150 results on '"Sasanakul,Werasak"'
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2. Phenotypic and genotypic analysis of patients with congenital factor VII deficiency in a multicenter study in Thailand
3. Alleviated bleeding phenotypes in a child with severe haemophilia A and thalassemia disease
4. Response to Prolonged Duration of Therapeutic Dose Oral Iron Therapy in a Girl With Novel TMPRSS6 Gene Variants: A Case Report and Review Literature
5. Novel Pathogenic Variants of TMPRSS6 Gene in a Girl with Iron Refractory Iron Deficiency Anemia (IRIDA)
6. Benefits of prophylactic emicizumab in enhancing immune tolerance induction in a hemophiliac boy with very high inhibitor titer
7. Abnormal red blood cell indices increase the risk of arterial ischemic stroke in children
8. Identifying Two Novel Mutations and MDS/AML Outcome of Severe Congenital Neutropenia/Cyclic Neutropenia
9. Phenotypic and genotypic analysis of patients with congenital factor VII deficiency in a multicenter study in Thailand
10. Response to Prolonged Duration of Therapeutic Dose Oral Iron Therapy in a Girl With Novel TMPRSS6 Gene Variants: A Case Report and Review Literature
11. Three-Decade Successive Establishment of Care for Women/Girls from Families with Haemophilia
12. Global Fibrinolytic Activity, PAI-1 Level, and 4G/5G Polymorphism in Thai Children with Arterial Ischemic Stroke
13. Whole‐exome sequencing uncovered genetic diagnosis of severe inherited haemolytic anaemia: Correlation with clinical phenotypes
14. Three-Decade Successive Establishment of Care for Women/Girls from Families with Haemophilia
15. Prominent Mutation of Intron 22 Inversion in Sporadic Hemophilia: Is It Worth the Antenatal Screening?
16. Prominent Mutation of Intron 22 Inversion in Sporadic Hemophilia: Is It Worth the Antenatal Screening?
17. Lipoprotein(a) and the risk of thromboembolism in Thai children
18. Report on effective treatment and genetic predisposition in two children with refractory probable catastrophic antiphospholipid syndrome
19. Combined Chelation Therapy with Daily Oral Deferiprone and Twice-Weekly Subcutaneous Infusion of Desferrioxamine in Children with β-Thalassemia: 3-Year Experience
20. Response to Prolonged Duration of Therapeutic Dose Oral Iron Therapy in a Girl With Novel TMPRSS6Gene Variants: A Case Report and Review Literature
21. Benefits of prophylactic emicizumab in enhancing immune tolerance induction in a boy with hemophilia A and very high inhibitor titer
22. PROC Promoter Single Nucleotide Polymorphisms Associated With Low Protein C Activity But Not Increased Risk of Thromboembolism in Pediatric Population
23. The Effect of Blood Transfusion on Growth of Patients with Hb E/β-Thalassemia
24. Coagulant activity of recombinant human factor VII produced by lentiviral human F7 gene transfer in immortalized hepatocyte-like cell line
25. Generation of a human induced pluripotent stem cell line (MUi010-A) from skin fibroblast of patient carrying a c.2104C>T mutation in MYH9 gene
26. No evidence of hemostasis disturbance in Thai children with iron deficiency anemia
27. Novel mutation of the TINF2 gene resulting in severe phenotypic Revesz syndrome
28. R147W in PROC Gene Is a Risk Factor of Thromboembolism in Thai Children
29. Incidences, risk factors and outcomes of neonatal thromboembolism
30. Genotypes and phenotypes of protein S deficiency in Thai children with thromboembolism
31. Normal hemostatic parameters in children and young adults with α-thalassemia diseases
32. Safety profile of a liquid formulation of deferiprone in young children with transfusion-induced iron overload: a 1-year experience
33. R147W in PROC Gene Is a Risk Factor of Thromboembolism in Thai Children.
34. Incidences, risk factors and outcomes of neonatal thromboembolism.
35. Genotypes and phenotypes of protein S deficiency in Thai children with thromboembolism.
36. Protein C deficiency in Thai children with thromboembolism: A report of clinical presentations and mutation analysis
37. Combined Chelation Therapy with Daily Oral Deferiprone and Twice-Weekly Subcutaneous Infusion of Desferrioxamine in Children with β-Thalassemia: 3-Year Experience
38. High Factor VIII and Von Willebrand Factor Levels Are Not Risk Factors of Cryptogenic Arterial Ischemic Stroke in Thai Children
39. The Correlation Of Hepatic Iron Loading Determined By Magnetic Resonance Image and Serum Ferritin In Patients With Beta-Thalassemia Intermedia
40. Tumour necrosis factor gene polymorphism in dengue infection: association with risk of bleeding
41. The effect of polymorphisms of MTHFR C677T, A1298C, MS A2756G and CBS 844ins68bp on plasma total homocysteine level and the risk of ischemic stroke in Thai children
42. Establishment of Carrier Detection and Prenatal Diagnosis Service for Hemophilia in a Developing Country: Experience From International Hemophilia Training Center-Bangkok.
43. No evidence of hemostasis disturbance in Thai children with iron deficiency anemia
44. Activation of a cryptic splice site in a potentially lethal coagulation defect accounts for a functional protein variant
45. Association of HLA class II Alleles and the Occurrence of Factor VIII Inhibitor in Thai Patients with Hemophilia A
46. New Formula for the Differentiation Between Iron Deficiency Anemia and Thalassemic Carrier in Thalassemic Prevalence Areas: A Study in Healthy School-Age Children.
47. A Novel Mutation of Cystathionine β-synthase Gene in a Thai Boy With Homocystinuria
48. Genetic Polymorphisms in the Homocysteine Metabolism Pathway and Thrombosis in Thai Children: A Case Control Study.
49. Comparison of Phenotypic Assessment and Mutation Detection in the Diagnosis of Carrier State in Hemophilia: Identification of 10 Novel Mutations.
50. Frequency of thiopurine S-methyltransferase genetic variation in Thai children with acute leukemia
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