Evaluation of (HPLC) Patterns of Sickle Cell Anaemia patients in comparison with apparently healthy individuals

Evaluation of (HPLC) Patterns of Sickle Cell Anaemia patients in comparison with apparently healthy individuals

Background: Sickle cell haemoglobin (HbS) results from an autosomal recessively inherited mutation in which the amino-acid glutamine is replaced by valine at position 6 in the beta globin chain of haemoglobin (Hb). Sickle cells have a reduced deformability and are easily destroyed, causing occl...

Full description

Bibliographic Details
Main Author:	R Manasa Reddy1 , Srilatha K 2
Format:	Article
Language:	English
Published:	Prathima Institute of Medical Sciences 2017-12-01
Series:	Perspectives In Medical Research
Subjects:	sickle cell anemia hbs hplc variant hb testing system
Online Access:	http://www.pimr.org.in/manasa_vol5-issue3-2017.PDF

Similar Items

The spleen in sickle cell anaemia during early childhood
by: Rogers, DW
Published: (1982)

Epidemiology of sickle cell disease in tribal population of Southern Rajasthan, India
by: Anil Purohit, et al.
Published: (2025-01-01)

A Rare Hemoglobinopathy Presenting as Chronic Hyperbilirubinemia
by: Lenaa Sakthiyavathy Manivannan, et al.
Published: (2021-08-01)

Antioxidant vitamins and glycatedhaemoglobin status in sickle cell anaemia
by: Johnkennedy Nnodim, et al.
Published: (2014-04-01)

Molecular Detection of Hemoglobin O-Arab in the Sudanese Population
by: Elbashir I, et al.
Published: (2023-08-01)

Drug discovery by a basic research scientist
by: William A. Eaton
Published: (2022-11-01)

Sickle Cell Anaemia with Antiglobulin Positive Autoimmune Haemolytic Crisis
by: Saniya Khan, et al.
Published: (2023-09-01)

Hematological Indices of Sickle Cell Anaemia Patients with Pulmonary Tuberculosis in Northern Nigeria.
by: Sagir G. Ahmed, et al.
Published: (2010-06-01)

Sickle cell anemia: An update on diagnosis, management and prevention strategies
by: Shruti Mishra, et al.
Published: (2018-01-01)

Fetal hemoglobin modifies the disease manifestation of severe Plasmodium falciparum malaria in adult patients with sickle cell anemia.
by: Prasanta Purohit
Published: (2016-11-01)

Sickle cell disease /
by: Jones, Phill, 1953-
Published: (2008)

PULMONARY FUNCTIONS IN ADOLESCENTS WITH SICKLE CELL ANAEMIA: A CASE-CONTROL STUDY
by: Lajwanti L Lalwani, et al.
Published: (2017-06-01)

Management of COVID-19 in a Sickle Cell Anaemia Patient: A Case Report
by: Ammar Tarig Elgadi, et al.
Published: (2023-12-01)

CHRONIC KIDNEY DISEASE AMONGST SICKLE CELL ANAEMIA PATIENT AT THE UNIVERSITY OF MAIDUGURI TEACHING HOSPITAL, NORTH EASTERN NIGERIA: A STUDY OF PREVALENCE AND RISK FACTORS
by: Audu Abdullahi Bukar, et al.
Published: (2019-01-01)

High Performance Liquid Chromatography (HPLC): An Essential Tool for Diagnosis of Compound Heterozygous Form (HbSD) of Hemoglobin-D (HbD) with Hemoglobin-S (HbS)
by: Bhushan Warpe, et al.
Published: (2024-07-01)

PREVALENCE OF SICKLE CELL TRAIT IN THE SOUTHERN SUBURBS OF BEIRUT, LEBANON
by: Abdel Badih El Ariss, et al.
Published: (2016-02-01)

A hospital-based prospective study of sickle cell disease in children of Eastern India
by: Bighneswar Senapati, et al.
Published: (2023-01-01)

Sickle cell-induced ischemic priapism
by: Salma AlDallal, et al.
Published: (2016-12-01)

Erythroid Adhesion Molecules in Sickle Cell Anaemia Infants: Insights Into Early Pathophysiology
by: Valentine Brousse, et al.
Published: (2015-02-01)

Levels of inflammatory markers are differentially expressed in sickle cell anemia and sickle cell trait
by: Ingrid Cristiane Pereira Gomes, et al.
Published: (2023-08-01)

ELEVATED MEAN CELL VOLUME IN SICKLE CELL ANAEMIA: ONE STORY, TOO MANY?
by: Jeremiah Zaccheaus, et al.
Published: (2024-04-01)

Identification of Sickle Cell Anemia Using Deep Neural Networks
by: Sagar Yeruva, et al.
Published: (2021-04-01)

Elevated homocysteine and crises state in patients with sickle cell anemia: A comparative study
by: Adebukola K Orolu, et al.
Published: (2022-01-01)

Phenotypic expression of HbO Indonesia in two Indian families and its interaction with sickle hemoglobin
by: Amar Das Gupta, et al.
Published: (2017-01-01)

Bibliometric analysis of global sickle cell disease research from 1997 to 2017
by: Henshaw Uchechi Okoroiwu, et al.
Published: (2022-04-01)

Hemoglobinopathies in Iran: An Updated Review
by: Abolfazl Nasiri, et al.
Published: (2020-04-01)

Incidence, demographic characteristics, and geographic distribution of sickle cell trait and sickle cell anemia births in Michigan, 1997–2014
by: Sarah L. Reeves, et al.
Published: (2019-08-01)

Total antioxidant status in sickle cell anemia
by: Tolulase Aderayo Olutogun, et al.
Published: (2018-01-01)

The use of hydroxycarbamide in children with sickle cell anemia
by: Hafsat Rufai Ahmad, et al.
Published: (2018-01-01)

ADULT SICKLE CELL ANAEMIA PATIENTS IN BONE PAIN CRISIS HAVE ELEVATED PRO-INFLAMMATORY CYTOKINES
by: Adekunle Emmanuel Alagbe, et al.
Published: (2018-03-01)

A model for gene therapy : gene replacement in the treatment of sickle cell anemia and B thalassemia /
by: 234771 Merkeley, Ward
Published: (2005)

Impact of Sickle Cell Disease on Affected Individuals in Nigeria: A Critical Review
by: Adigwe OP, et al.
Published: (2023-08-01)

REDUCTION OF INTRAMEDULLARY APOPTOSIS AFTER STEM CELL TRANSPLANTATION IN BLACK AFRICAN VARIANT OF PEDIATRIC SICKLE CELL ANEMIA.
by: Antonella Isgrò, et al.
Published: (2014-07-01)

Clinical and laboratory profile of patients with sickle cell anemia
by: Phelipe Gabriel dos Santos Sant'Ana, et al.

COVID‐19 and the pulmonary complications of sickle cell disease
by: Thivya Sivalingam, et al.
Published: (2020-11-01)

Sickle cell anemia and pregnancy: Profile of hemodynamic changes in sickle cell pregnant women in Kinshasa
by: Tite Minga Mikobi, et al.
Published: (2023-11-01)

Jaw Osteomyelitis as a Complication of Sickle Cell Anaemia in Three Omani Patients : Case reports and literature review
by: Hilal Al-Ismaili, et al.
Published: (2017-02-01)

Factors Effecting Hospitalization Frequency of Sickle Cell Anemia Patients
by: Gul Ilhan, et al.
Published: (2014-02-01)

Experiences and Problems Encountered by Families of Children with Sickle Cell Anemia
by: Gülendam Karadağ, et al.
Published: (2018-09-01)

Evaluation of pediatric hydroxyurea prescriptions for patients with sickle cell disease
by: Fernanda Alice Tanimoto Duque, et al.
Published: (2022-11-01)