Research Topics
| D BeschSummaryCountry: Germany Publications
| Collaborators
|
Detail Information
Publications
Leber's hereditary optic neuropathy: clinical and molecular genetic findings in a patient with a new mutation in the ND6 geneD Besch
Abteilung für Pathophysiologie des Sehens und Neuroophthalmologie, Universitats Augenklinik, Schleichstrasse 12, D 72076 Tubingen, Germany
Graefes Arch Clin Exp Ophthalmol 237:745-52. 1999..We describe the clinical and molecular genetic findings in a LHON patient and his family with a new mtDNA mutation at np14568 in the ND6 gene...
Visual field constriction and electrophysiological changes associated with vigabatrinDorothea Besch
Department of Neuro Ophthalmology and Pathophysiology of Vision, University Eye Hospital, Tubingen, Germany
Doc Ophthalmol 104:151-70. 2002..We investigated functional, morphological and electrophysiological changes in patients under anti-epileptic therapy with vigabatrin (VGB), a GABA aminotransferase inhibitor...
Mutation analysis of the ND6 gene in patients with Lebers hereditary optic neuropathyB Wissinger
Molekulargenetisches Labor, Universitats Augenklinik, Tubingen, Germany
Biochem Biophys Res Commun 234:511-5. 1997..None of 170 analyzed control subjects carried this mutation. These findings provide evidence that several allelic ND6 gene mutations may be involved in Lebers hereditary optic neuropathy...
Extraocular surgery for implantation of an active subretinal visual prosthesis with external connections: feasibility and outcome in seven patientsD Besch
Centre for Ophthalmology, University of Tubingen, Tubingen, Germany
Br J Ophthalmol 92:1361-8. 2008....
Novel rhodopsin mutations and genotype-phenotype correlation in patients with autosomal dominant retinitis pigmentosaA Schuster
University Eye Hospital, Department of Neuroophthalmology, Schleichstr 12 16, D 72076 Tuebingen, Germany
Br J Ophthalmol 89:1258-64. 2005..To identify novel or rare rhodopsin gene mutations in patients with autosomal dominant retinitis pigmentosa and description of their clinical phenotype...
[Spontaneous ocular pulsation]D Besch
Augenklinik, ,
Ophthalmologe 102:1000-1, 1002. 2005
[Genetic diseases of the eye]D Besch
Universitäts Augenklinik Tübingen, Tubingen
Klin Monbl Augenheilkd 222:955-71. 2005..In this article, current knowledge on the clinical manifestations, aetiology and management of genetic diseases of the eye has been summarised...
[Arthrogryposis multiplex congenita and retinitis pigmentosa]N Stubiger
Department für Augenheilkunde, Universitäts Augenklinik Tübingen, Schleichstrasse 12 16, 72076, Tubingen, Deutschland
Ophthalmologe 106:1121-5. 2009..In such syndromes retinopathy as an ophthalmological manifestation of AMC has been described in the literature in only two patients...
[Bilateral tumors of the eyebrows]D Süsskind
Department für Augenheilkunde, Eberhard Karls Universitat Tubingen
Ophthalmologe 107:558-61. 2010..The bilateral or multiple manifestation of pilomatrixoma is uncommon and can be associated with myotonic dystrophy, sarcoidosis or Gardner's syndrome...
Visual field defects in acute optic neuritis--distribution of different types of defect pattern, assessed with threshold-related supraliminal perimetry, ensuring high spatial resolutionJ Nevalainen
University Eye Hospital Oulu, Oulu, Finland
Graefes Arch Clin Exp Ophthalmol 246:599-607. 2008....
[Evaluation of extensive visual field defects with computer-assisted kinetic perimetry]U Schiefer
, , Schleichstr. 12-16,
Klin Monatsbl Augenheilkd 218:13-20. 2001..1 degree and 3.0 degrees. CONCLUSION: Computer assisted kinetic perimetry is a new, useful, examiner-independent, reliable method for effective evaluation and monitoring of advanced visual field loss...
