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Journal Articles

Physical Activities in Patients with β-Thalassemia As Measured By Fitbit in Association with Patient-Reported Outcomes

Antonis Kattamis, MD, Pranee Sutcharitchan, MD, Ali Taher, MDPhDFRCP, Maria Domenica Cappellini, MD, Dalia Mahmoud, Joseph Pariseau, PharmD, Abderrahmane Laadem, MD, Anzalee Khan, PhD, X. Henry Hu, MD PhD, Vip Viprakasit, MD PhD

Blood (2017) 130 (Supplement 1): 4731.

https://doi.org/10.1182/blood.V130.Suppl_1.4731.4731

Published: 2017

Journal Articles

Quality of Life in Patients with β-Thalassemia: Transfusion Dependent Versus Non-Transfusion Dependent

Maria Domenica Cappellini, MD, Antonis Kattamis, MD, Vip Viprakasit, MD PhD, Pranee Sutcharitchan, MD, Dalia Mahmoud, Joseph Pariseau, PharmD, Abderrahmane Laadem, MD, Anzalee Khan, PhD, X. Henry Hu, MD PhD, Ali Taher, MDPhDFRCP

Blood (2017) 130 (Supplement 1): 751.

https://doi.org/10.1182/blood.V130.Suppl_1.751.751

Published: 2017

Journal Articles

Osteopenia Is Commonly Present in Prepubertal Children with Severe Hb E/βthalassemia Despite Adequate Transfusion and Iron Chelation Therapy.

Vip Viprakasit, MD, PhD, Pairunya Sawathiparnich, MD, Tuangrat Sangpraypanm, BSc, Linda Weerakulwattana, MSc, Pornpimol Kiattisakthavee, BSc, Katharee Chaichanwatanakul, BSc, Natsawee Vatana, MD

Blood (2007) 110 (11): 3830.

https://doi.org/10.1182/blood.V110.11.3830.3830

Published: 2007

Journal Articles

Identification of a Novel IL7RA Mutation (444_450insA) Caused Marked Reduction in CD127 Expression from a Cohort Molecular Analysis of Severe Combined Immunodeficiency (T − , B + , NK + SCID) in Thailand.

Vip Viprakasit, MD, PhD, Yuwarat Monteerarat, BSc, Orathai Piboonpocanun, MD, Kleebsabai Sanpakit, MD, Worrawut Chinchang, MSc, Kalaya Tachavanich, MSc, Nualanong Visitsunthorn, MD, Visith Thongboonkerd, MD, Prakit Vichyanond, MD

Blood (2006) 108 (11): 1247.

https://doi.org/10.1182/blood.V108.11.1247.1247

Published: 2006

Journal Articles

An Entirely Novel Form of α Thalassemia in Patients from the South Pacific Linked to Chromosome 16.

Vip Viprakasit, MD, PhD, Marco De Gobbi, MD, Helena Ayyub, BSc, Ioannis Ragoussis, PhD, William G. Wood, PhD, Donald K. Bowden, MD, Douglas R. Higgs, MD, DSc

Blood (2005) 106 (11): 2688.

https://doi.org/10.1182/blood.V106.11.2688.2688

Published: 2005

Journal Articles

Identification of a Gain-of-Function SNP Causing a New Model of α-Thalassaemia.

Marco De Gobbi, MD, Vip Viprakasit, MD, PhD, Pieter J. de Jong, PhD, Yuko Yoshinaga, PhD, Jan-Fang Cheng, PhD, Jim R. Hughes, PhD, Chris A. Fisher, PhD, William G. Wood, PhD, Donald K. Bowden, PhD, Douglas R. Higgs, MD

Blood (2005) 106 (11): 523.

https://doi.org/10.1182/blood.V106.11.523.523

Published: 2005

Journal Articles

Molecular Diagnosis of the First Ferroportin Mutation (C326Y) in the Far East Causing a Dominant Form of Inherited Iron Overload.

Vip Viprakasit, MD, PhD, Alison T. Merryweather-Clarke, PhD, Yingyong Chinthammitr, MD, Lisa Schimanski, PhD, Hal Drakesmith, PhD, Somdet Srichairatanakool, PhD, Chanin Limwongse, MD, Alain Townsend, MD, Kathryn J.H. Robson, PhD

Blood (2004) 104 (11): 3204.

https://doi.org/10.1182/blood.V104.11.3204.3204

Published: 2004

NARROW

Physical Activities in Patients with β-Thalassemia As Measured By Fitbit in Association with Patient-Reported Outcomes

Quality of Life in Patients with β-Thalassemia: Transfusion Dependent Versus Non-Transfusion Dependent

Osteopenia Is Commonly Present in Prepubertal Children with Severe Hb E/βthalassemia Despite Adequate Transfusion and Iron Chelation Therapy.

Identification of a Novel IL7RA Mutation (444_450insA) Caused Marked Reduction in CD127 Expression from a Cohort Molecular Analysis of Severe Combined Immunodeficiency (T − , B + , NK + SCID) in Thailand.

An Entirely Novel Form of α Thalassemia in Patients from the South Pacific Linked to Chromosome 16.

Identification of a Gain-of-Function SNP Causing a New Model of α-Thalassaemia.

Molecular Diagnosis of the First Ferroportin Mutation (C326Y) in the Far East Causing a Dominant Form of Inherited Iron Overload.

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ASH Publications

American Society of Hematology

Physical Activities in Patients with β-Thalassemia As Measured By Fitbit in Association with Patient-Reported Outcomes

Quality of Life in Patients with β-Thalassemia: Transfusion Dependent Versus Non-Transfusion Dependent

Osteopenia Is Commonly Present in Prepubertal Children with Severe Hb E/βthalassemia Despite Adequate Transfusion and Iron Chelation Therapy.

Identification of a Novel IL7RA Mutation (444_450insA) Caused Marked Reduction in CD127 Expression from a Cohort Molecular Analysis of Severe Combined Immunodeficiency (T − , B + , NK + SCID) in Thailand.

An Entirely Novel Form of α Thalassemia in Patients from the South Pacific Linked to Chromosome 16.

Identification of a Gain-of-Function SNP Causing a New Model of α-Thalassaemia.

Molecular Diagnosis of the First Ferroportin Mutation (C326Y) in the Far East Causing a Dominant Form of Inherited Iron Overload.

Email alerts

ASH Publications

American Society of Hematology

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