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1

Clinical Classification, Screening and Diagnosis for Thalassemia

Viprakasit, Vip, Ekwattanakit, Supachai

Journal:

Hematology/Oncology Clinics of North America

Année:

2018

Langue:

english

Fichier:

PDF, 1.67 MB

english, 2018

2

A paradigm shift on beta-thalassaemia treatment: How will we manage this old disease with new therapies?

Cappellini, Maria Domenica, Porter, John B., Viprakasit, Vip, Taher, Ali T.

Journal:

Année:

2018

Langue:

english

Fichier:

PDF, 948 KB

english, 2018

3

Validation of a patient-reported outcomes symptom measure for patients with non-transfusion-dependent thalassemia (NTDT-PRO©)

Taher, Ali, Cappellini, Maria Domenica, Viprakasit, Vip, Sutcharitchan, Pranee, Mahmoud, Dalia, Laadem, Abderrahmane, Khan, Anzalee, Gwaltney, Chad, Harding, Gale, Attie, Kenneth, Zhang, Xiaosha, Zou,

Journal:

American Journal of Hematology

Année:

2018

Langue:

english

Fichier:

PDF, 1.34 MB

english, 2018

4

Development of a patient-reported outcomes symptom measure for patients with non-transfusion-dependent thalassemia (NTDT-PRO©)

Taher, Ali, Viprakasit, Vip, Cappellini, Maria Domenica, Sutcharitchan, Pranee, Ward, Richard, Mahmoud, Dalia, Laadem, Abderrahmane, Khan, Anzalee, Gwaltney, Chad, Harding, Gale, Attie, Kenneth, Zhang

Journal:

American Journal of Hematology

Année:

2018

Langue:

english

Fichier:

PDF, 1.42 MB

english, 2018

5

A Phase 3 Trial of Luspatercept in Patients with Transfusion-Dependent Î²-Thalassemia

Cappellini, M. Domenica, Viprakasit, Vip, Taher, Ali T., Georgiev, Pencho, Kuo, Kevin H.M., Coates, Thomas, Voskaridou, Ersi, Liew, Hong-Keng, Pazgal-Kobrowski, Idit, Forni, G.L., Perrotta, Silverio,

Journal:

New England Journal of Medicine

Année:

2020

Langue:

english

Fichier:

PDF, 629 KB

english, 2020

6

Clinical efficacy and safety evaluation of tailoring iron chelation practice in thalassaemia patients from Asia-Pacific: a subanalysis of the EPIC study of deferasirox

Vip 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. Bo

Journal:

International Journal of Hematology

Année:

2011

Langue:

english

Fichier:

PDF, 277 KB

english, 2011

7

Problems in determining thalassemia carrier status in a program for prevention and control of severe thalassemia syndromes: a lesson from Thailand

Viprakasit, Vip, Limwongse, Chanin, Sukpanichnant, Sathein, Ruangvutilert, Pornpimol, Kanjanakorn, Chompunut, Glomglao, Waraporn, Sirikong, Monchan, Utto, Witayakarn, Tanphaichitr, Voravarn S.

Journal:

Clinical Chemistry and Laboratory Medicine

Année:

2013

Langue:

english

Fichier:

PDF, 603 KB

english, 2013

8

A Single-Tube Multiplex Gap-Polymerase Chain Reaction for the Detection of Eight β-Globin Gene Cluster Deletions Common in Southeast Asia

Tritipsombut, Jaruwan, Phylipsen, Marion, Viprakasit, Vip, Chalaow, Nipon, Sanchaisuriya, Kanokwan, Giordano, Piero C., Fucharoen, Supan, Harteveld, Cornelis L.

Journal:

Année:

2012

Langue:

english

Fichier:

PDF, 211 KB

english, 2012

9

COMPOUND HETEROZYGOSITY FOR α 0 -THALASSEMIA (−− THAI ) AND Hb CONSTANT SPRING CAUSES SEVERE Hb H DISEASE

Viprakasit, Vip, Tanphaichitr, Voravarn S.

Journal:

Année:

2002

Langue:

english

Fichier:

PDF, 220 KB

english, 2002

10

Identification and key management of non-transfusion-dependent thalassaemia patients: not a rare but potentially under-recognised condition

Viprakasit, Vip, Tyan, Paul, Rodmai, Sarayuth, Taher, Ali T

Journal:

Orphanet Journal of Rare Diseases

Année:

2014

Langue:

english

Fichier:

PDF, 439 KB

english, 2014

11

Validation of a reverse-hybridization StripAssay for the simultaneous analysis of common α-thalassemia point mutations and deletions

Puehringer, Helene, Najmabadi, Hossein, Law, Hai-Yang, Krugluger, Walter, Viprakasit, Vip, Pissard, Serge, Baysal, Erol, Taher, Ali, Farra, Chantal, Al-Ali, Amein, Al-Ateeq, Suad, Oberkanins, Christia

Journal:

Clinical Chemistry and Laboratory Medicine

Année:

2007

Langue:

english

Fichier:

PDF, 239 KB

english, 2007

12

Iron overload across the spectrum of non-transfusion-dependent thalassaemias: role of erythropoiesis, splenectomy and transfusions

Porter, John B., Cappellini, Maria Domenica, Kattamis, Antonis, Viprakasit, Vip, Musallam, Khaled M., Zhu, Zewen, Taher, Ali T.

Journal:

British Journal of Haematology

Année:

2017

Langue:

english

Fichier:

PDF, 367 KB

english, 2017

13

Serum ferritin in the diagnosis of cardiac and liver iron overload in thalassaemia patients real-world practice: a multicentre study

Krittayaphong, Rungroj, Viprakasit, Vip, Saiviroonporn, Pairash, Wangworatrakul, Wipaporn, Wood, John C.

Journal:

British Journal of Haematology

Année:

2017

Langue:

english

Fichier:

PDF, 451 KB

english, 2017

14

Co-inheritance of Southeast Asian Ovalocytosis (SAO) and G6PD deficiency associated with acute hemolysis in a Thai patient

Prayongratana, Kannadit, Viprakasit, Vip

Journal:

Blood Cells, Molecules, and Diseases

Année:

2019

Langue:

english

Fichier:

PDF, 467 KB

english, 2019

15

Baseline levels of plasma endothelin-1 (ET-1) and changes during transfusion in thalassemic patients

Vip Viprakasit, Suthida Kankirawatana, Pravit Akarasereenont, Kritvikrom Durongpisitkul, Sirikul Chotewuttakorn, Voravarn S. Tanphaichitr

Journal:

American Journal of Hematology

Année:

2002

Langue:

english

Fichier:

PDF, 57 KB

english, 2002

16

Co-inheritance of Hb Pak Num Po, a novel α1 gene mutation, and α0 thalassemia associated with transfusion-dependent Hb H disease

Vip Viprakasit, Voravarn S. Tanphaichitr, Gavivann Veerakul, Worrawut Chinchang, Siripan Petrarat, Parichat Pung-Amritt, Douglas R. Higgs

Journal:

American Journal of Hematology

Année:

2004

Langue:

english

Fichier:

PDF, 200 KB

english, 2004

17

Hb H hydrops fetalis syndrome associated with the interaction of two common determinants of α thalassaemia (--MED/αTSaudiα)

Vip Viprakasit, Sarah Green, Sue Height, Helena Ayyub, Douglas R. Higgs

Journal:

British Journal of Haematology

Année:

2002

Langue:

english

Fichier:

PDF, 112 KB

english, 2002

18

De novo deletion within the telomeric region flanking the human α globin locus as a cause of α thalassaemia

Vip Viprakasit, Alexa M. J. Kidd, Helena Ayyub, Sharon Horsley, Jim Hughes, Douglas R. Higgs

Journal:

British Journal of Haematology

Année:

2003

Langue:

english

Fichier:

PDF, 351 KB

english, 2003

19

Hemoglobin H disease induced by the common SEA deletion and the rare hemoglobin Quong Sze in a Thai female: longitudinal clinical course, molecular characterization, and development of a PCR/RFLP-based detection method

Thanyachai Sura, Objoon Trachoo, Vip Viprakasit, Prin Vathesatogkit, Atchara Tunteeratum, Manisa Busabaratana, Raewadee Wisedpanichkij, Parttraporn Isarangkura

Journal:

Annals of Hematology

Année:

2007

Langue:

english

Fichier:

PDF, 192 KB

english, 2007

20

Clinical features and molecular analysis in Thai patients with HbH disease

Vichai Laosombat, Vip Viprakasit, Thirachit Chotsampancharoen, Malai Wongchanchailert, Sudarat Khodchawan, Worawut Chinchang, Benjamas Sattayasevana

Journal:

Annals of Hematology

Année:

2009

Langue:

english

Fichier:

PDF, 156 KB

english, 2009

21

Inhibition of H5N1 highly pathogenic influenza virus by suppressing a specific sialyltransferase

Yuwarat Monteerarat, Ornpreya Suptawiwat, Chompunuch Boonarkart, Mongkol Uiprasertkul, Prasert Auewarakul, Vip Viprakasit

Journal:

Archives of Virology

Année:

2010

Langue:

english

Fichier:

PDF, 278 KB

english, 2010

22

Iron chelation therapy in the management of thalassemia: the Asian perspectives

Vip Viprakasit, Chan Lee-Lee, Quah Thuan Chong, Kai-Hsin Lin, Archrob Khuhapinant

Journal:

International Journal of Hematology

Année:

2009

Langue:

english

Fichier:

PDF, 241 KB

english, 2009

23

Molecular analysis of unknown β-globin gene mutations using polymerase chain reaction-single strand conformation polymorphism (PCR-SSCP) technique and its application in Thai families with β-thalassemias and β-globin variants

Worrawut Chinchang, Vip Viprakasit, Parichat Pung-Amritt, Voravarn S. Tanphaichitr, Pa-thai Yenchitsomanus

Journal:

Clinical Biochemistry

Année:

2005

Langue:

english

Fichier:

PDF, 440 KB

english, 2005

24

Immune-mediated hemolytic anemia in pediatric renal transplantation

Anirut Pattaragarn, Vip Viprakasit, Suroj Supavekin, Achra Sumboonnanonda

Journal:

Pediatric Transplantation

Année:

2006

Langue:

english

Fichier:

PDF, 513 KB

english, 2006

25

Complex interactions of δβ hybrid haemoglobin (Hb Lepore-Hollandia) Hb E (β26 G→A) and α+ thalassaemia in a Thai family

Vip Viprakasit, Parichat Pung-Amritt, Lerlugh Suwanthon, Kevin Clark, Voravarn S. Tanphaichitr

Journal:

European Journal of Haematology

Année:

2002

Langue:

english

Fichier:

PDF, 134 KB

english, 2002

26

Dinucleotide deletion in –α3.7 allele causes a severe form of α+ thalassaemia

Vip Viprakasit, Helena Ayyub, Alison May

Journal:

European Journal of Haematology

Année:

2003

Langue:

english

Fichier:

PDF, 114 KB

english, 2003

27

Distal Renal Tubular Acidosis Associated With Anion Exchanger 1 Mutations in Children in Thailand

Sookkasem Khositseth, Apiwan Sirikanerat, Kulruedee Wongbenjarat, Sauwalak Opastirakul, Siri Khoprasert, Ratikorn Peuksungnern, Duangrurdee Wattanasirichaigoon, Wanna Thongnoppakhun, Vip Viprakasit, P

Journal:

American Journal of Kidney Diseases

Année:

2007

Langue:

english

Fichier:

PDF, 641 KB

english, 2007

28

Hb Woodville, a rare α-globin variant, caused by codon 6 mutation of the α1 gene

Vip Viprakasit, Worrawut Chinchang, Pipat Chotimarat

Journal:

European Journal of Haematology

Année:

2006

Langue:

english

Fichier:

PDF, 128 KB

english, 2006

29

Prevalence of HFE mutations among the Thai population and correlation with iron loading in haemoglobin E disorder

Vip Viprakasit, Prin Vathesathokit, Worrawut Chinchang, Kalaya Tachavanich, Parichat Pung-Amritt, Victoria L. C. Wimhurst, Pa-Thai Yenchitsomanus, Alison T. Merryweather-Clarke, Voravarn S. Tanphaichi

Journal:

European Journal of Haematology

Année:

2004

Langue:

english

Fichier:

PDF, 129 KB

english, 2004

30

Haemoglobin Hope in a northern Thai family: first identification of homozygous haemoglobin Hope associated with haemoglobin H disease

Thanyachai Sura, Manisa Busabaratana, Supak Youngcharoen, Raewadee Wisedpanichkij, Vip Viprakasit, Objoon Trachoo

Journal:

European Journal of Haematology

Année:

2007

Langue:

english

Fichier:

PDF, 458 KB

english, 2007

31

Molecular heterogeneity of glucose-6-phosphate dehydrogenase (G6PD) variants in the south of Thailand and identification of a novel variant (G6PD Songklanagarind)

Vichai Laosombat, Benjamas Sattayasevana, Waricha Janejindamai, Vip Viprakasit, Taku Shirakawa, Kaoru Nishiyama, Masafumi Matsuo

Journal:

Blood Cells, Molecules, and Diseases

Année:

2005

Langue:

english

Fichier:

PDF, 141 KB

english, 2005

32

Natural history of Southeast Asian Ovalocytosis during the first 3 years of life

Vichai Laosombat, Vip Viprakasit, Supaporn Dissaneevate, Roengsak Leetanaporn, Thirachit Chotsampancharoen, Malai Wongchanchailert, Sudarat Kodchawan, Warangkana Thongnoppakun, Sarapee Duangchu

Journal:

Blood Cells, Molecules, and Diseases

Année:

2010

Langue:

english

Fichier:

PDF, 323 KB

english, 2010

33

Two independent origins of Hb Dhonburi (Neapolis) [β 126 (H4) Val→Gly]: An electrophoretically silent hemoglobin variant

Vip Viprakasit, Worrawut Chinchang

Journal:

Clinica Chimica Acta

Année:

2007

Langue:

english

Fichier:

PDF, 350 KB

english, 2007

34

ATR-X Syndrome Protein Targets Tandem Repeats and Influences Allele-Specific Expression in a Size-Dependent Manner

Martin 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

Journal:

Année:

2010

Langue:

english

Fichier:

PDF, 1.01 MB

english, 2010

35

Unusual phenotype of Hemoglobin EE with Hemoglobin H disease: a pitfall in clinical diagnosis and genetic counseling

Vip Viprakasit, Voravarn S. Tanphaichitr

Journal:

The Journal of Pediatrics

Année:

2004

Langue:

english

Fichier:

PDF, 186 KB

english, 2004

36

Hemochromatosis gene (HFE) mutations in South East Asia: a potential for iron overload☆

Jennifer J Pointon, Vip Viprakasit, Katie L Miles, Karen J Livesey, Michael Steiner, Sean O’Riordan, Tran T Hien, Alison T Merryweather-Clarke, Kathryn J.H Robson

Journal:

Blood Cells, Molecules, and Diseases

Année:

2003

Langue:

english

Fichier:

PDF, 114 KB

english, 2003

37

IRON CHELATION THERAPY WITH DEFERASIROX (EXJADE®) IN REDUCING CARDIAC SIDEROSIS IN β-THALASSEMIA PATIENTS: 2-YEAR RESULTS FROM THE EPIC CARDIAC SUBSTUDY

Dudley J. Pennell, John Porter, Domenica Cappellini, Lee Lee Chan, Amal El-Beshlawy, Yesim Aydinok, Hishamshah Ibrahim, Chi-Kong Li, Vip Viprakasit, Mohsen Elalfy, Antonis Kattamis, Gillian Smith, Dan

Journal:

Journal of the American College of Cardiology

Année:

2010

Langue:

english

Fichier:

PDF, 68 KB

english, 2010

38

Prince Wongsa Dhiraj Snid—Thai Physician and Diplomat

David P. Steensma, Vip Viprakasit, Robert A. Kyle, Marc A. Shampo

Journal:

Mayo Clinic Proceedings

Année:

2012

Langue:

english

Fichier:

PDF, 247 KB

english, 2012

39

Treating iron overload in patients with non-transfusion-dependent thalassemia

Taher, Ali T., Viprakasit, Vip, Musallam, Khaled M., Cappellini, M. Domenica

Journal:

American Journal of Hematology

Année:

2013

Langue:

english

Fichier:

PDF, 181 KB

english, 2013

40

Deferasirox effectively reduces iron overload in non-transfusion-dependent thalassemia (NTDT) patients: 1-year extension results from the THALASSA study

Ali T. Taher, John B. Porter, Vip Viprakasit, Antonis Kattamis…

Journal:

Annals of Hematology

Année:

2013

Langue:

english

Fichier:

PDF, 404 KB

english, 2013

41

Deferasirox demonstrates a dose-dependent reduction in liver iron concentration and consistent efficacy across subgroups of non-transfusion-dependent thalassemia patients

Taher, Ali T., Porter, John B., Viprakasit, Vip, Kattamis, Antonis, Chuncharunee, Suporn, Sutcharitchan, Pranee, Siritanaratkul, Noppadol, Galanello, Renzo, Karakas, Zeynep, Lawniczek, Tomasz, Habr, D

Journal:

American Journal of Hematology

Année:

2013

Langue:

english

Fichier:

PDF, 268 KB

english, 2013

42

Iron chelation therapy for non-transfusion-dependent thalassemia (NTDT): A status quo

Taher, Ali T., Musallam, Khaled M., Viprakasit, Vip, Porter, John B., Cappellini, Maria Domenica

Journal:

Blood Cells, Molecules, and Diseases

Année:

2014

Langue:

english

Fichier:

PDF, 444 KB

english, 2014

43

Non-transfusion dependent hemoglobin E/β thalassemia had high prevalence of vitamin D deficiency than more severe patients who received regular blood transfusion and iron chelation therapy

Nakavachara, Pairunyar, Chaichanwattanakul, Katharee, Viprakasit, Vip

Journal:

International Journal of Pediatric Endocrinology

Année:

2013

Langue:

english

Fichier:

PDF, 322 KB

english, 2013

44

Current approach to iron chelation in children

Aydinok, Yesim, Kattamis, Antonis, Viprakasit, Vip

Journal:

British Journal of Haematology

Année:

2014

Langue:

english

Fichier:

PDF, 124 KB

english, 2014

45

Clinical Presentation and Molecular Identification of Four Uncommon Alpha Globin Variants in Thailand

Viprakasit, Vip, Ekwattanakit, Supachai, Chalaow, Nipon, Riolueang, Suchada, Wijit, Sirirat, Tanyut, Porntep, Chat-Uthai, Nunthawut, Tachavanich, Kalaya

Journal:

Acta Haematologica

Année:

2014

Langue:

english

Fichier:

PDF, 657 KB

english, 2014

46

An overview of current treatment strategies for β-thalassemia

Cappellini, Maria Domenica, Viprakasit, Vip, Taher, Ali T

Journal:

Expert Opinion on Orphan Drugs

Année:

2014

Langue:

english

Fichier:

PDF, 581 KB

english, 2014

47

Twice daily deferasirox significantly improves clinical efficacy in transfusion dependent thalassaemias who were inadequate responders to standard once daily dose

Pongtanakul, Bunchoo, Viprakasit, Vip

Journal:

Blood Cells, Molecules, and Diseases

Année:

2013

Langue:

english

Fichier:

PDF, 177 KB

english, 2013

48

Incidence of Ototoxicity in Pediatric Patients with Transfusion-Dependent Thalassemia Who Are Less Well-Chelated by Mono- and Combined Therapy of Iron Chelating Agents

Tanphaichitr, Archwin, Kusuwan, Thisarat, Limviriyakul, Siriporn, Atipas, Suvajana, Pooliam, Julaporn, Sangpraypan, Tuangrat, Tanphaichitr, Voravarn S., Viprakasit, Vip

Journal:

Année:

2014

Langue:

english

Fichier:

PDF, 248 KB

english, 2014

49

A Rare Association of α 0 -Thalassemia (– – SEA ) and an Initiation Codon Mutation (ATG→A-G) of the α2 Gene Causes Hb H Disease in Thailand

Viprakasit, Vip, Chinchang, Worrawut, Glomglao, Waraporn, Tanphaichitr, Voravarn S

Journal:

Année:

2005

Langue:

english

Fichier:

PDF, 339 KB

english, 2005

50

Hb G-MAKASSAR [ β 6(A3)Glu→Ala; CODON 6 (G A G→G C G)]: MOLECULAR CHARACTERIZATION, CLINICAL, AND HEMATOLOGICAL EFFECTS

Viprakasit, Vip, Wiriyasateinkul, Aranya, Sattayasevana, Benjamas, Miles, Katie L., Laosombat, Vichai

Journal:

Année:

2002

Langue:

english

Fichier:

PDF, 299 KB

english, 2002