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Browsing by Author Vip Viprakasit

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Issue DateTitleAuthor(s)
1-Sep-2013The 12.6 kb-deletion in the β-globin gene cluster is the known Thai/Vietnamese (δβ)0-thalassemia commonly found in Southeast AsiaNipon Chalaow; Swee Lay Thein; Vip Viprakasit; Mahidol University; King's College London; Faculty of Medicine, Siriraj Hospital, Mahidol University
1-Dec-2004Acute haemolytic crisis in a Thai patient with homozygous haemoglobin Constants Spring (Hb CS/CS): A case reportVip Viprakasit; Gavivann Veerakul; Kleebsabai Sanpakit; Bunchoo Pongtanakul; Worrawut Chinchang; Voravarn S. Tanphaichitr; Mahidol University
1-Dec-2013Adrenal insufficiency is prevalent in HbE/β-thalassaemia paediatric patients irrespective of their clinical severity and transfusion requirementPairunyar Nakavachara; Vip Viprakasit; Mahidol University
22-Dec-2009Adventitious changes in long-range gene expression caused by polymorphic structural variation and promoter competitionKaren M. Lower; Jim R. Hughes; Marco De Gobbi; Shirley Henderson; Vip Viprakasit; Chris Fisher; Anne Goriely; Helena Ayyub; Jackie Sloane-Stanley; Douglas Vernimmen; Cordelia Langford; David Garrick; Richard J. Gibbons; Douglas R. Higgs; John Radcliffe Hospital; Oxford Radcliffe Hospitals NHS Trust; Mahidol University; Wellcome Trust Sanger Institute
1-Aug-2002Allele Related Mutation Specific-Polymerase Chain Reaction for rapid diagnosis of Hb New York (beta 113 (G15) Val→Glu, β<sup>CD113 GTG→GAG</sup>)Vip Viprakasit; Lerlugsn Suwantol; Worawut Chinchang; Kalaya Tachavanich; Parichat Pung-Amritt; Voravarn S. Tanphaichitr; Weatherall Institute of Molecular Medicine; Mahidol University
1-Jan-2014Approaching low liver iron burden in chelated patients with non-transfusion-dependent thalassemia: The safety profile of deferasiroxAli T. Taher; John B. Porter; Vip Viprakasit; Antonis Kattamis; Suporn Chuncharunee; Pranee Sutcharitchan; Noppadol Siritanaratkul; Raffaella Origa; Zeynep Karakas; Dany Habr; Zewen Zhu; M. Domenica Cappellini; American University of Beirut; UCL; Mahidol University; University of Athens; King Chulalongkorn Memorial Hospital, Faculty of Medicine Chulalongkorn University; Ospedale Regional Microcitemie; Istanbul Tip Fakultesi; Novartis Pharmaceuticals; Universita degli Studi di Milano
1-May-2005Argininosuccinate synthetase deficiency: Mutation analysis in 3 Thai patientsPornswan Wasant; Vip Viprakasit; Chantragan Srisomsap; Somporn Liammongkolkul; Pisanu Ratanarak; Achara Sathienkijakanchai; Jisnuson Svasti; Mahidol University; Weatherall Institute of Molecular Medicine; Chulabhorn Research Institute
17-Oct-2012Association of Xmn i polymorphism and hemoglobin e haplotypes on postnatal gamma globin gene expression in homozygous hemoglobin eSupachai Ekwattanakit; Yuwarat Monteerarat; Suchada Riolueang; Kalaya Tachavanich; Vip Viprakasit; Mahidol University
29-Oct-2010ATR-X syndrome protein targets tandem repeats and influences allele-specific expression in a size-dependent mannerMartin J. Law; Karen M. Lower; Hsiao P.J. Voon; Jim R. Hughes; David Garrick; Vip Viprakasit; Matthew Mitson; Marco De Gobbi; Marco Marra; Andrew Morris; Aaron Abbott; Steven P. Wilder; Stephen Taylor; Guilherme M. Santos; Joe Cross; Helena Ayyub; Steven Jones; Jiannis Ragoussis; Daniela Rhodes; Ian Dunham; Douglas R. Higgs; Richard J. Gibbons; John Radcliffe Hospital; Mahidol University; Wellcome Trust Centre for Human Genetics; Wellcome Trust; The Medical Research Council Laboratory of Molecular Biology; The University of British Columbia
1-May-2018An Automated Segmentation of R2∗ Iron-Overloaded Liver Images Using a Fuzzy C-Mean Clustering SchemePairash Saiviroonporn; Pornpim Korpraphong; Vip Viprakasit; Rungroj Krittayaphong; Mahidol University; Faculty of Medicine, Siriraj Hospital, Mahidol University
4-Jul-2002Baseline levels of plasma endothelin-1 (ET-1) and changes during transfusion in thalassemic patientsVip Viprakasit; Suthida Kankirawatana; Pravit Akarasereenont; Kritvikrom Durongpisitkul; Sirikul Chotewuttakorn; Voravarn S. Tanphaichitr; Weatherall Institute of Molecular Medicine; Mahidol University; John Radcliffe Hospital; University of Oxford
1-Oct-2013Children with hemoglobin E/β-thalassemia have a high risk of being vitamin D deficient even if they get abundant sun exposure: A study from ThailandPairunyar Nakavachara; Vip Viprakasit; Mahidol University
1-Mar-2009Clinical and hematological phenotype of homozygous hemoglobin E: revisit of a benign condition with hidden reproductive riskKalaya Tachavanich; Vip Viprakasit; Worawut Chinchang; Waraporn Glomglao; Parichat Pung-Amritt; Voravarn S. Tanphaichitr; Mahidol University
1-Apr-2018Clinical Classification, Screening and Diagnosis for ThalassemiaVip Viprakasit; Supachai Ekwattanakit; Faculty of Medicine, Siriraj Hospital, Mahidol University
1-Mar-2011Clinical efficacy and safety evaluation of tailoring iron chelation practice in thalassaemia patients from Asia-Pacific: A subanalysis of the EPIC study of deferasiroxVip Viprakasit; Hishamshah Ibrahim; Shau Yin Ha; Phoebe Joy Ho; Chi Kong Li; Lee Lee Chan; Chang Fang Chiu; Pranee Sutcharitchan; Dany Habr; Gabor Domokos; Bernard Roubert; Hong Ling Xue; Donald K. Bowden; Kai Hsin Lin; Mahidol University; Kuala Lumpur Hospital; The University of Hong Kong; Royal Prince Alfred Hospital; Prince of Wales Hospital Hong Kong; University of Malaya Medical Centre; China Medical University Hospital Taichung; Chulalongkorn University; Novartis Pharmaceuticals Corporation; Novartis International AG; Novartis Asia Pacific Pharmaceuticals Pte Ltd; Monash Medical Centre; National Taiwan University Hospital
24-Apr-2009Clinical features and molecular analysis in Thai patients with HbH diseaseVichai Laosombat; Vip Viprakasit; Thirachit Chotsampancharoen; Malai Wongchanchailert; Sudarat Khodchawan; Worawut Chinchang; Benjamas Sattayasevana; Prince of Songkla University; Mahidol University
1-Aug-2005Clinical phenotypes and molecular diagnosis in a hitherto interaction of Hb E/β thalassemia syndrome (β<sup>E</sup>/ β<sup>-31, A→G</sup>)Nassawee Vathana; Vip Viprakasit; Kleebsabi Sanpakit; Worrawut Chinchang; Gavivann Veerakul; Voravarn Tanphaichitr; Mahidol University
1-Jan-2014Clinical presentation and molecular identification of four uncommon alpha globin variants in Thailand: Initiation codon mutation of α2-Globin Gene (HBA2:c.1delA), donor splice site mutation of α1-globin gene (IVSI-1, HBA1:c.95 + 1G&gt;A), hemoglobin Queens Park/Chao Pra Ya (HBA1:c.98T&gt;A) and hemoglobin Westmead (HBA2:c.369C&gt;G)Vip Viprakasit; Supachai Ekwattanakit; Nipon Chalaow; Suchada Riolueang; Sirirat Wijit; Porntep Tanyut; Nunthawut Chat-Uthai; Kalaya Tachavanich; Mahidol University
1-Mar-2004Co-inheritance of Hb Pak Num Po, a Novel α1 Gene Mutation, and α<sup>0</sup>Thalassemia Associated with Transfusion-Dependent Hb H DiseaseVip Viprakasit; Voravarn S. Tanphaichitr; Gavivann Veerakul; Worrawut Chinchang; Siripan Petrarat; Parichat Pung-Amritt; Douglas R. Higgs; Mahidol University; University of Oxford; John Radcliffe Hospital
1-Dec-2005Common origin of a rare β-globin initiation codon mutation (ATG → AGG) in AsiansVip Viprakasit; W. Chinchang; L. Suwanthol; V. S. Tanphaichitr; Mahidol University