Voravarn S Tanphaichitr - JoVE Visualize

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Journal of the Medical Association of Thailand = Chotmaihet Thangphaet|October 31, 2002

Thrombotic complications during induction chemotherapy of acute childhood lymphoblastic leukemiaSuthida Kankirawatana, Gavivann Veerakul, Kleebsabai Sanpakit, et al.

Journal of the Medical Association of Thailand = Chotmaihet Thangphaet|October 31, 2002

Effect of red blood cell glucose-6-phosphate dehydrogenase deficiency on patients with dengue hemorrhagic feverVoravarn S Tanphaichitr, Rachaneekorn Chonlasin, Lerlugsn Suwantol, et al.

Haematologica|February 12, 2002

Clinical phenotypes and molecular characterization of Hb H-Paksé diseaseVip Viprakasit, Voravarn S Tanphaichitr, Parichat Pung-Amritt, et al.

Hemoglobin|July 23, 2014

Incidence of ototoxicity in pediatric patients with transfusion-dependent thalassemia who are less well-chelated by mono- and combined therapy of iron chelating agentsArchwin Tanphaichitr, Thisarat Kusuwan, Siriporn Limviriyakul, et al.

American Journal of Hematology|February 24, 2004

Co-inheritance of Hb Pak Num Po, a novel alpha1 gene mutation, and alpha0 thalassemia associated with transfusion-dependent Hb H diseaseVip Viprakasit, Voravarn S Tanphaichitr, Gavivann Veerakul, et al.

Clinical Chemistry and Laboratory Medicine|March 26, 2013

Problems in determining thalassemia carrier status in a program for prevention and control of severe thalassemia syndromes: a lesson from ThailandVip Viprakasit, Chanin Limwongse, Sathein Sukpanichnant, et al.

European Journal of Haematology|June 9, 2004

Prevalence of HFE mutations among the Thai population and correlation with iron loading in haemoglobin E disorderVip Viprakasit, Prin Vathesathokit, Worrawut Chinchang, et al.

American Journal of Hematology|March 6, 2013

Deferiprone (GPO-L-ONE(®) ) monotherapy reduces iron overload in transfusion-dependent thalassemias: 1-year results from a multicenter prospective, single arm, open label, dose escalating phase III pediatric study (GPO-L-ONE; A001) from ThailandVip Viprakasit, Issarang Nuchprayoon, Ampaiwan Chuansumrit, et al.

Blood|January 21, 2014

Mutations in Kruppel-like factor 1 cause transfusion-dependent hemolytic anemia and persistence of embryonic globin gene expressionVip Viprakasit, Supachai Ekwattanakit, Suchada Riolueang, et al.

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Showing results (21-30 of 29) with videos related to

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You have reached the last page of results.This site can display upto 29 results.

Journal of the Medical Association of Thailand = Chotmaihet Thangphaet|October 31, 2002

Thrombotic complications during induction chemotherapy of acute childhood lymphoblastic leukemiaSuthida Kankirawatana, Gavivann Veerakul, Kleebsabai Sanpakit, et al.

Journal of the Medical Association of Thailand = Chotmaihet Thangphaet|October 31, 2002

Effect of red blood cell glucose-6-phosphate dehydrogenase deficiency on patients with dengue hemorrhagic feverVoravarn S Tanphaichitr, Rachaneekorn Chonlasin, Lerlugsn Suwantol, et al.

Haematologica|February 12, 2002

Clinical phenotypes and molecular characterization of Hb H-Paksé diseaseVip Viprakasit, Voravarn S Tanphaichitr, Parichat Pung-Amritt, et al.

Hemoglobin|July 23, 2014

Incidence of ototoxicity in pediatric patients with transfusion-dependent thalassemia who are less well-chelated by mono- and combined therapy of iron chelating agentsArchwin Tanphaichitr, Thisarat Kusuwan, Siriporn Limviriyakul, et al.

American Journal of Hematology|February 24, 2004

Co-inheritance of Hb Pak Num Po, a novel alpha1 gene mutation, and alpha0 thalassemia associated with transfusion-dependent Hb H diseaseVip Viprakasit, Voravarn S Tanphaichitr, Gavivann Veerakul, et al.

Clinical Chemistry and Laboratory Medicine|March 26, 2013

Problems in determining thalassemia carrier status in a program for prevention and control of severe thalassemia syndromes: a lesson from ThailandVip Viprakasit, Chanin Limwongse, Sathein Sukpanichnant, et al.

European Journal of Haematology|June 9, 2004

Prevalence of HFE mutations among the Thai population and correlation with iron loading in haemoglobin E disorderVip Viprakasit, Prin Vathesathokit, Worrawut Chinchang, et al.

American Journal of Hematology|March 6, 2013

Deferiprone (GPO-L-ONE(®) ) monotherapy reduces iron overload in transfusion-dependent thalassemias: 1-year results from a multicenter prospective, single arm, open label, dose escalating phase III pediatric study (GPO-L-ONE; A001) from ThailandVip Viprakasit, Issarang Nuchprayoon, Ampaiwan Chuansumrit, et al.

Blood|January 21, 2014

Mutations in Kruppel-like factor 1 cause transfusion-dependent hemolytic anemia and persistence of embryonic globin gene expressionVip Viprakasit, Supachai Ekwattanakit, Suchada Riolueang, et al.

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