نتایج جستجو برای: pellucid marginal degeneration

تعداد نتایج: 102937  

2005
Michal Laclavik Zoltan Balogh Emil Gatial Ladislav Hluchy

In this paper we describe a semantic knowledge model of an agent as well as implementation and use of such model using the Jena semantic library and the JADE agent system. The solution has been used and evaluated in the Pellucid and K-Wf Grid projects.

Journal: :Journal of Evolution of Medical and Dental Sciences 2015

Journal: :European journal of ophthalmology 2013
Luis F Mejía Juan P Santamaría Ana M Gaviria Ana M Rodríguez

PURPOSE To report a case of Fuchs' superficial marginal keratitis managed with circumferential marginal corneoscleral lamellar patch graft. METHODS Interventional case report. RESULTS A 34-year-old man presented with several years' history of ill-defined symptoms of binocular ocular irritation associated with vision loss, mostly in the left eye. A superior marginal corneal thinning was foun...

2007
Ryszard Ochyra

1. Plants acrocarpous, growing erect in tufts. Capsule immersed with columella falling with attached operculum after dehiscence. Annulus absent. Central strand present. Lamina cells with straight walls, irregularly quadrate throughout and only short rectangular at the base .........................................Schistidium rivulare 1. Plants cladocarpous, prostrate in mats. Capsule exserted w...

Journal: :Revista Colombiana de Computación 2005
Simon C. Lambert Álvaro Enrique Arenas Alistair J. Miles

The Pellucid project developed an adaptable and customisable platform for enabling experience management in public organisations. A framework for experience management has been developed based on the generation of ‘active hints’ that are presented to the user according to working context. Working context encompasses both position in the work process and domain-specific characteristics. The pape...

Journal: :BMC Medicine 2006
Sairam V Jabba Alisha Oelke Ruchira Singh Rajanikanth J Maganti Sherry Fleming Susan M Wall Lorraine A Everett Eric D Green Philine Wangemann

BACKGROUND Pendred syndrome, an autosomal-recessive disorder characterized by deafness and goiter, is caused by a mutation of SLC26A4, which codes for the anion exchanger pendrin. We investigated the relationship between pendrin expression and deafness using mice that have (Slc26a4+/+ or Slc26a4+/-) or lack (Slc26a4-/-) a complete Slc26a4 gene. Previously, we reported that stria vascularis of a...

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