Results 71 to 80 of about 5,241 (198)
As anemias hereditárias, que englobam as hemoglobinopatias e talassemias são doenças determinadas geneticamente. Na maioria dos casos os heterozigotos são assintomáticos e desconhecem o defeito genético do qual são portadores.
Paulo R. Melo-Reis +5 more
doaj +1 more source
Anaemia Among Mother–Child Dyads in India: Trends, Drivers, and Future Projections
ABSTRACT Anaemia among mothers and their children is a widespread public health challenge with profound consequences for individuals and societies. While anaemia has been studied separately in women and children, there remains a literature gap examining anaemia in mother‐child dyads, limiting insights on interventions that may simultaneously address ...
Sarang Pedgaonker +8 more
wiley +1 more source
Association of XmnI Polymorphism with Foetal Haemoglobin Level and Severity of Thalassaemia in Children: A Cross-sectional Study [PDF]
Introduction: The North-eastern Region of India has been a rich reservoir of haemoglobinopathies and thalassaemias. Genetic modifiers, commonly known as ameliorating factors, like co-inheritance of α-thalassaemia, excess α genes, the presence of the XmnI
Aditi Baruah +5 more
doaj +1 more source
Abstract Background Massive fetomaternal hemorrhage can lead to significant fetal morbidity or mortality. RhD negative patients require appropriate treatment to prevent alloimmunization in subsequent pregnancies. Few cases with follow‐up into future pregnancies have been reported.
Sajjad Hassan +4 more
wiley +1 more source
A global survey of blood transfusion practices for patients with sickle cell disease
Abstract Background Sickle cell disease (SCD) affects over 7 million people globally, with blood transfusion remaining a cornerstone of management. However, contemporary transfusion practices across diverse settings remain poorly characterized. We evaluated global transfusion practices for patients with SCD to identify gaps and inform resource ...
Jeremy W. Jacobs +18 more
wiley +1 more source
ITHANET: Information and database community portal for haemoglobinopathies
Haemoglobinopathies are the commonest monogenic diseases, with millions of carriers and patients worldwide. Online resources for haemoglobinopathies are largely divided into specialised sites catering for patients, researchers and clinicians separately ...
Jacques Elion +11 more
core +1 more source
Quantification of haemoglobin A2 for mass screening of major haemoglobinopathies [PDF]
Haemoglobinopathies are the most prevalent single-gene disorders and include a wide range of disorders most commonly thalassaemia and sickle cell disease (SCD).
Sant, Desiree
core
Codocytosis in the Dog: 345 Cases (2020–2022)
ABSTRACT Introduction Codocytes, or target cells, are a morphologic variation of erythrocytes characterized by increased membrane surface area relative to volume. In dogs, codocytosis is frequently noted on blood smear evaluation, but its clinical significance remains poorly understood. Objectives To characterize the clinical conditions associated with
Sarena M. Krojanker +5 more
wiley +1 more source
Abstract figure legend Metabolic stimulation improves bioenergetics, redox state, hydration and hematologic indices of circulating erythrocytes from sickle cell mice. Retained mitochondria in circulating RBCs from sickle mice are a source of RBC ATP as mitochondria function (ETC, electron transport chain) inhibitors [rotenone, a mitochondrial complex I
Luis E. F. Almeida +4 more
wiley +1 more source
Increasing the involvement of diverse populations in genomics-based health care—lessons from haemoglobinopathies [PDF]
Integrating genomic medicine into health care delivery poses significant challenges to health professionals. To draw clinical benefit from genomic information, there is a need to build an evidence-based relationship between genotype and the physical ...
Helen M. Robinson, Robinson, HM
core +1 more source

