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List of works by Patrik Schatz

Accommodative esotropia and Brown syndrome in a girl with recessive geleophysic dysplasia

scientific article published on 08 November 2018

Analysis of retinal function and structure in autosomal recessive retinal-renal ciliopathy

scientific article published on 07 January 2020

Analysis of retinal structure and function in cone dystrophy with supernormal rod response

scientific article published on 20 January 2020

Association between Sickle Cell Trait and the Prevalence and Severity of Diabetic Retinopathy

scientific article

Clinical evaluation of two consanguineous families with homozygous mutations in BEST1

scientific article

Clinical phenotype in a Swedish family with a mutation in the IMPDH1 gene

scientific article

Comparison of outcomes of four different treatment modalities for diabetic vitreous haemorrhage

scientific article published on 28 February 2020

Congenital stationary night blindness associated with morning glory disc malformation: a novel hemizygous mutation in CACNA1F

scientific article published on 01 August 2018

Congenital stationary night blindness with hypoplastic discs, negative electroretinogram and thinning of the inner nuclear layer.

scientific article published on 15 April 2016

Congenital stationary night blindness: an update and review of the disease spectrum in Saudi Arabia

scientific article published on 26 December 2020

Evaluation of macular structure and function by OCT and electrophysiology in patients with vitelliform macular dystrophy due to mutations in BEST1.

scientific article published on 7 April 2010

Frequency, genotype, and clinical spectrum of best vitelliform macular dystrophy: data from a national center in Denmark

scientific article

Fundus albipunctatus associated with compound heterozygous mutations in RPE65.

scientific article published on 6 January 2011

Genetic Testing for Wolfram Syndrome Mutations in a Sample of 71 Patients with Hereditary Optic Neuropathy and Negative Genetic Test Results for

scientific article published on 18 August 2017

Improved retinal function after trabeculectomy in glaucoma patients

scientific article published on 29 October 2009

Incidence and Natural History of Retinochoroidal Neovascularization in Enhanced S-Cone Syndrome

scientific article published on 14 September 2020

Incidence of Intraocular Lens Exchange after Cataract Surgery

scientific article published on 09 September 2019

Lack of autofluorescence in fundus albipunctatus associated with mutations in RDH5.

scientific article published on November 2010

Late presentation of RPE65 retinopathy in three siblings

scientific article published on 10 January 2020

Long-term follow-up of retinal function and structure in TRPM1-associated complete congenital stationary night blindness

scientific article published on 19 December 2019

Long-term resolution of chronic macular edema after a single dose of intravitreal dexamethasone in familial retinal arterial macroaneurysm

scientific article published on 19 May 2020

Macular appearance by means of OCT and electrophysiology in members of two families with different mutations in RDS (the peripherin/RDS gene).

scientific article published in October 2003

Morphological and functional changes in multifocal vitelliform retinopathy and biallelic mutations in BEST1

scientific article published on 30 December 2010

Multifocal electroretinography and optical coherence tomography in two patients with solar retinopathy

scientific article

Multimodal imaging in CABP4-related retinopathy

scientific article published in March 2017

Multimodal imaging in serologically confirmed Rubella retinopathy

scientific article published on 22 June 2018

Multimodal retinal imaging in MFSD8-neuronal ceroid lipofuscinosis

scientific article published on 01 December 2019

Non-syndromic retinal dystrophy associated with homozygous mutations in the ALMS1 gene

scientific article published on 29 November 2018

Novel causative variants in patients with achromatopsia

scientific article published on 05 October 2018

Ocular phenotype analysis of a family with biallelic mutations in the BEST1 gene

scientific article published on 15 December 2013

Poretti-Boltshauser syndrome: a rare differential diagnosis to consider in pediatric high myopia with retinal degeneration

scientific article published on 29 November 2020

Preservation of macular structure and function after intravitreal aflibercept for choroidal neovascularization associated with serpiginous choroiditis

scientific article published on 18 January 2016

Prevalence of Diabetic Retinopathy in a Population of Diabetics From the Middle East With Microvascular Ocular Motor Palsies.

scientific article

Response of inflammatory markers to balloon angioplasty in peripheral arterial occlusive disease

scientific article published on 01 December 2000

Retinal function after scleral buckling for recent onset rhegmatogenous retinal detachment: assessment with electroretinography and optical coherence tomography

scientific article published on 01 January 2007

Retinal structure in young patients aged 10 years or less with Best vitelliform macular dystrophy

scientific article published on 5 May 2015

Rhegmatogenous Retinal Detachment in Nonsyndromic High Myopia Associated with Recessive Mutations in LRPAP1

scientific article published on 22 August 2019

Serous retinal detachment after panretinal photocoagulation for proliferative diabetic retinopathy: a case report

scientific article published on 19 September 2017

Severe retinal degeneration at an early age in Usher syndrome type 1B associated with homozygous splice site mutations in MYO7A gene

scientific article

Sickle cell retinopathy. A focused review

scientific article published on 20 March 2019

Teleophthalmology image-based navigated retinal laser therapy for diabetic macular edema: a concept of retinal telephotocoagulation

scientific article published on 26 April 2017

Three New PAX2 Gene Mutations in Patients with Papillorenal Syndrome.

scientific article published on 8 May 2017

Unilateral central retinal vein occlusion as a first manifestation of diabetes mellitus in a ten-year-old girl

scientific article published on 27 February 2018

Update on Clinical Trials in Dry Age-related Macular Degeneration

scientific article

Variable Familial Exudative Vitreoretinopathy in a family harbouring variants in both FZD4 and TSPAN12.

scientific article published on 16 February 2017

Variant phenotype of Best vitelliform macular dystrophy associated with compound heterozygous mutations in VMD2.

scientific article

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