Zobrazeno 1 - 10
of 31
pro vyhledávání: '"Kittikalayawong A"'
Autor:
Poparn H, Kittikalayawong Y, Techavichit P, Lauhasurayotin S, Chiengthong K, Chaweephisal P, Sosothikul D
Publikováno v:
Pediatric Health, Medicine and Therapeutics, Vol Volume 15, Pp 333-338 (2024)
Hansamon Poparn,1,2 Yaowaree Kittikalayawong,1,2 Piti Techavichit,1,2 Supanun Lauhasurayotin,1,2 Kanhatai Chiengthong,1,2 Phumin Chaweephisal,2 Darintr Sosothikul1,2 1Division of Pediatric Hematology and Oncology, Department of Pediatrics, Faculty of
Externí odkaz:
https://doaj.org/article/4789e8d213204058876af2c2d39a0b7b
Autor:
Chatphatai Moonla MD, MSc, Benjaporn Akkawat BSc, Yaowaree Kittikalayawong PhD, Autcharaporn Sukperm BSc, Mukmanee Meesanun BSc, Noppacharn Uaprasert MD, Darintr Sosothikul MD, Ponlapat Rojnuckarin MD, PhD
Publikováno v:
Clinical and Applied Thrombosis/Hemostasis, Vol 25 (2019)
Correlations between bleeding symptoms and von Willebrand factor (VWF) levels may help to predict hemorrhagic severity in the Westerners with von Willebrand disease (VWD), but data in Asians are lacking. In this study, Thai patients with VWF levels
Externí odkaz:
https://doaj.org/article/24c8c2496f214d1ca1e58c1f1b990caa
Autor:
Karan Prasopsanti, Vorasuk Shotelersuk, Pintip Suchartlikitwong, Kanya Suphapeetiporn, Darintr Sosothikul, Rungnapa Ittiwut, Yaowaree Kittikalayawong, Chupong Ittiwut
Publikováno v:
European Journal of Haematology. 99:520-524
Objectives Glanzmann thrombasthenia (GT) is an autosomal recessive platelet disorder, caused by defects of the platelet integrin αIIbβ3 (GPIIb/IIIa) resulting from pathogenic mutations in either ITGA2B or ITGB3. It is characterized by spontaneous m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::70387009a5980d3d6f4e6bb4c69c42dc
https://doi.org/10.1111/ejh.12965
https://doi.org/10.1111/ejh.12965
Autor:
Mukmanee Meesanun, Darintr Sosothikul, Noppacharn Uaprasert, Chatphatai Moonla, Ponlapat Rojnuckarin, Yaowaree Kittikalayawong, Autcharaporn Sukperm, Benjaporn Akkawat
Publikováno v:
Clinical and Applied Thrombosis/Hemostasis
Clinical and Applied Thrombosis/Hemostasis, Vol 25 (2019)
Clinical and Applied Thrombosis/Hemostasis, Vol 25 (2019)
Correlations between bleeding symptoms and von Willebrand factor (VWF) levels may help to predict hemorrhagic severity in the Westerners with von Willebrand disease (VWD), but data in Asians are lacking. In this study, Thai patients with VWF levels
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eaa7b9e0f5f6646b38285cb5b4eb1f37
https://pubmed.ncbi.nlm.nih.gov/31359769
https://pubmed.ncbi.nlm.nih.gov/31359769
Akademický článek
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Akademický článek
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Autor:
Pattramon Aungbamnet, Panya Seksarn, Darintr Sosothikul, Chatchai Buphachat, Yaowaree Kittikalayawong
Publikováno v:
Blood coagulationfibrinolysis : an international journal in haemostasis and thrombosis. 23(3)
Thromboembolic events are an increasingly common problem encountered in children. The laboratory diagnosis of thrombotic disorders in children differs from that in adults. To establish the normal reference of natural anticoagulant parameters in child
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::70a2d820565cbd55fed01879e8ad8729
https://pubmed.ncbi.nlm.nih.gov/22322138
https://pubmed.ncbi.nlm.nih.gov/22322138
Publikováno v:
The Southeast Asian journal of tropical medicine and public health. 36(5)
Upon erythroid cell maturation in vivo, beta-thalassemic erythroid cells accumulate unmatched unstable alpha-globin chains that are believed to be a causal factor in such cell destruction. This study showed that beta-thalassemia/Hb E erythroid precur
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::89ef193a090c8607ce95c74156fde9f0
https://pubmed.ncbi.nlm.nih.gov/16438161
https://pubmed.ncbi.nlm.nih.gov/16438161
Publikováno v:
Journal of the Medical Association of Thailand = Chotmaihet thangphaet. 84
Glucose 6-phosphate dehydrogenase (G-6-PD) deficiency is common in the Thai population and is the cause of neonatal hyperbilirubinemia and hemolytic anemia. This X-linked disorder is much more common in males than females. The objectives of this stud
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1a08d12f687c28923ed09ddce217ab26
https://pubmed.ncbi.nlm.nih.gov/11529386
https://pubmed.ncbi.nlm.nih.gov/11529386
Autor:
R, Udomsangpetch, T, Sueblinvong, K, Pattanapanyasat, A, Dharmkrong-at, A, Kittikalayawong, H K, Webster
Publikováno v:
Blood. 82(12)
Hemoglobinopathies have a protective role in malaria that appears to be related to alterations in red blood cell (RBC) properties. Thalassemic RBCs infected with Plasmodium falciparum showed greatly reduced cytoadherence and rosetting properties as w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a54df9dd4d08e429c9eff20f771152d6
https://pubmed.ncbi.nlm.nih.gov/8260712
https://pubmed.ncbi.nlm.nih.gov/8260712