[HTML][HTML] Infection and potential challenge of childhood mortality in sickle cell disease: a comprehensive review of the literature from a global perspective

T Sahu, B Pande, HK Verma, L Bhaskar, M Sinha… - Thalassemia …, 2023 - mdpi.com
Sickle cell disease (SCD) is a complex genetic disorder associated with multiple clinical
manifestations, including increased susceptibility to bacterial and viral infections. This …

Myopia in India

A Pujari, S Modaboyina, D Agarwal, G Saluja… - Clinical …, 2022 - Taylor & Francis
India is a culturally and geographically diverse nation. Its vast demographic nature does not
allow a single definition for any of the given medical conditions in its territory. One important …

Erythrocyte microRNAs: a tiny magic bullet with great potential for sickle cell disease therapy

HK Verma, YK Ratre, L Bhaskar, R Colombatti - Annals of Hematology, 2021 - Springer
Sickle cell disease (SCD) is a severe hereditary blood disorder caused by a mutation of the
beta-globin gene, which results in a substantial reduction in life expectancy. Many studies …

Ocular Presentations of Sickle Cell Disease Patients in a Nigerian Hospital

CC Efobi, OS Ejiofor, BC Ochiogu… - … of Advances in …, 2020 - archive.paparesearch.co.in
Introduction: Sickle Cell Disease (SCD) is an inherited haemolytic disorder that affects
virtually all body systems including the eye. Ocular complications of SCD could have dire …

[PDF][PDF] ACE I/D polymorphism is not a genetic modifier of renal features in sickle cell anemia patients

L Bhaskar, S Pattnaik - Journal of Renal Endocrinology, 2022 - pdfs.semanticscholar.org
Introduction: Sickle cell anemia (SCA) exhibits a host of complications that contribute to
increased morbidity and mortality at the youngest ages. Objectives: The aim of this …

High Systolic Blood Pressure, Anterior Segment Changes and Visual Impairment Independently Predict Sickle Cell Retinopathy

IM Idris, AA Yusuf, DH Gwarzo, MS Kurawa… - …, 2021 - Taylor & Francis
Sickle cell disease is often complicated by retinopathy, which can be proliferative or non
proliferative. Proliferative sickle cell retinopathy potentially leads to blindness. There is a …

Genetic association of GSTM1, GSTT1, and GSTP1 polymorphisms with sickle cell disease complications: A systematic review and meta-analysis

HK Verma, S Swarnakar, L Bhaskar - Meta Gene, 2020 - Elsevier
Background Sickle cell disease (SCD) is a monogenic blood disorder characterized by vaso-
occlusive crises (VOC) also recurrent episodes of severe pain. Glutathione S-transferase …

[PDF][PDF] A SYSTEMATIC REVIEW ON ABNORMAL HEMOGLOBIN OF SICKLE CELL DISORDER PATIENTS

S Das, BP Dash - researchgate.net
With a populace of over 1.2 billion people, it is anticipated that our country is domestic to
over fifty percent of the arena's SCD (Sickle Cell Disease) sufferers (Kate et. al., 2002) …

[HTML][HTML] Ocular Complications in Sickle Cell Disease: A Neglected Issue

H Al-Jafar, N Abul, Y Al-Herz, N Kumar - Open Journal of Ophthalmology, 2020 - scirp.org
Sickle cell disease is a common genetic blood disorder. It causes severe systemic
complications including ocular involvement. The degree of ocular complications is not …

[PDF][PDF] Coinheritance of-3.7 Alpha-Thalassaemia Deletions Among Sickle Cell Anaemia Patients in Chhattisgarh, India

S Swarnakar, PK Patra, PK Khodiar… - Malaysian Journal of …, 2020 - researchgate.net
Abstract Background: Alpha (α)-thalassaemia is inherited as an autosomal recessive
disorder characterised by microcytic hypochromic anaemia. In children with homozygous …