Zobrazeno 1 - 10
of 94
pro vyhledávání: '"Teruo HARANO"'
Autor:
Kyaw-Shwe, Shigeru Okada, Aye-Aye-Myint, Ne-Win, Keiko Harano, Teruo Harano, Khin-Thander-Aye
Publikováno v:
Hemoglobin. 32:454-461
Hb Constant Spring (Hb CS), the gene (αCS) of which arises from a point mutation in the termination codon of the α2-globin gene, is the most prevalent variety of nondeletional α-thalassemia (α-thal) in Asian populations. It is a major cause of Hb
Autor:
Hiroshi Nakahara, Hiroto Matsuoka, Yoshihiro Oka, Isao Tachibana, Seiji Hayashi, Mitsunori Sakatani, Keiko Harano, Hiroshi Kida, Tomio Kawasaki, Shingo Kyotani, Teruo Harano, Ichiro Kawase
Publikováno v:
Lung. 184:223-227
Pulmonary infarction is an entity of medical significance that develops concurrently in beta-thalassemia but not in alpha-thalassemia. The reason for this difference is yet to be elucidated. We have evaluated a 21-year-old male alpha-thalassemia-2 pa
Autor:
Teruo Harano, Akira Shimizu, Akira Morimoto, Shigeyoshi Hibi, Ayako Miyazaki, Shinjiro Todo, Tohru Sugimoto, Shinsaku Imashuku, Chika Tokuda, Gen Kano
Publikováno v:
International Journal of Hematology. 80:410-415
Hemoglobin (Hb) Bristol-Alesha is caused by a GTG --ATG mutation at codon 67 in the Hb beta chain, resulting in abnormal beta globin chains with mutated molecules from normal beta67 valine (Val) to beta67 methionine (Met) or beta67 aspartate (Asp). W
Publikováno v:
Journal of Nippon Medical School. 71:297-300
We present two Japanese students with thalassemia identified during screening for anemia in their junior high school. Blood test results revealed marked hypochromic and microcytic erythrocytosis in one patient and microcytic anemia in the other. Both
Publikováno v:
Hemoglobin. 27:117-121
Abnormal hemoglobins (Hbs) are often discovered during glycated Hb (Hb A1c) assays by using cation exchange high performance liquid chromatography (HPLC) [[1]]. We observed an abnormal HPLC elution...
Autor:
Rai-Mra, Keiko Harano, Shigeru Okada, Aye-Aye-Myint, Ne-Win, Thein-Thein-Myint, Kunio Shimono, Teruo Harano
Publikováno v:
British Journal of Haematology. 117:988-992
Two hundred and nine beta-thalassaemia (beta-Thal) alleles of 158 unrelated Myanmar patients (107 HbE-beta-Thal; 51 beta-Thal major) were analysed for beta-globin gene mutations. Amplification refractory mutation system (ARMS) characterized six beta-
Autor:
R. Hanada, G. Yoshimichi, Toshiie Sakata, Kazuyuki Hamaguchi, Teruo Harano, Yoichiro Kusuda, Keiko Harano
Publikováno v:
Hemoglobin. 24:153-156
(2000). Hb I-High Wycombe [β59(E3)Lys→Glu]: The First Instance in Japan. Hemoglobin: Vol. 24, No. 2, pp. 153-156.
Autor:
Keiko Harano, Y Oribe, Kazuyuki Hamaguchi, Y Iwasaki, Toshiie Sakata, K Kotegawa, Yoichiro Kusuda, Teruo Harano
Publikováno v:
Hemoglobin. 24:117-123
We accidentally observed an abnormal elution pattern on high performance liquid chromatogram when we examined the Hb A1c level in a 65-year-old male patient who suffered from pneumoconiosis and alcoholic liver injury. The value of the glycated fracti
Autor:
Keiko, Harano, Teruo, Harano
Publikováno v:
Rinsho byori. The Japanese journal of clinical pathology. 61(3)
This study was done to detect and diagnose beta-thalassemia (beta-Thal) gene quickly. We applied sequence specific Amplification (SSA) method to the analysis. 13 kinds of beta-Thal and two kinds of hemoglobin variants were able to detect under the sa
Publikováno v:
Hemoglobin. 20:361-369
We describe a silent and unstable hemoglobin variant, Hb Toranomon, which was discovered by high performance liquid chromatography in an apparently healthy Japanese male during a Hb A1c assay. Isoelectrofocusing of his hemolysate and chromatographic