D Besch

Summary

Country: Germany

Publications

  1. ncbi request reprint Leber's hereditary optic neuropathy: clinical and molecular genetic findings in a patient with a new mutation in the ND6 gene
    D 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
  2. ncbi request reprint Visual field constriction and electrophysiological changes associated with vigabatrin
    Dorothea Besch
    Department of Neuro Ophthalmology and Pathophysiology of Vision, University Eye Hospital, Tubingen, Germany
    Doc Ophthalmol 104:151-70. 2002
  3. ncbi request reprint Mutation analysis of the ND6 gene in patients with Lebers hereditary optic neuropathy
    B Wissinger
    Molekulargenetisches Labor, Universitats Augenklinik, Tubingen, Germany
    Biochem Biophys Res Commun 234:511-5. 1997
  4. doi request reprint Extraocular surgery for implantation of an active subretinal visual prosthesis with external connections: feasibility and outcome in seven patients
    D Besch
    Centre for Ophthalmology, University of Tubingen, Tubingen, Germany
    Br J Ophthalmol 92:1361-8. 2008
  5. pmc Novel rhodopsin mutations and genotype-phenotype correlation in patients with autosomal dominant retinitis pigmentosa
    A Schuster
    University Eye Hospital, Department of Neuroophthalmology, Schleichstr 12 16, D 72076 Tuebingen, Germany
    Br J Ophthalmol 89:1258-64. 2005
  6. ncbi request reprint [Spontaneous ocular pulsation]
    D Besch
    Augenklinik, Eberhard Karls Universitat, Tubingen
    Ophthalmologe 102:1000-1, 1002. 2005
  7. ncbi request reprint [Genetic diseases of the eye]
    D Besch
    Universitäts Augenklinik Tübingen, Tubingen
    Klin Monbl Augenheilkd 222:955-71. 2005
  8. doi request reprint [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
  9. doi request reprint [Bilateral tumors of the eyebrows]
    D Süsskind
    Department für Augenheilkunde, Eberhard Karls Universitat Tubingen
    Ophthalmologe 107:558-61. 2010
  10. doi request reprint Visual field defects in acute optic neuritis--distribution of different types of defect pattern, assessed with threshold-related supraliminal perimetry, ensuring high spatial resolution
    J Nevalainen
    University Eye Hospital Oulu, Oulu, Finland
    Graefes Arch Clin Exp Ophthalmol 246:599-607. 2008

Collaborators

Detail Information

Publications11

  1. ncbi request reprint Leber's hereditary optic neuropathy: clinical and molecular genetic findings in a patient with a new mutation in the ND6 gene
    D 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...
  2. ncbi request reprint Visual field constriction and electrophysiological changes associated with vigabatrin
    Dorothea 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...
  3. ncbi request reprint Mutation analysis of the ND6 gene in patients with Lebers hereditary optic neuropathy
    B 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...
  4. doi request reprint Extraocular surgery for implantation of an active subretinal visual prosthesis with external connections: feasibility and outcome in seven patients
    D Besch
    Centre for Ophthalmology, University of Tubingen, Tubingen, Germany
    Br J Ophthalmol 92:1361-8. 2008
    ....
  5. pmc Novel rhodopsin mutations and genotype-phenotype correlation in patients with autosomal dominant retinitis pigmentosa
    A 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...
  6. ncbi request reprint [Spontaneous ocular pulsation]
    D Besch
    Augenklinik, Eberhard Karls Universitat, Tubingen
    Ophthalmologe 102:1000-1, 1002. 2005
  7. ncbi request reprint [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...
  8. doi request reprint [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...
  9. doi request reprint [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...
  10. doi request reprint Visual field defects in acute optic neuritis--distribution of different types of defect pattern, assessed with threshold-related supraliminal perimetry, ensuring high spatial resolution
    J Nevalainen
    University Eye Hospital Oulu, Oulu, Finland
    Graefes Arch Clin Exp Ophthalmol 246:599-607. 2008
    ....
  11. ncbi request reprint [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...