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Page 1
Genetic variations of type 2 and type 3 von Willebrand diseases in Thailand.
Lauhasurayotin S, Moonla C, Ittiwut R, Ittiwut C, Songthawee N, Komvilaisak P, Natesirinilkul R, Sirachainan N, Rojnuckarin P, Sosothikul D, Suphapeetiporn K. Lauhasurayotin S, et al. Among authors: natesirinilkul r. J Clin Pathol. 2024 Dec 18;78(1):57-63. doi: 10.1136/jcp-2023-209123. J Clin Pathol. 2024. PMID: 38053262
Pulmonary hypertension in non-transfusion-dependent thalassemia: Correlation with clinical parameters, liver iron concentration, and non-transferrin-bound iron.
Inthawong K, Charoenkwan P, Silvilairat S, Tantiworawit A, Phrommintikul A, Choeyprasert W, Natesirinilkul R, Siwasomboon C, Visrutaratna P, Srichairatanakool S, Chattipakorn N, Sanguansermsri T. Inthawong K, et al. Among authors: natesirinilkul r. Hematology. 2015 Dec;20(10):610-7. doi: 10.1179/1607845415Y.0000000014. Epub 2015 May 12. Hematology. 2015. PMID: 25964094 Free article.
Development of a Thai version of the paediatric bleeding assessment tool (Thai paediatric-BAT) suitable for use in children with inherited mucocutaneous bleeding disorders.
Pakdeeto S, Natesirinilkul R, Komwilaisak P, Rand ML, Blanchette VS, Vallibhakara SA, Sirachainan N. Pakdeeto S, et al. Among authors: natesirinilkul r. Haemophilia. 2017 Nov;23(6):e539-e542. doi: 10.1111/hae.13358. Epub 2017 Oct 10. Haemophilia. 2017. PMID: 28994494 No abstract available.
Efficacy and safety of low-dose prophylaxis of highly purified plasma-derived factor VIII concentrate produced by the National Blood Centre, Thai Red Cross Society.
Chuansumrit A, Sosothikul D, Natesirinilkul R, Lektrakul Y, Charoonruangrit U; Factor VIII Study Group. Chuansumrit A, et al. Among authors: natesirinilkul r. Haemophilia. 2018 Sep;24(5):e387-e390. doi: 10.1111/hae.13601. Epub 2018 Aug 17. Haemophilia. 2018. PMID: 30117632 Clinical Trial. No abstract available.
Novel mutations in SPTA1 and SPTB identified by whole exome sequencing in eight Thai families with hereditary pyropoikilocytosis presenting with severe fetal and neonatal anaemia.
Ittiwut C, Natesirinilkul R, Tongprasert F, Sathitsamitphong L, Choed-Amphai C, Fanhchaksai K, Charoenkwan P, Suphapeetiporn K, Shotelersuk V. Ittiwut C, et al. Among authors: natesirinilkul r. Br J Haematol. 2019 May;185(3):578-582. doi: 10.1111/bjh.15559. Epub 2018 Sep 10. Br J Haematol. 2019. PMID: 30198572 Free article. No abstract available.
A Novel GNAS Mutation Causing Isolated Infantile Cushing's Syndrome.
Dejkhamron P, Ittiwut C, TangNgam H, Sunkonkit K, Natesirinilkul R, Suphapeetiporn K, Shotelersuk V. Dejkhamron P, et al. Among authors: natesirinilkul r. Horm Res Paediatr. 2019;92(3):196-202. doi: 10.1159/000501169. Epub 2019 Jul 30. Horm Res Paediatr. 2019. PMID: 31362300
49 results