Results 31 to 40 of about 129,591 (344)

Fetomaternal hemorrhage - case report

open access: yesJournal of Education, Health and Sport, 2022
Maternal fetal leakage (FMH) is a well-known cause of fetal anemia. We define it as the transition of the fetal erythrocytes into the maternal circulation. Its severity is determined by measuring the level of fetal hemoglobin in the mother's blood using
Jakub Gruszka   +3 more
doaj   +1 more source

Efficacy of lactoferrin oral administration in the treatment of anemia and anemia of inflammation in pregnant and non-pregnant women: an interventional study [PDF]

open access: yes, 2018
The discovery of the ferroportin-hepcidin complex has led to a critical review on the treatment of anemia and anemia of inflammation (AI). Ferroportin, the only known mammalian iron exporter from cells to blood, is negatively regulated by hepcidin, a ...
Antimo Cutone   +6 more
core   +2 more sources

Doppler middle cerebral artery peak systolic velocity measurement as diagnostic tool for fetal anemia after in-utero transfusions in red blood cell alloimmunisation [PDF]

open access: yesVojnosanitetski Pregled, 2020
Background/Aim. Doppler sonography of fetal middle cerebral artery peak systolic velocity (MCA-PSV) can be used to predict fetal anemia and the need for in utero intravascular transfusion (IUIT) in red blood cell (RBC) alloimmunisation pregnancies.
Marjanović-Cvjetićanin Mirjana   +5 more
doaj   +1 more source

A novel mutation in NDUFB11 unveils a new clinical phenotype associated with lactic acidosis and sideroblastic anemia [PDF]

open access: yes, 2017
NDUFB11, a component of mitochondrial complex I, is a relatively small integral membrane protein, belonging to the 'supernumerary' group of subunits, but proved to be absolutely essential for the assembly of an active complex I.
Bertini, Enrico   +21 more
core   +2 more sources

Transfusión intrauterina para el tratamiento del Hidrops fetal causado por anemia: Reporte de caso y revisión de la literatura

open access: yesRevista de la Facultad de Ciencias de la Salud, 2020
OBJETIVO Reportar un caso de hidrops fetal no inmune  causado por anemia. Además realizar una revisión de la literatura sobre anemia fetal asociada a hidrops.
Cristian Hincapié-Porras   +5 more
doaj   +1 more source

Novel use Of Hydroxyurea in an African Region with Malaria (NOHARM): a trial for children with sickle cell anemia [PDF]

open access: yes, 2017
Hydroxyurea treatment is recommended for children with sickle cell anemia (SCA) living in high-resource malaria-free regions, but its safety and efficacy in malaria-endemic sub-Saharan Africa, where the greatest sickle-cell burden exists, remain unknown.
Hodges, James S.   +8 more
core   +2 more sources

Management of severe epistaxis during pregnancy: a case report and review of the literature [PDF]

open access: yes, 2019
Epistaxis is a common problem during pregnancy. Few cases of severe epistaxis, not associated with nasal lesions or clotting disorders, were described in the literature.
Brunelli, Roberto   +6 more
core   +1 more source

Noninvasive Diagnostics of Fetal Anemia

open access: yesDonald School Journal of Ultrasound in Obstetrics and Gynecology, 2011
ABSTRACT Even though the use of anti-D immunoglobulin has dramatically decreased the incidence of hemolytic disease of fetus and newborn, it still remains a significant cause of fetal and neonatal morbidity and mortality. The main challenge facing fetal medicine specialists today is not the skill required for invasive therapy, but rather the ...
Badreldeen Ahmed, Oliver Vasilj
openaire   +2 more sources

Successful Management of the Fetal Severe Anemia Associated with Jra Alloimmunization by Intrauterine Transfusion of Jr(a+) Red Blood Cells

open access: yesCase Reports in Obstetrics and Gynecology, 2019
Objective. We present a case of fetal severe anemia associated with Jra alloimmunization, which was managed using Doppler measurement of the peak systolic velocity of the fetal middle cerebral artery (MCA-PSV) and intrauterine transfusion (IUT) of Jr(a+)
Masatake Toshimitsu   +4 more
doaj   +1 more source

Nonimmune hydrops fetalis due to autosomal recessive hereditary spherocytosis

open access: yesCase Reports in Women's Health, 2017
Background: Hereditary spherocytosis is the most common form of inherited hemolytic anemia and is characterized by a structural defect in the RBC membrane.
Dawn M. Hannah   +2 more
doaj   +1 more source

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