Results 21 to 30 of about 20,282 (239)

Acute fetal anemia diagnosed by middle cerebral artery Doppler velocimetry in stage v twin-twin transfusion syndrome. [PDF]

open access: yes, 2011
In stage V twin-twin transfusion syndrome (TTTS), up to 50% of surviving twins die or experience permanent disabilities, likely due to acute intertwin hemorrhage resulting in sudden severe anemia of the survivor.
Friedrich, Esther   +3 more
core   +2 more sources

FEATURES OF ADAPTATION OF NEWBORNS WHO HAVE HAD INTRAUTERINE BLOOD TRANSFUSIONS

open access: yesКубанский научный медицинский вестник, 2018
Aim. To assess the adaptive capacity of newborns who have had intrauterine blood transfusions.Materials and methods. The study included 40 newborns who underwent intrauterine intravascular blood transfusion due to hemolytic disease of the fetus RH-factor.
N. V. BOYKO   +2 more
doaj   +1 more source

Usefulness of absorption techniques in doubtful cases of incompatibility Rh maternal fetal: a case report

open access: yesJournal of Biomedical Practitioners, 2023
INTRODUCTION This case report traces the diagnostic and therapeutic process of the Immuno-Transfusion Service in a case of fetal anaemia characterized by various inconsistencies between clinical and laboratory data.
Eleonora Donno   +11 more
doaj   +1 more source

Intrauterine Blood Transfusion: Current Indications and Associated Risks [PDF]

open access: yesFetal Diagnosis and Therapy, 2014
Fetal anemia is a serious complication in pregnancy and associated with perinatal mortality and morbidity. During 25 years of worldwide experience with intravascular intrauterine blood transfusion, a variety of indications have been described. Intrauterine transfusion (IUT) treatment is considered most successful for fetal anemia due to red cell ...
Lindenburg, I.T.M.   +2 more
openaire   +3 more sources

MANAGEMENT OF FETAL ANEMIA AND THROMBOCYTOPENIA WITH INTRAUTERINE BLOOD TRANSFUSION

open access: yesInternational Journal of Advanced Research, 2022
Fetal anemia and fetal thrombocytopenia are two of the most unsmiling complications in pregnant women, and they can lead to perinatal mortality and morbidity. After long years of study with intravascular intrauterine blood transfusion, a number of varieties of implications have been described.
Rohan Pal   +5 more
openaire   +2 more sources

Early invasive prenatal diagnosis in HBsAg-positive women [PDF]

open access: yes, 1994
From 1982 to 1989, pregnant women in two large city hospitals in The Netherlands had serum samples screened for hepatitis B surface antigen (HBsAg). Infants of mothers found to be HBsAg-positive received hepatitis B immune globulin immediately after ...
Alter   +25 more
core   +5 more sources

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

Foetal Haemoglobin as a Marker of Bone Marrow Suppression Secondary to Anti-Kell Alloimmunisation

open access: yesInternational Journal of Neonatal Screening, 2023
Anti-Kell alloimmunisation is a potentially severe minor blood group type incompatibility, not only as a cause of haemolytic disease of the foetus and newborn, but also due to the destruction of red blood cells (RBC) and mature form in the bone marrow ...
Rodrigo Alfredo Morales Painamil   +7 more
doaj   +1 more source

Detecção de parvovírus humano B19 em casos de hydropsia fetal em São Paulo, Brasil [PDF]

open access: yes, 2008
Human parvovirus B19 infection is known to be one of the causes of hydrops fetalis. The maternal infection caused by the virus may be symptomatic or asymptomatic.
AFONSO, Ana Maria Sardinha   +6 more
core   +2 more sources

Severe hereditary spherocytosis presenting with non-immune fetal hydrops

open access: yesIndian Pediatrics Case Reports, 2023
Background: Hereditary spherocytosis (HS) is characterized by spherocytes on the peripheral smear and heterogeneous clinical presentation (mild, moderate, moderate/severe, and severe) depending upon the severity of hemolytic anemia, jaundice, and ...
Snehal Mallakmir   +3 more
doaj   +1 more source

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