Literature DB >> 11545326

Inherited haemoglobin disorders: an increasing global health problem.

D J Weatherall1, J B Clegg.   

Abstract

Despite major advances in our understanding of the molecular pathology, pathophysiology, and control and management of the inherited disorders of haemoglobin, thousands of infants and children with these diseases are dying through lack of appropriate medical care. This problem will undoubtedly increase over the next 20 years because, as the result of a reduction in childhood mortality due to infection and malnutrition, more babies with haemoglobin disorders will survive to present for treatment. Although WHO and various voluntary agencies have tried to disseminate information about these diseases, they are rarely mentioned as being sufficiently important to be included in setting health care priorities for the future. It takes considerable time to establish expertise in developing programmes for the control and management of these conditions, and the lessons learned in developed countries will need to be transmitted to those countries in which they occur at a high frequency.

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Year:  2001        PMID: 11545326      PMCID: PMC2566499     

Source DB:  PubMed          Journal:  Bull World Health Organ        ISSN: 0042-9686            Impact factor:   9.408


  277 in total

1.  Molecular prenatal diagnosis of alpha and beta thalassemia in pregnant Hakka women in southern China.

Authors:  Pingsen Zhao; Heming Wu; Zhixiong Zhong; Liubing Lan; Mei Zeng; Hualan Lin; Huaxian Wang; Zhiyuan Zheng; Luxian Su; Wei Guo
Journal:  J Clin Lab Anal       Date:  2017-08-03       Impact factor: 2.352

2.  The Diagnosis of α-Thalassaemia: A Case of Hemoglobin H -α Deletion.

Authors:  Vijay S Bhat; Kalyan Kumar Dewan; Patnam Rajagopalan Krishnaswamy
Journal:  Indian J Clin Biochem       Date:  2010-09-14

3.  Profiling β-thalassaemia mutations in India at state and regional levels: implications for genetic education, screening and counselling programmes.

Authors:  S Sinha; M L Black; S Agarwal; R Colah; R Das; K Ryan; M Bellgard; A H Bittles
Journal:  Hugo J       Date:  2010-02-10

4.  Psychosocial burden of sickle cell disease on parents with an affected child in Cameroon.

Authors:  Ambroise Wonkam; Caryl Zameyo Mba; Dora Mbanya; Jeanne Ngogang; Raj Ramesar; Fru F Angwafo
Journal:  J Genet Couns       Date:  2013-07-24       Impact factor: 2.537

5.  Dental and periodontal health status of Beta thalassemia major and sickle cell anemic patients: a comparative study.

Authors:  Jaideep Singh; Nitin Singh; Amit Kumar; Neal Bharat Kedia; Anil Agarwal
Journal:  J Int Oral Health       Date:  2013-10-26

Review 6.  Hemoglobin variants: biochemical properties and clinical correlates.

Authors:  Christopher S Thom; Claire F Dickson; David A Gell; Mitchell J Weiss
Journal:  Cold Spring Harb Perspect Med       Date:  2013-03-01       Impact factor: 6.915

7.  Impaired Collateral Vessel Formation in Sickle Cell Disease.

Authors:  Derick Okwan-Duodu; Laura Hansen; Giji Joseph; Alicia N Lyle; Daiana Weiss; David R Archer; W Robert Taylor
Journal:  Arterioscler Thromb Vasc Biol       Date:  2018-03-15       Impact factor: 8.311

8.  Psychosocial stressors of sickle cell disease on adult patients in Cameroon.

Authors:  Ambroise Wonkam; Caryl Zameyo Mba; Dora Mbanya; Jeanne Ngogang; Raj Ramesar; Fru F Angwafo
Journal:  J Genet Couns       Date:  2014-02-21       Impact factor: 2.537

Review 9.  Regulation of iron absorption in hemoglobinopathies.

Authors:  Gideon Rechavi; Stefano Rivella
Journal:  Curr Mol Med       Date:  2008-11       Impact factor: 2.222

10.  Global epidemiology of haemoglobin disorders and derived service indicators.

Authors:  Bernadette Modell; Matthew Darlison
Journal:  Bull World Health Organ       Date:  2008-06       Impact factor: 9.408

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