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Prevention of thalassemia: a necessity in India.

作者信息

Verma I C, Choudhry V P, Jain P K

机构信息

Department of Pediatrics, All India Institute of Medical Sciences, New Delhi.

出版信息

Indian J Pediatr. 1992 Nov-Dec;59(6):649-54. doi: 10.1007/BF02859390.

DOI:10.1007/BF02859390
PMID:1340849
Abstract
摘要

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A demographic prevalence of β Thalassemia carrier and other hemoglobinopathies in adolescent of Tharu population.

本文引用的文献

1
Effectiveness of one tube osmotic fragility screening in detecting beta-thalassaemia trait.单管渗透脆性筛查在检测β地中海贫血特征中的有效性。
J Med Genet. 1981 Aug;18(4):266-70. doi: 10.1136/jmg.18.4.266.
2
Molecular characterization of seven beta-thalassemia mutations in Asian Indians.亚洲印度人中七种β地中海贫血突变的分子特征分析
EMBO J. 1984 Mar;3(3):593-6. doi: 10.1002/j.1460-2075.1984.tb01853.x.
3
Community control of hereditary anaemias: memorandum from a WHO meeting.遗传性贫血的社区控制：世界卫生组织会议纪要
塔鲁族青少年中β地中海贫血携带者和其他血红蛋白病的人口统计学患病率。
J Family Med Prim Care. 2020 Aug 25;9(8):4305-4310. doi: 10.4103/jfmpc.jfmpc_879_20. eCollection 2020 Aug.
4
Comparative Evaluation of BMI, Dental Age, Salivary Alkaline Phosphatase Levels, and Oral Health Status in Children with β Thalassemia Major.重型β地中海贫血患儿的体重指数、牙龄、唾液碱性磷酸酶水平及口腔健康状况的比较评估
Int J Clin Pediatr Dent. 2019 Jul-Aug;12(4):303-306. doi: 10.5005/jp-journals-10005-1641.
5
Clinico-Haematological Profile of Hereditary Haemolytic Anaemias in a Tertiary Health Care Hospital in South India.印度南部一家三级医疗保健医院遗传性溶血性贫血的临床血液学概况
J Clin Diagn Res. 2017 Jun;11(6):EC17-EC21. doi: 10.7860/JCDR/2017/25366.10023. Epub 2017 Jun 1.
6
The role of discriminant functions in screening beta thalassemia trait and iron deficiency anemia among laboratory samples.判别函数在实验室样本中筛查β地中海贫血特征和缺铁性贫血的作用。
J Lab Physicians. 2017 Jul-Sep;9(3):195-201. doi: 10.4103/0974-2727.208256.
7
Attitudes and beliefs among high- and low-risk population groups towards β-thalassemia prevention: a cross-sectional descriptive study from India.高风险和低风险人群对β地中海贫血预防的态度和信念：来自印度的一项横断面描述性研究。
J Community Genet. 2017 Jul;8(3):159-166. doi: 10.1007/s12687-017-0298-4. Epub 2017 Apr 6.
8
Evaluation of carotid artery dynamics & correlation with cardiac & hepatic iron in β-thalassaemia patients.β地中海贫血患者颈动脉动力学评估及其与心脏和肝脏铁含量的相关性
Indian J Med Res. 2016 Apr;143(4):443-8. doi: 10.4103/0971-5916.184302.
9
Health Related Quality of Life and its Predictors among Bengali Thalassemic Children Admitted to a Tertiary Care Hospital.一家三级护理医院收治的孟加拉国地中海贫血儿童的健康相关生活质量及其预测因素
Indian J Pediatr. 2015 Oct;82(10):909-16. doi: 10.1007/s12098-014-1670-6. Epub 2015 Feb 26.
10
Descriptive profile of β-thalassemia mutations in West Bengal population: a hospital-based study.
Int J Hematol. 2014 Mar;99(3):345-53. doi: 10.1007/s12185-014-1511-4. Epub 2014 Feb 1.
Bull World Health Organ. 1983;61(1):63-80.
4
Distribution and control of some genetic disorders.某些遗传性疾病的分布与控制
World Health Stat Q. 1988;41(3-4):209-18.
5
Rapid and non-radioactive prenatal diagnosis of beta thalassaemia and sickle cell disease: application of the polymerase chain reaction (PCR).
Br J Haematol. 1988 Dec;70(4):455-8. doi: 10.1111/j.1365-2141.1988.tb02516.x.
6
The molecular basis of thalassaemia major and thalassaemia intermedia in Asian Indians: application to prenatal diagnosis.
Br J Haematol. 1988 Oct;70(2):225-31. doi: 10.1111/j.1365-2141.1988.tb02468.x.
7
Thalassemia in Bombay: the role of medical genetics in developing countries.孟买的地中海贫血：医学遗传学在发展中国家的作用。
Bull World Health Organ. 1990;68(1):75-81.
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The thalassemia syndromes: molecular basis and prenatal diagnosis in 1990.地中海贫血综合征：1990年的分子基础与产前诊断
Semin Hematol. 1990 Jul;27(3):209-28.
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The spectrum of beta-thalassaemia mutations on the Indian subcontinent: the basis for prenatal diagnosis.
Br J Haematol. 1991 Jun;78(2):242-7. doi: 10.1111/j.1365-2141.1991.tb04423.x.
10
Rapid detection and prenatal diagnosis of beta-thalassaemia: studies in Indian and Cypriot populations in the UK.
Lancet. 1990 Oct 6;336(8719):834-7. doi: 10.1016/0140-6736(90)92338-i.