Found: 45
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Thalassaemia—A global view.
- Published in:
- British Journal of Haematology, 2023, v. 201, n. 2, p. 199, doi. 10.1111/bjh.18671
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- Publication type:
- Article
Magnitude of cumulative iron overload correlates with the severity of anemia in untreated non-transfusion-dependent β-thalassemia.
- Published in:
- Annals of Hematology, 2023, v. 102, n. 2, p. 467, doi. 10.1007/s00277-022-05046-9
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- Publication type:
- Article
Glucose Homeostasis and Assessment of β-Cell Function by 3-hour Oral Glucose Tolerance (OGTT) in Patients with β-Thalassemia Major with Serum Ferritin below 1,000 ng/dL: Results from a Single ICET-A Centre.
- Published in:
- Mediterranean Journal of Hematology & Infectious Diseases, 2023, v. 15, n. 1, p. 1, doi. 10.4084/MJHID.2023.006
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- Publication type:
- Article
A Multicenter ICET-A Study on Age at Menarche and Menstrual Cycles in Patients with Transfusion-Dependent Thalassemia (TDT) who Started Early Chelation Therapy with Different Chelating Agents.
- Published in:
- Mediterranean Journal of Hematology & Infectious Diseases, 2023, v. 15, n. 1, p. 1, doi. 10.4084/MJHID.2023.058
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- Publication type:
- Article
Random Forest Clustering Identifies Three Subgroups of β-Thalassemia with Distinct Clinical Severity.
- Published in:
- Thalassemia Reports, 2022, v. 12, n. 1, p. 14, doi. 10.3390/thalassrep12010004
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- Publication type:
- Article
Risk of mortality from anemia and iron overload in nontransfusion‐dependent β‐thalassemia.
- Published in:
- American Journal of Hematology, 2022, v. 97, n. 2, p. E78, doi. 10.1002/ajh.26428
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- Publication type:
- Article
Primary HBB gene mutation severity and long‐term outcomes in a global cohort of β‐thalassaemia.
- Published in:
- British Journal of Haematology, 2022, v. 196, n. 2, p. 414, doi. 10.1111/bjh.17897
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- Publication type:
- Article
Morbidity-free survival and hemoglobin level in non-transfusion-dependent β-thalassemia: a 10-year cohort study.
- Published in:
- 2022
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- Publication type:
- Letter
Cognitive Function in Adults with Beta-Thalassemia Major in Oman: A Pilot Study.
- Published in:
- Oman Medical Journal, 2021, v. 36, n. 6, p. 40, doi. 10.5001/omj.2021.101
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- Publication type:
- Article
A complication risk score to evaluate clinical severity of thalassaemia syndromes.
- Published in:
- British Journal of Haematology, 2021, v. 192, n. 3, p. 626, doi. 10.1111/bjh.17203
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- Publication type:
- Article
Abnormal diastolic function and Global longitudinal strain in patients with Thalassemia Major on long term chelation therapy.
- Published in:
- International Journal of Cardiovascular Imaging, 2021, v. 37, n. 2, p. 643, doi. 10.1007/s10554-020-02036-8
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- Publication type:
- Article
Glucose Metabolism and Insulin Response to Oral Glucose Tolerance Test (OGTT) in Prepubertal Patients with Transfusion-Dependent ß-thalassemia (TDT): A Long-Term Retrospective Analysis.
- Published in:
- Mediterranean Journal of Hematology & Infectious Diseases, 2021, v. 13, n. 1, p. 1, doi. 10.4084/MJHID.2021.051
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- Publication type:
- Article
Long-Term Follow-up of β-Transfusion-Dependent Thalassemia (TDT) Normoglycemic Patients with Reduced Insulin Secretion to Oral Glucose Tolerance Test (OGTT): A Pilot Study.
- Published in:
- Mediterranean Journal of Hematology & Infectious Diseases, 2021, v. 13, n. 1, p. 1, doi. 10.4084/mjhid.2021.051
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- Publication type:
- Article
Cardiac T2* MR in patients with thalassemia major: a 10-year long-term follow-up.
- Published in:
- 2020
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- Publication type:
- journal article
Evaluation of endocrine complications in beta-thalassemia intermedia (β-TI): a cross-sectional multicenter study.
- Published in:
- Endocrine (1355008X), 2020, v. 69, n. 1, p. 220, doi. 10.1007/s12020-019-02159-6
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- Publication type:
- Article
A Concise Review on the Frequency, Major Risk Factors and Surveillance of Hepatocellular Carcinoma (HCC) in β-Thalassemias: Past, Present and Future Perspectives and the ICET-A Experience.
- Published in:
- Mediterranean Journal of Hematology & Infectious Diseases, 2020, v. 12, n. 1, p. 1, doi. 10.4084/MJHID.2020.006
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- Publication type:
- Article
Risks of red blood cell alloimmunization in transfusion-dependent β-thalassemia in Oman: a 25-year experience of a university tertiary care reference center and a literature review.
- Published in:
- 2018
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- Publication type:
- journal article
Transfusion in Haemoglobinopathies: Review and recommendations for local blood banks and transfusion services in Oman.
- Published in:
- Sultan Qaboos University Medical Journal, 2018, v. 18, n. 1, p. 3, doi. 10.18295/squmj.2018.18.01.002
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- Publication type:
- Article
Understanding Iron Metabolism: Lessons from Transfusion-dependent Thalassemia.
- Published in:
- Oman Medical Journal, 2018, v. 33, n. 1, p. 1, doi. 10.5001/omj.2018.01
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- Publication type:
- Article
Does Testosterone Replacement Therapy Promote an Augmented Risk of Thrombotic Events in Thalassemia Major Male Patients with Hypogonadism?
- Published in:
- Indian Journal of Endocrinology & Metabolism, 2017, v. 21, n. 4, p. 636, doi. 10.4103/ijem.IJEM_73_17
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- Publication type:
- 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.
- Published in:
- American Journal of Hematology, 2017, v. 92, n. 3, p. E35, doi. 10.1002/ajh.24628
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- Publication type:
- Article
First Implementation of Transfusion Consent Policy in Oman.
- Published in:
- Sultan Qaboos University Medical Journal, 2016, v. 16, n. 3, p. e293, doi. 10.18295/SQUMJ.2016.16.03.005
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- Publication type:
- Article
Transfusion Consent in Oman: Physicians' Perception at a Tertiary Care University Hospital.
- Published in:
- Oman Medical Journal, 2016, v. 31, n. 4, p. 253, doi. 10.5001/omj.2016.50
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- Publication type:
- Article
Single Breath-Hold Physiotherapy Technique.
- Published in:
- Sultan Qaboos University Medical Journal, 2016, v. 16, n. 1, p. e78, doi. 10.18295/SQUMJ.2016.16.01.014
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- Publication type:
- Article
Aetiological profile of women presenting with premature ovarian failure to a single tertiary care center in Oman.
- Published in:
- Post Reproductive Health, 2015, v. 21, n. 2, p. 63, doi. 10.1177/2053369115587419
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- Publication type:
- Article
Multicenter validation of spin-density projection-assisted R2-MRI for the noninvasive measurement of liver iron concentration.
- Published in:
- Magnetic Resonance in Medicine, 2014, v. 71, n. 6, p. 2215, doi. 10.1002/mrm.24854
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- Publication type:
- Article
A stepwise α-thalassemia screening strategy in high-prevalence areas.
- Published in:
- European Journal of Haematology, 2013, v. 91, n. 2, p. 164, doi. 10.1111/ejh.12136
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- Publication type:
- Article
First reported case of compound heterozygosity for HbA-Yialousa (HBD: c.82 G>C) and HbA-Wrens (HBD: c.295 G>A) in Oman.
- Published in:
- 2013
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- Publication type:
- Report
First reported case of compound heterozygosity for HbA2-Yialousa (HBD: c.82 G>C) and HbA2-Wrens (HBD: c.295 G>A) in Oman.
- Published in:
- 2013
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- Publication type:
- journal article
Side effects of Deferasirox Iron Chelation in Patients with Beta Thalassemia Major or Intermedia.
- Published in:
- Oman Medical Journal, 2013, v. 28, n. 2, p. 121, doi. 10.5001/omj.2013.31
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- Publication type:
- Article
Side effects of Deferasirox Iron Chelation in Patients with Beta Thalassemia Major or Intermedia.
- Published in:
- 2013
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- Publication type:
- Journal Article
Deferasirox and renal dysfunction in children.
- Published in:
- 2012
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- Publication type:
- Letter
The β-globin promoter −71 C>T mutation is a β+ thalassemic allele.
- Published in:
- European Journal of Haematology, 2011, v. 87, n. 5, p. 457, doi. 10.1111/j.1600-0609.2011.01687.x
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- Publication type:
- Article
Achieving treatment goals of reducing or maintaining body iron burden with deferasirox in patients with β-thalassaemia: results from the ESCALATOR study.
- Published in:
- European Journal of Haematology, 2011, v. 87, n. 4, p. 349, doi. 10.1111/j.1600-0609.2011.01661.x
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- Publication type:
- Article
Importance of optimal dosing ≥30 mg/kg/d during deferasirox treatment: 2.7-yr follow-up from the ESCALATOR study in patients with β-thalassaemia.
- Published in:
- European Journal of Haematology, 2011, v. 87, n. 4, p. 355, doi. 10.1111/j.1600-0609.2011.01662.x
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- Publication type:
- Article
Severity ranking of non-deletional alpha thalassemic alleles: insights from an Omani family study.
- Published in:
- European Journal of Haematology, 2011, v. 86, n. 6, p. 507, doi. 10.1111/j.1600-0609.2011.01606.x
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- Publication type:
- Article
Age-related complications in treatment-naïve patients with thalassaemia intermedia.
- Published in:
- 2010
- By:
- Publication type:
- Letter
Improved Treatment Satisfaction and Convenience with Deferasirox in Iron-Overloaded Patients with β-Thalassemia: Results from the ESCALATOR Trial.
- Published in:
- Acta Haematologica, 2010, v. 123, n. 4, p. 220, doi. 10.1159/000313447
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- Publication type:
- Article
Deferasirox (Exjade) significantly improves cardiac T2* in heavily iron-overloaded patients with beta-thalassemia major.
- Published in:
- 2010
- By:
- Publication type:
- journal article
Reduction in labile plasma iron during treatment with deferasirox, a once-daily oral iron chelator, in heavily iron-overloaded patients with β-thalassaemia.
- Published in:
- European Journal of Haematology, 2009, v. 82, n. 6, p. 454, doi. 10.1111/j.1600-0609.2008.01204.x
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- Publication type:
- Article
Efficacy and safety of deferasirox, an oral iron chelator, in heavily iron-overloaded patients with β-thalassaemia: the ESCALATOR study.
- Published in:
- European Journal of Haematology, 2009, v. 82, n. 6, p. 458, doi. 10.1111/j.1600-0609.2009.01228.x
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- Publication type:
- Article
Haematological and clinical features of β-thalassaemia associated with Hb Dhofar.
- Published in:
- European Journal of Haematology, 2008, v. 80, n. 1, p. 67, doi. 10.1111/j.1600-0609.2007.00989.x
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- Publication type:
- Article
Cytokine profile of sickle cell disease in Oman.
- Published in:
- American Journal of Hematology, 2004, v. 77, n. 4, p. 323, doi. 10.1002/ajh.20196
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- Publication type:
- Article
Genetic epidemiology of HbS in Oman: Multicentric origin for the β<sup>S</sup> gene.
- Published in:
- American Journal of Hematology, 2000, v. 64, n. 1, p. 39, doi. 10.1002/(SICI)1096-8652(200005)64:1<39::AID-AJH7>3.0.CO;2-#
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- Publication type:
- Article
Molecular Characterization of G6PD Deficiency in Oman.
- Published in:
- Human Heredity, 1996, v. 46, n. 3, p. 172, doi. 10.1159/000154348
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- Publication type:
- Article