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  • 1
    Electronic Resource
    Electronic Resource
    studies of renal homotransplantation in man (1965)
    Oxford, UK : Blackwell Publishing Ltd
    Annals of the New York Academy of Sciences 120 (1965), S. 0 
    Details
    ISSN: 1749-6632
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Natural Sciences in General
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1111/j.1749-6632.1965.tb30686.x
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  • 2
    Electronic Resource
    Electronic Resource
    STUDIES OF RENAL HOMOTRANSPLANTATION IN MAN (1964)
    Oxford, UK : Blackwell Publishing Ltd
    Annals of the New York Academy of Sciences 120 (1964), S. 0 
    Details
    ISSN: 1749-6632
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Natural Sciences in General
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1111/j.1749-6632.1964.tb34754.x
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    Paper (German National Licenses)
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  • 3
    Electronic Resource
    Electronic Resource
    CT in the evaluation of pleural versus pulmonary disease in children (1988)
    Springer
    Pediatric radiology 18 (1988), S. 14-19 
    Details
    ISSN: 1432-1998
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Post pneumonic empyema in children is the result of infection by Staphylococcus aureus in approximately 80% of cases. Approximately 93% of children with empyema respond well to treatment with appropriate antibiotics and drainage of the pleural space. We present seven children in whom such therapy failed to produce an adequate response. Computed tomography alone clearly excluded persistent pneumonia as a cause of symptoms while in all seven patients revealing an unexpectedly extensive empyema rind. This information, coupled with the lack of clinical improvement and the specific organism isolated, led to a change in clinical management. These children were infected by organisms other than Staphylococcus aureus and required surgical decortication of the fibrinous pleural rind to alleviate persistent symptoms.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF02395753
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    Paper (German National Licenses)
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  • 4
    Electronic Resource
    Electronic Resource
    Familial superior mesenteric artery syndrome (1990)
    Springer
    Pediatric radiology 20 (1990), S. 588-589 
    Details
    ISSN: 1432-1998
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Five members of a family of eight, including the father and four daughters, presented with symptoms previously attributed to the superior mesenteric artery syndrome. The four daughters also had radiographic studies supporting that diagnosis. This familial clustering raises the possibility of a genetic predisposition to this symptom and radiographic complex.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF02129061
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    Paper (German National Licenses)
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  • 5
    Electronic Resource
    Electronic Resource
    A radiologic update on medical diseases of the newborn chest (1995)
    Springer
    Pediatric radiology 25 (1995), S. 631-637 
    Details
    ISSN: 1432-1998
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract This paper reviews the common spectrum of medical diseases of the neonatal chest. Emphasis is on radiographic changes that have been produced by the introduction of new therapeutic maneuvers, particularly the use of artificial surfactant in treating hyaline membrane disease and the survival of profoundly premature newborns (less than 650 g). A discussion of meconium aspiration syndrome, neonatal pneumonia, transient tachypnea of the newborn, congenital lymphangiectasia, and congenital heart disease is also included. The effects on the neonatal chest radiograph of extracorporeal membrane oxygenation and high-frequency ventilation are also mentioned.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF02011835
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  • 6
    Electronic Resource
    Electronic Resource
    Retained fetal lung liquid in congenital lobar emphysema: A possible predictor of polyalveolar lobe (1993)
    Springer
    Pediatric radiology 23 (1993), S. 291-295 
    Details
    ISSN: 1432-1998
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract The purpose of this study was to determine whether retention of fetal lung liquid is more prevalent in polyalveolar congenital lobar emphysema than in conventional congenital lobar emphysema. Two patients with congenital lobar emphysema were prospectively identified in a 3-year period. Twenty-five such patients were identified in a retrospective study covering 39 years. Medical records were available for 22 patients who had 23 emphysematous lobes. Both babies from the prospective study and six subjects from the retrospective group had respiratory symptoms and underwent chest X-ray in the first day of life. Six of the eight babies with respiratory symptoms and chest imaging in the first day of life had retention of fetal lung liquid in an emphysematous lobe. All six of these lobes were polyalveolar. The lobe in one child was a polyalveolar lobe but without retained fetal lung liquid, and one child exhibited conventional lobar emphysema also without retained fetal lung liquid. One polyalveolar lobe caused no neonatal symptoms and was not imaged until the child was 3 months old. No baby with conventional lobar emphysema was shown to have retained fetal lung liquid. There seems to be a correlation between polyalveolar lobe and onset of respiratory symptoms in the first day of life. Retention of fetal lung liquid within the affected lobe was documented only in cases of polyalveolar lobe.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF02010918
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    Paper (German National Licenses)
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  • 7
    Electronic Resource
    Electronic Resource
    Esophageal stricture secondary to drug-induced toxic epidermal necrolysis (1984)
    Springer
    Pediatric radiology 14 (1984), S. 439-440 
    Details
    ISSN: 1432-1998
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Toxic epidermal necrolysis is a cutaneous disorder with high morbidity and mortality. Esophageal stricture has rarely been reported following recovery from this abnormality. A case is presented demonstrating the occurrence of an esophageal stricture following successful therapy. New methods of treatment are changing the mortality and morbidity such that esophageal stricture will be observed more frequently.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF02343438
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  • 8
    Electronic Resource
    Electronic Resource
    Small carpal bone surface area, a characteristic of Turner's syndrome (1985)
    Springer
    Pediatric radiology 15 (1985), S. 168-172 
    Details
    ISSN: 1432-1998
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract An abnormality which has received little attention but may be easily recognized on radiographs of the hand of patients with Turner's syndrome is described. Eleven of thirty-one patients (35.5%) with Turner's syndrome were shown on radiographs of the hand to have a visually detectable smallness of the bone surface area of the carpus when compared to the area of the second through fifth metacarpals. Values for the “C/M” ratio (the area of the carpals divided by the area of the second through fifth metacarpals) were calculated for films of 31 individuals with gonadal dysgenesis and compared with those from bone age-matched films of seventy-six individuals with normal development of the hand and wrist. A consistent difference with minimal overlap was documented. For all of the films of patients with Turner's syndrome the C/M ratio averaged 89% of the value in the films of the controls. In the 11 patients in whose films smallness was visually apparent, the C/M ratio averaged 82% of controls while in those where the diminution was detected only by planimetry the C/M ratio averaged 91% of controls. The incidence of a diminished C/M ratio was compared with the incidence of four other previously described signs of Turner's syndrome; although not seen as often as the coarse reticular pattern or delayed bone age, the C/M sign was recognizable without planimetry at least as commonly as the “metacarpal sign,” and a decreased carpal angle and/or Madelung's deformity. Taken together, these several criteria suggest the radiographic diagnosis of Turner's syndrome in more than 93% of cases.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF02388604
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  • 9
    Electronic Resource
    Electronic Resource
    Premature sternal fusion in gonadal dysgenesis with coarctation (1985)
    Springer
    Pediatric radiology 15 (1985), S. 350-352 
    Details
    ISSN: 1432-1998
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Gonadal dysgenesis and coarctation of the aorta were found in four patients to be associated with premature sternal fusion but possible etiologic relationship to shield chest deformity is suggested.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF02386775
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  • 10
    Electronic Resource
    Electronic Resource
    Hand-foot-genital syndrome: the importance of hallux varus (1990)
    Springer
    Pediatric radiology 20 (1990), S. 339-343 
    Details
    ISSN: 1432-1998
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract The hand-foot-genital syndrome is an autosomal dominant disorder previously reported in six families. This report of the seventh family identified with this syndrome is presented to emphasize the frequent occurrence of medial deviation of the first toes (hallux varus).
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF02013170
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