Results 211 to 220 of about 22,152 (250)
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CONGENITAL ATRESIA OF THE INTESTINE

Archives of Pediatrics & Adolescent Medicine, 1929
Although rare, congenital atresia of the intestine occurs with sufficient frequency to be of clinical importance. Calder 1 first called attention to this condition in 1733, and case reports, discussions of etiology, symptomatology and treatment have appeared at intervals since, more frequently during the past quarter century. Attention should be called
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Origin of Intestinal Atresia of Newborn

JAMA, 1964
Current concepts of the pathogenesis of intestinal atresia of the newborn cast considerable doubt on the classical theory of failure of recanalization. Clinical and experimental evidence make it probable that atresias are the consequence of intrauterine abdominal catastrophes occurring late in fetal life.
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CONGENITAL INTESTINAL ATRESIA

Archives of Pediatrics & Adolescent Medicine, 1931
Congenital atresia and stenosis of the intestine, exclusive of the pylorus, rectum and anal canal, is a relatively rare condition, occurring in about 1 of 20,000 infants. We have been able to find mention of more than 500 instances previously reported in the literature, though this number probably does not include all the recorded cases.
C. H. Webb, Owen H. Wangensteen
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Intestinal Atresia

2010
Milestones in Pediatric Surgery.- Milestones in Pediatric Surgery.- Principles of Surgical Science.- Fluids, Electrolytes, and Dehydration.- Metabolic Response to Injury and Sepsis.- Shock.- Parenteral Nutrition.- Hematology for Surgeons.- Postoperative Problems.- Neonatal Physiology and Care.- Fetal and Neonatal Surgery.- Fetal Surgery: General ...
Sinha, Chandrasen K.   +2 more
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Intestinal Atresia

Archives of Surgery, 1968
G, Dykstra   +2 more
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Atresia of the Small Intestine

Southern Medical Journal, 1969
Levy Jl, Linder Lh
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Congenital atresia of the small intestine

The American Journal of Surgery, 1962
Abstract Congenital atresia of the small intestine is rare, uniformly fatal if untreated and demands early diagnosis and careful preoperative preparation. Corrective surgery must be precise, designed to remedy the lesion in a single procedure and conducted with careful attention to blood replacement and maintenance of body warmth.
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Acquired intestinal atresia

Journal of Pediatric Surgery, 1971
Meredith Alrich   +2 more
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Intestinal Atresia and Stenosis

2016
Congenital atresia and stenosis of the small intestine are classified into the four groups. Type I: The obstruction is caused by a membrane or web. Type II: Blind-ending proximal loop connected by a fibrous cord. Type III(a): The atresia ends blindly with no fibrous connecting with a mesenteric defect. Type III(b): “Apple peel-type”
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