日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

The Potential and Challenges of Online Genetic Counseling in Japan

日本在线基因咨询的潜力和挑战

Fukushima, Yoshimitsu

Novel evaluation of pulmonary hypertension associated with chronic lung disease using perfusion SPECT/CT: A pilot study

利用灌注SPECT/CT对慢性肺病相关肺动脉高压进行新型评估:一项初步研究

Atsumi, Kenichiro; Fukushima, Yoshimitsu; Tanaka, Yosuke; Nishima, Shunichi; Tanaka, Toru; Seike, Masahiro; Kubota, Yoshiaki; Kimura, Hiroshi

Prognostic Implications of Sarcoidosis Granulomas - Insights From the Multicenter Registry, the Japanese Cardiac Sarcoidosis Prognostic Study

结节病肉芽肿的预后意义——来自多中心注册研究(日本心脏结节病预后研究)的启示

Yoshida, Shohei; Nakata, Tomoaki; Naya, Masanao; Momose, Mitsuru; Taniguchi, Yasuyo; Fukushima, Yoshimitsu; Moroi, Masao; Okizaki, Atsutaka; Hashimoto, Akiyoshi; Kiko, Takatoyo; Hida, Satoshi; Takehana, Kazuya; Nakajima, Kenichi

Serial change in perfusion-metabolism mismatch after coronary artery bypass grafting

冠状动脉旁路移植术后灌注-代谢不匹配的连续变化

Morishima, Motoko; Kiriyama, Tomonari; Miyagi, Yasuo; Otsuka, Toshiaki; Fukushima, Yoshimitsu; Kumita, Shin-Ichiro; Ishii, Yosuke

Correction to: Serial change in perfusion-metabolism mismatch after coronary artery bypass grafting

更正:冠状动脉旁路移植术后灌注-代谢不匹配的连续变化

Morishima, Motoko; Kiriyama, Tomonari; Miyagi, Yasuo; Otsuka, Toshiaki; Fukushima, Yoshimitsu; Kumita, Shin-Ichiro; Ishii, Yosuke

Multicenter Registry in the Japanese Cardiac Sarcoidosis Prognostic (J-CASP) Study: Baseline Characteristics and Validation of the Non-invasive Approach Using (18)F-FDG PET

日本心脏结节病预后(J-CASP)研究的多中心注册研究:基线特征及使用(18)F-FDG PET的非侵入性方法的验证

Nakata, Tomoaki; Nakajima, Kenichi; Naya, Masanao; Yoshida, Shohei; Momose, Mitsuru; Taniguchi, Yasuyo; Fukushima, Yoshimitsu; Moroi, Masao; Okizaki, Atsutaka; Hashimoto, Akiyoshi; Kiko, Takatoyo; Hida, Satoshi; Takehana, Kazuya

Clinical Genetics in Japan: Efforts of Human Genetics Societies and Related Organizations

日本临床遗传学:人类遗传学会及相关组织的努力

Fukushima, Yoshimitsu; Takada, Fumio

Frequency and clinical features of hearing loss caused by STRC deletions

STRC基因缺失引起的听力损失的发生率和临床特征

Yokota, Yoh; Moteki, Hideaki; Nishio, Shin-Ya; Yamaguchi, Tomomi; Wakui, Keiko; Kobayashi, Yumiko; Ohyama, Kenji; Miyazaki, Hiromitsu; Matsuoka, Rina; Abe, Satoko; Kumakawa, Kozo; Takahashi, Masahiro; Sakaguchi, Hirofumi; Uehara, Natsumi; Ishino, Takashi; Kosho, Tomoki; Fukushima, Yoshimitsu; Usami, Shin-Ichi

Myelodysplastic syndrome in an infant with constitutional pure duplication 1q41-qter

一名患有先天性纯重复1q41-qter的婴儿被诊断为骨髓增生异常综合征。

Morokawa, Hirokazu; Kamiya, Motoko; Wakui, Keiko; Kobayashi, Mikiko; Kurata, Takashi; Matsuda, Kazuyuki; Kawamura, Rie; Kanno, Hiroyuki; Fukushima, Yoshimitsu; Nakazawa, Yozo; Kosho, Tomoki

Diagnostic performance of hybrid cardiac SPECT/CT imaging for patients with takotsubo cardiomyopathy

混合心脏SPECT/CT成像对Takotsubo心肌病患者的诊断性能

Sugihara, Yasuro; Fukushima, Yoshimitsu; Kumita, Shin-Ichiro; Takano, Hitoshi; Shimizu, Wataru