β° Thalassemia Trait in Sardinia-Reference-Cited by-同舟云学术

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β° Thalassemia Trait in Sardinia

Published:1979-01 Issue:1 Volume:3 Page:33-46
ISSN:0363-0269
Container-title:Hemoglobin
language:en
Short-container-title:Hemoglobin

Author:

Galanello R.,Melis M. A.,Ruggeri R.,Addis N.,Scalas M. T.,Maccioni L.,Furbetta M.,Angius A.,Tuveri T.,Cao A.

Publisher

Informa UK Limited

Subject

Biochemistry (medical),Clinical Biochemistry,Genetics (clinical),Hematology

Link

http://www.tandfonline.com/doi/pdf/10.3109/03630267909069153

Reference34 articles.

1. MOLECULAR BASIS OF THALASSAEMIA

2. Absence of Messenger RNA for Beta Globin Chain in β°-Thalassaemia

3. Absence of functional messenger RNA activity for beta globin chain synthesis in beta 0-thalassemia

4. Presence of gene for β globin in homozygous β0 thalassaemia

5. Demonstration of non-functional beta-globin mRNA in homozygous beta (0) thalassemia.

Cited by 27 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Challenging the dogma of the healthy heterozygote: Implications for newborn screening policies and practices;Molecular Genetics and Metabolism;2021-09

2. Drug safety in thalassemia: lessons from the present and directions for the future;Expert Opinion on Drug Safety;2021-05-04

3. Correlation of Cytogenetic, Molecular and Clinical Findings in Thalassemia Patients at a Tertiary Care Hospital;Journal of Evolution of Medical and Dental Sciences;2019-11-18

4. Evaluation of Renal Function Disorder With Urinary Neutrophil Gelatinase–associated Lipocalin Level in Patients With β-Thalassemia Major;Journal of Pediatric Hematology/Oncology;2019-10

5. Role of Genomic Biomarkers in Increasing Fetal Hemoglobin Levels Upon Hydroxyurea Therapy and in β-Thalassemia Intermedia: A Validation Cohort Study;Hemoglobin;2019-01-02

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