Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Kaoru Nishiyama"'
Autor:
Masafumi Matsuo, Benjamas Sattayasevana, Taku Shirakawa, Kaoru Nishiyama, Waricha Janejindamai, Vichai Laosombat, Vip Viprakasit
Publikováno v:
Blood Cells, Molecules, and Diseases. 34:191-196
Two hundred and twenty-five G6PD-deficient subjects in Songklanagarind Hospital in the south of Thailand comprising 210 males and 15 females were studied. Neonatal jaundice was detected in 85% of these patients. Acute hemolysis related to infection w
Publikováno v:
Japanese Journal of Human Genetics. 42:417-423
We have developed a fast and comprehensive method to scan for point mutations in a gene on X chromosome. A target region of the gene is first amplified. Then, using the amplified product as a template, PCR is carried out with multiple short-length fo
Autor:
Masafumi, Matsuo, Kaoru, Nishiyama, Taku, Shirakawa, Carmencita David, Padilla, Lai Poh, San, Purnomo, Suryantoro, Narazah Mohd, Yusoff, Nguyen Thi Ngoc, Dao
Publikováno v:
The Southeast Asian journal of tropical medicine and public health. 34
Glucose-6-phosphate dehydrogenase (G6PD) deficiency is common in malaria endemic regions and is estimated to affect more than 400 million people worldwide. Deficient subjects are mostly asymptomatic but clinical manifestations range from neonatal jau
Publikováno v:
Pediatrics international : official journal of the Japan Pediatric Society. 45(1)
Background: Glucose-6-phosphate dehydrogenase (G6PD) deficiency has increased prevalence rates in tropical Africa, tropical and subtropical Asia and some parts of the Mediterranean. Earlier studies on G6PD deficiency in the Philippines have shown pre
Autor:
Masafumi Matsuo, Mohd Nizam Isa, Hans Van Rostenberghe, Selamah Ghazali, Ayako Orita, Wan Zaidah Abdullah, Kaoru Nishiyama, Choo Keng Ee, Taku Shirakawa, Narazah Mohd Yusoff
Publikováno v:
International journal of hematology. 76(2)
Multiplex polymerase chain reaction (PCR) using multiple tandem forward primers and a common reverse primer (MPTP) was recently established as a comprehensive screening method for mutations in X-linked recessive diseases. In the work reported here, M