Results 91 to 100 of about 23,191 (234)
Identification of Hemoglobins and Hemoglobinopathies by Electrophoresis on Cellulose Acetate Plates Impregnated with Citrate Agar [PDF]
, 1974 Rose G. Schneider +3 more
openalex +1 more source
Maternal &Child Nutrition, EarlyView.Coupling a multilevel participatory‐ludic BCC strategy with the use of unsweetened SQ‐LNS reduces the risk of being overweight or obese in infants and young children from Guatemala. Yet, complementary interventions to address non‐nutritional factors related to stunting in Guatemala are needed. ABSTRACT The co‐existence of childhood stunting and obesity
Carolina Gonzalez Acero +3 more
wiley +1 more source
Assessment of Thyroid Hormones and Vitamin D Levels in Patients with Hereditary Hemoglobinopathies
مجلة علوم ذي قار, 2023 Background: Hemoglobinopathies are ultimately developed many complications with a high of morbidity, secondary to iron overload. Thyroid dysfunction and bone disorders are the most common clinical manifestations.
Ghfran A. Kadim +1 more
doaj
Rastreio neonatal de hemoglobinopatias numa população residente em Portugal.
Acta Médica Portuguesa, 1996 The primary objective of newborn screening of hemoglobinopathies is the early identification of infants with sickle cell disease, as they are at increased clinical risk.
M J Peres +7 more
doaj +1 more source
Experimental Hematology & Oncology, 2019 The word of hemoglobinopathy is described for an array of disorders that affecting hemoglobin (Hb) functions. Hb is a molecule with 68 kDa molecular weight, serving as oxygen carrying metalloprotein.
Z. Mousavi +4 more
semanticscholar +1 more source
The Hemoglobinopathies. Techniques of Identification. [PDF]
, 1978 Titus H.J. Huisman, J. H. P. Jonxis
openalex +1 more source
Maternal &Child Nutrition, EarlyView.Micronutrient powders (MNPs) are recommended by the World Health Organization to address and prevent anaemia among children in nutritionally vulnerable settings with a high prevalence of anaemia (> 40%); however, following a 24‐week intervention of daily MNP provision among young Bangladeshi children, anaemia was associated with factors related to ...
Lauren Thompson +8 more
wiley +1 more source
Human Mutation, 2019 Hemoglobinopathies are the most common monogenic disorders worldwide. Substantial effort has been made to establish databases to record complete mutation spectra causing or modifying this group of diseases.
Li Zhang +28 more
semanticscholar +1 more source
Hemoglobinopathy screening: approaches to diagnosis, education and counseling. [PDF]
, 1974 Robert M. Schmidt
openalex +1 more source
Breaking down barriers: Recruiting donors of African ancestry in Ireland
Vox Sanguinis, EarlyView.Abstract Background and Objectives The diversity of the donor pool has an impact on blood provision for patients with inherited blood disorders, such as sickle cell anaemia. Many patients are critically dependent on red cell transfusions and due to uneven antigen distribution among different ethnic groups, they are at high risk of red cell ...
Allison Waters +5 more
wiley +1 more source