Variable genotype-phenotype correlations in patients with a rare nondeletional α-thalassemia; Hb Pak Num Po (HBA1: C.396-397insT)

بواسطة Kleebsabai Sanpakit, Vip Viprakasit
منشور في 2018

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

بواسطة Bunchoo Pongtanakul, Vip Viprakasit
منشور في 2018

Further identification of Hb G-Coushatta [β22(B4)Glu→Ala (GAA→GCA)] in Thailand by the polymerase chain reaction-single-strand conformation polymorphism technique and by amplificat...

بواسطة Worrawut Chinchang, Vip Viprakasit
منشور في 2018

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

بواسطة Pairunyar Nakavachara, Vip Viprakasit
منشور في 2018

Adrenal insufficiency is prevalent in HbE/β-thalassaemia paediatric patients irrespective of their clinical severity and transfusion requirement

بواسطة Pairunyar Nakavachara, Vip Viprakasit
منشور في 2018

Clinical Classification, Screening and Diagnosis for Thalassemia

بواسطة Vip Viprakasit, Supachai Ekwattanakit
منشور في 2019

Compound heterozygosity for α⁰-thalassemia (--^THAI) and Hb constant spring causes severe Hb H disease

بواسطة Vip Viprakasit, Voravarn S. Tanphaichitr
منشور في 2018

Hb H disease: clinical course and disease modifiers.

بواسطة Suthat Fucharoen, Vip Viprakasit
منشور في 2018

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

بواسطة Kannadit Prayongratana, Vip Viprakasit
منشور في 2020

Deferiprone for transfusional iron overload and its roles in developing countries

بواسطة Vip Viprakasit, Sarayuth Rodmai, Somdet Srichairatanakool
منشور في 2018

Deferiprone for transfusional iron overload and its roles in developing countries

بواسطة Vip Viprakasit, Sarayuth Rodmai, Somdet Srichairatanakool
منشور في 2018

Deferiprone for transfusional iron overload and its roles in developing countries

بواسطة Vip Viprakasit, Sarayuth Rodmai, Somdet Srichairatanakool
منشور في 2018

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

بواسطة Supachai Ekwattanakit, Suchada Riolueang, Vip Viprakasit
منشور في 2019

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

بواسطة Supachai Ekwattanakit, Noppadol Siritanaratkul, Vip Viprakasit
منشور في 2019

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

بواسطة Pairash Saiviroonporn, Vip Viprakasit, Rungroj Krittayaphong
منشور في 2018

Current approach to iron chelation in children

بواسطة Yesim Aydinok, Antonis Kattamis, Vip Viprakasit
منشور في 2018

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

بواسطة Vip Viprakasit, Worrawut Chinchang, Pipat Chotimarat
منشور في 2018

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

بواسطة Pairash Saiviroonporn, Vip Viprakasit, Rungroj Krittayaphong
منشور في 2017

The 12.6 kb-deletion in the β-globin gene cluster is the known Thai/Vietnamese (δβ)0-thalassemia commonly found in Southeast Asia

بواسطة Nipon Chalaow, Swee Lay Thein, Vip Viprakasit
منشور في 2018

An overview of current treatment strategies for β-thalassemia

بواسطة Maria Domenica Cappellini, Vip Viprakasit, Ali T. Taher
منشور في 2018