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  • 1
    Electronic Resource
    Electronic Resource
    s.l. ; Stafa-Zurich, Switzerland
    Materials science forum Vol. 150-151 (Jan. 1994), p. 297-306 
    ISSN: 1662-9752
    Source: Scientific.Net: Materials Science & Technology / Trans Tech Publications Archiv 1984-2008
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Acta neurochirurgica 104 (1990), S. 21-26 
    ISSN: 0942-0940
    Keywords: ACTH ; basophil proliferation ; ectopic pituitary adenoma ; pituitary adenoma
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Proliferation of pituitary basophil cells and occasional chromophobe and eosinophil cells into the posterior lobe was found in 61.8±6.9% (α=0.05) in routine necropsy series. The incidence and intensity of proliferation increased in accordance with increasing age. There were no sex differences. The cells were for the most part ACTH-productive; only a few were found to produce somatotropic hormone (STH) or prolactin in exceptional cases, when examined immunocytochemically. Proliferation of these cells appears to take place postnatally, probably in young adult ages. Basophil proliferation, stemming from the pars intermedia, was not related to any clinical features. However, in 6 out of 191 examined cases (3.1±2.5%), the proliferating cells displayed neoplastic potentiality, demonstrated as a combination of mitoses, multinuclear cells, polymorphism, and hypertrophy of the protoplasma in addition to intense proliferation. This finding, described for the first time, may contribute to a better understanding of the origin of silent corticotrophic cell adenomas.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1432-0533
    Keywords: Fetal brain development ; Immunohistochemistry ; Intrauterine growth retardation ; Microcephaly ; Seckel syndrome
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Marked intrauterine developmental retardation in a fetal case of Seckel syndrome was morphologically defined in the 29th week of gestation by comparing with a large number of length-matched and age-matched controls. Telencephalic micrencephaly with reduced neuroblast production, retarded functional differentiation of the pituitary gland, and generalized hypotrophy with craniofacial stigmata were observed.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Acta neuropathologica 25 (1973), S. 89-94 
    ISSN: 1432-0533
    Keywords: Intraspinal Schwannosis ; Zona terminalis Lissauer ; Recklinghausen's Disease ; Generalized Neurofibromatosis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Five cases of intraspinal schwannosis in the zona terminalis Lissauer were found in a series of 163 spinal cords and were discussed. They showed no tumors in the posterior roots and no Recklinghausen's symptomes. Whether this lesion is due to “formes frustes” of Recklinghausen's neurofibromatosis or a reactive change, is still undetermined.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Acta neuropathologica 65 (1984), S. 158-162 
    ISSN: 1432-0533
    Keywords: Anencephaly ; Cantrell-Haller-Ravitsch syndrome ; Dysraphism ; Ectopic germinal islets ; Exencephaly ; Heterotopia ; Iniencephaly
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary A case of exencephaly associated with spinal dysraphism and Cantrell-Haller-Ravitsch syndrome is described. Significant findings included exencephaly, multiple subcortical neuroepithelial islets with active proliferation, cerebellar aplasia, and abnormal flexion of the neuraxis, with spinal dysraphism of the cervicothoracic region. The various features of exencephaly, anencephaly, and iniencephaly are discussed. The significance of subcortical growth zones is evaluated in the light of experimental observations.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Acta neuropathologica 58 (1982), S. 78-80 
    ISSN: 1432-0533
    Keywords: Fetal leptomeningitis ; Intrauterine purulent leptomeningitis ; Streptococcal meningitis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary This may be the first report of intrauterine purulent leptomeningitis, the infection of which has been caused by amnio-chorionitis via the umbilical route. The fetus was stillborn at the 35th week of gestation. Neuropathologic features did not differ from those of neonatal meningitis.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Acta neuropathologica 64 (1984), S. 72-74 
    ISSN: 1432-0533
    Keywords: Encephalitis ; Intrauterine purulent encephalitis ; Hydranencephaly
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Intrauterine purulent necrotizing encephalitis was found in a stillborn male of the 30th gestational week. The necrotizing process in the brain, prominent in the white matter, suggested an early stage of hydranencephaly.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Acta neuropathologica 76 (1988), S. 212-215 
    ISSN: 1432-0533
    Keywords: Amyloidosis ; Cerebral amyloid ; Cerebral amyloidoma
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The brain of a 60-year-old patient with bronchial carcinoma presented a focal amyloid deposit in the white matter associated with myelin and axonal destruction. An additional lesion was found in the basal ganglia. This silent focal intracerebral accumulation of amyloid substance may be a prestadium of a “cerebral amyloidoma”. The histochemical chemical and immunohistochemical analysis of the accumulated amyloid indicated that it may belong to a novel type of amyloid.
    Type of Medium: Electronic Resource
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  • 9
    ISSN: 1432-0533
    Keywords: Gruber's syndrome ; Heterotopia in spinal cord ; Micropolygyria in neocortex ; Purkinje cell heterotopia
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary A macrosomic male infant with multiple malformations survived for 4 days. His external dysplasias comprised macrocephalus, cheilopalatoschisis, auricular anomalies, and unilateral hexadactyly; his internal dysplasias included cysts of kidneys and pancreas, and a patent foramen ovale. The child had frequent generalized convulsions and died of bronchopneumonia. Chromosomal analysis was normal. The main neuropathological findings were a cleft foramen magnum, micropolygyria and heterotopia of the neocerebrum, hypoplasia of the vermis and central white matter of the cerebellum, diffuse heterotopia of Purkinje cells, and unique heterotopic gray matter in the central cervical cord. The infant's disorder was classified as Gruber's syndrome, and this report may be the first detailed description of CNS malformations in this syndrome which, however, are probably not specific for this syndrome. The neuropathological findings were compatible with a heterochronic pathogenesis. This and the familial occurrence of malformations suggest a genetic nature of the syndrome.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Springer
    Acta neuropathologica 59 (1983), S. 150-154 
    ISSN: 1432-0533
    Keywords: Double hypophysis ; Dysraphism ; Frontonasal dysplasia ; Harmartoma of Hypothalamus ; Heterotopia ; Median cleft face syndrome
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary An unusual duplication of the hypophysis is described in a female baby aged 26 days with a median cleft face syndrome. Malformations of the cranium, brain, and spinal cord were confined to the ventral midline. These findings contrast to dysraphism, in which anomalies of dorsal neural and/or mesodermal structures are common. This rare condition of double hypophysis should also be classified among the midline cleft face syndrome in contrast to the formerly recorded cases of double hypophysis in partial twinning.
    Type of Medium: Electronic Resource
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