Literature DB >> 9333404

[Albinism. Current clinical and molecular genetic aspects of an important differential congenital nystagmus diagnosis].

B Lorenz1.   

Abstract

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Year:  1997        PMID： 9333404     DOI： 10.1007/s003470050155

Source DB:  PubMed          Journal:  Ophthalmologe        ISSN： 0941-293X            Impact factor:   1.059


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  3 in total

1.  Deletion in the OA1 gene in a family with congenital X linked nystagmus.

Authors:  M Preising; J P Op de Laak; B Lorenz
Journal:  Br J Ophthalmol       Date:  2001-09       Impact factor: 4.638

2.  Monocular visual activation patterns in albinism as revealed by functional magnetic resonance imaging.

Authors:  Bernd Schmitz; Barbara Käsmann-Kellner; Torsten Schäfer; Christoph M Krick; Georg Grön; Martin Backens; Wolfgang Reith
Journal:  Hum Brain Mapp       Date:  2004-09       Impact factor: 5.038

Review 3.  [Abnormal representations in the visual cortex of patients with albinism: diagnostic aid and model for the investigation of the self-organisation of the visual cortex].

Authors:  M B Hoffmann; L C Schmidtborn; A B Morland
Journal:  Ophthalmologe       Date:  2007-08       Impact factor: 1.059
  3 in total

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