Common, but neglected: A comprehensive review of leg ulcers in sickle cell disease
Common, But Neglected: A Comprehensive Review of Leg Ulcers... : Advances in Skin &
Wound Care Common, But Neglected: A Comprehensive Review of Leg Ulcers in Sickle Cell …
Wound Care Common, But Neglected: A Comprehensive Review of Leg Ulcers in Sickle Cell …
[PDF][PDF] Prevalence of β-S globin haplotypes in Jazan Region of Saudi Arabia
Prevalence of β-S Globin Haplotypes in Jazan Region of Saudi Arabia Page 1 Clin. Lab. 8/2021
1 Clin. Lab. 2021;67:XXX-XXX ©Copyright ORIGINAL ARTICLE Prevalence of β-S Globin …
1 Clin. Lab. 2021;67:XXX-XXX ©Copyright ORIGINAL ARTICLE Prevalence of β-S Globin …
Sickle ß-globin haplotypes among patients with sickle cell anemia in Basra, Iraq: A cross-sectional study
NT Yaseen, HS Al-Mamoori… - Iraqi Journal of …, 2020 - journals.lww.com
BACKGROUND: Sickle cell disease is a monogenic disease with heterogeneous clinical
course. Many genetic factors such as inheritance of α-thalassemia trait and fetal hemoglobin …
course. Many genetic factors such as inheritance of α-thalassemia trait and fetal hemoglobin …
[PDF][PDF] HBB gene cluster haplotype diversity in sickle cell anemia patients of Chhattisgarh, India
B Lakkakula, S Pattnaik - J Appl Biol Biotechnol, 2021 - academia.edu
Sickle cell anemia (SCA) is one of the hereditary hemoglobin disorders in Indian
populations. An exceptionally high prevalence of SCA is observed in the populations of …
populations. An exceptionally high prevalence of SCA is observed in the populations of …
[PDF][PDF] Genetic screening in sickle cell anemia
L Bhaskar - Polymorphism, 2019 - peerpublishers.com
Sickle cell anemia (SCA) is a monogenic genetic disorder characterized by sickle-shaped
red blood cells and chronic anemia (Bhaskar and Patra, 2015). SCA is caused by mutations …
red blood cells and chronic anemia (Bhaskar and Patra, 2015). SCA is caused by mutations …
Genetic association of GSTM1, GSTT1, and GSTP1 polymorphisms with sickle cell disease complications: A systematic review and meta-analysis
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 …
occlusive crises (VOC) also recurrent episodes of severe pain. Glutathione S-transferase …
[PDF][PDF] Clinical Implications of Neutrophil-to-Lymphocyte Ratio in Sickle Cell Disease
Abstract Sickle Cell Disease (SCD) is a hereditary hemoglobinopathy characterized by
chronic hemolytic anemia and vaso-occlusive events. In recent years, the Neutrophil-to …
chronic hemolytic anemia and vaso-occlusive events. In recent years, the Neutrophil-to …
Tracing the Indian Population Ancestry by cis-linked Mutations in HBB Gene
A Panja, P Chowdhury, A basu - bioRxiv, 2021 - biorxiv.org
Background Human left their genetic footprints during the time of migration throughout the
different countries all over the world. Human evolution was studied through various markers …
different countries all over the world. Human evolution was studied through various markers …
[HTML][HTML] A Cross-Sectional Study of Detection of Beta Globin (HBB) Haplotypes Among Beta Thalassemia Patients
A Alsamiri, F Alzahrani, N Filimban, A Khojah… - Cureus, 2021 - ncbi.nlm.nih.gov
Methods We analyzed 60 β-thalassemia patients. Male/female distribution for β-thalassemia
was 58.33%/41.66%. Results of hematological parameters and indices were obtained from …
was 58.33%/41.66%. Results of hematological parameters and indices were obtained from …
Sickle Cell Anemia Diagnosis Using Microscopic Images
S Aloni, P Adivarekar, M Jain, S Takmare… - …, 2022 - search.proquest.com
Sickle cell anemia is a red blood cell disorder that causes a shortage of oxy-gen due to the
sickling of red blood cells in the body. Sickle cell disease is a genetic disorder and typically …
sickling of red blood cells in the body. Sickle cell disease is a genetic disorder and typically …