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  • Failure to thrive  (1)
  • Gaussian random fields  (1)
  • Mitochondrial myopathy  (1)
  • 1
    Digitale Medien
    Digitale Medien
    Corticosterone methyl oxidase type II deficiency: a cause of failure to thrive and recurrent dehydration in early infancy (1992)
    Springer
    European journal of pediatrics 151 (1992), S. 170-173 
    Details
    ISSN: 1432-1076
    Schlagwort(e): Corticosterone methyl oxidase type II ; Failure to thrive ; Salt wasting
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Medizin
    Notizen: Abstract Corticosterone methyl oxidase type II (CMO II) deficiency is an uncommon cause of salt-wasting in infancy. We describe a boy who presented with recurrent dehydration and severe failure to thrive in the first 3 months of life, associated with mild hyponatraemia (serum Na+ 127–132 mEq/l) and hyperkalaemia (serum K+ 5.3–5.9 mEq/l). The diagnosis was suggested by an elevated plasma renin activity (PRA): serum aldosterone ratio, and subsequently confirmed by an elevated serum 18-hydroxycorticosterone: aldosterone ratio. Treatment with 9α-fluorohydroxycortisone normalized growth parameters and PRA levels. CMO II deficiency should be considered in infants with recurrent dehydration and failure to thrive, even when serum sodium and potassium levels are not strikingly abnormal.
    Materialart: Digitale Medien
    URL: http://dx.doi.org/10.1007/BF01954376
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 2
    Digitale Medien
    Digitale Medien
    On the invariant measures for the two-dimensional euler flow (1987)
    Springer
    Journal of statistical physics 46 (1987), S. 729-742 
    Details
    ISSN: 1572-9613
    Schlagwort(e): Invariant measures for the Euler flow ; vortices ; Gaussian random fields
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Physik
    Notizen: Abstract It is proven that the canonical Gibbs measure associated with a gas of vortices of intensity ±√σ converges, in the limitN→∞, √σ→0,Nσ→const, to a Gaussian measure, which is invariant for the two-dimensional Euler equation.
    Materialart: Digitale Medien
    URL: http://dx.doi.org/10.1007/BF01013382
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 3
    Digitale Medien
    Digitale Medien
    Familial megaconial myopathy: A real nosologic entity (1983)
    Springer
    Acta neuropathologica 59 (1983), S. 70-74 
    Details
    ISSN: 1432-0533
    Schlagwort(e): Mitochondrial myopathy ; Giant mitochondria ; Familial mitochondrial myopathy
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Medizin
    Notizen: Summary The most prominent ultrastructural feature of muscle tissue in two siblings with a childhood-onset myopathy was the presence of giant mitochondria of up to 4 μm in length. The mitochondria had no tendency to aggregate and kept their normal localization among the myofibrils. Such a megaconial myopathy was first described by Shy and Gonatas (1964), In our family two members had the disease and consanguinity between their parents was present. These data suggest that megaconial myopathy might be a real nosologic entity genetically transmitted as an autosomal recessive trait.
    Materialart: Digitale Medien
    URL: http://dx.doi.org/10.1007/BF00690319
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