Skip to search formSkip to main contentSkip to account menu

Erythroblastosis, Fetal

Known as: Erythroblastosis Fetali, disease haemolytic newborn, diseases hemolytic newborn 
A condition characterized by the abnormal presence of ERYTHROBLASTS in the circulation of the FETUS or NEWBORNS. It is a disorder due to BLOOD GROUP… 
National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2009
Highly Cited
2009
Fabry disease (α‐galactosidase A (α‐Gal A, GLA) deficiency) is a panethnic inborn error of glycosphingolipid metabolism. Because… 
Highly Cited
2008
Highly Cited
2008
In recent years, gene‐targeting studies in mice have elucidated many molecular mechanisms in vascular biology. However, it has… 
Review
2000
Review
2000
Cerebral hypoxia-ischemia (asphyxia) occurring in the fetus and newborn infant is a major cause of acute mortality and chronic… 
Highly Cited
2000
Highly Cited
2000
Antigens of the Rh blood group system are encoded by 2 homologous genes, RHD and RHCE, that produce 2 red cell membrane proteins… 
Highly Cited
1989
Highly Cited
1989
Newborn animals recover from neurological injury to a greater extent than adults in spite of the greater vulnerability of… 
Highly Cited
1988
Highly Cited
1988
Newborn screening for sickle cell disease has been recommended as a method of decreasing patient mortality. However, its… 
Highly Cited
1981
Highly Cited
1981
Pigmented naevi (PN) were clinically diagnosed in 1083 newborn infants from a series of 531,831 consecutive livebirths examined… 
Highly Cited
1964
Highly Cited
1964
Large populations (up to 600/cell) of spherical, electron-opaque granules ∼0.3 to 0.4 µ in diameter are characteristically found… 
Highly Cited
1933
Highly Cited
1933
Broth cultures of hemolytic streptococci derived from patients are capable of rapidly liquefying normal human fibrin clot. The…