Barend F T Hogewind

Summary

Publications

  1. pmc Autosomal dominant optic neuropathy and sensorineual hearing loss associated with a novel mutation of WFS1
    Barend F T Hogewind
    Department of Ophthalmology, Radboud University Nijmegen Medical Centre, Nijmegen, The Netherlands
    Mol Vis 16:26-35. 2010
  2. doi request reprint Variable clinical spectrum of the myocilin Gln368X mutation in a Dutch family with primary open angle glaucoma
    Barend F T Hogewind
    Department of Ophthalmology, Radboud University Nijmegen Medical Centre, Nijmegen, The
    Curr Eye Res 35:31-6. 2010

Detail Information

Publications2

  1. pmc Autosomal dominant optic neuropathy and sensorineual hearing loss associated with a novel mutation of WFS1
    Barend F T Hogewind
    Department of Ophthalmology, Radboud University Nijmegen Medical Centre, Nijmegen, The Netherlands
    Mol Vis 16:26-35. 2010
    ..To describe the phenotype of a novel Wolframin (WFS1) mutation in a family with autosomal dominant optic neuropathy and deafness. The study is designed as a retrospective observational case series...
  2. doi request reprint Variable clinical spectrum of the myocilin Gln368X mutation in a Dutch family with primary open angle glaucoma
    Barend F T Hogewind
    Department of Ophthalmology, Radboud University Nijmegen Medical Centre, Nijmegen, The
    Curr Eye Res 35:31-6. 2010
    ..To describe the clinical phenotype in a family with primary open angle glaucoma harboring a p.Gln368X mutation in MYOC...