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Träfflista för sökning "WFRF:(Etienne Mathieu) srt2:(2008-2009)"

Search: WFRF:(Etienne Mathieu) > (2008-2009)

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1.
  • Baudrier, Etienne, et al. (author)
  • Retrieval of the ornaments from the Hand-Press Period : An overview
  • 2009
  • In: Proceedings of the International Conference on Document Analysis and Recognition, ICDAR. - : IEEE. - 9780769537252 ; , s. 496-500
  • Conference paper (peer-reviewed)abstract
    • This paper deals with the topic of the retrieval of document images focused on a specific application: the ornaments of the Hand-Press period. It presents an overview as a result of the work and the discussions undertaken by a workgroup on this subject. The paper starts by giving a general view about digital libraries of ornaments and associated retrieval problematics. Two main issues are underlined: content based image retrieval (CBIR) and image difference visualization. Several contributions are summarized, commented and compared. Conclusions and open problems arising from this overview are twofold: 1. contributions on CBIR miss scale-invariant methods and don't provide significative evaluation results. 2. robust registration is the open problem for visual comparison.
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2.
  • Simon-Bouy, Brigitte, et al. (author)
  • Hypophosphatasia: molecular testing of 19 prenatal cases and discussion about genetic counseling.
  • 2008
  • In: Prenatal diagnosis. - : Wiley. - 0197-3851 .- 1097-0223. ; 28:11, s. 993-8
  • Journal article (peer-reviewed)abstract
    • OBJECTIVE: We studied hypophosphatasia (HP) mutations in 19 cases prenatally detected by ultrasonography without familial history of HP. We correlated the mutations with the reported ultrasound signs, and discussed genetic counseling with regard to the particular dominantly inherited prenatal benign form of HP. METHOD: The coding sequence of the tissue nonspecific alkaline phosphatase (TNSALP) gene was analyzed by DNA sequencing, and 3D modeling was used to locate the mutated amino acids with regard to the functional domains of TNSALP. RESULTS: Although reported ultrasound signs were heterogeneous, two mutated alleles were found in 18 of the 19 cases studied, indicating recessive transmission of the disease. Functional domains of TNSALP were affected by 74% of missense mutations. In all the cases, including one with only a heterozygous mutation, molecular, biological, and familial data do not corroborate the hypothesis of prenatal benign HP. The mutation c.1133A>T observed in the prenatal benign form of HP and common in USA was not found in this series. CONCLUSION: The results point out the prenatally detectable allelic heterogeneity of HP. The nature of the detected mutations and the evidence of recessive inheritance do not support these cases being affected with prenatal benign HP.
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