Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Nirut Siriratmanawong"'
Autor:
Nirut Siriratmanawong, Charnchai Pinmuang-ngam, Supan Fucharoen, Goonnapa Fucharoen, Thanet Prajantasen
Publikováno v:
Molecular Biology Reports. 40:3173-3179
We have developed methods based on PCR and denaturing high performance liquid chromatography (DHPLC) for rapid identifications of common β-thalassemia mutations found in Thailand. The β-globin gene was separately amplified by PCR on four different
Autor:
Nirut Siriratmanawong, Sanita Singsanan, Goonnapa Fucharoen, Wichuda Chansri, Supan Fucharoen
Publikováno v:
Hemoglobin. 33:507-514
A pregnant Thai woman with mild hypochromic microcytic anemia caused by alpha- and beta- globin defects is described. The proband was a 26-year-old pregnant woman discovered through our ongoing thalassemia screening program. Initial hemoglobin (Hb) h
Publikováno v:
Fetal Diagnosis and Therapy. 22:264-268
Objective: To describe prenatal diagnosis of hemoglobin (Hb) Bart’s hydrops fetalis caused by a previously undescribed condition in Thailand of the interaction of αo-thalassemia with the Southeast Asian (–SEA) and the THAI (–THAI) deletions in
Autor:
Yossombat Changtrakun, Goonnapa Fucharoen, Kanokwan Sanchaisuriya, Nirut Siriratmanawong, K. Ayukarn, Supan Fucharoen
Publikováno v:
Annals of Hematology. 81:389-393
Hemoglobin (Hb) Korle-Bu (beta73; Asp-Asn) is the most frequent of the rare beta-chain variants in the population of West Africa whereas Hb E (beta26; Glu-Lys) is common among the Southeast Asian population. We report a hitherto undescribed condition
Autor:
Kanokwan Sanchaisuriya, Nirut Siriratmanawong, Supan Fucharoen, Thawalwong Ratanasiri, Goonnapa Fucharoen
Publikováno v:
Clinical Biochemistry. 34:377-380
Objective: To establish a rapid PCR method for simultaneous detection of β-thalassemia and α-thalassemia 1 genes for diagnosis of complex αβ-thalassemia syndrome. Design and methods: Using multiplex allele specific PCR approach, we evaluated a si
Publikováno v:
European journal of haematology. 92(1)
Background Deletions of δ- and β-globin genes are associated with different Hb F levels. To address this, we have examined hematological and molecular characteristics in a large cohort of high Hb F determinants in Thailand. Methods A total of 160 u
Publikováno v:
Fetal diagnosis and therapy. 22(4)
To describe prenatal diagnosis of hemoglobin (Hb) Bart's hydrops fetalis caused by a previously undescribed condition in Thailand of the interaction of alpha(o)-thalassemia with the Southeast Asian (-(SEA)) and the THAI (-(THAI)) deletions in a Thai
Publikováno v:
Fetal Diagnosis & Therapy; 2007, Vol. 22 Issue 4, p264-268, 5p, 2 Diagrams, 1 Chart