Shinichi Hirose
Fukuoka University
H-index: 59
Asia-Japan
Top articles of Shinichi Hirose
Title | Journal | Author(s) | Publication Date |
|---|---|---|---|
Frequency of iduronate-2-sulfatase gene variants detected in newborn screening for mucopolysaccharidosis type II in Japan | Molecular Genetics and Metabolism Reports | Yusuke Hattori Takaaki Sawada Jun Kido Keishin Sugawara Shinichiro Yoshida | 2023/12/1 |
Developmental changes in brain activity of heterozygous Scn1a knockout rats | Frontiers in Neurology | Mayu Tahara Norimichi Higurashi Junichi Hata Masako Nishikawa Ken Ito | 2023/3/14 |
Astrocyte Ca2+ signaling is facilitated in Scn1a+/− mouse model of Dravet syndrome | Biochemical and Biophysical Research Communications | Kouya Uchino Yasuyoshi Tanaka Wakana Ikezawa Masanobu Deshimaru Kaori Kubota | 2023/2/5 |
Burden of seizures and comorbidities in patients with epilepsy: a survey based on the tertiary hospital‐based Epilepsy Syndrome Registry in Japan | Epileptic Disorders | Yushi Inoue Shin‐ichiro Hamano Masaharu Hayashi Hiroshi Sakuma Shinichi Hirose | 2022/2 |
Establishment of autaptic culture with human-induced pluripotent stem cell-derived astrocytes | Iscience | Kouya Uchino Yasuyoshi Tanaka Sayaka Kawaguchi Kaori Kubota Takuya Watanabe | 2022/8/19 |
Invasive candidiasis in a neonatal intensive care unit in Fukuoka | Nigerian Postgraduate Medical Journal | Beatrice Nkolika Ezenwa Rita Okeoghene Oladele Patricia Eyanya Akintan Iretiola Bamikeolu Fajolu Phillip Olayiwola Oshun | 2017/7/1 |
Newborn screening for Gaucher disease in Japan | Molecular Genetics and Metabolism Reports | Takaaki Sawada Jun Kido Keishin Sugawara Shinichiro Yoshida Shirou Matsumoto | 2022/6/1 |
Genetics and gene therapy in Dravet syndrome | Norimichi Higurashi Vania Broccoli Shinichi Hirose | 2022/6/1 | |
CUX2 deficiency causes facilitation of excitatory synaptic transmission onto hippocampus and increased seizure susceptibility to kainate | Scientific reports | Toshimitsu Suzuki Tetsuya Tatsukawa Genki Sudo Caroline Delandre Yun Jin Pai | 2022/5/17 |
The effectiveness of intravenous benzodiazepine for status epilepticus in Dravet syndrome | Brain and Development | Kenjiro Kikuchi Shin-ichiro Hamano Ryuki Matsuura Hazuki Nonoyama Atsuro Daida | 2022/5/1 |
Mutation in the STXBP1 Gene Associated with Early Onset West Syndrome: A Case Report and Literature Review | Pediatric Reports | Kanako Takeda Yusaku Miyamoto Hisako Yamamoto Toshiyuki Iwasaki Noriko Sumitomo | 2022/9/20 |
Multicentric glioblastoma in a 4‑year‑old female patient: A case report | Molecular and Clinical Oncology | Toshiyuki Enomoto Mikiko Aoki Takamichi Kouzaki Masaki Takahara Hiroshi Abe | 2021/5/1 |
Sub-genic intolerance, ClinVar, and the epilepsies: A whole-exome sequencing study of 29,165 individuals | The American Journal of Human Genetics | Joshua E Motelow Gundula Povysil Ryan S Dhindsa Kate E Stanley Andrew S Allen | 2021/6/3 |
MicroRNAs miR-4535 and miR-1915-5p in amniotic fluid as predictive biomarkers for chorioamnionitis | Future Science OA | Chihiro Kiyoshima Naoto Shirasu Daichi Urushiyama Satoshi Fukagawa Toyofumi Hirakawa | 2021/6 |
DCTN1 binds to TDP-43 and regulates TDP-43 aggregation | International journal of molecular sciences | Manami Deshimaru Mariko Kinoshita-Kawada Kaori Kubota Takuya Watanabe Yasuyoshi Tanaka | 2021/4/13 |
Current status of newborn screening for Pompe disease in Japan | Orphanet Journal of Rare Diseases | Takaaki Sawada Jun Kido Keishin Sugawara Ken Momosaki Shinichiro Yoshida | 2021/12/18 |
Physical, cognitive, and social status of patients with urea cycle disorders in Japan | Molecular Genetics and Metabolism Reports | Jun Kido Shirou Matsumoto Tetsuya Ito Shinichi Hirose Kaori Fukui | 2021/6/1 |
The excitatory/inhibitory balance of synaptic transmission is impaired at higher extracellular Ca2+ concentrations in Scn1a+/− mouse model of Dravet syndrome | bioRxiv | Kouya Uchino Hiroyuki Kawano Yasuyoshi Tanaka Yuna Adaniya Ai Asahara | 2021/2/4 |
Genome sequencing and RNA‐seq analyses of mitochondrial complex I deficiency revealed Alu insertion‐mediated deletion in NDUFV2 | Human Mutation | Yoshihito Kishita Masaru Shimura Masakazu Kohda Takuya Fushimi Kazuhiro R Nitta | 2021/11 |
Comparative characterization of PCDH19 missense and truncating variants in PCDH19-related epilepsy | Journal of human genetics | Mami Shibata Atsushi Ishii Ayako Goto Shinichi Hirose | 2021/6 |
