A longitudinal study of growth and relation with anemia and iron overload in pediatric patients with transfusion-dependent thalassemia

A longitudinal study of growth and relation with anemia and iron overload in pediatric patients with transfusion-dependent thalassemia

Copyright © 2016 Wolters Kluwer Health, Inc. All rights reserved. Short stature is one of the most common endocrinopathies in transfusion-dependent thalassemia (TDT). This study aimed to determine the longitudinal pattern of growth in pediatric patients with TDT and study the relationship between gr...

وصف كامل

محفوظ في:

التفاصيل البيبلوغرافية
المؤلفون الرئيسيون:	Nokeaingtong K., Charoenkwan P., Silvilairat S., Saekho S., Pongprot Y., Dejkhamron P.
التنسيق:	دورية
منشور في:	2017
الوصول للمادة أونلاين:	https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84979737388&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/41708
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مواد مشابهة

A longitudinal study of growth and relation with anemia and iron overload in pediatric patients with transfusion-dependent thalassemia
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Tissue Doppler echocardiography reliably reflects severity of iron overload in pediatric patients with β thalassemia
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Treating iron overload in patients with non-transfusion-dependent thalassemia
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Iron overload in non-transfusion-dependent thalassemia: association with genotype and clinical risk factors
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Tissue Doppler echocardiography reliably reflects severity of iron overload in pediatric patients with β thalassemia
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Heart rate variability for early detection of cardiac iron deposition in patients with transfusion-dependent thalassemia
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Iron overload in non-transfusion-dependent thalassemia: association with genotype and clinical risk factors
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Heart rate variability for early detection of cardiac iron deposition in patients with transfusion-dependent thalassemia
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Iron Overload in Transfusion-Dependent Indonesian Thalassemic Patients
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Early detection of ventricular dysfunction by tissue Doppler echocardiography related to cardiac iron overload in patients with thalassemia
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MRI for the diagnosis of cardiac and liver iron overload in patients with transfusion-dependent thalassemia: An algorithm to guide clinical use when availability is limited
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Curcuminoids supplementation ameliorates iron overload, oxidative stress, hypercoagulability, and inflammation in non-transfusion-dependent β-thalassemia/Hb E patients
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Deferasirox effectively reduces iron overload in non-transfusion-dependent thalassemia (NTDT) patients: 1-year extension results from the THALASSA study
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Thalassemia-related complications in pediatric, adolescent, and young adult patients with transfusion-dependent thalassemia: A multicenter study in Thailand
بواسطة: Surapolchai P.
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Heart rate variability as an alternative indicator for identifying cardiac iron status in non-transfusion dependent thalassemia patients
بواسطة: Karn Wijarnpreecha, وآخرون
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Heart rate variability as an alternative indicator for identifying cardiac iron status in non-transfusion dependent thalassemia patients
بواسطة: Karn Wijarnpreecha, وآخرون
منشور في: (2018)

Incidence of ototoxicity in pediatric patients with transfusion-dependent thalassemia who are less well-chelated by mono- and combined therapy of iron chelating agents
بواسطة: Archwin Tanphaichitr, وآخرون
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Prevalence and risk factors for cardiac iron overload and cardiovascular complications among patients with thalassemia in Northern Thailand
بواسطة: Tantiworawit A., وآخرون
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Impact of splenectomy on outcomes of hematopoietic stem cell transplantation in pediatric patients with transfusion-dependent thalassemia
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Heart rate variability for early detection of iron overload cardiomyopathy in β-thalassemia patients
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Heart rate variability for early detection of iron overload cardiomyopathy in β-thalassemia patients
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Deferasirox in iron-overloaded patients with transfusion-dependent myelodysplastic syndromes: Results from the large 1-year EPIC study
بواسطة: Gattermann,N., وآخرون
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Impact of iron overload on bone remodeling in thalassemia
بواسطة: Pokpong Piriyakhuntorn, وآخرون
منشور في: (2020)

Leukocyte telomere length in patients with transfusion-dependent thalassemia
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Prevalence and risk factors for cardiac iron overload and cardiovascular complications among patients with thalassemia in Northern Thailand
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An association between fibroblast growth factor 21 and cognitive impairment in iron-overload thalassemia
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Using of deferasirox and deferoxamine in refractory iron overload thalassemia
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Gene therapy in patients with transfusion-dependent β-thalassemia
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No Difference in the Incidence of Complications in Pediatric Patients with Moderate Anemia 30 Days after Pediatric Hip Surgery with and without Blood Transfusion
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Differences in longitudinal growth patterns of children and adolescents with transfusion-dependent hemoglobin E/β-thalassemia and those achieving successful hematopoietic stem-cell transplantation
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Differences in longitudinal growth patterns of children and adolescents with transfusion-dependent hemoglobin E/β-thalassemia and those achieving successful hematopoietic stem-cell transplantation
بواسطة: Jitpirasakun S.
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