Viprakasit, Vip: search on Z-Library

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1

Clinical Classification, Screening and Diagnosis for Thalassemia

Viprakasit, Vip, Ekwattanakit, Supachai

Journal:

Hematology/Oncology Clinics of North America

Year:

2018

Language:

english

File:

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:

Year:

2018

Language:

english

File:

PDF, 948 KB

english, 2018

3

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

Year:

2018

Language:

english

File:

PDF, 1.42 MB

english, 2018

4

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

Year:

2018

Language:

english

File:

PDF, 1.34 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

Year:

2020

Language:

english

File:

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

Year:

2011

Language:

english

File:

PDF, 277 KB

english, 2011

7

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

Viprakasit, Vip, Tanphaichitr, Voravarn S.

Journal:

Year:

2002

Language:

english

File:

PDF, 220 KB

english, 2002

8

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

Year:

2017

Language:

english

File:

PDF, 451 KB

english, 2017

9

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

Year:

2007

Language:

english

File:

PDF, 239 KB

english, 2007

10

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

Year:

2019

Language:

english

File:

PDF, 467 KB

english, 2019

11

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:

Year:

2012

Language:

english

File:

PDF, 211 KB

english, 2012

12

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

Year:

2014

Language:

english

File:

PDF, 439 KB

english, 2014

13

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

Year:

2013

Language:

english

File:

PDF, 603 KB

english, 2013

14

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

Year:

2017

Language:

english

File:

PDF, 367 KB

english, 2017

15

185: Recurrent Hemoglobin H hydrops Caused by a Compound Heterozygosity of HBA2: c.* 93_* 94delAA and É0- thalassemia (-- SEA)

Anuwutnavin, Sanitra, Watananirun, Kanokwaroon, Riolueang, Suchada, Ekwattanakit, Supachai, Ruangvutilert, Pornpimol, Viprakasit, Vip

Journal:

American Journal of Obstetrics and Gynecology

Year:

2020

File:

PDF, 526 KB

2020

16

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

Year:

2013

Language:

english

File:

PDF, 404 KB

english, 2013

17

Current approach to iron chelation in children

Aydinok, Yesim, Kattamis, Antonis, Viprakasit, Vip

Journal:

British Journal of Haematology

Year:

2014

Language:

english

File:

PDF, 124 KB

english, 2014

18

Regular Article Mutations in Kr uppel-like factor 1 cause transfusion-dependent hemolytic anemia and persistence of embryonic globin gene expression

Cells, R E D, Viprakasit, Vip, Ekwattanakit, Supachai, Riolueang, Suchada, Chalaow, Nipon, Fisher, Chris, Lower, Karen, Kanno, Hitoshi, Tachavanich, Kalaya, Bejrachandra, Sasithorn, Saipin, Jariya, Ju

Year:

2014

Language:

english

File:

PDF, 1.05 MB

english, 2014

19

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

Vip Viprakasit, Helena Ayyub, Alison May

Journal:

European Journal of Haematology

Year:

2003

Language:

english

File:

PDF, 114 KB

english, 2003

20

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:

Year:

2010

Language:

english

File:

PDF, 1.01 MB

english, 2010

21

Serum ferritin values between 300 and 800 ng/mL in nontransfusion-dependent thalassemia: A probability curve to guide clinical decision making when MRI is unavailable

Saliba, Antoine N., Musallam, Khaled M., Cappellini, Maria D., Graziadei, Giovanna, Daar, Shahina, Viprakasit, Vip, Taher, Ali T.

Journal:

American Journal of Hematology

Year:

2017

Language:

english

File:

PDF, 675 KB

english, 2017

22

An integration-free iPSC line (MUSIi008-A) derived from a patient with severe hemolytic anemia carrying compound heterozygote mutations in KLF1 gene for disease modeling

Potirat, Ponthip, Wattanapanitch, Methichit, Viprakasit, Vip, Kheolamai, Pakpoom, Issaragrisil, Surapol

Journal:

Stem Cell Research

Year:

2019

Language:

english

File:

PDF, 2.30 MB

english, 2019

23

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

Year:

2002

Language:

english

File:

PDF, 57 KB

english, 2002

24

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

Year:

2009

Language:

english

File:

PDF, 156 KB

english, 2009

25

Detection of cardiac iron overload with native magnetic resonance T1 and T2 mapping in patients with thalassemia

Krittayaphong, Rungroj, Zhang, Shuo, Saiviroonporn, Pairash, Viprakasit, Vip, Tanapibunpon, Prajak, Komoltri, Chulaluk, Wangworatrakul, Wipaporn

Journal:

International Journal of Cardiology

Year:

2017

Language:

english

File:

PDF, 717 KB

english, 2017

26

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

Year:

2002

Language:

english

File:

PDF, 134 KB

english, 2002

27

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

Year:

2006

Language:

english

File:

PDF, 128 KB

english, 2006

28

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:

Year:

2014

Language:

english

File:

PDF, 248 KB

english, 2014

29

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 Thailand

Viprakasit, Vip, Nuchprayoon, Issarang, Chuansumrit, Ampaiwan, Torcharus, Kitti, Pongtanakul, Bunchoo, Laothamatas, Jiraporn, Srichairatanakool, Somdet, Pooliam, Julaporn, Supajitkasem, Siriwat, Suriy

Journal:

American Journal of Hematology

Year:

2013

Language:

english

File:

PDF, 536 KB

english, 2013

30

Efficacy and safety of iron-chelation therapy with deferoxamine, deferiprone, and deferasirox for the treatment of iron-loaded patients with nontransfusion-dependent thalassemia syndromes

Taher, Ali, Porter, John, Kattamis, Antonis, Viprakasit, Vip, Cappellini, Domenica

Journal:

Drug Design Development and Therapy

Year:

2016

Language:

english

File:

PDF, 318 KB

english, 2016

31

A prospective analysis for prevalence of complications in Thai non-transfusion-dependent Hb E/β-thalassemia and α-thalassemia (Hb H disease)

Ekwattanakit, Supachai, Siritanaratkul, Noppadol, Viprakasit, Vip

Journal:

American Journal of Hematology

Year:

2018

Language:

english

File:

PDF, 713 KB

english, 2018

32

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

Year:

2007

Language:

english

File:

PDF, 350 KB

english, 2007

33

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

Year:

2013

Language:

english

File:

PDF, 181 KB

english, 2013

34

Improved R2* liver iron concentration assessment using a novel fuzzy c-mean clustering scheme

Saiviroonporn, Pairash, Viprakasit, Vip, Krittayaphong, Rungroj

Journal:

BMC Medical Imaging

Year:

2015

Language:

english

File:

PDF, 2.22 MB

english, 2015

35

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

Year:

2010

Language:

english

File:

PDF, 278 KB

english, 2010

36

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

Year:

2007

Language:

english

File:

PDF, 641 KB

english, 2007

37

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:

Year:

2005

Language:

english

File:

PDF, 339 KB

english, 2005

38

[Side Effects of Drugs Annual] A worldwide yearly survey of new data in adverse drug reactions and interactions Volume 35 || Metal antagonists

Viprakasit, Vip

Year:

2014

Language:

english

File:

PDF, 307 KB

english, 2014

39

Children with hemoglobin E/β-thalassemia have a high risk of being vitamin D deficient even if they get abundant sun exposure: A study from thailand

Nakavachara, Pairunyar, Viprakasit, Vip

Journal:

Pediatric Blood & Cancer

Year:

2013

Language:

english

File:

PDF, 286 KB

english, 2013

40

Prevalence and predictors of cardiac and liver iron overload in patients with thalassemia: A multicenter study based on real-world data

Krittayaphong, Rungroj, Viprakasit, Vip, Saiviroonporn, Pairash, Siritanaratkul, Noppadol, Siripornpitak, Suvipaporn, Meekaewkunchorn, Arunotai, Kirawittaya, Thawatchai, Sripornsawan, Pornpun, Jetsris

Journal:

Blood Cells, Molecules, and Diseases

Year:

2017

Language:

english

File:

PDF, 404 KB

english, 2017

41

Prevalence of left ventricular diastolic dysfunction by cardiac magnetic resonance imaging in thalassemia major patients with normal left ventricular systolic function

Chinprateep, Benjaporn, Ratanasit, Nithima, Kaolawanich, Yodying, Karaketklang, Khemajira, Saiviroonporn, Pairash, Viprakasit, Vip, Krittayaphong, Rungroj

Journal:

BMC Cardiovascular Disorders

Year:

2019

Language:

english

File:

PDF, 1.51 MB

english, 2019

42

An overview of current treatment strategies for β-thalassemia

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

Journal:

Expert Opinion on Orphan Drugs

Year:

2014

Language:

english

File:

PDF, 581 KB

english, 2014

43

A Normal Reference of Bone Mineral Density (BMD) Measured by Dual Energy X-Ray Absorptiometry in Healthy Thai Children and Adolescents Aged 5–18 Years: A New Reference for Southeast Asian Populations

Nakavachara, Pairunyar, Pooliam, Julaporn, Weerakulwattana, Linda, Kiattisakthavee, Pornpimol, Chaichanwattanakul, Katharee, Manorompatarasarn, Racahnee, Chokephaibulkit, Kulkanya, Viprakasit, Vip, He

Journal:

Year:

2014

Language:

english

File:

PDF, 1.33 MB

english, 2014

44

Defining serum ferritin thresholds to predict clinically relevant liver iron concentrations for guiding deferasirox therapy when MRI is unavailable in patients with non-transfusion-dependent thalassaemia

Taher, Ali T., Porter, John B., Viprakasit, Vip, Kattamis, Antonis, Chuncharunee, Suporn, Sutcharitchan, Pranee, Siritanaratkul, Noppadol, Origa, Raffaella, Karakas, Zeynep, Habr, Dany, Zhu, Zewen, Ca

Journal:

British Journal of Haematology

Year:

2015

Language:

english

File:

PDF, 289 KB

english, 2015

45

Optimising iron chelation therapy with deferasirox for non-transfusion-dependent thalassaemia patients: 1-year results from the THETIS study

Taher, Ali T., Cappellini, M. Domenica, Aydinok, Yesim, Porter, John B., Karakas, Zeynep, Viprakasit, Vip, Siritanaratkul, Noppadol, Kattamis, Antonis, Wang, Candace, Zhu, Zewen, Joaquin, Victor, Uwam

Journal:

Blood Cells, Molecules, and Diseases

Year:

2016

Language:

english

File:

PDF, 952 KB

english, 2016

46

Interaction between Hb E and Hb Yala (HBB:c.129delT); a novel frameshift beta globin gene mutation, resulting in Hemoglobin E/β 0 thalassemia

Ekwattanakit, Supachai, Riolueang, Suchada, Viprakasit, Vip

Journal:

Hematology (Maney Publishing)

Year:

2017

Language:

english

File:

PDF, 1014 KB

english, 2017

47

Recent advances in molecular understanding of NTDT: 2012

Viprakasit, Vip

Journal:

Thalassemia Reports

Year:

2013

File:

PDF, 499 KB

2013

48

Immune-mediated hemolytic anemia in pediatric renal transplantation

Anirut Pattaragarn, Vip Viprakasit, Suroj Supavekin, Achra Sumboonnanonda

Journal:

Pediatric Transplantation

Year:

2006

Language:

english

File:

PDF, 513 KB

english, 2006

49

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

Year:

2010

Language:

english

File:

PDF, 68 KB

english, 2010

50

Utility of labile plasma iron and transferrin saturation in addition to serum ferritin as iron overload markers in different underlying anemias before and after deferasirox treatment

Porter, John B., El-Alfy, Mohsen, Viprakasit, Vip, Giraudier, Stephane, Chan, Lee Lee, Lai, Yongrong, El-Ali, Ali, Han, Jackie, Cappellini, Maria D.

Journal:

European Journal of Haematology

Year:

2015

Language:

english

File:

PDF, 298 KB

english, 2015

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