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Kinetics of surfactant in respiratory diseases of the newborn infant

The Journal of Maternal-Fetal & Neonatal Medicine, 2004
Deficiency or dysfunction of pulmonary surfactant plays a critical role in the pathogenesis of respiratory diseases in the newborn. We describe the studies made by applying two recently developed methods to measure surfactant kinetics. The first allows the measurement of endogenous surfactant phosphatidylcholine (PC) synthesis and kinetics by a ...
Verlato, G.   +5 more
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Manifestations of Disease in Newborns and Infants [PDF]

open access: possible, 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 ...
openaire   +1 more source

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.
openaire   +3 more sources

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.
C. Chintu   +4 more
openaire   +3 more sources

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.
Birdsong M   +3 more
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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.
Bernard J. Fogel   +2 more
openaire   +3 more sources

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 ...
Robert Guthrie   +2 more
openaire   +3 more sources

Skin disease of the newborn infant

The Journal of Pediatrics, 1943
Summary 1. A case of skin disease in an infant is presented with the clinicaland the post-mortem findings. 2. A discussion of the relation of pemphigus neonatorum, Ritter'sdisease, and Leiner's disease is presented, and consideration is given to the possible underlying causes.
openaire   +2 more sources

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.
Peter A. M. Auld   +4 more
openaire   +3 more sources

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.
Benjamin H. Landing   +2 more
openaire   +3 more sources

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