Zobrazeno 1 - 10
of 130
pro vyhledávání: '"Teruo Kitagawa"'
Autor:
Kauznari Kaneko, Takahisha Kimata, Shoji Tsuji, Kazumi Shiraishi, Kuniaki Yamauchi, Mutsumi Murakami, Teruo Kitagawa
Publikováno v:
Pediatric Reports, Vol 3, Iss 4, Pp e27-e27 (2011)
Obese patients are known to have greater risks to develop hypertension, coronary vascular disease, and insulin resistance, and more attention has been recently paid to the impact of obesity on kidney. This study was conducted to investigate whether o
Externí odkaz:
https://doaj.org/article/c88f682d32844adf97832e518529d996
Autor:
Hiroshi Hataya, Nahoko Yata, Shuichi Ito, Takuhito Nagai, Teruo Kitagawa, Kenji Ishikura, Takeshi Matsuyama, Naoya Fujita, Mari Saito, Tetsuji Keneko, Kazumoto Iijima, Masataka Honda, Yohei Ikezumi, Osamu Uemura
Publikováno v:
Clinical and Experimental Nephrology. 17:872-876
The data available on reference ranges for cystatin C in children are limited, and there are discrepancies among the available data. The aim of this study was to describe the reference ranges for cystatin C in Japanese children by using 4 automated a
Autor:
Takayuki Inomata, Eiji Kusano, Tomoyoshi Yanagisawa, Toya Ohashi, Yoshikatsu Eto, Hiroyuki Ida, Takashi Nagaoka, Masahisa Kobayashi, Takahiro Fukuda, Teruo Kitagawa
Publikováno v:
Molecular Genetics and Metabolism. 107:711-715
Background Fabry disease is an X-linked lysosomal disorder resulting from mutations in the α-galactosidase A (GLA) gene. Recent reports described that the E66Q mutation of GLA is not a disease-causing mutation. However, no pathological study was rep
Autor:
Teruo Kitagawa, Misao Owada
Publikováno v:
Journal of The Society of Japanese Women Scientists. 12:22-31
Autor:
Teruo KITAGAWA
Publikováno v:
Proceedings of the Japan Academy. Series B, Physical and Biological Sciences
In 1957 Sakai and Kitagawa in Japan reported the clinical and biochemical findings in a patient with tyrosinemia, tyrosyluria, liver cirrhosis, and renal rickets. Subsequently, reports were published from various countries of other patients with hepa
Autor:
Atsumi Tsuji, Teruo Kitagawa, Kaoru Konishi, Tomohiro Morio, Satomi Hasegawa, Makoto Ono, Toshikazu Onishi, Akira Anazawa, Kenichi Kashimada
Publikováno v:
BMC Pediatrics
Background Congenital adrenal hyperplasia (CAH) cause life-threatening adrenal crisis. It also affects fetal sex development and can result in incorrect sex assignment at birth. In 1989, a newborn screening program for congenital adrenal hyperplasia
Autor:
Shuichi Ito, Yohei Ikezumi, Teruo Kitagawa, Hiroshi Hataya, Kazumoto Iijima, Osamu Uemura, Masataka Honda, Kenji Ishikura, Takeshi Matsuyama, Takuhito Nagai, Naoya Fujita, Nahoko Yata
Publikováno v:
Clinical and Experimental Nephrology. 15:694-699
Enzymatic methods have recently been used to measure creatinine (Cr) instead of the Jaffe method. Therefore, it is necessary to determine the reference serum Cr value for these enzymatic methods to evaluate renal function in Japanese children. To det
Autor:
Teruo Kitagawa, Nobuyuki Ishige, Takashi Kodama, Toshihiro Suzuki, Toya Ohashi, Hitoshi Sakuraba, Kanako Sugawara, Tadayasu Togawa, Takahiro Tsukimura, Ken Suzuki
Publikováno v:
Molecular Genetics and Metabolism. 100:257-261
Fabry disease is an X-linked genetic disorder caused by a deficiency of α-galactosidase A (GLA) activity. As enzyme replacement therapy (ERT) involving recombinant GLAs has been introduced for this disease, a useful biomarker for diagnosis and monit
Autor:
Toshiharu Jinbo, Teruo Kitagawa, Yoshiaki Yagami, Sachio Ogita, Masahiko Matsumoto, Kaoru Suzumori, Tadashi Sugawa, Keiya Tada
Publikováno v:
Asia-Oceania Journal of Obstetrics and Gynaecology. 6:55-71
Prenatal diagnosis of genetic disease in Japan today, as of the end of 1978, and results of a follow-up study of infants born after genetic amniocentesis are reported. Of the 585 amniocentesis in 523 women, 568 cases contributed data for the results
Autor:
May-Chin Chao, Shu-Chuan Chiang, Robert J. Desnick, Hui-Ying Yeh, Shio Jean Lin, Wuh-Liang Hwu, Robert Dobrovolny, Yin-Hsiu Chien, Ai-Chu Huang, Li-Wen Hsu, Ni-Chung Lee, Teruo Kitagawa
Publikováno v:
Human Mutation. 30:1397-1405
Fabry disease (alpha-galactosidase A (alpha-Gal A, GLA) deficiency) is a panethnic inborn error of glycosphingolipid metabolism. Because optimal therapeutic outcomes depend on early intervention, a pilot program was designed to assess newborn screeni