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Human Genome Variation
|
April 16, 2016
Prenatal genetic testing for familial severe congenital protein C deficiency
Shinya Tairaku, Mariko Taniguchi-Ikeda, Yoko Okazaki, et al.
Brain & Development
|
August 27, 2018
Fosphenytoin vs. continuous midazolam for pediatric febrile status epilepticus
Masahiro 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-Analysis
Kaori 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 etiology
Kazumi Tomioka, Hiroaki Nagase, Tsukasa Tanaka, et al.
Brain & Development
|
March 9, 2016
Short and long-term outcomes in children with suspected acute encephalopathy
Masahiro 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 children
Kaori Maeyama, Ichiro Morioka, Sota Iwatani, et al.
Human Mutation
|
May 17, 2018
De novo variants in RHOBTB2, an atypical Rho GTPase gene, cause epileptic encephalopathy
Hazrat 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 Proliferation
Sota Iwatani, Akemi Shono, Makiko Yoshida, et al.
Journal of Human Genetics
|
October 28, 2016
Cryptic exon activation in SLC12A3 in Gitelman syndrome
Kandai 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 genitalia
Rie Kawamura, Takema Kato, Shunsuke Miyai, et al.
Page
of 10
Search research articles
Search
Showing results (71-80 of 91) with videos related to
Sort By:
Page
of 10
Human Genome Variation
|
April 16, 2016
Prenatal genetic testing for familial severe congenital protein C deficiency
Shinya Tairaku, Mariko Taniguchi-Ikeda, Yoko Okazaki, et al.
Brain & Development
|
August 27, 2018
Fosphenytoin vs. continuous midazolam for pediatric febrile status epilepticus
Masahiro 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-Analysis
Kaori 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 etiology
Kazumi Tomioka, Hiroaki Nagase, Tsukasa Tanaka, et al.
Brain & Development
|
March 9, 2016
Short and long-term outcomes in children with suspected acute encephalopathy
Masahiro 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 children
Kaori Maeyama, Ichiro Morioka, Sota Iwatani, et al.
Human Mutation
|
May 17, 2018
De novo variants in RHOBTB2, an atypical Rho GTPase gene, cause epileptic encephalopathy
Hazrat 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 Proliferation
Sota Iwatani, Akemi Shono, Makiko Yoshida, et al.
Journal of Human Genetics
|
October 28, 2016
Cryptic exon activation in SLC12A3 in Gitelman syndrome
Kandai 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 genitalia
Rie Kawamura, Takema Kato, Shunsuke Miyai, et al.
Page
of 10