Zobrazeno 1 - 10
of 53
pro vyhledávání: '"Voravarn S, Tanphaichitr"'
Autor:
Suthida Kankirawatana, Vinai Suvatte, Chularatana Mahasandana, Voravarn S. Tanphaichitr, Gavivann Veerakul, Vip Viprakasit
Publikováno v:
Siriraj Medical Journal, Vol 51, Iss 3 (1999)
We carried out a retrospective analysis of the outcome of treatment in patients with severe aplastic anemia who attended the Department of Pediatrics, Siriraj Hospital, during 1972- 1998. There were 31 patients, 17 boys and 14 girls, by Camittaâ€
Externí odkaz:
https://doaj.org/article/7c8db68c95064ba4afeefce360abf240
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::365a755e1e87cd1fe795dc5b0260f06f
https://doi.org/10.1111/ijlh.12282
https://doi.org/10.1111/ijlh.12282
Autor:
Vip Viprakasit, Suvajana Atipas, Tuangrat Sangpraypan, Thisarat Kusuwan, Siriporn Limviriyakul, Julaporn Pooliam, Archwin Tanphaichitr, Voravarn S. Tanphaichitr
Publikováno v:
Hemoglobin. 38:345-350
Ototoxicity due to iron chelation therapy, especially deferoxamine (DFO), is frequently observed in patients who have a higher chelation index (0.025). However, there is limited data on patients who are less well-chelated and on other chelating regim
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::96af81cdee3bba57650fa2596328fb98
https://doi.org/10.3109/03630269.2014.940462
https://doi.org/10.3109/03630269.2014.940462
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::12991c1fa54b69f02ff2b5c5803d4563
https://doi.org/10.1111/ijlh.12264
https://doi.org/10.1111/ijlh.12264
Autor:
Kleebsabai Sanpakit, Sjaak Philipsen, Vip Viprakasit, Hitoshi Kanno, Christian Babbs, Monthana Juntharaniyom, Jariya Saipin, Sasithorn Bejrachandra, Voravarn S. Tanphaichitr, Kalaya Tachavanich, Richard J. Gibbons, Karen M. Lower, Nipon Chalaow, Douglas R. Higgs, Duantida Songdej, Chris Fisher, Suchada Riolueang, Supachai Ekwattanakit
Publikováno v:
Blood, 123(10), 1586-1595. American Society of Hematology
In this study, we report on 8 compound heterozygotes for mutations in the key erythroid transcription factor Krüppel-like factor 1 in patients who presented with severe, transfusion-dependent hemolytic anemia. In most cases, the red cells were hypoc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2916ecd3bd01f0564e1d03382a3d0698
https://doi.org/10.1182/blood-2013-09-526087
https://doi.org/10.1182/blood-2013-09-526087
Autor:
Akira Hirono, Parichat Pung-Amritt, Wanchai Wanachiwanawin, Ajjima Treesucon, Voravarn S. Tanphaichitr
Publikováno v:
Annals of Hematology. 90:769-775
Glucose-6-phosphate dehydrogenase (G6PD) deficiency is one of the most common hereditary enzymopathies worldwide. Mostly G6PD deficient cases are asymptomatic though they may have the risk of neonatal jaundice (NNJ) and acute intravascular hemolysis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e5742edcf655d0c70621d194d791948d
https://doi.org/10.1007/s00277-010-1153-4
https://doi.org/10.1007/s00277-010-1153-4
Publikováno v:
Clinical and Laboratory Haematology. 27:409-415
In this report, we describe two Thai siblings presenting with mild hypochromic microcytic anaemia and splenomegaly since 2(1/2) years of age. However, both patients were otherwise well with normal weight and height development and did not require tra
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::06402be1887c92431dd60b9c74e5b7b7
https://doi.org/10.1111/j.1365-2257.2005.00734.x
https://doi.org/10.1111/j.1365-2257.2005.00734.x
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::901e7a7a1590f441257fff5edd3d15e4
https://doi.org/10.1081/hem-200066339
https://doi.org/10.1081/hem-200066339
Autor:
Voravarn S. Tanphaichitr, Bunchoo Pongtanakul, Kleebsabai Sanpakit, Gavivann Veerakul, Worrawut Chinchang, Vip Viprakasit
Publikováno v:
Annals of Tropical Paediatrics. 24:323-328
Acute haemolysis associated with mild upper respiratory tract infection was observed in a Thai boy who presented with a rapid decline in haemoglobin (Hb) levels, haemoglobinuria and evidence of intravascular haemolysis. Several possible causes giving
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8aaee36b2ea7ba691e80fc60ac6a4d6e
https://doi.org/10.1179/027249304225019145
https://doi.org/10.1179/027249304225019145
Autor:
Worrawut Chinchang, Prin Vathesathokit, Alison T. Merryweather-Clarke, Pa-thai Yenchitsomanus, Vip Viprakasit, Voravarn S. Tanphaichitr, Kalaya Tachavanich, Parichat Pung-Amritt, Victoria L. C. Wimhurst
Publikováno v:
European Journal of Haematology. 73:43-49
Co-inheritance of HFE mutations has a substantial role in iron overload in beta-thalassaemia carriers in north European populations where two HFE mutations, C282Y and H63D, are prevalent. In Thailand, there was little information about the allele fre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::76eb8e1691831f6ac777dc5ff082a7ce
https://doi.org/10.1111/j.1600-0609.2004.00246.x
https://doi.org/10.1111/j.1600-0609.2004.00246.x