Works matching DE "THALASSEMIA treatment"
Results: 245
Emodin can induce K562 cells to erythroid differentiation and improve the expression of globin genes.
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- Molecular & Cellular Biochemistry, 2013, v. 382, n. 1/2, p. 127, doi. 10.1007/s11010-013-1726-3
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- Article
Cecal Perforation in a Child with Cooley's Anemia.
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- World Journal of Colorectal Surgery, 2023, v. 12, n. 1, p. 22, doi. 10.4103/wjcs.wjcs_9_23
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- Article
Development of a new real-time PCR screening kit for HbS and common beta-thalassemia mutations observed in Turkey.
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- Turkish Journal of Medical Sciences, 2017, v. 47, n. 3, p. 973, doi. 10.3906/sag-1606-49
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- Article
A Cross-Sectional, Multicentric, Disease-Specific, Health-Related Quality of Life Study in Greek Transfusion Dependent Thalassemia Patients.
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- Healthcare (2227-9032), 2024, v. 12, n. 5, p. 524, doi. 10.3390/healthcare12050524
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- Article
Study of Alloimmunization in Transfusion‑dependent Thalassemia Patients at a Tertiary Care Hospital.
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- Journal of Applied Hematology, 2024, v. 15, n. 2, p. 121, doi. 10.4103/joah.joah_26_24
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- Article
Patient activation measure among transfusion-Dependent patients with hemoglobinopathies.
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- Journal of Applied Hematology, 2022, v. 13, n. 4, p. 263, doi. 10.4103/joah.joah_12_22
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- Article
Clinical Management of Patients With Thalassemia Syndromes.
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- Clinical Journal of Oncology Nursing, 2016, v. 20, n. 3, p. 310, doi. 10.1188/16.CJON.310-317
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- Article
Non-Transfusion-Dependent Thalassemia: A Complex Mix of Genetic Entities Yet to Be Fully Discovered.
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- BioMed Research International, 2015, v. 2015, p. 1, doi. 10.1155/2015/161434
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- Article
Efficacy of Deferasirox for the treatment of iron overload in Chinese thalassaemia major patients: results from a prospective, open-label, multicentre clinical trial.
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- Transfusion Medicine, 2013, v. 23, n. 6, p. 389, doi. 10.1111/tme.12077
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- Article
Gene therapy breakthrough for β-thalassemia.
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- BioEssays, 2010, v. 32, n. 10, p. A1
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- Article
Summaries for patients. Reversibility of liver scarring in patients who are cured of thalassemia.
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- 2002
- Publication type:
- journal article
Reversibility of cirrhosis in patients cured of thalassemia by bone marrow transplantation.
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- 2002
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- Publication type:
- journal article
Psychosocial Disorders in Childhood, Adolescence and Young Adult Life of Patients with Thalassaemia.
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- Nosileftiki, 2016, v. 55, n. 2, p. 132
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- Publication type:
- Article
A family empowerment program for families having children with thalassemia, Thailand.
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- 2015
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- Publication type:
- Journal Article
DEMOGRAPHIC DATA OF THALASSEMIA PATIENTS.
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- Erciyes Medical Journal / Erciyes Tip Dergisi, 2018, v. 40, n. 1, p. S17
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- Publication type:
- Article
Chorionic Villus Sampling Complications in Prenatal Diagnosis of Thalassemia Major.
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- Iranian Journal of Radiology, 2010, v. 7, n. 2, p. 101
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- Publication type:
- Article
Thalassemia major. A report of two cases with severe skeletal involvement.
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- Acta Chirurgica Iugoslavica, 2010, v. 57, n. 2, p. 99, doi. 10.2298/ACI1002099L
- Publication type:
- Article
Thalassemia: The Facts and the Controversies.
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- Pediatric Nursing, 2003, v. 29, n. 6, p. 447
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- Article
Predictors of Red Cell Alloimmunization in Multitransfused Egyptian Patients With β-Thalassemia.
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- Archives of Pathology & Laboratory Medicine, 2014, v. 138, n. 5, p. 684, doi. 10.5858/arpa.2013-0016-OA
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- Article
Non-transfusion Dependent Thalassemias: A Developing Country Perspective.
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- Current Pediatric Reviews, 2015, v. 11, n. 2, p. 87
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- Publication type:
- Article
Necrotizing Arteritis Due to Emerging Pythium insidiosum Infection in Patients With Thalassemia: Rapid Diagnosis with PCR and Serological Tests — Case Reports.
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- International Journal of Angiology (Springer Science & Business Media B.V.), 2005, v. 14, n. 3, p. 123, doi. 10.1007/s00547-005-2012-3
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- Publication type:
- Article
What are the occupational implications of thalassaemia?
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- Occupational Medicine, 1999, v. 49, n. 2, p. 117, doi. 10.1093/occmed/49.2.117
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- Publication type:
- Article
Seroprevalence and geographical distribution of hepatitis C virus in Iranian patients with thalassemia: a systematic review and meta-analysis.
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- Journal of Laboratory Medicine, 2019, v. 43, n. 2, p. 45, doi. 10.1515/labmed-2018-0150
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- Publication type:
- Article
STUDY ON ALTERS IN SOME HEMATOLOGICAL AND BIOCHEMICAL BIOMARKERS IN THALASSEMIA PATIENTS IN DIAYLA GOVERNORATE, IRAQ.
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- Biochemical & Cellular Archives, 2021, v. 21, n. 1, p. 599
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- Publication type:
- Article
MOLECULAR DETECTION OF HEPATITIS C VIRUS BY NESTED PCR FROM THE THALASSEMIC PATIENTS IN AL-AMARA PROVINCE IN IRAQ.
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- Biochemical & Cellular Archives, 2020, v. 20, n. 2, p. 6289
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- Publication type:
- Article
EVALUATION OF SOME ELECTROLYTE IN IRAQI PATIENTS WITH MAJOR THALASSEMIA IN BAGHDAD CITY.
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- Biochemical & Cellular Archives, 2018, v. 18, n. 1, p. 803
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- Article
Issue Information.
- Published in:
- 2018
- Publication type:
- Cover Art
Population pharmacokinetics and dosing recommendations for the use of deferiprone in children younger than 6 years.
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- British Journal of Clinical Pharmacology, 2017, v. 83, n. 3, p. 593, doi. 10.1111/bcp.13134
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- Publication type:
- Article
Iron chelation therapy in transfusion-dependent thalassemia patients: current strategies and future directions.
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- Journal of Blood Medicine, 2015, v. 6, p. 197, doi. 10.2147/JBM.S72463
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- Publication type:
- Article
Treating thalassemia major-related iron overload: the role of deferiprone.
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- Journal of Blood Medicine, 2012, v. 3, p. 119, doi. 10.2147/JBM.S27400
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- Publication type:
- Article
Detection of β-Thalassemia Carriers by Red Cell Parameters Obtained from Automatic Counters using Mathematical Formulas.
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- Mediterranean Journal of Hematology & Infectious Diseases, 2018, v. 10, n. 1, p. 1, doi. 10.4084/MJHID.2018.008
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- Publication type:
- Article
An Observational Study of the Effect of Hemoglobinopathy, Alpha Thalassemia and Hemoglobin E on P. Vivax Parasitemia.
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- Mediterranean Journal of Hematology & Infectious Diseases, 2018, v. 10, n. 1, p. 1, doi. 10.4084/MJHID.2018.015
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- Publication type:
- Article
Modulating Effect of the -158 <sup>G</sup>γ (C→T) Xmn1 Polymorphism in Indian Sickle Cell Patients.
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- Mediterranean Journal of Hematology & Infectious Diseases, 2012, v. 4, n. 1, p. 1, doi. 10.4084/MJHID.2012.001
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- Publication type:
- Article
Plasma microRNA-451 as a novel hemolytic marker for β<sup>0</sup>-thalassemia/HbE disease.
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- Molecular Medicine Reports, 2017, v. 15, n. 5, p. 2495, doi. 10.3892/mmr.2017.6326
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- Publication type:
- Article
Bronze Diabetes.
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- 2015
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- Publication type:
- Case Study
Understanding Iron Metabolism: Lessons from Transfusion-dependent Thalassemia.
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- Oman Medical Journal, 2018, v. 33, n. 1, p. 1, doi. 10.5001/omj.2018.01
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- Publication type:
- Article
Alpha Thalassemia and General Anesthesia.
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- 2009
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- Publication type:
- Case Study
Management of Transfusion-Dependent Thalassaemia Patients in Emergency Situations.
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- 2022
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- Publication type:
- Letter
Initial Dosage Optimization of Tacrolimus in Pediatric Patients With Thalassemia Major Undergoing Hematopoietic Stem Cell Transplantation Based on Population Pharmacokinetics.
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- Annals of Pharmacotherapy, 2021, v. 55, n. 4, p. 440, doi. 10.1177/1060028020959039
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- Article
SINUS OBLITERATION IN DWARFISM.
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- Acta Endocrinologica (1841-0987), 2005, v. 1, n. 4, p. 489, doi. 10.4183/aeb.2005.489
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- Publication type:
- Article
Intrathoracic extramedullary hematopoiesis related spontaneous hemothorax.
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- QJM: An International Journal of Medicine, 2015, v. 108, n. 12, p. 989, doi. 10.1093/qjmed/hcv143
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- Publication type:
- Article
Haploidentical haematopoietic stem cell transplantation for thalassaemia major based on an FBCA conditioning regimen.
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- British Journal of Haematology, 2018, v. 182, n. 4, p. 554, doi. 10.1111/bjh.15438
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- Publication type:
- Article
The new era of chelation treatments: effectiveness and safety of 10 different regimens for controlling iron overloading in thalassaemia major.
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- British Journal of Haematology, 2017, v. 178, n. 5, p. 676, doi. 10.1111/bjh.14712
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- Publication type:
- Article
Increased iron stores prolong the QT interval - a general population study including 20 261 individuals and meta-analysis of thalassaemia major.
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- British Journal of Haematology, 2016, v. 174, n. 5, p. 776, doi. 10.1111/bjh.14099
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- Publication type:
- Article
HbA<sub>2</sub>: biology, clinical relevance and a possible target for ameliorating sickle cell disease.
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- British Journal of Haematology, 2015, v. 170, n. 6, p. 781, doi. 10.1111/bjh.13570
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- Publication type:
- Article
Hematopoietic stem cell gene therapy with drug resistance genes: an update.
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- Cancer Gene Therapy, 2005, v. 12, n. 11, p. 849, doi. 10.1038/sj.cgt.7700866
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- Publication type:
- Article
Haemoglobin disorders.
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- Eastern Mediterranean Health Journal, 2011, v. 17, n. 9, p. 713
- Publication type:
- Article
Outcome and management of pregnancy in women with thalassaemia in Cyprus.
- Published in:
- 2008
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- Publication type:
- Journal Article
The experience of thalassemic adults with their treatment.
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- Revista Latino-Americana de Enfermagem (RLAE), 2011, v. 19, n. 4, p. 968, doi. 10.1590/S0104-11692011000400016
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- Publication type:
- Article
Cost Structure and Clinical Outcome of a Stem Cell Transplantation Program in a Developing Country: The Experience in Northeast Mexico.
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- Oncologist, 2015, v. 20, n. 4, p. 386, doi. 10.1634/theoncologist.2014-0218
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- Publication type:
- Article