Lifestyle modification is associated with improving estimated glomerular filtration rate (eGFR) and proteinuria in Japanese with proteinuria [0.03%]
行为干预可以改善蛋白尿日本受试者的肾小球滤过率(eGFR)和蛋白尿
Nobuyuki Miyatake,Kenichi Shikata,Hirofumi Makino et al.
Nobuyuki Miyatake et al.
The link between lifestyle modification and changes in both proteinuria and estimated glomerular filtration rates (eGFRs) was evaluated in Japanese subjects with proteinuria who were not taking medications. We used data from 51 men (35.8±1...
Robot-assisted radical prostatectomy: modified ultradissection reduces pT2 positive surgical margins on the bladder neck [0.03%]
机器人辅助的根治性前列腺切除术：改良式的超游离可减少膀胱颈pT2阳性切缘
Motoo Araki,Wooju Jeong,Sung Yul Park et al.
Motoo Araki et al.
The purpose of this study was to compare the positive surgical margin (PSM) rates of 2 techniques of robot-assisted radical prostatectomy (RARP) for pT2 (localized) prostate cancer. A retrospective analysis was conducted of 361 RARP cases, ...
Association of blood pressure and body mass index with intraocular pressure in middle-aged and older Japanese residents: a cross-sectional and longitudinal study [0.03%]
中老年人群收缩压和体质指数与眼压的相关性分析：横断面及纵向队列研究
Masao Yoshida,Mamoru Ishikawa,Kanae Karita et al.
Masao Yoshida et al.
To clarify whether high blood pressure (BP) and high body mass index (BMI) are associated with elevated intraocular pressure (IOP), a cross-sectional and longitudinal study was conducted. This epidemiological study analyzed health examinati...
Preclinical evaluation of microRNA-34b/c delivery for malignant pleural mesothelioma [0.03%]
恶性胸膜间皮瘤的microRNA-34b/c递送的临床前评估
Tsuyoshi Ueno,Shinichi Toyooka,Takuya Fukazawa et al.
Tsuyoshi Ueno et al.
The microRNA-34s (miR-34s) have p53 response elements in their 5'-flanking regions and demonstrate tumor-suppressive functions. In malignant pleural mesothelioma (MPM), we previously reported that expression of miR-34b and miR-34c (miR-34b/...
Impact of comorbid hepatic steatosis on treatment of chronic hepatitis C in Japanese patients and the relationship with genetic polymorphism of IL28B, PNPLA3 and LDL receptor [0.03%]
肝脂变并存对日本丙型肝炎患者治疗的影响以及与IL28B、PNPLA3和LDL受体基因多态性的关系
Yuki Moritou,Fusao Ikeda,Yoshiaki Iwasaki et al.
Yuki Moritou et al.
The impact of hepatic steatosis on interferon therapy for patients with chronic hepatitis C (CHC) has been associated with single-nucleotide polymorphisms (SNP) of IL28B, patatin-like phospholipase domain-containing protein 3 (PNPLA3), and ...
Mizoribine inhibits the proliferation of renal stem/progenitor cells by G1/S arrest during renal regeneration [0.03%]
霉利素通过G1 / S停滞抑制肾再生过程中的肾干细胞/前体细胞增殖
Naoya Horimoto,Shinji Kitamura,Kenji Tsuji et al.
Naoya Horimoto et al.
Immunosuppressive agents are generally administered to treat kidney diseases. However, it is unclear whether renal stem/progenitor cells are directly affected by the immunosuppressive agents. We used normal rat kidney cells, ureteric bud ce...
Assessment of medical expenditures for sepsis:differentiating between cases with and without ruled-out diagnoses [0.03%]
脓毒症医疗费用评估：区分排除诊断的病例与未排除诊断的病例
Shinichi Tanihara,Takuya Imatoh,Yoshito Momose
Shinichi Tanihara
Setting public health priorities requires precise estimation of the burden of disease, including disease-specific medical expenditure. Information on multiple and ruled-out diagnoses on health insurance claims (HICs) has been ignored in tra...
A case of acute superior mesenteric artery embolism with severe ischemic liver injury successfully treated by endovascular treatment [0.03%]
急性肠系膜上动脉栓塞致重症肝缺血一例及血管内治疗经验
Yusuke Matsui,Hidefumi Mimura,Takuya Fukazawa et al.
Yusuke Matsui et al.
We describe an interesting clinical course of a patient who developed severe ischemic liver injury due to acute embolism of the superior mesenteric artery (SMA) and celiac artery. A 70-year-old man was hospitalized for abdominal pain and di...
Kenjiro Hasegawa,Yuzaburo Namba,Yoshihiro Kimata
Kenjiro Hasegawa
Thumb polydactyly is reported to be the most common congenital anomaly of the hand in Japan. The floating type is not particularly rare, accounting for 0.9 to 15% of all cases of thumb polydactyly. However, to the best of our knowledge, the...
Case Reports
Acta medica Okayama. 2013;67(6):391-5. DOI:10.18926/AMO/52013 2013
Masato Tanaka,Shinya Arataki,Yoshihisa Sugimoto et al.
Masato Tanaka et al.
Craniometaphyseal dysplasia is a rare genetic condition characterized by progressive thickening of bones in the skull and metaphyseal abnormalities in the long bones. This disorder often causes progressively symptomatic cranial nerve compre...