Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Kanokwan Jaiping"'
Autor:
Jiraporn Gatedee, Kanokwan Jaiping, Sumana Kasemsawasdi, Aungsana Yothinarak, Janjuree Netsawang, Supanit Angsirikul, Rachasak Somyanonthanakul
Publikováno v:
2022 17th International Joint Symposium on Artificial Intelligence and Natural Language Processing (iSAI-NLP).
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7984f903300a78e2cafb17b0225742a2
https://doi.org/10.1109/isai-nlp56921.2022.9960276
https://doi.org/10.1109/isai-nlp56921.2022.9960276
Autor:
Dararat Dankai, Kanokwan Jaiping, Panthong Singboottra, Sarayut Nualkeaw, Patcharapong Pantiya, Sakorn Pornprasert, Saowanit Chairatanapiwong
Publikováno v:
Clinical Chemistry and Laboratory Medicine (CCLM). 58:e44-e46
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::82bd053ccfea127cfe40157c0f67a948
https://doi.org/10.1515/cclm-2019-0827
https://doi.org/10.1515/cclm-2019-0827
Publikováno v:
Indian J Hematol Blood Transfus
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a67a217ae58669fc50d65aeb3cb73570
https://pubmed.ncbi.nlm.nih.gov/32158104
https://pubmed.ncbi.nlm.nih.gov/32158104
Autor:
Manoo Punyamung, Kritsanee Maneewong, Siriporn Nanta, Sanchai Wongwiwatthananukit, Sakorn Pornprasert, Jintana Yanola, Soontharee Plengsuree, Kanokwan Jaiping
Publikováno v:
Hemoglobin. 39:235-239
β-Thalassemia (β-thal) and iron deficiency cause most microcytic anemias. Red cell indices and formulas have been established as simple, fast, and inexpensive in discrimination between these two hematological disorders in school children. However,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::af3de59dce5f5c62ac5a1cd04a9f4c20
https://doi.org/10.3109/03630269.2015.1048352
https://doi.org/10.3109/03630269.2015.1048352
Publikováno v:
Hemoglobin. 39:292-295
We report the molecular and hematological feature of a Thai woman who had clinical diagnosis of β-thalassemia intermedia (β-TI). Hemoglobin (Hb) high performance liquid chromatography (HPLC) analysis identified Hb A (64.4%), Hb F (12.3%) and Hb A2/
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e9bea50a9c952bbc12b5575140b1de81
https://doi.org/10.3109/03630269.2015.1047513
https://doi.org/10.3109/03630269.2015.1047513
Autor:
Pisuttinee Khantarag, Nopphadol Permsripong, Sakorn Pornprasert, Sitthichai Panyasai, Kanokwan Jaiping
Hemoglobin (Hb) J-Buda [α61(E10)Lys → Asn, AAG > AAT] is a very rare α-chain variant found in South-East Asia. We analyzed hematological parameters and provided a rapid molecular analysis method for detection of this hemoglobinopathy in two Thai
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6de77e1f8a9de96de0912f3c08040ae1
https://europepmc.org/articles/PMC4925550/
https://europepmc.org/articles/PMC4925550/
Publikováno v:
Hemoglobin. 39(4)
We report the molecular and hematological feature of a Thai woman who had clinical diagnosis of β-thalassemia intermedia (β-TI). Hemoglobin (Hb) high performance liquid chromatography (HPLC) analysis identified Hb A (64.4%), Hb F (12.3%) and Hb A2/
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9837580a0746dac4e4b8effcd2615a49
https://pubmed.ncbi.nlm.nih.gov/26029792
https://pubmed.ncbi.nlm.nih.gov/26029792
Autor:
Sakorn Pornprasert, Monthathip Tookjai, Manoo Punyamung, Kanokwan Jaiping, Panida Pongpunyayuen
Publikováno v:
Clinical chemistry and laboratory medicine. 54(1)
Background To date, the hemoglobin (Hb) typing control materials for laboratory investigation of thalassemia with low (1.8%-3.2%) and high (4%-6%) levels of HbA2 are available but there are no Hb typing quality control materials for analysis of thala
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eaafbea66fb2ff31ca65d8d3417c5a57
https://pubmed.ncbi.nlm.nih.gov/25996485
https://pubmed.ncbi.nlm.nih.gov/25996485
Autor:
Sakorn Pornprasert, Kanokwan Jaiping
Publikováno v:
Hemoglobin. 38(4)
A subject with Hb E (HBB: c.79G A) trait is asymptomatic and can become a blood donor. However, a blood transfusion from a Hb E trait donor can affect β-thalassemia (β-thal) diagnosis. Blood samples from three Thai women were sent to the Associated
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::688821e844f0ca18c3cc0deaf129af6d
https://pubmed.ncbi.nlm.nih.gov/24940968
https://pubmed.ncbi.nlm.nih.gov/24940968
Autor:
Asami Moriyama, Kallayanee Treesuwan, Kanyakan Kongthai, Sakorn Pornprasert, Kanokwan Jaiping, Jarurin Waneesorn, Yukio Hattori
Publikováno v:
Clinical Laboratory. 59
Background Differentiation of beta-thalassemia/HbE disease from homozygous HbE in samples containing HbA2/E > 75% and HbF Methods Multiplex amplification refractory mutation system (MARMS)-PCR for beta-thalassemia codons 17 (A > T), 41/42 (-TCTT), 71
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f4c8bd62ecee679783efe56ac0e4faa5
https://doi.org/10.7754/clin.lab.2012.120920
https://doi.org/10.7754/clin.lab.2012.120920