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  • 1
    Electronic Resource
    Electronic Resource
    The spectrum of X-ray manifestations in Cockayne's syndrome (1981)
    Springer
    Skeletal radiology 7 (1981), S. 173-177 
    Details
    ISSN: 1432-2161
    Keywords: Cockayne's syndrome ; Bone deformities ; Children, growth and development ; Premature aging ; Thymic hormone
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Cockayne's syndrome is a rare familial disorder characterised clinically by premature aging, appearing progressively from the third year on. The radiological manifestations of eight affected children have been studied and summarised. It is concluded that a skeletal survey can provide a roentgenologic pattern suggesting the diagnosis, even when it is inconclusive from the clinical signs during the first years of life. The aetiology of this syndrome is unknown, but the authors postulate the possible role of a defect of thymic hormone which has been found in all their cases.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00361860
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  • 2
    Electronic Resource
    Electronic Resource
    Case report 336 (1985)
    Springer
    Skeletal radiology 14 (1985), S. 296-300 
    Details
    ISSN: 1432-2161
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00352623
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    Paper (German National Licenses)
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  • 3
    Electronic Resource
    Electronic Resource
    Effect of Vibration Frequency and Sample Composition on Acoustic Properties of Y-Ba-Cu-O High-T〈sub〉C〈/sub〉 Superconductors (1989)
    s.l. ; Stafa-Zurich, Switzerland
    Solid state phenomena Vol. 6-7 (Jan. 1989), p. 501-506 
    Details
    ISSN: 1662-9779
    Source: Scientific.Net: Materials Science & Technology / Trans Tech Publications Archiv 1984-2008
    Topics: Physics
    Type of Medium: Electronic Resource
    URL: http://www.tib-hannover.de/fulltexts/2011/0528/02/25/transtech_doi~10.4028%252Fwww.scientific.net%252FSSP.6-7.501.pdf
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  • 4
    Electronic Resource
    Electronic Resource
    The proteus syndrome (1983)
    Springer
    European journal of pediatrics 140 (1983), S. 5-12 
    Details
    ISSN: 1432-1076
    Keywords: Proteus syndrome ; Macrodactyly ; Hemihypertrophy ; Pigmented nevi ; Skull anomalies ; Lipomas
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Four boys are described with partial gigantism of the hands and/or feet, pigmented nevi, hemihypertrophy, subcutaneous hamartomatous tumors and macrocephaly, and/or other skull anomalies. Three of these patients showed an accelerated growth in their first years of life. Two suffered from cystiform pulmonary abnormalities. The children showed normal mental development with the exception of one with traumatic brain damage. Parental consanguinity was not disclosed. As a result of a review of the literature, we can say that these cases do not conform to any well defined entity and would appear to represent a ‘new’ syndrome to be categorized under congenital hamartomatous disorders. The mode of inheritance of the undoubtedly genetically determined syndrome is yet not clearly understood. We propose the term Proteus syndrome for this ‘new’ syndrome.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00661895
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  • 5
    Electronic Resource
    Electronic Resource
    A new familial skeletal dysplasia with severely retarded ossification and abnormal modeling of bones especially of the epiphyses, the hands, and feet (1984)
    Springer
    European journal of pediatrics 141 (1984), S. 231-235 
    Details
    ISSN: 1432-1076
    Keywords: New skeletal dysplasia ; Multiple epiphyseal dysplasia ; Delayed maturation of hand feet pelvis sacrum
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Three brothers with a constitutional skeletal dysplasia characterized by an excessively retarded ossification, principally of the epiphyses, the pelvis, the hands and the feet, are reported. In the hands and feet the retarded ossification is combined with an abnormal modeling of the bones. All the children appeared normal at birth. At the time of examination a moderate degree of dwarfism could be predicted. There was no mental retardation. All laboratory investigations including chromosomal analyses and examination for acid mucopolysaccharides in the urine were normal. Parental consanguinity suggest an autosomal recessive inheritance. There is no resemblance of this disorder to any of the hitherto described groups of constitutional diseases of bones.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00572767
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  • 6
    Electronic Resource
    Electronic Resource
    Osteomalacia of the mother —rickets of the newborn (1987)
    Springer
    European journal of pediatrics 146 (1987), S. 292-293 
    Details
    ISSN: 1432-1076
    Keywords: Osteomalacia ; Neonatal rickets ; 25-hydroxy-vitamin D
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract During the last 4 years we observed four cases of neonatal rickets. The mothers of the infants suffered from osteomalacia for 1–3 years prior to its diagnosis shortly after the birth of their children. All four infants were born with craniotabes, and one infant had, in addition, a radial fracture. The diagnoses were confirmed by radiological and laboratory tests which revealed a rarefied bone structure, decreased serum 25-hydroxy-vitamin D and increased alkaline phosphatase levels in all patients. The disorder regressed under low-dose vitamin D3 therapy. As osteomalacia seems to be predominant in oriental women living in Berlin, it is necessary to consider vitamin D deficiency when clinical symptoms of this disease arise and to treat these women at least during pregnancy.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00716477
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  • 7
    Electronic Resource
    Electronic Resource
    Arteriovenous malformation of the great cerebral vein (of Galen) in a newborn (1987)
    Springer
    European journal of pediatrics 146 (1987), S. 87-89 
    Details
    ISSN: 1432-1076
    Keywords: a.v. malformation ; DSA ; Ultrasound
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract This is a report of a case with an arteriovenous (a.v.) malformation of the great cerebral vein. Applicable diagnostic procedures are reviewed. The initial diagnostic procedure in the approach to an a.v. malformation of the great vein of Galen is cerebral ultrasound. The findings in our patient are compared with those reported in the literature.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00647298
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  • 8
    Electronic Resource
    Electronic Resource
    Therapeutic approach to ingested Button-type batteries (1989)
    Springer
    Pediatric radiology 19 (1989), S. 114-118 
    Details
    ISSN: 1432-1998
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Button-type batteries ingested by 13 children were removed from the esophagus and the upper gastro-intestinal tract by means of the FE-EX® “OGTM-technique”. An initial radiogram from the nasopharynx to the anus was performed. We used the FE-EX® tube magnet with a cylindric Vacomax®/Vacodym® magnet. In all cases the button type battery was easily detected and retracted under fluoroscopic control with the magnet. All patients tolerated the procedure without subjective complaints and were discharged soon without a need of anesthesia, surgery/endoscopy or more radiography. The FE-EX® “OGTM” procedure is a relatively non-invasive approach to a potentially catastrophic pediatric problem.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF02387899
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  • 9
    Electronic Resource
    Electronic Resource
    Primary (isolated) bilateral pulmonary hypoplasia: a comparative study of radiologic findings and autopsy results (1986)
    Springer
    Pediatric radiology 16 (1986), S. 175-179 
    Details
    ISSN: 1432-1998
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Comparative radiologic/pathologic study of 45 newborns with primary and secondary pulmonary hypoplasia is presented and 43 cases were proven at autopsy. From 9 cases with primary pulmonary hypoplasia, 7 could be identified by 3 independent observers on chest radiographs. The roentgen criteria of primary pulmonary hypoplasia are evaluated and should serve in future to diagnose this condition clinically.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF02456280
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  • 10
    Electronic Resource
    Electronic Resource
    Pulmonary alveolar microlithiasis in pediatric patients — review of the world literature and two new observations (1987)
    Springer
    Pediatric radiology 17 (1987), S. 439-442 
    Details
    ISSN: 1432-1998
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Report of two new pediatric cases of pulmonary alveolar microlithiasis (PAM). PAM is a rare disease of unknown etiology; not more than 38 cases have been reported aged less than 18 years. The essential features of this disease are (1) a characteristic radiographic appearance of a sand-like opacity of both lungs and linear densities like “beads on a string» along the heart, pleura and interlobar fissures; this is best visualized by fluoroscopy in combination with magnification technique; (2) extremely few clinical signs and almost no laboratory abnormalities.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF02388272
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