Results 31 to 40 of about 9,064,819 (381)
Fourier Transform of Percoll Gradients Boosts CNN Classification of Hereditary Hemolytic Anemias [PDF]
arXiv, 2021 Hereditary hemolytic anemias are genetic disorders that affect the shape and density of red blood cells. Genetic tests currently used to diagnose such anemias are expensive and unavailable in the majority of clinical labs. Here, we propose a method for identifying hereditary hemolytic anemias based on a standard biochemistry method, called Percoll ...
arxiv
Editorial: Inflammatory Mechanisms of Hemolytic Diseases [PDF]
Frontiers in Immunology, 2022 No abstract available.
Sesti-Costa, Renata +4 more
openaire +4 more sources
Rh-incompatible hemolytic disease of the newborn in Hefei
World Journal of Clinical Cases, 2019 BACKGROUND Anti-D antibody is not the common cause of Rh-isoimmunization in Chinese neonatal jaundice. Recent change in national population policy has followed by an increase in Rh-isoimmunization related hemolytic disease of the newborn (HDN ...
Shaohua Bi +13 more
semanticscholar +1 more source
Edematous form of the Hemolytic Disease of the Fetus and Newborn
Медицинский вестник Юга России, 2019 Clinical observation of a premature newborn patient with an edematous form of the Hemolytic Disease is presented. A feature of this case is its relative rarity in view of the favorable outcome of the most severe form of hemolytic disease in an extremely ...
M. G. Pukhtinskaya +3 more
doaj +1 more source
Transfusion, 2018 Alloanti‐M was once regarded as not clinically significant, with a few exceptions in extremely rare cases. However, an increasing number of cases of severe hemolytic disease of the fetus and newborn (HDFN), resulting in fetal hydrops and recurrent ...
Si Li +6 more
semanticscholar +1 more source
Neonatal management and outcome in alloimmune hemolytic disease
Expert Review of Hematology, 2017 Introduction: Hemolytic disease of the fetus and newborn (HDFN) occurs when fetal and neonatal erythroid cells are destroyed by maternal erythrocyte alloantibodies, it leads to anemia and hydrops in the fetus, and hyperbilirubinemia and kernicterus in ...
I. Ree +5 more
semanticscholar +1 more source
ABO incompatibility in newborn babies
مجلة كلية الطب, 2012 Bacjground: hemolytic disease of the newborn due to ABO icompatibility (HDN-ABO) is the most common cause of hemolytic disease of the newborn.
Numan N. Hameed +2 more
doaj +1 more source
Nephrotic syndrome associated with primary atypical hemolytic uremic syndrome
Brazilian Journal of Nephrology, 2020 Primary atypical hemolytic-uremic syndrome is a rare disease characterized by non-immune microangiopathic hemolytic anemia, thrombocytopenia, and renal dysfunction; it is related to alterations in the regulation of the alternative pathway of complement ...
Diana Carolina Bello-Marquez +3 more
doaj +2 more sources
Kasabach-Merritt syndrome arising from an Enteroatmospheric Fistula [PDF]
arXiv, 2022 Kasabach-Merritt syndrome (KMS) is a rare, life-threatening condition that is characterized by profound thrombocytopenia, hypofibrinogenemia, elevated partial thromboplastin time, and may also be associated with microangiopathic hemolytic anemia. It is well established that this phenomenon is notably associated with the vascular tumors kaposiform ...
arxiv
Expert Review of Hematology, 2017 Introduction: Hemolytic disease of the fetus and newborn (HDFN) remains a serious pregnancy complication which can lead to severe fetal anemia, hydrops and perinatal death. Areas covered: This review focusses on the current prenatal management, treatment
C. Zwiers +3 more
semanticscholar +1 more source