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Träfflista för sökning "WFRF:(Mohammadi M.) srt2:(2005-2009)"

Search: WFRF:(Mohammadi M.) > (2005-2009)

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1.
  • Ebrahimi, M., et al. (author)
  • An Efficient Dynamic Multicast Routing Protocol for Distributing Traffic in NOCs
  • 2009
  • In: 2009 Design, Automation and Test in Europe Conference and Exhibition, DATE '09. ; , s. 1064-1069
  • Conference paper (peer-reviewed)abstract
    • Nowadays, in MPSoCs and NoCs, multicast protocol is significantly used for many parallel applications such as cache coherency in distributed shared-memory architectures, clock synchronization, replication, or barrier synchronization. Among several multicast schemes proposed in on chip interconnection networks, path-based multicast scheme has been proven to be more efficient than the tree-based, and unicast-based. In this paper a low distance path-based multicast scheme is proposed. The proposed method takes advantage of the network partitioning, and utilizing of an efficient destination ordering algorithm. The results in performance, and power consumption show that the proposed method outstands the previous on chip path-based multicasting algorithms.
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  • Aghamohammadi, A, et al. (author)
  • Progression of selective IgA deficiency to common variable immunodeficiency
  • 2008
  • In: International archives of allergy and immunology. - : S. Karger AG. - 1423-0097 .- 1018-2438. ; 147:2, s. 87-92
  • Journal article (peer-reviewed)abstract
    • Selective IgA deficiency (IgAD) is the most common primary immunodeficiency in Caucasians. Although it is often asymptomatic, selected patients show an increased frequency of infections, allergies and autoimmune manifestations. Common variable immunodeficiency (CVID) is a primary antibody deficiency disease that shares many clinical features with IgAD. A common genetic basis for IgAD and CVID has been suggested based on their occurrence in members of the same family and the similarity of the underlying B cell defects. Progression from IgAD to CVID has also been reported in several cases. Here we present 4 patients with IgAD and autoimmune features who subsequently developed CVID. All symptomatic IgAD patients, especially those with associated IgG subclass deficiency or autoimmune features, should be monitored for evolution to CVID. Early diagnosis of this conversion and institution of immunoglobulin therapy is effective in preventing severe bacterial infections and pulmonary insufficiency.
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  • Result 1-10 of 14

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