Is Hemoglobin Variant Analysis Helpful in the Diagnostic Work-up of Patients Revealing Microcytic Erythrocytosis on Complete Blood Count? [PDF]
Introduction: Microcytic erythrocytosis is an abnormal CBC (complete blood count) finding that is under-recognized, poorly understood, and consequently under-utilized in patient care. It is characterized by decreased MCV and increased RBC count.
Dulau-Florea, Alina +3 more
core +1 more source
Bridging the Gaps in Thalassemia Care in Sri Lanka: Challenges and Way Forward
ABSTRACT Thalassemia is the most common monogenic disease reported in Sri Lanka and has been a major health issue for decades. Although thalassemia major is preventable, there are about 60–80 births reported annually across the country. In Sri Lanka, the majority of them are managed at government hospitals, and healthcare facilities are provided free ...
L. H. M. R. L. Ambillapitiya +7 more
wiley +1 more source
Predictors of anemia in preschool children: Biomarkers Reflecting Inflammation and Nutritional Determinants of Anemia (BRINDA) project. [PDF]
Background: A lack of information on the etiology of anemia has hampered the design and monitoring of anemia-control efforts.Objective: We aimed to evaluate predictors of anemia in preschool children (PSC) (age range: 6-59 mo) by country and infection ...
Aaron, Grant J +13 more
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Hemoglobinopathy screening and prevention in primary care in the Netherlands: informing further research within the US? [PDF]
Elisa J. F. Houwink, Nathaniel E. Miller
openalex +1 more source
ABSTRACT Introduction Maternal birth satisfaction is correlated to long‐term outcomes and is influenced by the place of birth. In Italy, most births occur in hospitals. Our study aimed to assess whether the organizational level (I vs. II) of the Maternity Unit (MU) had any impact on birth satisfaction.
Simona Fumagalli +27 more
wiley +1 more source
IMPORTANCE OF IMPLEMENTING PROGRAM SCREENING NEONATAL HEMOGLOBINOPATHIES IN CAPE VERDE
Hemoglobinopathies are hereditary blood diseases, the most frequent sickle cell anemia. To date not have curative treatment, unless bone marrow transplant, which has yet been carried out experimentally.
Leonel Barbosa Gonçalves
doaj
Background: Hemoglobinopathies are the most commonly inherited red cell disorder around the world. In India, hemoglobinopathies show wide variation of prevalence in different regions and different populations.
Arnab Sinha +2 more
doaj +1 more source
Abstract Introduction Misperceptions about blood donation eligibility can deter individuals from donating. In Australia, misperceptions of one's eligibility status may be exacerbated by recent changes to donor criteria. However, public knowledge of these criteria remains underexplored.
Yasmin Mowat +8 more
wiley +1 more source
Erythrocytapheresis as a novel treatment option for adult patients with pyruvate kinase deficiency
Rawia F.G. Jensen +4 more
doaj +1 more source
Microalbuminuria as Predictor of Early Glomerular Injury in Children and Adolescents with Sickle Cell Anaemia at Muhimbili National Hospital Dar es Salaam, Tanzania 2012 [PDF]
Microalbuminuria (MA) is the earliest marker of various diseases affecting the renal system. Its relevance in children and adolescents with sickle cell anaemia (SCA), who are known to be prone to renal complications, has not been fully explored in our ...
Christopher, Richard
core

