Louise Eksandh

Summary

Country: Sweden

Publications

  1. ncbi request reprint Full-field ERG in patients with Batten/Spielmeyer-Vogt disease caused by mutations in the CLN3 gene
    L B Eksandh
    Department of Ophthalmology, University Hospital, Lund, Sweden
    Ophthalmic Genet 21:69-77. 2000
  2. ncbi request reprint Phenotypic expression of juvenile X-linked retinoschisis in Swedish families with different mutations in the XLRS1 gene
    L C Eksandh
    Department of Ophthalmology, University Hospital, Lund, Sweden
    Arch Ophthalmol 118:1098-104. 2000
  3. ncbi request reprint Best's vitelliform macular dystrophy caused by a new mutation (Val89Ala) in the VMD2 gene
    L Eksandh
    Department of Ophthalmology, University Hospital, Lund, Sweden
    Ophthalmic Genet 22:107-15. 2001
  4. ncbi request reprint Different clinical expressions in two families with Stargardt's macular dystrophy (STGD1)
    L Eksandh
    Department of Ophthalmology, University Hospital of Lund, Sweden
    Acta Ophthalmol Scand 79:524-30. 2001
  5. ncbi request reprint Clinical features of achromatopsia in Swedish patients with defined genotypes
    Louise Eksandh
    Department of Ophthalmology, University Hospital, Lund, Sweden
    Ophthalmic Genet 23:109-20. 2002
  6. ncbi request reprint Juvenile X-linked retinoschisis with normal scotopic b-wave in the electroretinogram at an early stage of the disease
    Louise Eksandh
    Department of Ophthalmology, University Hospital of Lund, Sweden
    Ophthalmic Genet 26:111-7. 2005
  7. ncbi request reprint Clinical studies of X-linked retinitis pigmentosa in three Swedish families with newly identified mutations in the RP2 and RPGR-ORF15 genes
    Sten Andreasson
    Department of Ophthalmology, University Hospital of Lund, Lund, Sweden
    Ophthalmic Genet 24:215-23. 2003
  8. ncbi request reprint Macular appearance by means of OCT and electrophysiology in members of two families with different mutations in RDS (the peripherin/RDS gene)
    Patrik Schatz
    Department of Ophthalmology, Lund University Hospital, 221 85 Lund, Sweden
    Acta Ophthalmol Scand 81:500-7. 2003
  9. doi request reprint Autoantibodies against bestrophin in a patient with vitelliform paraneoplastic retinopathy and a metastatic choroidal malignant melanoma
    Louise Eksandh
    Arch Ophthalmol 126:432-5. 2008

Detail Information

Publications9

  1. ncbi request reprint Full-field ERG in patients with Batten/Spielmeyer-Vogt disease caused by mutations in the CLN3 gene
    L B Eksandh
    Department of Ophthalmology, University Hospital, Lund, Sweden
    Ophthalmic Genet 21:69-77. 2000
    ..To investigate, using full-field ERG, the retinal function in patients with Batten/Spielmeyer-Vogt disease caused by mutations in the CLN(3) gene...
  2. ncbi request reprint Phenotypic expression of juvenile X-linked retinoschisis in Swedish families with different mutations in the XLRS1 gene
    L C Eksandh
    Department of Ophthalmology, University Hospital, Lund, Sweden
    Arch Ophthalmol 118:1098-104. 2000
    ..To describe the clinical phenotype of juvenile X-linked retinoschisis in patients with different mutations in the XLRS1 gene...
  3. ncbi request reprint Best's vitelliform macular dystrophy caused by a new mutation (Val89Ala) in the VMD2 gene
    L Eksandh
    Department of Ophthalmology, University Hospital, Lund, Sweden
    Ophthalmic Genet 22:107-15. 2001
    ..To describe the clinical phenotype in a family with Best's vitelliform macular dystrophy (BMD) and a new mutation (Val89Ala) in the VMD2 gene...
  4. ncbi request reprint Different clinical expressions in two families with Stargardt's macular dystrophy (STGD1)
    L Eksandh
    Department of Ophthalmology, University Hospital of Lund, Sweden
    Acta Ophthalmol Scand 79:524-30. 2001
    ..To describe the clinical expressions, with emphasis on electrophysiological examinations, in two Swedish families with Stargardt's macular dystrophy (STGD1)...
  5. ncbi request reprint Clinical features of achromatopsia in Swedish patients with defined genotypes
    Louise Eksandh
    Department of Ophthalmology, University Hospital, Lund, Sweden
    Ophthalmic Genet 23:109-20. 2002
    ..To describe the clinical phenotype, with emphasis on the electrophysiological findings, of patients with autosomal recessive rod monochromacy (RM) and defined mutations in the CNGA3/CNGB3 genes...
  6. ncbi request reprint Juvenile X-linked retinoschisis with normal scotopic b-wave in the electroretinogram at an early stage of the disease
    Louise Eksandh
    Department of Ophthalmology, University Hospital of Lund, Sweden
    Ophthalmic Genet 26:111-7. 2005
    ..To report four cases of genetically verified juvenile X-linked retinoschisis (XLRS) with normal scotopic b-waves in full-field ERG, including one patient with a novel mutation (W50X) in the RS1 gene...
  7. ncbi request reprint Clinical studies of X-linked retinitis pigmentosa in three Swedish families with newly identified mutations in the RP2 and RPGR-ORF15 genes
    Sten Andreasson
    Department of Ophthalmology, University Hospital of Lund, Lund, Sweden
    Ophthalmic Genet 24:215-23. 2003
    ....
  8. ncbi request reprint Macular appearance by means of OCT and electrophysiology in members of two families with different mutations in RDS (the peripherin/RDS gene)
    Patrik Schatz
    Department of Ophthalmology, Lund University Hospital, 221 85 Lund, Sweden
    Acta Ophthalmol Scand 81:500-7. 2003
    ..To describe the phenotype using electroretinography and optical coherence tomography (OCT) in members of two families with different mutations in RDS...
  9. doi request reprint Autoantibodies against bestrophin in a patient with vitelliform paraneoplastic retinopathy and a metastatic choroidal malignant melanoma
    Louise Eksandh
    Arch Ophthalmol 126:432-5. 2008