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Early‐onset reduced bone mineral density in patients with pyruvate kinase deficiency.
- Published in:
- American Journal of Hematology, 2023, v. 98, n. 3, p. E57, doi. 10.1002/ajh.26830
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- Publication type:
- Article
Crushed deferasirox film‐coated tablets in pediatric patients with transfusional hemosiderosis: Results from a single‐arm, interventional phase 4 study (MIMAS).
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- American Journal of Hematology, 2022, v. 97, n. 8, p. E292, doi. 10.1002/ajh.26598
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- Publication type:
- Article
An open‐label, multicenter, efficacy, and safety study of deferasirox in iron‐overloaded patients with non‐transfusion‐dependent thalassemia (THETIS): 5‐year results.
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- American Journal of Hematology, 2022, v. 97, n. 8, p. E281, doi. 10.1002/ajh.26592
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- Article
Revisiting the non‐transfusion‐dependent (NTDT) vs. transfusion‐dependent (TDT) thalassemia classification 10 years later.
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- American Journal of Hematology, 2021, v. 96, n. 2, p. E54, doi. 10.1002/ajh.26056
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- Article
Quality of life in patients with β‐thalassemia: A prospective study of transfusion‐dependent and non‐transfusion‐dependent patients in Greece, Italy, Lebanon, and Thailand.
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- American Journal of Hematology, 2019, v. 94, n. 10, p. E261, doi. 10.1002/ajh.25584
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- Publication type:
- Article
Validation of a patient‐reported outcomes symptom measure for patients with nontransfusion‐dependent thalassemia (NTDT‐PRO<sup>©</sup>).
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- American Journal of Hematology, 2019, v. 94, n. 2, p. 177, doi. 10.1002/ajh.25344
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- Publication type:
- Article
Development of a patient‐reported outcomes symptom measure for patients with nontransfusion‐dependent thalassemia (NTDT‐PRO<sup>©</sup>).
- Published in:
- American Journal of Hematology, 2019, v. 94, n. 2, p. 171, doi. 10.1002/ajh.25343
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- Publication type:
- Article
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.
- Published in:
- American Journal of Hematology, 2018, v. 93, n. 6, p. E135, doi. 10.1002/ajh.25075
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- Article
A prospective analysis for prevalence of complications in Thai nontransfusion‐dependent Hb E/β‐thalassemia and α‐thalassemia (Hb H disease).
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- American Journal of Hematology, 2018, v. 93, n. 5, p. 623, doi. 10.1002/ajh.25046
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- Article
Safety and pharmacokinetics of the oral iron chelator SP-420 in β-thalassemia.
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- American Journal of Hematology, 2017, v. 92, n. 12, p. 1356, doi. 10.1002/ajh.24914
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- Article
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.
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- American Journal of Hematology, 2017, v. 92, n. 3, p. E35, doi. 10.1002/ajh.24628
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- Publication type:
- Article
Deferasirox demonstrates a dose-dependent reduction in liver iron concentration and consistent efficacy across subgroups of non-transfusion-dependent thalassemia patients.
- Published in:
- American Journal of Hematology, 2013, v. 88, n. 6, p. 503, doi. 10.1002/ajh.23445
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- Publication type:
- Article
Treating iron overload in patients with non-transfusion-dependent thalassemia.
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- American Journal of Hematology, 2013, v. 88, n. 5, p. 409, doi. 10.1002/ajh.23405
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- Publication type:
- Article
Deferiprone (GPO-L-ONE<sup>®</sup>) 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
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- American Journal of Hematology, 2013, v. 88, n. 4, p. 251, doi. 10.1002/ajh.23386
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- Publication type:
- Article
Co-inheritance of Hb Pak Num Po, a novel α1 gene mutation, and α<sup>0</sup> thalassemia associated with transfusion-dependent Hb H disease.
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- American Journal of Hematology, 2004, v. 75, n. 3, p. 157, doi. 10.1002/ajh.10479
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- Publication type:
- Article
A genome-wide association identified the common genetic variants influence disease severity in β<sup>0</sup>-thalassemia/hemoglobin E.
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- Human Genetics, 2010, v. 127, n. 3, p. 303, doi. 10.1007/s00439-009-0770-2
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- Publication type:
- Article
Justification of Universal Iron Supplementation for Infants 6-12 months in Regions with a High Prevalence of Thalassemia.
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- Mediterranean Journal of Hematology & Infectious Diseases, 2023, v. 15, n. 1, p. 1, doi. 10.4084/MJHID.2023.056
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- Publication type:
- Article
Long-Term Effectiveness, Safety, and Tolerability of Twice-Daily Dosing with Deferasirox in Children with Transfusion-Dependent Thalassemias Unresponsive to Standard Once-Daily Dosing.
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- Mediterranean Journal of Hematology & Infectious Diseases, 2021, v. 13, n. 1, p. 1, doi. 10.4084/MJHID.2021.065
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- Publication type:
- Article
Health‐related quality of life in patients with β‐thalassemia: Data from the phase 3 BELIEVE trial of luspatercept.
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- European Journal of Haematology, 2023, v. 111, n. 1, p. 113, doi. 10.1111/ejh.13975
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- Article
Changing patterns in the epidemiology of β‐thalassemia.
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- European Journal of Haematology, 2020, v. 105, n. 6, p. 692, doi. 10.1111/ejh.13512
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- Publication type:
- Article
Improved R2* liver iron concentration assessment using a novel fuzzy c-mean clustering scheme.
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- BMC Medical Imaging, 2015, v. 15, p. 1, doi. 10.1186/s12880-015-0097-5
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- Article
Inhibition of H5N1 highly pathogenic influenza virus by suppressing a specific sialyltransferase.
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- Archives of Virology, 2010, v. 155, n. 6, p. 889, doi. 10.1007/s00705-010-0658-4
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- Article
Problems in determining thalassemia carrier status in a program for prevention and control of severe thalassemia syndromes: a lesson from Thailand.
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- Clinical Chemistry & Laboratory Medicine, 2013, v. 51, n. 8, p. 1605, doi. 10.1515/cclm-2013-0098
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- Publication type:
- Article
Association of Xmn I Polymorphism and Hemoglobin E Haplotypes on Postnatal Gamma Globin Gene Expression in Homozygous Hemoglobin E.
- Published in:
- Advances in Hematology, 2012, p. 1, doi. 10.1155/2012/528075
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- Article
Clinical Presentation and Molecular Identification of Four Uncommon Alpha Globin Variants in Thailand.
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- Acta Haematologica, 2014, v. 131, n. 2, p. 88, doi. 10.1159/000353119
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- Article
Baseline levels of plasma endothelin-1 (ET-1) and changes during transfusion in thalassemic patients.
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- American Journal of Hematology, 2002, v. 70, n. 3, p. 260, doi. 10.1002/ajh.10129
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- Publication type:
- Article
Common Single Nucleotide Polymorphism of TMPRSS6 , an Iron Regulation Gene, Associated with Variable Red Blood Cell Indices in Deletional α-Globin Genotypes.
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- Genes, 2022, v. 13, n. 9, p. 1502, doi. 10.3390/genes13091502
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- Article
Prevalence of left ventricular diastolic dysfunction by cardiac magnetic resonance imaging in thalassemia major patients with normal left ventricular systolic function.
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- 2019
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- Publication type:
- journal article
De novo deletion within the telomeric region flanking the human α globin locus as a cause of α thalassaemia.
- Published in:
- British Journal of Haematology, 2003, v. 120, n. 5, p. 867, doi. 10.1046/j.1365-2141.2003.04197.x
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- Article
Hb H hydrops fetalis syndrome associated with the interaction of two common determinants of α thalassaemia (--<sup>MED</sup> /α<sup>TSaudi</sup> α).
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- British Journal of Haematology, 2002, v. 117, n. 3, p. 759, doi. 10.1046/j.1365-2141.2002.03427.x
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- Publication type:
- Article
Systematic review and evidence gap assessment of the clinical, quality of life, and economic burden of alpha‐thalassemia.
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- EJHaem, 2024, v. 5, n. 3, p. 541, doi. 10.1002/jha2.882
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- Publication type:
- Article
Efficacy and safety of iron-chelation therapy with deferoxamine, deferiprone, and deferasirox for the treatment of iron-loaded patients with nontransfusion-dependent thalassemia syndromes.
- Published in:
- Drug Design, Development & Therapy, 2016, v. 10, p. 4073, doi. 10.2147/DDDT.S117080
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- Publication type:
- Article
Non-transfusion dependent hemoglobin E/β thalassemia had high prevalence of vitamin D deficiency than more severe patients who received regular blood transfusion and iron chelation therapy.
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- 2013
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- Abstract
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.
- Published in:
- European Journal of Haematology, 2016, v. 96, n. 1, p. 19, doi. 10.1111/ejh.12540
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- Publication type:
- Article
Prevalence and distribution of iron overload in patients with transfusion-dependent anemias differs across geographic regions: results from the CORDELIA study.
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- European Journal of Haematology, 2015, v. 95, n. 3, p. 244, doi. 10.1111/ejh.12487
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- Publication type:
- Article
Approaching low liver iron burden in chelated patients with non-transfusion-dependent thalassemia: the safety profile of deferasirox.
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- European Journal of Haematology, 2014, v. 92, n. 6, p. 521, doi. 10.1111/ejh.12270
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- Publication type:
- Article
Haemoglobin Hope in a northern Thai family: first identification of homozygous haemoglobin Hope associated with haemoglobin H disease.
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- European Journal of Haematology, 2007, v. 79, n. 3, p. 251, doi. 10.1111/j.1600-0609.2007.00907.x
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- Publication type:
- Article
Hb Woodville, a rare α-globin variant, caused by codon 6 mutation of the α1 gene.
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- European Journal of Haematology, 2006, v. 76, n. 1, p. 79, doi. 10.1111/j.0902-4441.2005.t01-1-EJH2334.x
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- Publication type:
- Article
Prevalence of HFE mutations among the Thai population and correlation with iron loading in haemoglobin E disorder.
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- European Journal of Haematology, 2004, v. 73, n. 1, p. 43, doi. 10.1111/j.1600-0609.2004.00246.x
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- Publication type:
- Article
Dinucleotide deletion in –α<sup>3.7</sup> allele causes a severe form of α<sup>+</sup> thalassaemia.
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- European Journal of Haematology, 2003, v. 71, n. 2, p. 133, doi. 10.1034/j.1600-0609.2003.00106.x
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- Publication type:
- Article
Complex interactions of δβ hybrid haemoglobin (Hb Lepore-Hollandia) Hb E (β<sup>26 G→A</sup> ) and α<sup>+</sup> thalassaemia in a Thai family.
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- European Journal of Haematology, 2002, v. 68, n. 2, p. 107, doi. 10.1034/j.1600-0609.2002.01637.x
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- Publication type:
- Article
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.
- Published in:
- PLoS ONE, 2014, v. 9, n. 5, p. 1, doi. 10.1371/journal.pone.0097218
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- Publication type:
- Article
Severe neonatal haemolytic anaemia caused by compound heterozygous KLF1 mutations: report of four families and literature review.
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- British Journal of Haematology, 2021, v. 194, n. 3, p. 626, doi. 10.1111/bjh.17616
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- Publication type:
- Article
Haematological effects of oral administration of bitopertin, a glycine transport inhibitor, in patients with non‐transfusion‐dependent β‐thalassaemia.
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- British Journal of Haematology, 2021, v. 194, n. 2, p. 474, doi. 10.1111/bjh.17479
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- Article
Serum ferritin in the diagnosis of cardiac and liver iron overload in thalassaemia patients real‐world practice: a multicentre study.
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- British Journal of Haematology, 2018, v. 182, n. 2, p. 301, doi. 10.1111/bjh.14776
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- Publication type:
- Article
Iron overload across the spectrum of non-transfusion-dependent thalassaemias: role of erythropoiesis, splenectomy and transfusions.
- Published in:
- British Journal of Haematology, 2017, v. 176, n. 2, p. 288, doi. 10.1111/bjh.14373
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- Publication type:
- Article
The genetic basis of asymptomatic codon 8 frame-shift ( HBB:c25_26del AA) β<sup>0</sup>-thalassaemia homozygotes.
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- British Journal of Haematology, 2016, v. 172, n. 6, p. 958, doi. 10.1111/bjh.13909
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- Publication type:
- Article
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.
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- British Journal of Haematology, 2015, v. 168, n. 2, p. 284, doi. 10.1111/bjh.13119
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- Article
Current approach to iron chelation in children.
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- British Journal of Haematology, 2014, v. 165, n. 6, p. 745, doi. 10.1111/bjh.12825
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- Article
Iron chelation therapy for children with transfusion‐dependent β‐thalassemia: How young is too young?
- Published in:
- Pediatric Blood & Cancer, 2024, v. 71, n. 8, p. 1, doi. 10.1002/pbc.31035
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- Publication type:
- Article