原著2022年

1 Satomura T, Bessho K, Nawa N, Kondo H, Ito S, Togawa T, Yano M, Yamano Y, Inoue T, Fukui M, Onuma S, Fukuoka T, Yasuda K, Kimura T, Tachibana M, Kitaoka T, Nabatame S, Ozono K. Novel gene mutations in three Japanese patients with ARC syndrome associated mild phenotypes: a case series. J Med Case Rep. 2022 Feb 13;16:60
2 Imai K, Suzuki T, Fukaya S, Karasawa Y, Bando Y, Sawaki D, Araki Y, Saitoh S, Iwata O.  A New Quantitative Triage System for Hospitalized Neonates to Assist with Decisions of Hospital Evacuation Priorities. Prehosp Disaster Med. 2022 Jun;37(3):343-349.
3 Kato S, Ito M, Saito M, Miyahara N, Namba F, Ota E, Nakanishi H Severe bronchopulmonary dysplasia in extremely premature infants: a scoping review protocol for identifying risk factors. BMJ Open. 12:e062192; 2022
4 Michi Kamei, Mohamed Hamed Hussein, Ayako Hattori, Marwa Saleh, Hiroki Kakita, Ghada Abdel-Hamid Daoud, Akio Ishiguro, Fumihiko Namba, Makoto Yazaki, Ineko Kato, Hisanori Sobajima, Kabe Kazuhiko, Koichi Moriwaki, Hajime Togari, Haruo Goto Oxidative and Inflammatory Markers Are Higher in Full-Term Newborns Suffering Funisitis, and Higher Oxidative Markers Are Associated with Admission.  Children (Basel). 10;9(5):702; 2022
5 Shin Kato,  Osuke Iwata, Sachiko Iwata, Takaharu Yamada, Kennosuke Tsuda, Taihei Tanaka, Shinji Saitoh  Admission temperature of very low birth weight infants and outcomes at three years old. Sci Rep. 12: 11912 ;2022
6 Yamamoto K, Ohashi K, Fujimoto M, Ieda D, Nakamura Y, Hattori A, Kaname T, Ieda K, Nishino I, Saitoh S Long-term follow-up of a patient with autosomal dominant lower extremity-predominant spinal muscular atrophy-2 due to a BICD2 variant. Brain Dev. 2022 May 5;S0387-7604(22)00076-6.

[記事公開日]2022/04/01
[最終更新日]2022/08/05