[PDF][PDF] Nitric oxide and zinc levels in sickle cell hemoglobinopathies: a relationship with the markers of disease severity

AA Alaka, OO Alaka, AA Iyanda - Pomeranian Journal of Life Sciences, 2023 - sciendo.com
Introduction: Sickle cell disease is a genetically inherited disease affecting millions of people
worldwide. Patients with a severe form of the disease present with more complications and …

Clinical profile, dietary zinc content, and lifestyle habits of adult male and female hbss and hbsc patients.

AA Alaka, OO Alaka, AA Iyanda - Bangladesh Journal of …, 2024 - search.ebscohost.com
Objective: Males and females have been reported to show significant variation with respect
to clinical profile of sickle cell disease (SCD)(eg cardiovascular, musculoskeletal and …

[HTML][HTML] Low Uptake of Hydroxyurea among a Cohort of Sickle Cell Disease Patients in Nigeria

HC Okoye, CC Efobi, H Ommunakwe… - Nigerian Journal of …, 2023 - journals.lww.com
Background: Hydroxyurea (HU) is the first disease-modifying drug used in the treatment of
sickle cell disease (SCD). Despite its well-documented benefits, adoption and drug …

[PDF][PDF] KNOWLEDGE, BELIEFS, AND ATTITUDE TOWARDS SICKLE CELL DISEASE AMONG SENIOR HIGH SCHOOL STUDENTS IN TAMALE METROPOLIS

P Baba, A Yidana - UDS International Journal of Development, 2023 - ajol.info
Sickle cell disease (SCD) is a hereditary disease that comes with many complications, such
as vaso-occlusive crises and anemia. The SCD is now a public health problem due to its …

Knowledge and Beliefs, towards Sickle Cell Disease among Senior High School Students in Tamale Metropolis

P Baba, IZ Yakubu, A Yidana - Asian Journal of …, 2023 - archive.article4submit.com
Aim: Sickle cell disease is a public health problem with a global spread. As a hereditary
disease, sickle cell disease comes with many complications, including anemia. With the …

The Presentation of Acute Pancreatitis in Sickle Cell Disease Patients: A Single Hospital Experience

S Al-Hindi, Z Khalaf, ASN Al-Sousi - African Journal of Paediatric …, 2023 - journals.lww.com
Materials and Methods: Twenty-eight SCD patients who were diagnosed with AP during
their admission to the paediatric department at a tertiary hospital between January 2012 and …

A clinico-hematological study of sickle cell disease among adult patients in Makkah, Saudi Arabia.

AF Arbaeen - Al-Azhar International Medical Journal, 2023 - aimj.researchcommons.org
Background: Sickle cell disease is an autosomal recessive disease characterized by an
aberrant production of hemoglobin S (HbS). The disease's presentation and severity varied …

[PDF][PDF] Identification of Hematological Biomarkers and Assessment of Machine Learning Models for Sickle Cell Anemia Severity Classification

FA Ussher, EF Laing, AB Atta-Owusu, E Kissi - researchgate.net
Methods Our study involved 481 participants, including 356 SCA patients and 125 healthy
controls, who reported at the Korle-Bu Teaching Hospital, Accra, Ghana. Using a mixed …