Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Pranee Sucharitchan"'
Autor:
Yujie Cao, Shau-yin Ha, Chi-Chiu So, Ming-for Tony Tong, Clara Sze-man Tang, Huoru Zhang, Rui Liang, Jing Yang, Brian Hon-Yin Chung, Godfrey Chi-Fung Chan, Yu Lung Lau, Maria-Mercè Garcia-Barcelo, Edmond Shiu-Kwan Ma, Pranee Sucharitchan, Nattiya Hirankarn, Wanling Yang
Publikováno v:
The Journal of Molecular Diagnostics. 24:1089-1099
Thalassemia is one of the most common genetic diseases and a major health threat worldwide. Accurate, efficient, and scalable analysis of next-generation sequencing (NGS) data is much needed for its molecular diagnosis and carrier screening. We devel
Autor:
Amornchai Suksusut, Jiratchaya Sophonphan, Ponlapat Rojnuckarin, Pranee Sucharitchan, Chantana Polprasert, Rung Settapiboon, Noppacharn Uaprasert, Supaporn Amornsirivat, Piroonrut Wongprachar
Publikováno v:
Hematology. 25:276-279
Objectives: A sensitive screening for the coexistence of α0-thalassemia and the hemoglobin E (Hb E) trait is important to identify at-risk couples for hydrops fetalis. However, previous cutoff valu...
Autor:
Chantana, Polprasert, Piroonrut, Wongprachar, Amornchai, Suksusut, Rung, Settapiboon, Supaporn, Amornsirivat, Jiratchaya, Sophonphan, Noppacharn, Uaprasert, Pranee, Sucharitchan, Ponlapat, Rojnuckarin
Publikováno v:
Hematology (Amsterdam, Netherlands). 25(1)
Autor:
Juliano L Fernandes, Pranee Sucharitchan, Mark Westwood, Marianna Fontana, Yongkasem Vorasettakarnkij, Noppacharn Uaprasert, Emmanuel A. Ako, John B. Porter, Peter Kellman, Stefan K. Piechnik, Hataichanok Ngamkasem, James C. Moon, Charlotte Manisty, J Malcolm Walker, Amna Abdel-Gadir, Sabrina Nordin, Monravee Tumkosit
Thalassemia is the most common monogenetic disorder worldwide, with 60 000 infants with thalassemia major born annually.1 Survival often depends on regular blood transfusions to correct anemia and to reduce ineffective erythropoiesis, but these trans
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::33edca199362bad18ed8cec43aea1ce2
https://doi.org/10.1161/circulationaha.116.022803
https://doi.org/10.1161/circulationaha.116.022803