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44篇 您的检索式：作者名="VIPRAKASIT V"

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	题名	作者	年代	出处	被引量
1	Hb H disease:clinical course and disease modifiers 显示文摘	Fucharoen S Viprakasit V	2009	Hematology Am Soc Hematol Educ Program2009，，：	1
2	Common origin of a rara beta-globen initiation codon mutation (ATG-AGG)in Asians显示文摘	Viprakasit V Chinchang W Suwanthol L	2005	Clin Lab Haematol2005，27，6：	1
3	Hemoglobin H disease induced by the common SEA deletion and the rarehemoglobin Quong Sze in a Thai female:longitudinal clinical course,molecular characterization,and developmentof a PCR/RFLP-based detection method显示文摘	Sura T Trachoo O Viprakasit V	2007	Ann Hematol2007，86，9：	1
4	Children with hemoglobin EB-thalassemia have a high risk of being vitamin D deficient e yen if they get abundant sun exposure A study from Thai land显示文摘	Nakavachara P Viprakasit V	2013	Pediatr Blood Cancer2013，60，10：	1
5	Clinical features and molecular analysis in Thai patients with Hb H disease显示文摘	Laosombat V Viprakasit V Chotsampancharoen T ct al	2009	Ann Hematol2009，88，：	1
6	Clinical phenotypes and molecular characterization of Hb I-I -Pakse disease显示文摘	Viprakasit V Tanphaichitr VS Pung - Amritt P	2006	Haematologica2006，87，14：	1
7	Two independent origins of Hb Dhonburi (Neapolis) : an electrophoretically silent hemoglobin variant 显示文摘	Viprakasit V Chinchang W	2007	Clin Chim Acta2007，376，12：	1
8	Hematological parameters and red blood cell indices in healthy Thai children: A revision for 2005 显示文摘	Viprakasit V Suwanthol L Sangpraypan T	2005	J Med Assoc Thai2005，88，8：	1
9	Hemoglobin H disease induced by the common SEA deletion and the rare hemoglobin Quong Sze in a Thai female:longitudinal clin ical course,molecular characterization,and development of a PCR/RFLP-based detection method显示文摘	Sura T Trachoo O Viprakasit V		0，，09：	1
10	Deletion of the α-globin gene cluster as a cause of acquired α-thalassemia in myelodysplastic syndrome显示文摘	STEENSMA D P VIPRAKASIT V HENDRICK A	2004	Blood2004，1103，：	1
11	A regulatory ShIP causes a human genetic disease by creating a new transcriptional promoter显示文摘	De Gobhi M Viprakasit V Hughes JR	2006	Science2006，312，5777：	1
12	Clini cal phenotypes and molecular characterization of Hb H-Pakse disease显示文摘	Viprakasit V Tanphaiehitr V S Pung-Amritt P	2002	Haematologica2002，87，2：	1
13	Clinical features and molecular analysis in Thai patients with HbH disease显示文摘	LAOSOMBAT V VIPRAKASIT V CHOTSAMPANCHAROEN T	2009	Ann Hematol2009，88，12：	1
14	Clinical phenotypes and molecular characterization of Hb H-Pakse disease 显示文摘	Viprakasit V Tanphaichitr VS Pung-Amritt P	2002	Haematologica2002，87，2：	1
15	Clinical phenotypes and molecular characterization of Hb H - Paks6 disease显示文摘	VIPRAKASIT V TANPHAICHITR V S PUNG AMRITF P	2002	Haematologica2002，87，2：	1
16	Treating iron overload in patients with non-transfusion-dependent thalassemia显示文摘	Taher AT Viprakasit V Musallam KM	2013	Am J Hematol2013，88，5：	1
17	Immune- mediated hemolytic anemia in pediatric renal transplantation 显示文摘	Pattaragarn A Viprakasit V Supavekin S	2006	Pediatr Transplant2006，10，6：	1
18	A regulatory SNPcauses a human genetic disease by creating a new transcriptionalpromoter显示文摘	De Gobbi M Viprakasit V Hughes JR	2006	Science2006，312，5777：	1
19	Evaluation of alpha hemoglobin stabilizing protein(AHSP) as a genetic modifier in patients with beta thalassemia显示文摘	Viprakasit V Tanphaichitr V S Chinchang W	2004	Blood2004，103，：	1
20	Evaluation of alpha hemoglobin stabilizing protein as a genetic modifier in patients with Beta-thalassemia显示文摘	Viprakasit V Tanphaichitr V S Chinchang W	2004	Blood2004，103，9：	1

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