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Teruo Kitagawa

Showing results (21-30 of 25) with videos related to

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Clinical and Experimental Nephrology|April 21, 2011
Age, gender, and body length effects on reference serum creatinine levels determined by an enzymatic method in Japanese children: a multicenter studyOsamu Uemura, Masataka Honda, Takeshi Matsuyama, et al.
Pediatric Research|December 19, 2003
Long-term treatment and diagnosis of tetrahydrobiopterin-responsive hyperphenylalaninemia with a mutant phenylalanine hydroxylase geneHaruo Shintaku, Shigeo Kure, Toshihiro Ohura, et al.
Clinical and Experimental Nephrology|March 1, 2013
Reference ranges for serum cystatin C measurements in Japanese children by using 4 automated assaysNahoko Yata, Osamu Uemura, Masataka Honda, et al.
Human Mutation|July 22, 2009
Newborn screening for Fabry disease in Taiwan reveals a high incidence of the later-onset GLA mutation c.936+919G>A (IVS4+919G>A)Wuh-Liang Hwu, Yin-Hsiu Chien, Ni-Chung Lee, et al.
Clinical and Experimental Nephrology|July 23, 2015
Prevalence of Fabry disease in dialysis patients: Japan Fabry disease screening study (J-FAST)Osamu Saito, Eiji Kusano, Tetsu Akimoto, et al.
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Showing results (21-30 of 25) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 25 results.
Clinical and Experimental Nephrology|April 21, 2011
Age, gender, and body length effects on reference serum creatinine levels determined by an enzymatic method in Japanese children: a multicenter studyOsamu Uemura, Masataka Honda, Takeshi Matsuyama, et al.
Pediatric Research|December 19, 2003
Long-term treatment and diagnosis of tetrahydrobiopterin-responsive hyperphenylalaninemia with a mutant phenylalanine hydroxylase geneHaruo Shintaku, Shigeo Kure, Toshihiro Ohura, et al.
Clinical and Experimental Nephrology|March 1, 2013
Reference ranges for serum cystatin C measurements in Japanese children by using 4 automated assaysNahoko Yata, Osamu Uemura, Masataka Honda, et al.
Human Mutation|July 22, 2009
Newborn screening for Fabry disease in Taiwan reveals a high incidence of the later-onset GLA mutation c.936+919G>A (IVS4+919G>A)Wuh-Liang Hwu, Yin-Hsiu Chien, Ni-Chung Lee, et al.
Clinical and Experimental Nephrology|July 23, 2015
Prevalence of Fabry disease in dialysis patients: Japan Fabry disease screening study (J-FAST)Osamu Saito, Eiji Kusano, Tetsu Akimoto, et al.
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