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Regression of myocardial dysfunction after switching from desferrioxamine to deferiprone therapy in beta-thalassemia major patients.

• Authors : Huang YC; Division of Cardiology, Department of Pediatrics, China Medical University Hospital, Taichung, Taiwan.; Chang JS

Subjects: Chelation Therapy*; Cardiomyopathies/Cardiomyopathies/Cardiomyopathies/*drug therapy ; Deferoxamine/Deferoxamine/Deferoxamine/*therapeutic use

• Source: Hemoglobin [Hemoglobin] 2006; Vol. 30 (2), pp. 229-38.Publisher: Informa Healthcare Country of Publication: England NLM ID: 7705865 Publication Model: Print Cited Medium: Print ISSN: 0363-0269

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Regression of Myocardial Dysfunction After Switching from Desferrioxamine to Deferiprone Therapy in β-Thalassemia Major Patients

• Authors : Kang Hsi Wu; Jeng Sheng Chang; Ching-Tien Peng

Subjects: Adult; Male; Cardiac function curve

• Source: Hemoglobin. 30:229-238

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An Unusual Hydrops Fetalis Associated with Compound Heterozygosity for Krüppel-like Factor 1 mutations.

• Authors : Lee, Helena H. L.¹ (AUTHOR); Mak, Annisa S. L.¹ (AUTHOR); Kou, K. O.¹ (AUTHOR)

• Source: Hemoglobin. Nov2016, Vol. 40 Issue 6, p431-434. 4p.

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Fetal Anemia and Hydrops Fetalis Associated with Homozygous Hb Constant Spring ( HBA2 : c.427T > C).

• Authors : He, Yi¹ (AUTHOR); Zhao, Ying¹ (AUTHOR); Lou, Ji-Wu¹ (AUTHOR)

• Source: Hemoglobin. Mar2016, Vol. 40 Issue 2, p97-101. 5p.

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First Report of a Case with Nondeletional Hb H Disease Caused by IVS-I-116 (A>G) of the α2-Globin Gene.

• Authors : He, Xiao-Hong¹; Zhang, Rui¹; Mai, Guang-Xing¹

• Source: Hemoglobin. Sep-Nov2018, Vol. 42 Issue 5/6, p344-346. 3p.

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A Fetus with Hb Bart’s Disease Due to Maternal Uniparental Disomy for Chromosome 16.

• Authors : Au, Patrick K.C.¹ (AUTHOR) ; Kan, Anita S.Y.^1,2 (AUTHOR); Tang, Mary H.Y.^1,2 (AUTHOR)

• Source: Hemoglobin. Jan2016, Vol. 40 Issue 1, p66-69. 4p.

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Hb Lansing ( HBA2: c.264C > G) and a New β Promoter Transversion [−52 (G > T)]: An Attempt to Define the Phenotype of Two Mutations Found in the Omani Population.

• Authors : Hassan, Suha M.^1,2 (AUTHOR); Harteveld, Cornelis L.² (AUTHOR); Bakker, Engbert² (AUTHOR)

• Source: Hemoglobin. Apr2015, Vol. 39 Issue 2, p111-114. 4p.

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Hydrops Fetalis Associated with Compound Heterozygosity for Hb Zurich-Albisrieden ( HBA2 : C.178G > C) and the Southeast Asian (– – /) Deletion.

• Authors : Yang, Xin¹ (AUTHOR); Yan, Jin-Mei¹ (AUTHOR); Li, Jian¹ (AUTHOR)

• Source: Hemoglobin. Sep2016, Vol. 40 Issue 5, p353-355. 3p.

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Hb Lansing (HBA2: c.264C > G) and a NewβPromoter Transversion [−52 (G > T)]: An Attempt to Define the Phenotype of Two Mutations Found in the Omani Population

• Authors : Piero C. Giordano; Cornelis L. Harteveld; Suha M. Hassan

Subjects: Adult; Male; Heterozygote

• Source: Hemoglobin, 39(2), 111-114

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Hydrops Fetalis Associated with Compound Heterozygosity for Hb Zurich-Albisrieden (HBA2: C.178G > C) and the Southeast Asian (– –SEA/) Deletion

• Authors : Jian Li; Yan Li; Jin-Mei Yan

Subjects: Genetics; Fetus; medicine.medical_specialty

• Source: Hemoglobin. 40:353-355

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