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  • 1
    Digitale Medien
    Digitale Medien
    Oxford, UK : Blackwell Publishing Ltd
    Annals of the New York Academy of Sciences 501 (1987), S. 0 
    ISSN: 1749-6632
    Quelle: Blackwell Publishing Journal Backfiles 1879-2005
    Thema: Allgemeine Naturwissenschaft
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 2
    Digitale Medien
    Digitale Medien
    Springer
    Acta neuropathologica 50 (1980), S. 175-179 
    ISSN: 1432-0533
    Schlagwort(e): Arthrogryposis ; Facial anomalies
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Medizin
    Notizen: Summary An infant with the clinical syndrome of multiple joint ankyloses and facial anomalies was examined at autopsy. Neuropathologic analysis disclosed reduced numbers of spinal motor neurons and denervation atrophy of skeletal muscle as the basis for joint ankyloses. A comparison of the neuropathologic findings in this case to those of other clinically similar cases reported recently confirms that this phenotype is not specific, and occurs in a variety of neuro-muscular diseases only some of which are likely to be inherited as an autosomal recessive trait. Diagnostic evaluation of these disorders should include both chromosomal analysis and confirmation of the underlying pathologic process.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 3
    Digitale Medien
    Digitale Medien
    Springer
    Acta neuropathologica 42 (1978), S. 231-235 
    ISSN: 1432-0533
    Schlagwort(e): Porencephaly ; Perfusion failure ; Circle Willis
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Medizin
    Notizen: Summary An infant with multiple congenital anomalies was found at autopsy to have a porencencephalic defect on the ventral surface of the left frontal lobe. The intracranial defect was seen in association with an anomalous configuration of the circle of Willis. The zone of tissue destruction corresponded to the vascular territory of the anterior choroidal and lenticulo-striate branches of the proximal middle cerebral arteries, which were absent on the left. The developmental anomaly of the circle of Willis may have predisposed to tissue destruction by compromising cerebral perfusion at midgestation, a stage of rapid brain growth.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 4
    Digitale Medien
    Digitale Medien
    Springer
    Acta neuropathologica 36 (1976), S. 269-283 
    ISSN: 1432-0533
    Schlagwort(e): Microgyria ; Laminar necrosis ; Golgi study
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Medizin
    Notizen: Abstract A case of extensive classical four layered cerebral microgyria was examined in whole brain serial section using routine cell and fiber stains, and in Golgi impregnations. Golgi preparations demonstrate that microgyric cortex contains the spectrum of neurons characteristically found in normal cortex, and that they are segregated by class into horizontal laminae comparable to layers I–VI in the normal. In microgyric cortex neurons of the mid-cortical layers, variably layers III–V, are replaced by a tangential band of fibrous astrocytes. These findings confirm impressions from general cell and fiber stains that classical four layered microgyria is the result of a destructive process striking predominantly in mid-cortical regions. It must occur after migration is complete but before the development of secondary and tertiary gyri, that is, between the fifth and seventh fetal months. The cellular pathology as seen in Golgi impregnations establishes that neurons surviving above the scar are normally differentiated, aligned, and oriented. By exception, many surviving neurons at the border of the scar have attenuated dendritic arbors which are oriented tangentially. Very few axons or dendrites actually traverse the scar.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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