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The Psychosocial Burden of Cooley's Anemia in Affected Children and Their Parents.
- Published in:
- Annals of the New York Academy of Sciences, 1998, v. 850, n. 1, p. 512, doi. 10.1111/j.1749-6632.1998.tb10536.x
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- Article
Elimination of Transfusions Through Induction of Fetal Hemoglobin Synthesis in Cooley's Anemia<sup>a</sup>.
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- Annals of the New York Academy of Sciences, 1998, v. 850, n. 1, p. 100, doi. 10.1111/j.1749-6632.1998.tb10467.x
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- Article
Increase in Hemoglobin Concentration during Therapy with Hydroxyurea in Cooley's Anemia.
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- Annals of the New York Academy of Sciences, 1998, v. 850, n. 1, p. 459, doi. 10.1111/j.1749-6632.1998.tb10520.x
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- Article
Long-Term Trials of Deferiprone in Cooley's Anemia<sup>a</sup>.
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- Annals of the New York Academy of Sciences, 1998, v. 850, n. 1, p. 217, doi. 10.1111/j.1749-6632.1998.tb10477.x
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- Article
Hemoglobin H-constant spring in North America: An alpha thalassemia with frequent complications.
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- American Journal of Hematology, 2009, v. 84, n. 11, p. 759, doi. 10.1002/ajh.21523
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- Article
Adherence to deferoxamine therapy: Heeding Hippocrates and Osler.
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- American Journal of Hematology, 2004, v. 76, n. 4, p. 415, doi. 10.1002/ajh.20102
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- Article
Urinary iron excretion depends on the mode of administration of the oral iron chelator 1,2-dimethyl-3-hydroxypyrid-4-one in patients with homozygous β-thalassemia.
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- Clinical Pharmacology & Therapeutics, 1994, v. 55, n. 1, p. 70, doi. 10.1038/clpt.1994.12
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- Article
Emerging insights in the management of hemoglobin E beta thalassemia.
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- Annals of the New York Academy of Sciences, 2010, v. 1202, n. 1, p. 155, doi. 10.1111/j.1749-6632.2010.05579.x
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- Article
Methods for Noninvasive Measurement of Tissue Iron in Cooley's Anemia.
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- Annals of the New York Academy of Sciences, 2005, v. 1054, n. 1, p. 358, doi. 10.1196/annals.1345.044
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- Article
Single and Combination Drug Therapy for Fetal Hemoglobin Augmentation in Hemoglobin E-β<sup>o</sup>-Thalassemia: Considerations for Treatment.
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- Annals of the New York Academy of Sciences, 2005, v. 1054, n. 1, p. 250, doi. 10.1196/annals.1345.031
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- Article
Hemoglobin E-β-Thalassemia: Progress Report from the International Study Group.
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- Annals of the New York Academy of Sciences, 2005, v. 1054, n. 1, p. 33, doi. 10.1196/annals.1345.005
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- Article
Patients' Health or Company Profits? The Commercialisation of Academic Research.
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- Science & Engineering Ethics, 2003, v. 9, n. 1, p. 29, doi. 10.1007/s11948-003-0017-x
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- Article
Long-Term Therapy with Deferiprone.
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- Acta Haematologica, 1996, v. 95, n. 1, p. 37, doi. 10.1159/000203854
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- Article
Hemoglobin H (Hb H) disease in Canada: Molecular diagnosis and review of 116 cases.
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- American Journal of Hematology, 2001, v. 68, n. 1, p. 11, doi. 10.1002/ajh.1142
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- Publication type:
- Article
Severity of β-thalassemia due to genotypes involving the IVS-I-6 (T→C) mutation.
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- American Journal of Hematology, 1995, v. 50, n. 1, p. 15, doi. 10.1002/ajh.2830500104
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- Article
Hb E/Hb Lepore<sub>Hollandia</sub> in a family from Bangladesh.
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- American Journal of Hematology, 1994, v. 47, n. 4, p. 262, doi. 10.1002/ajh.2830470403
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- Article
DNA diagnosis of Hb S and Hb Caribbean (α<sub>2</sub>β<sub>2</sub><sup>91</sup> Leu→Arg) in a Jamaican family.
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- American Journal of Hematology, 1994, v. 47, n. 1, p. 33, doi. 10.1002/ajh.2830470107
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- Article
Reduction in tissue iron stores with a new regimen of continuous ambulatory intravenous deferoxamine.
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- American Journal of Hematology, 1992, v. 41, n. 1, p. 61, doi. 10.1002/ajh.2830410112
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- Article
A new frameshift β°-thalassemia mutation (codons 27-28 +C) found in a Chinese family.
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- American Journal of Hematology, 1991, v. 37, n. 1, p. 6, doi. 10.1002/ajh.2830370103
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- Article
Mycobacterial Brain Abscess Possibly Due to Bacille Calmette-Guérin in an Immunocompromised Child.
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- Clinical Infectious Diseases, 1992, v. 14, n. 3, p. 662
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- Publication type:
- Article
Disparity in the management of iron overload between patients with sickle cell disease and thalassemia who received transfusions.
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- Transfusion, 2008, v. 48, n. 9, p. 1971, doi. 10.1111/j.1537-2995.2008.01775.x
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- Article
Studies in haemoglobin E beta-thalassaemia.
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- British Journal of Haematology, 2008, v. 141, n. 3, p. 388, doi. 10.1111/j.1365-2141.2008.07126.x
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- Article
Fetal haemoglobin augmentation in E/ β<sup>0</sup> thalassaemia: clinical and haematological outcome.
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- British Journal of Haematology, 2005, v. 131, n. 3, p. 378, doi. 10.1111/j.1365-2141.2005.05768.x
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- Article
Identification of a novel β<sup>0</sup> - thalassaemia mutation in a greek family and subsequent prenatal diagnosis.
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- Prenatal Diagnosis, 1994, v. 14, n. 10, p. 929, doi. 10.1002/pd.1970141006
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- Article
Infection Due to Yersinia enterocolitica in a Series of Patients with α-Thalassemia: Incidence and Predisposing Factors.
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- Clinical Infectious Diseases, 1998, v. 27, n. 6, p. 1362
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- Article
Dysregulated arginine metabolism and cardiopulmonary dysfunction in patients with thalassaemia.
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- British Journal of Haematology, 2015, v. 169, n. 6, p. 887, doi. 10.1111/bjh.13452
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- Article
Reply.
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- Transfusion, 1995, v. 35, n. 3, p. 276, doi. 10.1111/j.1537-2995.1995.tb03410.x
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- Article
Identification of two novel β°-thalassemia mutations in a filipino family: Frameshift codon 67 (− TG) and a β-globin gene deletion.
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- Human Mutation, 1993, v. 2, n. 5, p. 375, doi. 10.1002/humu.1380020509
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- Article
Single-center retrospective study of the effectiveness and toxicity of the oral iron chelating drugs deferiprone and deferasirox.
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- PLoS ONE, 2019, v. 14, n. 2, p. 1, doi. 10.1371/journal.pone.0211942
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- Article
Evaluation of the Oral Iron Chelator 1,2-Dimethyl-3-hydroxypyrid-4-one (L1) in Iron-Loaded Patients<sup>a</sup>.
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- Annals of the New York Academy of Sciences, 1990, v. 612, n. 1, p. 369, doi. 10.1111/j.1749-6632.1990.tb24324.x
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- Article
Use of a Eutectic Mixture of Local Anesthetics for Prolonged Subcutaneous Drug Administration.
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- 1995
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- Other
Regression of extramedullary haemopoiesis and augmentation of fetal haemoglobin concentration during hydroxyurea therapy in β thalassaemia.
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- British Journal of Haematology, 1998, v. 101, n. 3, p. 416, doi. 10.1046/j.1365-2141.1998.00719.x
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- Article
Immune function in patients with β thalassaemia receiving the orally active iron-chelating agent deferiprone.
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- British Journal of Haematology, 1997, v. 98, n. 3, p. 597, doi. 10.1046/j.1365-2141.1997.2463064.x
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- Article
The therapeutic reactivation of fetal haemoglobin.
- Published in:
- Human Molecular Genetics, 1998, v. 7, n. 10, p. 1655, doi. 10.1093/hmg/7.10.1655
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- Article
The therapeutic reactivation of fetal haemoglobin.
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- Human Molecular Genetics, 1998, v. 7, n. 10, p. 1655, doi. 10.1093/hmg/7.10.1655
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- Publication type:
- Article
Engraftment of immune-deficient mice with primitive hematopoietic cells from β-thalassemia and sickle cell anemia patients: implications for evaluating human gene therapy protocols.
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- Human Molecular Genetics, 1995, v. 4, n. 2, p. 163
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- Article
Leg Ulcers: A Report in Patients with Hemoglobin E Beta Thalassemia and Review of the Literature in Severe Beta Thalassemia.
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- Acta Haematologica, 2022, v. 145, n. 3, p. 334, doi. 10.1159/000520731
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- Article
Hb E/beta-thalassaemia: a common & clinically diverse disorder.
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- Indian Journal of Medical Research, 2011, v. 134, n. 4, p. 522
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- Publication type:
- Article