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  • 1
    Electronic Resource
    Electronic Resource
    Black foam and emulsion films from nonionic surfactant solutions: rupture by hole formation (1988)
    Springer
    Colloid & polymer science 266 (1988), S. 921-925 
    Details
    ISSN: 1435-1536
    Keywords: Foam films ; emulsion films ; film rupture ; rupture theory ; hole nucleation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract The concept that rupture of bilayer films is caused by nucleation of holes was checked for foam and emulsion films stabilized by the same nonionic surfactant. Newtonian black (NB) films were formed in a ring-cell from a biconcave drop with air or nonane, respectively, as the ambient phase. The lifetime of the foam and emulsion films increases with surfactant concentration. This relation is analysed on the basis of above mentioned theory.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF01410847
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    Paper (German National Licenses)
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  • 2
    Electronic Resource
    Electronic Resource
    The value of family investigations in newly detected Charcot-Marie-Tooth disease in children (1995)
    Springer
    European journal of pediatrics 154 (1995), S. S40 
    Details
    ISSN: 1432-1076
    Keywords: Charcot-Marie-Tooth disease 1A ; Duplication on chromosome 17p11.2 ; Variable clinical phenotype
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Charcot-Marie-Tooth disease (CMT) was diagnosed by nerve conduction velocity and histology of the sural nerve in two boys aged 3 and 6 years with clinical signs of a severe neuromuscular disease. DNA analysis revealed the typical duplication on chromosome 17p 11.2 (2.7 kb allele) for CMT 1A. Although none of their family members reported symptoms of neuromuscular disease, the nerve conduction velocity was reduced in three members (father and two aunts). They were homozygous for the 2.7 kb allele and were assumed to carry three copies of this allele. The very differing clinical picture from one generation to the next in patients with identical neurophysiological and genetic results is discussed.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF02191504
    Library Location Call Number Volume/Issue/Year Availability
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    Paper (German National Licenses)
    Fulltext
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