Literature DB >> 17077770

Care of patients with haemoglobin abnormalities: history and biology.

Ahmed D Khattab1, Barry Rawlings, Ibtisam S Ali.   

Abstract

Haemoglobinopathies refer to a range of genetically inherited disorders of red blood cell haemoglobin and include sickle cell disorders and thalassaemias. They occur most commonly in populations whose ancestors come from Africa, Asia, Mediterranean Islands, and the Middle and Far East. Haemoglobin (Hb) abnormalities (or haemoglobinopathies) are caused by (i) abnormalities of the protein structure; (ii) imbalanced globin chain production owing to reduced rate of synthesis of normal a or b globin chains; or (iii) a combination of the two. This article will focus on the biological basis of sickle cell disorders and will discuss the history and pathology of the conditions.

Entities:  

Mesh:

Substances:

Year:  2006        PMID: 17077770     DOI: 10.12968/bjon.2006.15.18.22024

Source DB:  PubMed          Journal:  Br J Nurs        ISSN: 0966-0461


  1 in total

1.  Detection of the sickle hemoglobin allele using a surface plasmon resonance based biosensor.

Authors:  Giulia Breveglieri; Elisabetta D'Aversa; Lucia Carmela Cosenza; Effrossyni Boutou; Angeliki Balassopoulou; Ersi Voskaridou; Roberto Gambari; Monica Borgatti
Journal:  Sens Actuators B Chem       Date:  2019-10-01       Impact factor: 7.460

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.