Results 251 to 260 of about 177,391 (311)
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Management of hemolytic disease of the newborn infant

The Journal of Pediatrics, 1959
Summary The management of hemolytic diseaseof the newborn infant has been reviewed with respect to the three major problems which may be presented: the prevention of stillbirth, the management of the infant severely ill at birth, and the prevention of kernicterus in the infant with hyperbilirubinemia.
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Respiratory Diseases of the Newborn Infant

2021
So much of our lung health throughout life is determined by what happens before birth and when we are born. Managing respiratory problems in newborn infants requires experience and teamwork, an understanding of the background to the problems, and knowledge of the evidence behind the clinical options available.
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Urine screening for metabolic disease in newborn infants

The Journal of Pediatrics, 1980
A new method for urine screening for metabolic disease in newborn infants is described. A battery of bacterial inhibition assays to test urine-impregnated filter paper from 3- to 4-week-old infants for amino acids, purines, and pyrimidines was used. We were able to establish the accuracy and efficiency of the method by examining 289 unknown specimens ...
T D, Paul, E W, Naylor, R, Guthrie
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Hemoglobinuria associated with hemolytic disease of the newborn infant

The Journal of Pediatrics, 1967
An infant with ABO incompatibility and glucose-6-phosphate dehydrogenase deficiency developed severe intravascular hemolysis leading to hemoglobinuria in the immediate neonatal period. Severe intravascular hemolysis with resultant hemoglobinuria is rare in ABO hemolytic disease of the newborn.
J J, Angella, E N, Prieto, B J, Fogel
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GENERALIZED CYTOMEGALIC INCLUSION DISEASE IN NEWBORN INFANTS

Journal of the American Medical Association, 1956
• Generalized cytomegalic inclusion disease is an intrauterine infection that, in its most serious form, causes symptoms at or soon after birth. The two infants here described had icterus, extensive petechial or ecchymotic hemorrhages, hepatomegaly, splenomegaly, and various laboratory findings indicating a severe blood dyscrasia.
M, BIRDSONG   +3 more
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The spectrum of ABO hemolytic disease of the newborn infant

The Journal of Pediatrics, 1979
A series of 1,704 infants of blood group O mothers have been studied to determine the relation between the degree of red cell sensitization and the cord hemoglobin and bilirubin concentrations. The infants with blood group A or B had significantly higher cord bilirubin and lower cord hemoglobin concentrations than the group O babies.
L, Desjardins   +4 more
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Manifestations of Disease in Newborns and Infants

1980
Obstructed airways Choanal atresia Macroglossia Micrognathia (Robin’s syndrome) Laryngomalacia Laryngeal webs Vocal cord paralysis Tracheomalacia Thyroglossal duct cysts Anomalies of the aortic arch Cardiac enlargement Disturbed pulmonary ventilation Atelectasis Aspiration Lobar ...
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Central Nervous System Disease in a Newborn Infant

Archives of Pediatrics & Adolescent Medicine, 1968
THE POSSIBLE etiology of central nervous system (CNS) disease in a newborn infant is discussed by three physicians. A representative case is presented. This communication is the result of a clinical conference at the Childrens Hospital of Los Angeles. Report of a Case History.
H T, Wright, G, Reed, B H, Landing
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Phototherapy in ABO hemolytic disease of the newborn infant

The Journal of Pediatrics, 1971
Phototherapy for ABO hemolytic disease of the newborn infant usually reduces orprevents a further rise in serum bilirubin levels. In light-treated infants, peak bilirubin concentrations do not occur after the third day of life and exceed 20 mg. per cent in only 10 per cent of the infants.
E, Kaplan   +3 more
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Occlusive vascular disease in asphyxiated newborn infants

The Journal of Pediatrics, 1984
Six full-term severely asphyxiated newborn infants underwent evaluation with digital intravenous angiography. All infants were comatose and flaccid and had seizures, depressed brainstem function, and signs of intracranial hypertension. An initial brain CT scan revealed diffuse hypodensities and compressed ventricles.
T M, Voorhies   +4 more
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