Literature DB >> 16155673

Autosomal dominant Weill-Marchesani syndrome and glaucoma management.

Murat S Saricaoglu1, Ahmet Sengun, Ahmet Karakurt, Zeliha Colluoglu.   

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Year:  2005        PMID: 16155673

Source DB:  PubMed          Journal:  Saudi Med J        ISSN: 0379-5284            Impact factor:   1.484


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  2 in total

1.  Human eye development is characterized by coordinated expression of fibrillin isoforms.

Authors:  Dirk Hubmacher; Dieter P Reinhardt; Thomas Plesec; Katja Schenke-Layland; Suneel S Apte
Journal:  Invest Ophthalmol Vis Sci       Date:  2014-11-18       Impact factor: 4.799

2.  Geleophysic dysplasia associated with bilateral angle closure glaucoma.

Authors:  Murat Sinan Saricaoglu; Dilek Güven; Ahmet Karakurt; Hikmet Hasiripi
Journal:  Indian J Ophthalmol       Date:  2013-03       Impact factor: 1.848

  2 in total

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