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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Pediatric surgery international 2 (1987), S. 216-222 
    ISSN: 1437-9813
    Keywords: Oesophageal atresia ; Gasless abdomen ; Oesophageal replacement ; Long gap
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract At the Royal Children's Hospital, Melbourne, 553 babies with oesophageal atresia and/or tracheo-eesophageal fistula have been admitted during the past 39 years; 36 (6.5%) of these had oesophageal atresia without a tracheo-oesophageal fistula. Definitive surgery was performed in 27 patients: the primary definitive procedure was oesphageal anastomosis in 15 and oesophageal replacement in 12. Aspects of diagnosis and selection of the most appropriate treatment modality are discussed, with the results of treatment presented. Our current policy is to perform an oesphhageal anastomosis whenever possible, and this has been successful in 7 of the last 11 patients.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Pediatric surgery international 4 (1989), S. 238-240 
    ISSN: 1437-9813
    Keywords: Oesophageal atresia ; Livaditis procedure ; Oesophageal diverticulum
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract The findings and management in a male patient who developed a symptomatic oesophageal diverticulum 6 years after a circular myotomy was used to facilitate oesophageal anastomosis during repair of his oesophageal atresia are described.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Pediatric surgery international 2 (1987), S. 198-211 
    ISSN: 1437-9813
    Keywords: Tracheo-oesophageal fistula ; “H” fistula ; “N” fistula
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract At the Royal Children's Hospital, Melbourne, 28 patients with a congenital tracheo-oesophageal fistula were seen during a 38-year period, representing 5.2% of all babies seen with oesophageal atresia and/or tracheo-oesophageal fistula. Diagnostic delay occurred frequently because of failure to appreciate the significance of the clinical picture. There was variation in the level of the fistula; the basic pattern of investigation and management is now quite uniform.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Pediatric surgery international 2 (1987), S. 195-197 
    ISSN: 1437-9813
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Pediatric surgery international 4 (1989), S. 386-389 
    ISSN: 1437-9813
    Keywords: Achalasia ; Long-term results ; Oesophageal myotomy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Twenty children with achalasia of the cardia were seen at the Royal Children's Hospital, Melbourne in the years 1953 to 1986. The clinical presentation, investigations, and treatment are discussed. Ten children have been followed for 10 or more years and their late follow-up results are reported. The majority are symptomatic, and this is usually related to oesophageal dysmotility rather than gastro-oesophageal reflux.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Pediatric surgery international 1 (1986), S. 117-121 
    ISSN: 1437-9813
    Keywords: Esophagus: Atresia ; Tracheobronchial elements ; Stenosis abnormal motility
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract A histological study was conducted on unoperated specimens from six infants with esophageal atresia and tracheo-esophageal fistula. Sub-serial sections of the distal segment showed tracheobronchial elements in five cases, including cartilage in three. Normal esophageal layering was seen at a variable distance from the tracheobronchial end of the fistula. Tracheobronchial elements, including cartilage, were also seen in two other surgical specimens, which suggests that tracheobronchial elements may be very common in tracheo-esophageal fistula, and in some cases may lead to stenosis or abnormal motility following otherwise successful anastomosis.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Pediatric surgery international 2 (1987), S. 278-281 
    ISSN: 1437-9813
    Keywords: Oesophageal atresia ; Tracheo-oesophageal fistula ; Vertebra ; Spinal anomalies ; Rib
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Oesphageal atresia and/or tracheo-oesophageal fistula are relatively common congenital anomalies, occurring once in 3, 000 births [6, 10]. Associated anomalies are seen frequently, and in a series of 538 patients admitted to the Royal Children's Hospital, Melbourne, 256 had additional anomalies (47.5%). Evaluation of the spine was possible in 345 patients; in 57, structural vertebral anomalies were present (16.5%). Of the 57 with a structural abnormality of the spine, 40 had an abnormality of formation, 6 an abnormality of segmentation, and 10 had a combined defect. In the other patient, a bipartite cervical vertebra was present. Eight patients had scoliosis without a recognisable congenital spinal abnormality. In 81 there was a congenital rib abnormality; 56 of this group had a normal spine, 24 had a structural abnormality of the spine, and in 1 patient scoliosis was present without a structural abnormality of the spine. Comparison is made between our findings and the findings in other reported series and comments are made on the significance of spinal and/or rib anomalies in association with oesophageal atresia.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Pediatric surgery international 4 (1989), S. 193-198 
    ISSN: 1437-9813
    Keywords: Neurofibromatosis ; Neurofibrosarcoma ; Von Recklinghausen's disease
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract In patients with von Recklinghausen's disease or neurofibromatosis, a symptom of grave prognosis is the sudden increase in size of a previously static or slow-growing mass. We report five cases where such an increase in size heralded transformation of a plexiform neurofibroma into a malignant neurofibrosarcoma. CT scanning is a useful investigation in such patients, though little in our current surgical armamentarium appears to alter the dismal prognosis in these cases.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 316 (1985), S. 617-620 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] The FAO/UNEFs8'9 estimate of deforestation in the tropics is compared in Table 1 with estimates made by Myers10'12 and the FAO's Production Yearbook13. Comparison of the rates given by FAO/UNEP and the Production Yearbook assumes that deforestation of the open and closed forests of the former is ...
    Type of Medium: Electronic Resource
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