletion involving MAP2K2 in a patient with developmental delay, distinctive facial features, and lambdoid synostosisKeiko Shimojima, Yumiko Ondo, Mayumi Matsufuji, et al.
Pageof 2

Showing results (1-10 of 14) with videos related to

Sort By:
Pageof 2
Brain & Development|May 22, 2017
Neuroimaging and neuropathological characteristics of cerebellar injury in extremely low birth weight infantsMayumi Matsufuji, Nozomi Sano, Hisashi Tsuru, et al.
Journal of Clinical Neurophysiology : Official Publication of the American Electroencephalographic Society|October 21, 2016
Evaluation of Cognitive Function When Hearing One's Own Name in Patients With Brain Injuries in Early Developmental StagesKaori Tamura, Takaaki Mizuba, Tsuyoshi Okamoto, et al.
Brain & Development|December 23, 2014
Phase-locked theta activity evoked in patients with severe motor and intellectual disabilities upon hearing own namesKaori Tamura, Chihiro Karube, Takaaki Mizuba, et al.
Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE Engineering in Medicine and Biology Society. Annual International Conference|October 11, 2013
Measurement of brain activity responded by subjects'own name using EEGKaori Tamura, Chihiro Karube, Takaaki Mizuba, et al.
Pediatric Neurology|October 8, 2013
Partial PLP1 deletion causing X-linked dominant spastic paraplegia type 2Mayumi Matsufuji, Hitoshi Osaka, Leo Gotoh, et al.
Brain & Development|January 9, 2017
Aspartylglucosaminuria caused by a novel homozygous mutation in the AGA gene was identified by an exome-first approach in a patient from JapanToshiyuki Yamamoto, Keiko Shimojima, Mayumi Matsufuji, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|August 4, 2011
Magnetic resonance imaging volumetry and clinical analysis of epilepsy patients with unilateral hippocampal abnormalityMayumi Matsufuji, Hidetsuna Utsunomiya, Takahito Inoue, et al.
Brain & Development|May 12, 2010
A long-term survival case of arginase deficiency with severe multicystic white matter and compound mutationsYoshie Segawa, Mayumi Matsufuji, Naoya Itokazu, et al.
Brain & Development|October 13, 2019
Sodium phenylbutyrate improved the clinical state in an adult patient with arginase 1 deficiencyMayumi Matsufuji, Eiko Takeshita, Masayuki Nakashima, et al.
European Journal of Medical Genetics|November 7, 2016
Concurrent occurrence of an inherited 16p13.11 microduplication and a de novo 19p13.3 microdeletion involving MAP2K2 in a patient with developmental delay, distinctive facial features, and lambdoid synostosisKeiko Shimojima, Yumiko Ondo, Mayumi Matsufuji, et al.
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