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Circulation Journal : Official Journal of the Japanese Circulation Society|May 14, 2009
Predicting the efficacy of antiarrhythmic agents for interrupting persistent atrial fibrillation according to spectral analysis of the fibrillation waves on the surface ECGShinichi Niwano, Takeshi Sasaki, Sayaka Kurokawa, et al.
International Journal of Hematology|April 18, 2018
A characteristic flow cytometric pattern with broad forward scatter and narrowed side scatter helps diagnose immune thrombocytopenia (ITP)Raita Araki, Ryosei Nishimura, Rie Kuroda, et al.
American Journal of Ophthalmology|September 4, 2007
A novel variant lattice corneal dystrophy caused by association of mutation (V625D) in TGFBI geneXin Tian, Keiko Fujiki, Yan Zhang, et al.
Chemical Communications (Cambridge, England)|March 31, 2015
Pyrene magic: chiroptical enciphering and deciphering 1,3-dioxolane bearing two wirepullings to drive two remote pyrenesTomoyuki Amako, Kazuki Nakabayashi, Nozomu Suzuki, et al.
The Journal of Biological Chemistry|April 18, 2000
The mammalian peroxin Pex5pL, the longer isoform of the mobile peroxisome targeting signal (PTS) type 1 transporter, translocates the Pex7p.PTS2 protein complex into peroxisomes via its initial docking site, Pex14pH Otera, T Harano, M Honsho, et al.
American Journal of Ophthalmology|March 5, 2003
A novel mutation of M1S1 gene found in a Vietnamese patient with gelatinous droplike corneal dystrophyNguyen Thanh Ha, Hoang Minh Chau, Le Xuan Cung, et al.
Kaku Igaku. the Japanese Journal of Nuclear Medicine|May 1, 1990
[A three-headed SPECT system with high resolution and high sensitivity: application to myocardial imaging]K Nakajima, J Taki, K Hisada, et al.
Journal of Hepato-Biliary-Pancreatic Surgery|September 12, 2000
Adeno-endocrine cell carcinoma of the gallbladderN Eriguchi, S Aoyagi, T Noritomi, et al.
Japanese Circulation Journal|May 12, 2001
Relation of fibrillatory wave amplitude with hemostatic abnormality and left atrial appendage dysfunction in patients with chronic nonrheumatic atrial fibrillationK Nakagawa, T Hirai, N Shinokawa, et al.
Japanese Journal of Ophthalmology|December 12, 2018
In vivo histology and p.L132V mutation in KRT12 gene in Japanese patients with Meesmann corneal dystrophyTsubasa Nishino, Akira Kobayashi, Natsuko Mori, et al.
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