Zobrazeno 1 - 10
of 207
pro vyhledávání: '"T Sanguansermsri"'
Publikováno v:
ASEAN Journal on Science and Technology for Development, Vol 21, Iss 1, Pp 53-56 (2017)
This study aimed to characterize polymorphism of the b-globin gene (framework) among common b-thalassemia mutations found in northern Thailand. Thirty-one homozygous b-thalassemia major patients admitted to Chiang Mai University Hospital were identif
Externí odkaz:
https://doaj.org/article/f67e054040304656801ae920abf16929
Akademický článek
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Publikováno v:
Clinical and Laboratory Haematology. 27:47-49
Hb Constant Spring (HbCS), a nondeletional alpha-thalassemia, is most prevalent in southern Chinese and southeast Asian populations. In conjunction with alpha-thalassemia-1 or in the homozygous state, it is an important cause of HbH disease. The pres
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::46d27c5eff81b845f0a8e25c55ed1a24
https://doi.org/10.1111/j.1365-2257.2004.00658.x
https://doi.org/10.1111/j.1365-2257.2004.00658.x
Publikováno v:
Prenatal diagnosis. 32(1)
To investigate the use of cell-free fetal DNA (cff-DNA) to determine fetal status in pregnant women who were risk for having Hb Bart's.Plasma DNA was extracted from 10 mL of maternal blood from couples who both were alpha-thalassemia-1 carriers (SEA
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ec6d29118357778b8ac60252df0c9896
https://pubmed.ncbi.nlm.nih.gov/22031039
https://pubmed.ncbi.nlm.nih.gov/22031039
Autor:
MB Coleman, JG Adams, Stephen A. Liebhaber, F E Cash, A Pressley, T Sanguansermsri, Martin H. Steinberg, Ingrid Weiss
Publikováno v:
Blood. 76:2630-2636
Hemoglobin (Hb) Suan-Dok (alpha 109Arg) is a rare alpha-globin structural mutation that is linked to an alpha-thalassemia (alpha-thal) determinant. When inherited in trans to an alpha-thal-1 mutation (-), it results in Hb H disease associated with lo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4c649a647ea8e024cd06cae96a79a9e8
https://doi.org/10.1182/blood.v76.12.2630.bloodjournal76122630
https://doi.org/10.1182/blood.v76.12.2630.bloodjournal76122630
Autor:
Stephen A. Liebhaber, Ingrid Weiss, Annette Pressley, Mary B. Coleman, Junius G. Adams, T Sanguansermsri, Martin H. Steinberg, F E Cash
Publikováno v:
Blood. 76:2630-2636
Hemoglobin (Hb) Suan-Dok (alpha 109Arg) is a rare alpha-globin structural mutation that is linked to an alpha-thalassemia (alpha-thal) determinant. When inherited in trans to an alpha-thal-1 mutation (-), it results in Hb H disease associated with lo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5d135c70bb0bf16f24898cfcbe890a89
https://doi.org/10.1182/blood.v76.12.2630.2630
https://doi.org/10.1182/blood.v76.12.2630.2630
Autor:
T, Sanguansermsri, P, Thanaratanakorn, H F, Steger, T, Tongsong, P, Sirivatanapa, C, Wanapirak, S, Sirichotiyakul, P, Chanprapas, G, Flatz
Publikováno v:
The Southeast Asian journal of tropical medicine and public health. 32(1)
Since HbF and HbA are not found in fetuses with Hb Bart's hydrops fetalis the feasibility of prenatal diagnosis of homozygous alpha-thalassemia 1 by fetal hemoglobin typing was examined. Blood samples were obtained from fetuses at 18 to 22 weeks of g
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::048d8e9fb79122f8143898f142fed87c
https://pubmed.ncbi.nlm.nih.gov/11485083
https://pubmed.ncbi.nlm.nih.gov/11485083
Akademický článek
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Publikováno v:
The Southeast Asian journal of tropical medicine and public health. 27(2)
Abnormal linear growth (stunting) is characteristic of children with beta thalassemia major and has been variably and inconsistently attributed to multiple different mechanisms. Despite the coexistence of beta thalassemia with deficits of several mic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::7743add7ce7fb9c639cb05dc4ff83f1e
https://pubmed.ncbi.nlm.nih.gov/9280002
https://pubmed.ncbi.nlm.nih.gov/9280002