Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Satja Surapot"'
Publikováno v:
Acta Haematologica. 124:115-119
Secondary erythrocytosis may arise from several causes, but an association with oxygen transport is rare. We describe for the first time a form of secondary erythrocytosis caused by compound heterozygosity for hemoglobin (Hb) Tak and (δβ)⁰-thalas
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::74a92644940648f1cefa9ae7af03052c
https://doi.org/10.1159/000318015
https://doi.org/10.1159/000318015
Publikováno v:
Blood Cells, Molecules, and Diseases. 35:196-200
Hemoglobin (Hb) C (alpha2beta(2)6Glu-Lys) is a variant Hb found mainly in West Africa where individuals carrying both Hb C and Hb S (alpha2beta(2)6Glu-Val) usually have a disease similar to sickle cell disease. The Hb C molecule has reduced solubilit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ab247b5c2c8f0b906f9581cdd34104a9
https://doi.org/10.1016/j.bcmd.2005.05.004
https://doi.org/10.1016/j.bcmd.2005.05.004
Autor:
Satja Surapot, Kanokwan Sanchaisuriya, Goonnapa Fucharoen, Sitthichai Panyasai, Supan Fucharoen
Publikováno v:
American Journal of Hematology. 80:119-123
We report a hitherto undescribed interaction of a deletional (deltabeta) degrees -thalassemia and a deletional hereditary persistence of fetal hemoglobin (HPFH) in an adult Thai individual. He was a 40-year-old Thai male who had the following hematol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7b8d2b6001834e04212ff75b3d0edff4
https://doi.org/10.1002/ajh.20426
https://doi.org/10.1002/ajh.20426
Publikováno v:
European Journal of Haematology. 67:258-262
Two cases of the Thai thalassemia patients with compound heterozygosities for (deltabeta)(0)/beta(0)-thalassemia and (deltabeta)(0)-thalassemia/hemoglobin E have been reported. The first case was a 8-yr-old boy who had the following hematologic data:
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::710b4860ed70c265692f0f708e78371b
https://doi.org/10.1034/j.1600-0609.2001.00524.x
https://doi.org/10.1034/j.1600-0609.2001.00524.x
Autor:
Nattaphol, Prakobkaew, Sanita, Singsanan, Goonnapa, Fucharoen, Satja, Surapot, Supan, Fucharoen
Publikováno v:
Acta haematologica. 124(2)
Secondary erythrocytosis may arise from several causes, but an association with oxygen transport is rare. We describe for the first time a form of secondary erythrocytosis caused by compound heterozygosity for hemoglobin (Hb) Tak and (δβ)(0)-thalas
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::2a0699b14b50875a3aadd69ec1ffca11
https://pubmed.ncbi.nlm.nih.gov/20798489
https://pubmed.ncbi.nlm.nih.gov/20798489
Autor:
Supan, Fucharoen, Sitthichai, Panyasai, Satja, Surapot, Goonnapa, Fucharoen, Kanokwan, Sanchaisuriya
Publikováno v:
American journal of hematology. 80(2)
We report a hitherto undescribed interaction of a deletional (deltabeta) degrees -thalassemia and a deletional hereditary persistence of fetal hemoglobin (HPFH) in an adult Thai individual. He was a 40-year-old Thai male who had the following hematol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d02a74792599b7a6583b2ec752aa99ec
https://pubmed.ncbi.nlm.nih.gov/16184575
https://pubmed.ncbi.nlm.nih.gov/16184575
Autor:
Sitthichai, Panyasai, Supan, Fucharoen, Satja, Surapot, Goonnapa, Fucharoen, Kanokwan, Sanchaisuriya
Publikováno v:
Haematologica. 89(7)
Hereditary persistence of fetal hemoglobin (HPFH) and deltabeta-thalassemia are heterogeneous disorders characterized by increased levels of Hb F in adult life. The distinction between these two conditions is not always possible from routine hematolo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b405ba095bbaa55a4ff5f84671e3ed16
https://pubmed.ncbi.nlm.nih.gov/15257928
https://pubmed.ncbi.nlm.nih.gov/15257928
Publikováno v:
Acta haematologica. 108(3)
We report the molecular and hematological characterizations of thalassemia caused by interactions of the hereditary persistence of fetal hemoglobin (HPFH)-6 with β-thalassemia in 2 Thai patients and the HPFH-6 with Hb E in another Thai patient. Mark
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f824e5338e119460acbc003ae3e4dad3
https://pubmed.ncbi.nlm.nih.gov/12373089
https://pubmed.ncbi.nlm.nih.gov/12373089
Autor:
Supan, Fucharoen, Yutthana, Pengjam, Satja, Surapot, Goonnapa, Fucharoen, Kanokwan, Sanchaisuriya
Publikováno v:
American journal of hematology. 71(2)
The hereditary persistence of fetal hemoglobin (HPFH)-6 is sporadically found in Thailand whereas the deletion-inversion type (G)gamma((A)gamma delta beta)(0)-thalassemia is described among Indians. We report a hitherto un-described case in which the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b224266118941370396b099e312e97dd
https://pubmed.ncbi.nlm.nih.gov/12353310
https://pubmed.ncbi.nlm.nih.gov/12353310
Autor:
Supan Fucharoen, Sitthichai Panyasai, Satja Surapot, Goonnapa Fucharoen, Kanokwan Sanchaisuriya
Publikováno v:
American Journal of Hematology; Oct2005, Vol. 80 Issue 2, p119-123, 0p