Prevalence of low bone mass among adolescents with nontransfusion-dependent hemoglobin E/β-thalassemia and its relationship with anemia severity-Reference-Cited by-同舟云学术

Prevalence of low bone mass among adolescents with nontransfusion-dependent hemoglobin E/β-thalassemia and its relationship with anemia severity

Published:2017-08-12 Issue:1 Volume:65 Page:e26744
ISSN:1545-5009
Container-title:Pediatric Blood & Cancer
language:en
Short-container-title:Pediatr Blood Cancer

Author:

Nakavachara Pairunyar¹^ORCID,Petchkul Jaturat¹,Jeerawongpanich Krittha¹,Kiattisakthavee Pornpimol¹,Manpayak Teerarat¹,Netsakulnee Parichat¹,Chaichanwattanakul Katharee¹,Pooliam Julaporn²,Srichairatanakool Somdet³,Viprakasit Vip⁴

Affiliation:

1. Division of Pediatric Endocrinology; Faculty of Medicine Siriraj Hospital; Department of Pediatrics; Mahidol University; Bangkok Thailand

2. Clinical Epidemiology Unit; Office for Research and Development; Faculty of Medicine Siriraj Hospital; Mahidol University; Bangkok Thailand

3. Department of Biochemistry; Faculty of Medicine; Chiang Mai University; Chiang Mai Thailand

4. Thalassemia Center and Division of Pediatric Hematology and Oncology; Department of Pediatrics; Faculty of Medicine Siriraj Hospital; Mahidol University; Bangkok Thailand

Funder

Siriraj Research Development

Chalermprakiat Funding (PN and VV)

Mahidol University

Publisher

Wiley

Subject

Oncology,Hematology,Pediatrics, Perinatology and Child Health

Reference47 articles.

1. Identification and key management of non-transfusion-dependent thalassaemia patients: not a rare but potentially under-recognized condition;Viprakasit;Orphanet J Rare Dis,2014

2. Hemoglobin E syndromes;Vichinsky;Hematol Am Soc Hematol Educ Program,2007

3. Hb E/beta-thalassaemia: a common & clinically diverse disorder;Olivieri;Indian J Med Res,2011

4. Evaluation of alpha hemoglobin stabilizing protein (AHSP) as a genetic modifier in patients with β thalassemia;Viprakasit;Blood,2004

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