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The Journal of Infectious Diseases|July 10, 2004
Evaluation of systemic inflammatory responses in neonates with herpes simplex virus infectionJun-ichi Kawada, Hiroshi Kimura, Yoshinori Ito, et al.
Renal Failure|May 9, 2012
Identification of a novel mutation and prevalence study for fabry disease in Japanese dialysis patientsTomoya Nishino, Yoko Obata, Akira Furusu, et al.
Circulation Journal : Official Journal of the Japanese Circulation Society|December 21, 2018
Unexpectedly High Prevalence of Coronary Spastic Angina in Patients With Anderson-Fabry DiseaseYuya Kitani, Naoki Nakagawa, Naka Sakamoto, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|September 11, 2016
Amelioration by glycine of brain damage in neonatal rat brain following hypoxia-ischemiaHiroko Mori, Ken Momosaki, Jun Kido, et al.
Molecular Genetics and Metabolism|June 4, 2011
Time-dependent changes in the plasma amino acid concentration in diabetes mellitusTaiga Mochida, Takayuki Tanaka, Yasuko Shiraki, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|February 24, 2011
Exon-skipping events in candidates for clinical trials of morpholinoShiho Nakano, Shiro Ozasa, Kowashi Yoshioka, et al.
Genes to Cells : Devoted to Molecular & Cellular Mechanisms|October 21, 2005
Apical membrane and junctional complex formation during simple epithelial cell differentiation of F9 cellsSatoshi Komiya, Masayuki Shimizu, Junichi Ikenouchi, et al.
Journal of Human Genetics|March 15, 2013
Current status of hepatic glycogen storage disease in Japan: clinical manifestations, treatments and long-term outcomesJun Kido, Kimitoshi Nakamura, Shirou Matsumoto, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|December 17, 2013
VLCAD deficiency in a patient who recovered from ventricular fibrillation, but died suddenly of a respiratory syncytial virus infectionAkiko Yamamoto, Kimitoshi Nakamura, Shirou Matsumoto, et al.
Molecular Genetics and Metabolism|April 14, 2009
High frequency of acid alpha-glucosidase pseudodeficiency complicates newborn screening for glycogen storage disease type II in the Japanese populationShingo Kumamoto, Tatsuya Katafuchi, Kimitoshi Nakamura, et al.
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