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

How I Approach Hypokalemia, Polyuria, and Beyond: An Enigmatic Case of Caffeinated Proportions

我如何处理低钾血症、多尿症及其他问题:一个与咖啡因相关的疑难病例

Yamamura, Tomohiko; Nozu, Kandai; Velez, Juan Carlos Q

Clinical and Genetic Insights Into Isolated Proteinuria With CUBN Variants

CUBN变异引起的孤立性蛋白尿的临床和遗传学见解

Sakakibara, Nana; Ishiko, Shinya; Tanaka, Yu; Inoki, Yuta; Ichikawa, Yuta; Kitakado, Hideaki; Ueda, Chika; Kondo, Atsushi; Aoto, Yuya; Horinouchi, Tomoko; Yamamura, Tomohiko; Ishimori, Shingo; Onodera, Chinatsu; Inaba, Aya; Hamada, Riku; Harita, Yutaka; Nagano, China; Nozu, Kandai

Prevalence of Candidate Vaccine Targets and Genomic Features of Pediatric Invasive Streptococcus Agalactiae in Japan

日本儿童侵袭性无乳链球菌候选疫苗靶点流行情况及基因组特征

Kasai, Masashi; Nakano, Satoshi; Koide, Shota; Otake, Shogo; Shibata, Meiwa; Ishida-Kuroki, Kasumi; Sugawara, Yo; Akeda, Yukihiro; Nozu, Kandai; Sugai, Motoyuki

Functional Analysis of a Novel Pathogenic Glycine Amidinotransferase Mutant in Hereditary Fanconi Syndrome

遗传性范可尼综合征中一种新型致病性甘氨酸脒基转移酶突变体的功能分析

Takayanagi, Shunsuke; Mori, Keita P; Kang, Youngna; Araki, Mitsugu; Matsumoto, Shigeyuki; Sagae, Yukari; Sakakibara, Nana; Horinouchi, Tomoko; Higashi, Yoshiaki; Endo, Tomomi; Muso, Eri; Nozu, Kandai; Okuno, Yasushi; Yanagita, Motoko; Matsubara, Takeshi; Tsukamoto, Tatsuo

Serial Kidney Biopsies Reveal Progressive Pathology in Townes-Brocks Syndrome: A Case Report

连续肾活检揭示Townes-Brocks综合征的进行性病理改变:病例报告

Tsunoda, Susumu; Kurihara, Shigekazu; Ueno, Toshiharu; Oba, Yuki; Sekine, Akinari; Mizuno, Hiroki; Yamanouchi, Masayuki; Hasegawa, Eiko; Suwabe, Tatsuya; Kono, Kei; Ohashi, Kenichi; Yamaguchi, Yutaka; Morisada, Naoya; Nozu, Kandai; Ubara, Yoshifumi; Wada, Takehiko; Sawa, Naoki

Impact of the COVID-19 Pandemic on Child Development and Caregiving: A 7-Year Repeated Cross-Sectional Study of 3-Year-Old Children in Kobe City, Japan

新冠疫情对儿童发展和照护的影响:一项针对日本神户市3岁儿童的7年重复横断面研究

Suemune, Kazuki; Yamaguchi, Hiroshi; Nishiyama, Masahiro; Kyono, Yuki; Kawamura, Aoi; Oikawa, Shizuka; Imai, Takumi; Murakami, Sae; Mishina, Hiroki; Nozu, Kandai; Nagase, Hiroaki

Impact of the COVID-19 pandemic on infant neurodevelopmental outcomes

新冠疫情对婴儿神经发育结果的影响

Kyono, Yuki; Nishiyama, Masahiro; Yamaguchi, Hiroshi; Kawamura, Aoi; Oikawa, Shizuka; Tokumoto, Shoichi; Imai, Takumi; Murakami, Sae; Nozu, Kandai; Mishina, Hiroki; Nagase, Hiroaki

Risk factors and prognostic implications of upper or middle mediastinal lymph nodes metastasis and recurrence in esophagogastric junction carcinoma

食管胃交界癌上纵隔或中纵隔淋巴结转移和复发的危险因素及预后意义

Nozu, Shintaro; Fukuda, Takashi; Shiomi, Shinichiro; Oka, Daiji

Investigation of clinical and genetic characteristics of Alport syndrome using a national registry in Japan (JP-ALPS)

利用日本国家登记系统(JP-ALPS)研究阿尔波特综合征的临床和遗传特征

Okuda, Yusuke; Mikami, Naoaki; Hamada, Riku; Hataya, Hiroshi; Tanaka, Kazuki; Terano, Chikako; Fujita, Naoya; Miura, Kenichiro; Ishizuka, Kiyonobu; Shirai, Yoko; Kamei, Koichi; Ogura, Masao; Okamoto, Takayuki; Suzuki, Ryota; Shinozuka, Shunsuke; Shima, Yuko; Oka, Masafumi; Shimabukuro, Wataru; Tsukaguchi, Hiroyasu; Inagaki, Tetsuji; Nishiyama, Kei; Hashimoto, Taeko; Ito, Naoko; Yamamura, Tomohiko; Horinouchi, Tomoko; Ishikura, Kenji; Nakanishi, Koichi; Nozu, Kandai

Initial Suspicion of Autosomal Dominant Polycystic Kidney Disease Resulted in a Diagnosis of Autosomal Dominant Tubulointerstitial Kidney Disease Caused by a UMOD Mutation

最初怀疑为常染色体显性多囊肾病,最终确诊为由UMOD基因突变引起的常染色体显性肾小管间质性肾病。

Usui, Toshiaki; Ishibashi, Shun; Hattori, Akihisa; Nomura, Soichiro; Nakajima, Kentaro; Harada, Takuya; Akiyama, Tomoki; Tsunoda, Ryoya; Okada, Eri; Morito, Naoki; Mase, Kaori; Saito, Chie; Usui, Joichi; Kai, Hirayasu; Morisada, Naoya; Nozu, Kandai; Yamagata, Kunihiro