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  • 1
    Electronic Resource
    Electronic Resource
    Neonatal death dwarfism — a new form (1984)
    Springer
    Pediatric radiology 14 (1984), S. 451-452 
    Details
    ISSN: 1432-1998
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract A new type of neonatal death dwarfism is reported. Although it resembles superficially the metatropic dysplasia group of diseases it has some distinctive radiographic features which help to delineate it as a separate entity.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF02343443
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    Paper (German National Licenses)
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  • 2
    Electronic Resource
    Electronic Resource
    Mucolipidosis II: correlation between radiological features and histopathology of the bones (1989)
    Springer
    Pediatric radiology 19 (1989), S. 406-413 
    Details
    ISSN: 1432-1998
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Twelve cases of Mucolipidosis II (I-cell disease) with a wide range of severity of skeletal involvement were studied. Pathological findings in two cases provided helpful information in understanding the radiographic features of dysostosis multiplex. Inhibition of the growth plate cartilage calcification and rickets-like lesions were observed in the metaphyses. Enhanced subperiosteal remodelling and paratrabecular fibrosis were also evident in the diaphyses. High levels of parathormone were found in one case. This finding supports the hypothesis that bone lesions may be secondary, at least in part, to damage in such viscera as the kidney and/or the liver and that they are mediated by vitamin D and parathormone.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF02387638
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    Paper (German National Licenses)
    Fulltext
  • 3
    Electronic Resource
    Electronic Resource
    Melorheostosis: Presentation of a case followed up for 24 years (1987)
    Springer
    Archives of orthopaedic and trauma surgery 106 (1987), S. 123-125 
    Details
    ISSN: 1434-3916
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Zusammenfassung Es wird über einen Fall von Melorheostose des linken Armes bei einer Frau berichtet, dessen Verlauf über 24 Jahre beobachtet wurde. Die Autoren weisen auf die hauptsächlichen klinischen und radiologischen Erscheinungen, die mögliche Pathogenese und auf das langsame unaufhaltsame Fortschreiten der Veränderung hin und stellen fest, daß auch in dem von ehnen beobachteten Fall die Lokalisation der Veränderung der Sklerotomanordnung entspricht.
    Notes: Summary The case of a woman affected by Melorheostosis of the left arm, who was followed for 24 years, is presented. After a brief review of the main clinico-radiological features and the most likely pathogenetic theory, the authors point out the slow but inexorable progression of the alterations and their localization, which is strictly limited to the dermatome supplied by a spinal nerve.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00435426
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    Paper (German National Licenses)
    Fulltext
  • 4
    Electronic Resource
    Electronic Resource
    An unusual kind of muscular and skeletal involvement in a heroin addict (1984)
    Springer
    Archives of orthopaedic and trauma surgery 103 (1984), S. 140-141 
    Details
    ISSN: 1434-3916
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Zusammenfassung Es wird über einen Fall von beidseitiger Osteomyelitis der Ulna mit Verklebung und Sklerose der regionalen Haut mit Muskulatur und mit Beugekontrakturen der Fingerendgelenke 2–5 bei einem Heroin-Süchtigen berichtet.
    Notes: Summary After a brief review of the infectious complications that frequently occur in heroin users, the authors report a case of chronic osteomyelitis affecting the ulnar diaphysis bilaterally. Musculo-cutaneous dystrophic lesions were also present and resulted in forced flexion of the distal phalanges of fingers 2–5. The most likely pathogenetic development discussed.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00389589
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    Paper (German National Licenses)
    Fulltext
  • 5
    Electronic Resource
    Electronic Resource
    Premature epiphyseal fusion and extramedullary hematopoiesis in thalassemia (1987)
    Springer
    Skeletal radiology 16 (1987), S. 533-538 
    Details
    ISSN: 1432-2161
    Keywords: Premature epiphyseal fusion ; Extramedullary hematopoiesis ; Thalassemia ; Hemoglobin synthesis ; Low-transfusion regimen ; Hypertransfusion regimen
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract The main skeletal abnormalities in β-thalassemia are widening of medullary spaces, rarefaction of bone trabeculae, thinning of cortical bone, and perpendicular periosteal spiculation. Premature epiphyseal fusion (PEF) and extramedullary hematopoiesis (EH) are found, though more rarely. The incidence of PEF and EH in 64 patients affected by β-thalassemia is reported. The different incidence of such complications in thalassemia major and intermedia is reported, and a possible correlation with transfusion regimen is also considered.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00351267
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    Paper (German National Licenses)
    Fulltext
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