Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Waraporn Glomglao"'
Autor:
Patpetra Svasdisant, Waraporn Glomglao, Preeyanun Siraprapapat, Wiyakan Inthararujikul, Kalaya Tachavanich, Chetsada Boonthimat, Sakkarin Ardsiri, Kochpinchon Chansing, Suwimon Sriprach, Sasima Tongsai, Phakatip Sinlapamongkolkul, Kleebsabai Sanpakit, Jassada Buaboonnam
Publikováno v:
Mediterranean Journal of Hematology and Infectious Diseases, Vol 15, Iss 1 (2023)
Background: 6-Mercaptopurine (6-MP), a thiopurine agent, is an indispensable medication for treating pediatric acute lymphoblastic leukemia (ALL). However, its side effects of neutropenia and hepatotoxicity might interrupt treatment, resulting in poo
Externí odkaz:
https://doaj.org/article/9c0d003b73834e97a119d6b4aec30264
Publikováno v:
Genes, Vol 13, Iss 9, p 1502 (2022)
Red blood cell (RBC) indices, including mean corpuscular volume (MCV) and mean corpuscular haemoglobin (MCH), have been widely used for primary screening for thalassaemia (thal) syndromes. Recently, a single nucleotide polymorphism (SNP) rs855791 of
Externí odkaz:
https://doaj.org/article/72943955a30d43c5afeecae4d1801d88
Autor:
Bunchoo Pongtanakul, Phakatip Sinlapamongkolkul, Chayamon Takpradit, Nattee Narkbunnam, Pariwan Sripatanatadasakul, Sasima Tongsai, Waraporn Glomglao, Nassawee Vathana, Ajjima Treesucon, Kleebsabai Sanpakit, Kamon Phuakpet, Jassada Buaboonnam, Preeyanun Siraprapapat
Publikováno v:
Pediatrics international : official journal of the Japan Pediatric SocietyReferences. 61(8)
BACKGROUND 6-Mercaptopurine (6-MP) is considered the backbone of therapy in the maintenance phase of acute lymphoblastic leukemia (ALL). Gene polymorphisms involved in thiopurine degradation are predictors of toxicity in patients treated with 6-MP. W
Autor:
Thidarat Suksangpleng, Vip Viprakasit, Julia Z. Xu, Waraporn Glomglao, Kalaya Tachavanich, Supachai Ekwattanakit, Suchada Riolueang
Publikováno v:
International Journal of Laboratory Hematology. 41
Autor:
Voravarn S. Tanphaichitr, E. Roothumnong, L. Suwanthol, P. Siraprapapat, Ajjima Treesucon, W. Thongnoppakhun, Waraporn Glomglao, Kleebsabai Sanpakit
Publikováno v:
International Journal of Laboratory Hematology. 37:e44-e47
Autor:
Waraporn Glomglao, K. Chansing, Voravarn S. Tanphaichitr, P. Siraprapapat, W. Thongnoppakhun, Ajjima Treesucon, Kleebsabai Sanpakit
Publikováno v:
International Journal of Laboratory Hematology. 37:e21-e24
Autor:
Vip Viprakasit, Suchada Riolueang, Waraporn Glomglao, Sangkae Chamnanvanakij, Punyanuch Jindatanmanusan, Yaowapa Sukontharangsri, Kitti Torcharus
Publikováno v:
Annals of Clinical Biochemistry: International Journal of Laboratory Medicine. 51:237-247
Background Neonatal screening for haemoglobin (Hb) disorders is a standard of care in several developed countries with the main objective to detect Hb S. Such practice has not been established in Thailand where α-thalassaemia and haemoglobin E (Hb E
Publikováno v:
Hemoglobin. 29:235-240
Several rare and hitherto unidentified non deletional alpha-thalassemias (alphaTalpha or alphaalphaT) have been reported from Thailand within the past few years. Interactions of these determinants with alphaO-thalassemia (thal) (--/), which is highly
Autor:
Chanin Limwongse, Vip Viprakasit, Chompunut Kanjanakorn, Voravarn S. Tanphaichitr, Witayakarn Utto, Pornpimol Ruangvutilert, Sathein Sukpanichnant, Monchan Sirikong, Waraporn Glomglao
Publikováno v:
Clinical chemistry and laboratory medicine. 51(8)
Background: Prevention and control of severe β thalassemia by carrier detection and identification of couples at risk in developed countries is one of the most successful stories in modern medicine. Similar programs in developing countries especiall
Autor:
Kalaya, Tachavanich, Vip, Viprakasit, Worawut, Chinchang, Waraporn, Glomglao, Parichat, Pung-Amritt, Voravarn S, Tanphaichitr
Publikováno v:
The Southeast Asian journal of tropical medicine and public health. 40(2)
Hemoglobin E (HbE) is one of the most prevalent beta-globin variant, which is widely distributed in Southeast Asia especially in Thailand. Homozygosity for this variant is common and may occur with iron deficiency. In order to study clinical and hema