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Patrik Schatz

Department of Ophthalmology

Lund University Hospital

Sweden

[email]@telia.com

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Affiliation

Department of Ophthalmology, Lund University Hospital, Sweden. 2003 - 2010

References

Recovery of retinal function after recent-onset rhegmatogenous retinal detachment in relation to type of surgery. Schatz, P., Andréasson, S. Retina (Philadelphia, Pa.) (2010) [Pubmed]
Retinal function after scleral buckling for recent onset rhegmatogenous retinal detachment: assessment with electroretinography and optical coherence tomography. Schatz, P., Holm, K., Andréasson, S. Retina (Philadelphia, Pa.) (2007) [Pubmed]
Variant phenotype of Best vitelliform macular dystrophy associated with compound heterozygous mutations in VMD2. Schatz, P., Klar, J., Andréasson, S., Ponjavic, V., Dahl, N. Ophthalmic Genet. (2006) [Pubmed]
Clinical phenotype in a Swedish family with a mutation in the IMPDH1 gene. Schatz, P., Ponjavic, V., Andréasson, S., McGee, T.L., Dryja, T.P., Abrahamson, M. Ophthalmic Genet. (2005) [Pubmed]
Multifocal electroretinography and optical coherence tomography in two patients with solar retinopathy. Schatz, P., Eriksson, U., Ponjavic, V., Andréasson, S. Acta. Ophthalmol. Scand (2004) [Pubmed]
Macular appearance by means of OCT and electrophysiology in members of two families with different mutations in RDS (the peripherin/RDS gene). Schatz, P., Abrahamson, M., Eksandh, L., Ponjavic, V., Andréasson, S. Acta. Ophthalmol. Scand (2003) [Pubmed]