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Global Globin Network Consensus Paper: Classification and Stratified Roadmaps for Improved Thalassaemia Care and Prevention in 32 Countries.
- Published in:
- Journal of Personalized Medicine, 2022, v. 12, n. 4, p. 552, doi. 10.3390/jpm12040552
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- Publication type:
- Article
Geographical variations in current clinical practice on transfusions and iron chelation therapy across various transfusion-dependent anaemias.
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- Blood Transfusion (17232007), 2013, v. 11, n. 1, p. 108, doi. 10.2450/2012.0012-12
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- Publication type:
- Article
The origin of sickle cell disease in Thailand.
- Published in:
- 2019
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- Publication type:
- Letter to the Editor
Clinical efficacy and safety evaluation of tailoring iron chelation practice in thalassaemia patients from Asia-Pacific: a subanalysis of the EPIC study of deferasirox.
- Published in:
- 2011
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- Publication type:
- journal article
Iron chelation therapy in the management of thalassemia: the Asian perspectives.
- Published in:
- 2009
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- Publication type:
- journal article
Identification and key management of nontransfusion- dependent thalassaemia patients: not a rare but potentially under-recognised condition.
- Published in:
- Orphanet Journal of Rare Diseases, 2014, v. 9, n. 1, p. 2, doi. 10.1186/s13023-014-0131-7
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- Publication type:
- Article
Identification and key management of non-transfusion-dependent thalassaemia patients: not a rare but potentially under-recognised condition.
- Published in:
- 2014
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- Publication type:
- journal article
Prevalence of left ventricular diastolic dysfunction by cardiac magnetic resonance imaging in thalassemia major patients with normal left ventricular systolic function.
- Published in:
- 2019
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- Publication type:
- journal article
Using of deferasirox and deferoxamine in refractory iron overload thalassemia.
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- Pediatrics International, 2021, v. 63, n. 4, p. 404, doi. 10.1111/ped.14444
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- Publication type:
- Article
Hemophagocytic lymphohistiocytosis following dengue hemorrhagic fever in Hb H/ Hb Constant Spring patient.
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- Pediatrics International, 2015, v. 57, n. 4, p. 763, doi. 10.1111/ped.12617
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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
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
Validation of a reverse-hybridization StripAssay for the simultaneous analysis of common α-thalassemia point mutations and deletions.
- Published in:
- Clinical Chemistry & Laboratory Medicine, 2007, v. 45, n. 5, p. 605, doi. 10.1515/CCLM.2007.125
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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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- Publication type:
- 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.
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- 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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- Publication type:
- 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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- Publication type:
- Article
Disease burden, management strategies, and unmet needs in α‐thalassemia due to hemoglobin H disease.
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- American Journal of Hematology, 2024, v. 99, n. 11, p. 2164, doi. 10.1002/ajh.27440
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- Publication type:
- Article
Early‐onset reduced bone mineral density in patients with pyruvate kinase deficiency.
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- 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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- Publication type:
- 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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- 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.
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- PLoS ONE, 2014, v. 9, n. 5, p. 1, doi. 10.1371/journal.pone.0097218
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- Publication type:
- Article
Patient preference for deferasirox film-coated versus dispersible tablet formulation: a sequential-design phase 2 study in patients with thalassemia.
- Published in:
- Annals of Hematology, 2023, v. 102, n. 8, p. 2039, doi. 10.1007/s00277-023-05240-3
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- Publication type:
- Article
Deferasirox effectively reduces iron overload in non-transfusion-dependent thalassemia (NTDT) patients: 1-year extension results from the THALASSA study.
- Published in:
- Annals of Hematology, 2013, v. 92, n. 11, p. 1485, doi. 10.1007/s00277-013-1808-z
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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
Immune-mediated hemolytic anemia in pediatric renal transplantation.
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- Pediatric Transplantation, 2006, v. 10, n. 6, p. 740, doi. 10.1111/j.1399-3046.2006.00560.x
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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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- Publication type:
- 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
Diagnostic applications of newborn screening for [alpha]-thalassaemias, haemoglobins E and H disorders using isoelectric focusing on dry blood spots.
- Published in:
- 2014
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- Publication type:
- Journal Article
Diagnostic applications of newborn screening for α-thalassaemias, haemoglobins E and H disorders using isoelectric focusing on dry blood spots.
- Published in:
- Annals of Clinical Biochemistry, 2014, v. 51, n. 2, p. 237, doi. 10.1177/0004563213491078
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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.
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- Advances in Hematology, 2012, p. 1, doi. 10.1155/2012/528075
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- Publication type:
- Article
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.
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- 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.
- Published in:
- 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
Genetic association study of tumor necrosis factor-alpha with sepsis and septic shock in Thai pediatric patients.
- Published in:
- Jornal de Pediatria, 2012, v. 88, n. 5, p. 417, doi. 10.2223/JPED.2216
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- Publication type:
- Article
Identification of optimal thalassemia screening strategies for migrant populations in Thailand using a qualitative approach.
- Published in:
- BMC Public Health, 2021, v. 21, n. 1, p. 1, doi. 10.1186/s12889-021-11831-4
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- Publication type:
- Article
Identification of optimal thalassemia screening strategies for migrant populations in Thailand using a qualitative approach.
- Published in:
- 2021
- By:
- Publication type:
- journal article
Feasibility of and barriers to thalassemia screening in migrant populations: a cross-sectional study of Myanmar and Cambodian migrants in Thailand.
- Published in:
- 2021
- By:
- Publication type:
- journal article
Recent advances in molecular understanding of NTDT: 2012.
- Published in:
- Thalassemia Reports, 2013, v. 3, n. 1s, p. 43, doi. 10.4081/thal.2013.s1.e13
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- Publication type:
- Article
Clinical features and molecular analysis in Thai patients with HbH disease.
- Published in:
- Annals of Hematology, 2009, v. 88, n. 12, p. 1185, doi. 10.1007/s00277-009-0743-5
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- Publication type:
- Article