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Progression of liver fibrosis can be controlled by adequate chelation in transfusion-dependent thalassemia (TDT).
- Published in:
- 2017
- By:
- Publication type:
- journal article
Transcranial color Doppler in stroke-free adult patients with sickle cell disease.
- Published in:
- 2017
- By:
- Publication type:
- journal article
Bone quality in beta-thalassemia intermedia: relationships with bone quantity and endocrine and hematologic variables.
- Published in:
- 2017
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- Publication type:
- journal article
Spine Bone Texture Assessed by Trabecular Bone Score (TBS) to Evaluate Bone Health in Thalassemia Major.
- Published in:
- Calcified Tissue International, 2014, v. 95, n. 6, p. 540, doi. 10.1007/s00223-014-9919-7
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- Publication type:
- Article
Co-existence of two functional mutations on the same allele of the human ferrochelatase gene in erythropoietic protoporphyria.
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- Clinical Genetics, 2007, v. 71, n. 1, p. 84, doi. 10.1111/j.1399-0004.2007.00733.x
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- Publication type:
- Article
Laboratory diagnosis of thalassemia.
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- International Journal of Laboratory Hematology, 2016, v. 38, p. 32, doi. 10.1111/ijlh.12527
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- Publication type:
- Article
Nontransferrin-bound iron in transfused patients with sickle cell disease.
- Published in:
- International Journal of Laboratory Hematology, 2011, v. 33, n. 2, p. 133, doi. 10.1111/j.1751-553X.2010.01224.x
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- Publication type:
- Article
Effect of hydroxyurea on extramedullary haematopoiesis in thalassaemia intermedia: case reports and literature review.
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- International Journal of Laboratory Hematology, 2008, v. 30, n. 5, p. 425, doi. 10.1111/j.1751-553X.2007.00965.x
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- Publication type:
- Article
Iron overload and toxicity: the hidden risk of multiple blood transfusions.
- Published in:
- Vox Sanguinis, 2009, v. 97, n. 3, p. 185, doi. 10.1111/j.1423-0410.2009.01207.x
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- Publication type:
- Article
Redefining thalassemia as a hypercoagulable state.
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- Annals of the New York Academy of Sciences, 2010, v. 1202, n. 1, p. 231, doi. 10.1111/j.1749-6632.2010.05548.x
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- Publication type:
- Article
Cardiopulmonary testing in adult patients with β-thalassemia major in comparison to healthy subjects.
- Published in:
- 2022
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- Publication type:
- journal article
Pregnancy in patients with thalassemia major: a cohort study and conclusions for an adequate care management approach.
- Published in:
- 2017
- By:
- Publication type:
- journal article
A 5-year follow-up in deferasirox treatment: improvement of cardiac and hepatic iron overload and amelioration in cardiac function in thalassemia major patients.
- Published in:
- Annals of Hematology, 2015, v. 94, n. 6, p. 939, doi. 10.1007/s00277-014-2291-x
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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
Survival and Complications in Thalassemia.
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- Annals of the New York Academy of Sciences, 2005, v. 1054, n. 1, p. 40, doi. 10.1196/annals.1345.006
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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
Cholelithiasis in thalassemia major.
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- European Journal of Haematology, 2009, v. 82, n. 1, p. 22, doi. 10.1111/j.1600-0609.2008.01162.x
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- Publication type:
- Article
Iron deficiency anaemia revisited.
- Published in:
- 2020
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- Publication type:
- journal article
Effect of estrogens and progesterone on human peripheral erythroid burst-forming unit (BFU-E) growth.
- Published in:
- American Journal of Hematology, 1991, v. 38, n. 2, p. 81, doi. 10.1002/ajh.2830380202
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- Publication type:
- Article
The autophagy-activating kinase ULK1 mediates clearance of free α-globin in β-thalassemia.
- Published in:
- Science Translational Medicine, 2019, v. 11, n. 506, p. 1, doi. 10.1126/scitranslmed.aav4881
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- Publication type:
- Article
Management of non-neuronopathic Gaucher disease with special reference to pregnancy, splenectomy, bisphosphonate therapy, use of biomarkers and bone disease monitoring.
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- Journal of Inherited Metabolic Disease, 2008, v. 31, n. 3, p. 319, doi. 10.1007/s10545-008-0779-z
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- Publication type:
- Article
Pro-oxidant and antioxidant factors in acute intermittent porphyria: Family studies.
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- Journal of Inherited Metabolic Disease, 2004, v. 27, n. 2, p. 251, doi. 10.1023/B:BOLI.0000028795.84156.da
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- Publication type:
- Article
Red blood cell antioxidant and iron status in alcoholic and nonalcoholic cirrhosis.
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- European Journal of Clinical Investigation, 2002, v. 32, p. 21, doi. 10.1046/j.1365-2362.2002.0320s1021.x
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- Publication type:
- Article
Oxidative status and malondialdehyde in β-thalassaemia patients.
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- European Journal of Clinical Investigation, 2002, v. 32, p. 55, doi. 10.1046/j.1365-2362.2002.0320s1055.x
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- Publication type:
- Article
P426 Left atrial size and function assessment through CMR in thalassemia major patients.
- Published in:
- European Heart Journal - Cardiovascular Imaging, 2019, v. 20, p. N.PAG, doi. 10.1093/ehjci/jez118.014
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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
Hematologic malignancies in thalassemia: Adding new cases to the repertoire.
- Published in:
- American Journal of Hematology, 2017, v. 92, n. 5, p. E68, doi. 10.1002/ajh.24681
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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
Alternative splicing of human G6PD messenger RNA in K562 cells but not in cultured erythroblasts.
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- European Journal of Clinical Investigation, 1993, v. 23, n. 3, p. 188, doi. 10.1111/j.1365-2362.1993.tb00760.x
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- Publication type:
- Article
Venous thromboembolism and hypercoagulability in splenectomized patients with thalassaemia intermedia.
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- British Journal of Haematology, 2000, v. 111, n. 2, p. 467, doi. 10.1046/j.1365-2141.2000.02376.x
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- Publication type:
- Article
Deferasirox (Exjade®) for the Treatment of Iron Overload.
- Published in:
- Acta Haematologica, 2009, v. 122, n. 2/3, p. 165, doi. 10.1159/000243801
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- Publication type:
- Article
Lung Function in β-Thalassemia Patients: A Longitudinal Study.
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- Acta Haematologica, 2006, v. 116, n. 1, p. 25, doi. 10.1159/000092344
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- Publication type:
- Article
Comparison of the effects of β<sub>3</sub>-adrenoceptor agonism on urinary bladder function in conscious, anesthetized, and spinal cord injured rats.
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- Neurourology & Urodynamics, 2015, v. 34, n. 6, p. 578, doi. 10.1002/nau.22629
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- Publication type:
- Article
Beta-thalassaemia intermedia: evaluation of endocrine and bone complications.
- Published in:
- 2014
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- Publication type:
- Journal Article
Beta-Thalassaemia Intermedia: Evaluation of Endocrine and Bone Complications.
- Published in:
- BioMed Research International, 2014, v. 2014, p. 1, doi. 10.1155/2014/174581
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- Publication type:
- Article
Ribavirin suppresses erythroid differentiation and proliferation in chronic hepatitis C patients.
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- Journal of Viral Hepatitis, 2014, v. 21, n. 6, p. 416, doi. 10.1111/jvh.12158
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- Publication type:
- Article
Glucose 6-phosphate dehydrogenase deficiency and red cell membrane defects: additive or synergistic interaction in producing chronic haemolytic anaemia.
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- British Journal of Haematology, 1994, v. 87, n. 1, p. 148, doi. 10.1111/j.1365-2141.1994.tb04885.x
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- Publication type:
- Article
HEREDITARY SPHEROCYTOSIS CHARACTERIZED BY INCREASED SPECTRIN/BAND 3 RATIO.
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- British Journal of Haematology, 1992, v. 80, n. 1, p. 133, doi. 10.1111/j.1365-2141.1992.tb06417.x
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- Publication type:
- Article
Alpha thalassaemia in an Italian population.
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- British Journal of Haematology, 1986, v. 63, n. 3, p. 497, doi. 10.1111/j.1365-2141.1986.tb07526.x
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- Publication type:
- Article
Feasibility of prenatal diagnosis of β thalassaemia by DNA polymorphisms in an Italian population.
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- British Journal of Haematology, 1986, v. 62, n. 3, p. 495, doi. 10.1111/j.1365-2141.1986.tb02961.x
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- Publication type:
- Article
Long-term haemopoiesis in human fetal liver cell cultures.
- Published in:
- British Journal of Haematology, 1984, v. 57, n. 1, p. 61, doi. 10.1111/j.1365-2141.1984.tb02865.x
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- Publication type:
- Article
THE TRIPLICATED ALPHA-GENE LOCUS AND HETEROZYGOUS BETA THALASSAEMIA: A CASE OF THALASSAEMIA INTERMEDIA.
- Published in:
- British Journal of Haematology, 1983, v. 55, n. 4, p. 709, doi. 10.1111/j.1365-2141.1983.tb02854.x
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- Publication type:
- Article
IMPROVED CULTURE OF BFU-E AND CFC-GM BY THE USE OF AN OIL SEAL.
- Published in:
- British Journal of Haematology, 1983, v. 54, n. 1, p. 153, doi. 10.1111/j.1365-2141.1983.00153.x
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- Publication type:
- Article
Interaction between Homozygous β<sup>0</sup> Thalassaemia and the Swiss Type of Hereditary Persistence of Fetal Haemoglobin.
- Published in:
- British Journal of Haematology, 1981, v. 48, n. 4, p. 561, doi. 10.1111/j.1365-2141.1981.tb02753.x
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- Publication type:
- Article