Derivation of canopy light absorption coefficient from reflectance spectra of pigments in the plant canopy. It is
a useful metric for understanding the spatial and temporal dynamics
Exploratory trial of urethral submucosa injection therapy of deflux for stress urinary incontinence after radical prostatectomyFujihara Atsuko,
Shiraishi Takumi,
Miyashita Masatsugu,
Inoue Yuta,
Saito Yumiko,
Taga Hideto,
Naitoh Yasuyuki,
Iwami Yayoi,
Horiguchi Go,
Ito-Ihara Toshiko,
Ukimura Osamu patient quality-of-life (QOL).
A simple and less invasive treatment for SUI in these patients is urgently
Large XCH 4 anomaly in summer 2013 over northeast Asia observed by GOSATIshizawa, Misa,
Morino, Isamu,
Inoue, Makoto,
Yoshida, Yukio,
Mabuchi, Kazuo,
Shirai, Tomoko,
Tohjima, Yasunori,
Maksyutov, Shamil Sh,
Ohyama, Hirofumi,
Uchino, Osamu,
Kawakami, Shuji,
Takizawa, Atsushi,
Belikov, Dmitry A. over 2009–2012, after removing
a long-term trend), as being retrieved from the Short-Wavelength Infra
A new diagnostic indication device of a biomarker growth differentiation factor 15 for mitochondrial diseases: From laboratory to automated inspectionKoga Y.,
Povalko N.,
Inoue E.,
Ishii A.,
Fujii K.,
Fujii T.,
Murayama K.,
Mogami Y.,
Hata I.,
Ikawa M.,
Fukami K.,
Fukumoto Y.,
Nomura M.,
Ichikawa K.,
Yoshida K. differentiation factor 15 (GDF15) has been reported as
a biomarker useful for not only diagnosing MDs, but also
Enzalutamide versus abiraterone as a first-line endocrine therapy for castration-resistant prostate cancer (ENABLE study for PCa): a study protocol for a multicenter randomized phase III trialIzumi Kouji,
Mizokami Atsushi,
Namiki Mikio,
Inoue Shogo,
Tanaka Nobumichi,
Yoshio Yuko,
Ishibashi Kei,
Kamiyama Manabu,
Kawai Noriyasu,
Enokida Hideki,
Shima Takashi,
Takahara Shizuko for CRPC. The present study is
a phase III, investigator-initiated, multicenter, head-to-head, randomized
Biomarkers and clinical rating scales for sodium pyruvate therapy in patients with mitochondrial disease) that are appropriate in preparing the protocol for
a future clinical trial of sodium pyruvate (SP) therapy.
A 48-week