Results 131 to 140 of about 821,341 (299)
Potential New Non-Invasive Therapy Using Artificial Oxygen Carriers for Pre-Eclampsia
Journal of Functional Biomaterials, 2017 The molecular mechanisms of pre-eclampsia are being increasingly clarified in animals and humans. With the uncovering of these mechanisms, preventive therapy strategies using chronic infusion of adrenomedullin, vascular endothelial growth factor-121 ...
Hidenobu Ohta +5 more
doaj +1 more source
FETAL AND ADULT HEMOGLOBINS IN THE BLOOD OF INFANTS AFFECTED WITH HEMOLYTIC DISEASE OF THE NEWBORN [PDF]
, 1949 Eric Ponder, Philip Levine
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Revista Brasileira de Ginecologia e Obstetrícia, 2008 OBJETIVO: obter uma equação capaz de estimar o volume de concentrado de hemácias a ser infundido para correção da anemia em fetos de gestantes portadoras de isoimunização pelo fator Rh, baseado em parâmetros alcançados durante a cordocentese prévia à ...
Mônica Deolindo Santiago +5 more
doaj +1 more source
Molecular Therapy: Methods & Clinical Development, 2020 Sickle cell disease (SCD) and β-thalassemia are caused by structural abnormality or inadequate production of adult hemoglobin (HbA, α2β2), respectively.
Christopher B. Chambers +9 more
doaj
FetalDiffusion: Pose-Controllable 3D Fetal MRI Synthesis with Conditional Diffusion Model [PDF]
arXivThe quality of fetal MRI is significantly affected by unpredictable and substantial fetal motion, leading to the introduction of artifacts even when fast acquisition sequences are employed. The development of 3D real-time fetal pose estimation approaches on volumetric EPI fetal MRI opens up a promising avenue for fetal motion monitoring and prediction.
arxiv
Differences in Antigenic Specificity of Human Normal Adult, Fetal, and Sickle Cell Anemia Hemoglobin [PDF]
, 1953 Morris Goodman, Dan H. Campbell
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Revista Brasileira de Hematologia e Hemoterapia, 2008 A anemia falciforme está entre as doenças genéticas mais comuns e mais estudadas em todo o mundo. Ela é causada por mutação no gene β, produzindo alteração estrutural na molécula da hemoglobina.
Rita de Cassia Mousinho-Ribeiro +3 more
doaj +1 more source
The Postnatal Synthesis of Fetal Hemoglobin. I. Some Studies in Newborn Goats Using Radioactive Fe59 and Glycine-2-C14 [PDF]
, 1957 Henk Visser +2 more
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Fabrication and testing of microfluidic devices for blood cell separation [PDF]
, 2009 This paper was presented at the 2nd Micro and Nano Flows Conference (MNF2009), which was held at Brunel University, West London, UK. The conference was organised by Brunel University and supported by the Institution of Mechanical Engineers, IPEM, the ...
2nd Micro and Nano Flows Conference (MNF2009) +5 more
core
Brazilian Journal of Medical and Biological Research, 2001 Hereditary persistence of fetal hemoglobin is an uncommon, benign disorder in which the expression of gamma-globin genes persists into adult life. Several point mutations have been associated with the increased gamma-globin gene promoter activity.
Schreiber R. +5 more
doaj