Literature DB >> 3232409

Distribution and control of some genetic disorders.

B Modell1, V Bulyzhenkov.   

Abstract

The health burden of genetic disorders varies between ethnic groups within the same country or between countries to a large extent because of genotypic differences at the population level. Genetic services should recognize this variability in need and be developed within the traditional context of medical care. All practical approaches require a sound epidemiological basis and underline the importance of early diagnosis for both prevention and treatment. Effective control is now possible for some Mendelian conditions and some congenital malformations and should be incorporated into general health care. The development of genetic services within any country depends on the optimal utilization of available resources, both financial and intellectual.

Entities:  

Mesh:

Year:  1988        PMID: 3232409

Source DB:  PubMed          Journal:  World Health Stat Q        ISSN: 0379-8070


  12 in total

1.  Prevention of thalassemia: a necessity in India.

Authors:  I C Verma; V P Choudhry; P K Jain
Journal:  Indian J Pediatr       Date:  1992 Nov-Dec       Impact factor: 1.967

2.  Dynamic posttranscriptional regulation of epsilon-globin gene expression in vivo.

Authors:  Zhenning He; J Eric Russell
Journal:  Blood       Date:  2006-09-26       Impact factor: 22.113

3.  Developmental silencing of the embryonic zeta-globin gene: concerted action of the promoter and the 3'-flanking region combined with stage-specific silencing by the transcribed segment.

Authors:  S A Liebhaber; Z Wang; F E Cash; B Monks; J E Russell
Journal:  Mol Cell Biol       Date:  1996-06       Impact factor: 4.272

4.  A 3'-flanking NF-kappaB site mediates developmental silencing of the human zeta-globin gene.

Authors:  Z Wang; S A Liebhaber
Journal:  EMBO J       Date:  1999-04-15       Impact factor: 11.598

5.  Crystallographic analysis of human hemoglobin elucidates the structural basis of the potent and dual antisickling activity of pyridyl derivatives of vanillin.

Authors:  Osheiza Abdulmalik; Mohini S Ghatge; Faik N Musayev; Apurvasena Parikh; Qiukan Chen; Jisheng Yang; Ijeoma Nnamani; Richmond Danso-Danquah; Dorothy N Eseonu; Toshio Asakura; Donald J Abraham; Jurgen Venitz; Martin K Safo
Journal:  Acta Crystallogr D Biol Crystallogr       Date:  2011-10-19

Review 6.  Prevention and control of haemoglobinopathies.

Authors:  M Angastiniotis; B Modell; P Englezos; V Boulyjenkov
Journal:  Bull World Health Organ       Date:  1995       Impact factor: 9.408

7.  Frequency of β-thalassemia trait and other hemoglobinopathies in northern and western India.

Authors:  Nishi Madan; Satendra Sharma; S K Sood; Roshan Colah; Late H M Bhatia
Journal:  Indian J Hum Genet       Date:  2010-01

8.  Carrier Screening for β Thalassemia in Pregnant Indian Women: Experience at a Single Center in Madhya Pradesh.

Authors:  Asha Baxi; Kaushal Manila; Pooja Kadhi; Baxi Heena
Journal:  Indian J Hematol Blood Transfus       Date:  2012-06-22       Impact factor: 0.900

9.  Coexisting iron deficiency anemia and Beta thalassemia trait: effect of iron therapy on red cell parameters and hemoglobin subtypes.

Authors:  Sarika Verma; Ruchika Gupta; Madhur Kudesia; Alka Mathur; Gopal Krishan; Sompal Singh
Journal:  ISRN Hematol       Date:  2014-03-12

10.  Global migration and the changing distribution of sickle haemoglobin: a quantitative study of temporal trends between 1960 and 2000.

Authors:  Frédéric B Piel; Andrew J Tatem; Zhuojie Huang; Sunetra Gupta; Thomas N Williams; David J Weatherall
Journal:  Lancet Glob Health       Date:  2014-02       Impact factor: 26.763

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