Results 321 to 330 of about 9,064,819 (381)
Some of the next articles are maybe not open access.
Archives of Pediatrics & Adolescent Medicine, 1983
In Reply .—Dr Ozsoylu raised an interesting point regarding our article. We believe, however, that the patient whom we described did not have hemolytic disease. He had not been jaundiced at birth, and no evidence of hemolysis had been noted during the three-year follow-up. Moreover, the raised reticulocyte count was noted only once, and we assumed that
Lya Auslaender +5 more
openaire +2 more sources
In Reply .—Dr Ozsoylu raised an interesting point regarding our article. We believe, however, that the patient whom we described did not have hemolytic disease. He had not been jaundiced at birth, and no evidence of hemolysis had been noted during the three-year follow-up. Moreover, the raised reticulocyte count was noted only once, and we assumed that
Lya Auslaender +5 more
openaire +2 more sources
Serum Haptoglobin in Hemolytic Disease
JAMA: The Journal of the American Medical Association, 1980To the Editor.— Inadequate construction of study and control groups by Marchand et al (1980;243:1909) inflates the apparent sensitivity and specificity of their serum haptoglobin assay. More important, there is no reason to believe that the test has much practical value.
openaire +3 more sources
Hemolytic disease of the newborn
1967In the pathologic states, collectively known as “hemolytic disease of the newborn”, the placenta is an integral component of the reacting system, and often reflects injury shared with the fetus. Hellman and Hertig described the salient features of placentas associated with the hydropic and icteric forms of this disease.
Shirley G. Driscoll, Kurt Benirschke
openaire +2 more sources
Pathogenesis of ABO hemolytic disease
American Journal of Obstetrics and Gynecology, 1960Abstract 1.1. Observations on 51 families in which ABO hemolytic disease occurred are reviewed. In all but one of the families, the mothers were found to be Group O in conformity with previous reports. This is attributed to the ability of Group O mothers to form antibodies of specificity anti-C as well as anti-A and anti-B. 2.2.
Vincent J. Freda +3 more
openaire +3 more sources
Transfusion, 2013
BACKGROUND: The purpose of this study was to evaluate the efficacy of intravenous human immunoglobulin (IVIG) in the presence of high‐intensity phototherapy in decreasing the need for exchange transfusion in newborns with rhesus hemolytic disease.
Maria Cristina Batista dos Santos +4 more
semanticscholar +1 more source
BACKGROUND: The purpose of this study was to evaluate the efficacy of intravenous human immunoglobulin (IVIG) in the presence of high‐intensity phototherapy in decreasing the need for exchange transfusion in newborns with rhesus hemolytic disease.
Maria Cristina Batista dos Santos +4 more
semanticscholar +1 more source
The Journal of Pediatrics, 1962
Summary The serologic diagnosis of ABO hemolytic disease with the two stage direct antiglobulin test with the use of fresh serum is presented. In 127 infants who were incompatible with the mother in the ABO blood group system, 9 were clinically affected infants.
F. Chung, A.C. Chan, H.G. Keitel
openaire +2 more sources
Summary The serologic diagnosis of ABO hemolytic disease with the two stage direct antiglobulin test with the use of fresh serum is presented. In 127 infants who were incompatible with the mother in the ABO blood group system, 9 were clinically affected infants.
F. Chung, A.C. Chan, H.G. Keitel
openaire +2 more sources
Postnatal outcome in neonates with severe Rhesus c compared to Rhesus D hemolytic disease
Transfusion, 2013Neonates with Rhesus c (Rh c) hemolytic disease of the fetus and newborn (HDFN) are often managed in the same way as neonates with Rhesus D (Rh D) HDFN, although evidence to support this policy is limited.
M. Rath +8 more
semanticscholar +1 more source
Hemolytic Anemia in Wilson's Disease
Annals of Internal Medicine, 1970Abstract Penicillamine therapy was discontinued for a period of 200 days in a patient with Wilson's disease. Copper reaccumulated in the body at the rate of about 0.43 mg/day.
G. R. Lee, A Deiss, G E Cartwright
openaire +3 more sources
Neonatology, 2012
Background: Etiology of cholestatic liver disease in neonates with hemolytic disease of the newborn (HDN) has been associated with iron overload due to intrauterine red cell transfusions (IUTs).
V. E. Smits-Wintjens +6 more
semanticscholar +1 more source
Background: Etiology of cholestatic liver disease in neonates with hemolytic disease of the newborn (HDN) has been associated with iron overload due to intrauterine red cell transfusions (IUTs).
V. E. Smits-Wintjens +6 more
semanticscholar +1 more source
Neonatal Morbidity after Exchange Transfusion for Red Cell Alloimmune Hemolytic Disease
Neonatology, 2012Background: Exchange transfusion (ET) is a high-risk procedure. The type and rate of complications in neonatal red cell alloimmune hemolytic disease exclusively are not clear. Objectives: Our aim was to study the type and rate of complications associated
V. E. Smits-Wintjens +6 more
semanticscholar +1 more source