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Mariko Taniguchi

Showing results (71-80 of 91) with videos related to

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Human Genome Variation|April 16, 2016
Prenatal genetic testing for familial severe congenital protein C deficiencyShinya Tairaku, Mariko Taniguchi-Ikeda, Yoko Okazaki, et al.
Brain & Development|August 27, 2018
Fosphenytoin vs. continuous midazolam for pediatric febrile status epilepticusMasahiro Nishiyama, Hiroaki Nagase, Kazumi Tomioka, et al.
Journal of Autism and Developmental Disorders|November 30, 2017
Congenital Cytomegalovirus Infection in Children with Autism Spectrum Disorder: Systematic Review and Meta-AnalysisKaori Maeyama, Kazumi Tomioka, Hiroaki Nagase, et al.
Brain & Development|March 24, 2018
Early risk factors for mortality in children with seizure and/or impaired consciousness accompanied by fever without known etiologyKazumi Tomioka, Hiroaki Nagase, Tsukasa Tanaka, et al.
Brain & Development|March 9, 2016
Short and long-term outcomes in children with suspected acute encephalopathyMasahiro Nishiyama, Hiroaki Nagase, Tsukasa Tanaka, et al.
Scientific Reports|December 10, 2016
Gestational age-dependency of height and body mass index trajectories during the first 3 years in Japanese small-for-gestational age childrenKaori Maeyama, Ichiro Morioka, Sota Iwatani, et al.
Human Mutation|May 17, 2018
De novo variants in RHOBTB2, an atypical Rho GTPase gene, cause epileptic encephalopathyHazrat Belal, Mitsuko Nakashima, Hiroshi Matsumoto, et al.
Stem Cells International|November 16, 2017
Involvement of WNT Signaling in the Regulation of Gestational Age-Dependent Umbilical Cord-Derived Mesenchymal Stem Cell ProliferationSota Iwatani, Akemi Shono, Makiko Yoshida, et al.
Journal of Human Genetics|October 28, 2016
Cryptic exon activation in SLC12A3 in Gitelman syndromeKandai Nozu, Yoshimi Nozu, Keita Nakanishi, et al.
Journal of Human Genetics|April 12, 2020
A case of a parthenogenetic 46,XX/46,XY chimera presenting ambiguous genitaliaRie Kawamura, Takema Kato, Shunsuke Miyai, et al.
Pageof 10

Showing results (71-80 of 91) with videos related to

Sort By:
Pageof 10
Human Genome Variation|April 16, 2016
Prenatal genetic testing for familial severe congenital protein C deficiencyShinya Tairaku, Mariko Taniguchi-Ikeda, Yoko Okazaki, et al.
Brain & Development|August 27, 2018
Fosphenytoin vs. continuous midazolam for pediatric febrile status epilepticusMasahiro Nishiyama, Hiroaki Nagase, Kazumi Tomioka, et al.
Journal of Autism and Developmental Disorders|November 30, 2017
Congenital Cytomegalovirus Infection in Children with Autism Spectrum Disorder: Systematic Review and Meta-AnalysisKaori Maeyama, Kazumi Tomioka, Hiroaki Nagase, et al.
Brain & Development|March 24, 2018
Early risk factors for mortality in children with seizure and/or impaired consciousness accompanied by fever without known etiologyKazumi Tomioka, Hiroaki Nagase, Tsukasa Tanaka, et al.
Brain & Development|March 9, 2016
Short and long-term outcomes in children with suspected acute encephalopathyMasahiro Nishiyama, Hiroaki Nagase, Tsukasa Tanaka, et al.
Scientific Reports|December 10, 2016
Gestational age-dependency of height and body mass index trajectories during the first 3 years in Japanese small-for-gestational age childrenKaori Maeyama, Ichiro Morioka, Sota Iwatani, et al.
Human Mutation|May 17, 2018
De novo variants in RHOBTB2, an atypical Rho GTPase gene, cause epileptic encephalopathyHazrat Belal, Mitsuko Nakashima, Hiroshi Matsumoto, et al.
Stem Cells International|November 16, 2017
Involvement of WNT Signaling in the Regulation of Gestational Age-Dependent Umbilical Cord-Derived Mesenchymal Stem Cell ProliferationSota Iwatani, Akemi Shono, Makiko Yoshida, et al.
Journal of Human Genetics|October 28, 2016
Cryptic exon activation in SLC12A3 in Gitelman syndromeKandai Nozu, Yoshimi Nozu, Keita Nakanishi, et al.
Journal of Human Genetics|April 12, 2020
A case of a parthenogenetic 46,XX/46,XY chimera presenting ambiguous genitaliaRie Kawamura, Takema Kato, Shunsuke Miyai, et al.
Pageof 10