Patrik Schatz
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- 2024
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Mark
Effect of silicone oil versus gas tamponade on macular layer microstructure after pars plana vitrectomy for macula on rhegmatogenous retinal detachment
(
- Contribution to journal › Article
- 2023
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Mark
Leprel1-related Giant Retinal Tear Detachments Mimic the Phenotype of Ocular Stickler Syndrome
(
- Contribution to journal › Article
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Mark
Cone dystrophy associated with autoimmune polyglandular syndrome type 1
(
- Contribution to journal › Article
- 2022
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Mark
Unilateral Retinitis Pigmentosa Associated with Possible Ciliopathy and a Novel Mutation
(
- Contribution to journal › Article
- 2021
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Mark
Electrophysiological evaluation of fleck retina and temporal macular thinning in X-Linked alport's syndrome
(
- Contribution to journal › Article
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Mark
Comparison of posterior hyaloid assessment using preoperative optical coherence tomography and intraoperative triamcinolone acetonide staining during vitrectomy
(
- Contribution to journal › Article
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Mark
Recognizable Patterns of Submacular Fibrosis in Enhanced S-Cone Syndrome
(
- Contribution to journal › Article
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Mark
Surgical management of hemorrhagic retinal detachment secondary to peripheral exudative hemorrhagic chorioretinopathy
(
- Contribution to journal › Article
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Mark
Manifestation of panuveitis after intraocular surgery in a child with blau syndrome
(
- Contribution to journal › Article
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Mark
Clinical spectrum, genetic associations and management outcomes of Coats-like exudative retinal vasculopathy in autosomal recessive retinitis pigmentosa
(
- Contribution to journal › Article
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Mark
Association of the Recurrent Rare Variant c.415T>C p.Phe139Leu in CLN5 with a Recessively Inherited Macular Dystrophy
(
- Contribution to journal › Article
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Mark
Incidence and Natural History of Retinochoroidal Neovascularization in Enhanced S-Cone Syndrome
(
- Contribution to journal › Article
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Mark
Poretti-Boltshauser syndrome : a rare differential diagnosis to consider in pediatric high myopia with retinal degeneration
(
- Contribution to journal › Letter
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Mark
Congenital stationary night blindness : an update and review of the disease spectrum in Saudi Arabia
(
- Contribution to journal › Scientific review
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Mark
Comparison of short-pulse subthreshold (532 nm) and infrared micropulse (810 nm) macular laser for diabetic macular edema
(
- Contribution to journal › Article
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Mark
Evolution of macular hole in enhanced S-cone syndrome
(
- Contribution to journal › Article
- 2020
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Mark
Comparison of outcomes of four different treatment modalities for diabetic vitreous haemorrhage
(
- Contribution to journal › Article
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Mark
Rhegmatogenous Retinal Detachment in Nonsyndromic High Myopia Associated with Recessive Mutations in LRPAP1
(
- Contribution to journal › Published meeting abstract
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Mark
Long-term resolution of chronic macular edema after a single dose of intravitreal dexamethasone in familial retinal arterial macroaneurysm
(
- Contribution to journal › Letter
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Mark
Analysis of retinal structure and function in cone dystrophy with supernormal rod response
2020) In Documenta Ophthalmologica(
- Contribution to journal › Article
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Mark
Late presentation of RPE65 retinopathy in three siblings
(
- Contribution to journal › Article
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Mark
Analysis of retinal function and structure in autosomal recessive retinal-renal ciliopathy
(
- Contribution to journal › Letter
-
Mark
Severe retinitis pigmentosa phenotype associated with novel CNGB1 variants
(
- Contribution to journal › Article
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Mark
DIFFUSE RETINAL VASCULAR LEAKAGE AND CONE-ROD DYSTROPHY IN A FAMILY WITH THE HOMOZYGOUS MISSENSE C.1429G>A (P.GLY477ARG) MUTATION IN CRB1
(
- Contribution to journal › Article
- 2019
-
Mark
Non-syndromic retinal dystrophy associated with homozygous mutations in the ALMS1 gene
(
- Contribution to journal › Letter
-
Mark
Incidence of Intraocular Lens Exchange after Cataract Surgery
(
- Contribution to journal › Article
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Mark
Multimodal retinal imaging in MFSD8-neuronal ceroid lipofuscinosis
(
- Contribution to journal › Letter
-
Mark
Long-term follow-up of retinal function and structure in trpm1-associated complete congenital stationary night blindness
(
- Contribution to journal › Article
-
Mark
Sickle cell retinopathy. A focused review
(
- Contribution to journal › Scientific review
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Mark
Accommodative esotropia and Brown syndrome in a girl with recessive geleophysic dysplasia
(
- Contribution to journal › Article
- 2018
-
Mark
Unilateral central retinal vein occlusion as a first manifestation of diabetes mellitus in a ten-year-old girl
(
- Contribution to journal › Article
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Mark
Multimodal imaging in serologically confirmed Rubella retinopathy
(
- Contribution to journal › Article
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Mark
Novel causative variants in patients with achromatopsia
(
- Contribution to journal › Article
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Mark
Genetic Testing for Wolfram Syndrome Mutations in a Sample of 71 Patients with Hereditary Optic Neuropathy and Negative Genetic Test Results for OPA1/OPA3/LHON
(
- Contribution to journal › Article
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Mark
Severe retinal degeneration at an early age in Usher syndrome type 1B associated with homozygous splice site mutations in MYO7A gene
(
- Contribution to journal › Article
-
Mark
Congenital stationary night blindness associated with morning glory disc malformation : a novel hemizygous mutation in CACNA1F
(
- Contribution to journal › Letter
- 2017
-
Mark
Serous retinal detachment after panretinal photocoagulation for proliferative diabetic retinopathy : A case report
(
- Contribution to journal › Article
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Mark
Heterozygous mutation in OTX2 associated with early-onset retinal dystrophy with atypical maculopathy
(
- Contribution to journal › Article
-
Mark
Three New PAX2 Gene Mutations in Patients with Papillorenal Syndrome
(
- Contribution to journal › Article
-
Mark
Multimodal imaging in CABP4-related retinopathy
(
- Contribution to journal › Article
-
Mark
Teleophthalmology image-based navigated retinal laser therapy for diabetic macular edema : a concept of retinal telephotocoagulation
(
- Contribution to journal › Article
-
Mark
Variable Familial Exudative Vitreoretinopathy in a family harbouring variants in both FZD4 and TSPAN12
(
- Contribution to journal › Article
- 2016
-
Mark
Preservation of macular structure and function after intravitreal aflibercept for choroidal neovascularization associated with serpiginous choroiditis.
(
- Contribution to journal › Article
-
Mark
Update on Clinical Trials in Dry Age-related Macular Degeneration.
(
- Contribution to journal › Scientific review
-
Mark
Association between sickle cell trait and the prevalence and severity of diabetic retinopathy
(
- Contribution to journal › Article
-
Mark
Congenital stationary night blindness with hypoplastic discs, negative electroretinogram and thinning of the inner nuclear layer
(
- Contribution to journal › Article
-
Mark
Prevalence of diabetic retinopathy in a population of diabetics from the middle east with microvascular ocular motor palsies
(
- Contribution to journal › Article
- 2015
-
Mark
Retinal structure in young patients aged 10 years or less with Best vitelliform macular dystrophy.
2015) In Graefe's Archive for Clinical and Experimental Ophthalmology(
- Contribution to journal › Article
- 2014
-
Mark
Reappearance of the tapetal-like reflex after prolonged dark adaptation in a female carrier of RPGR ORF15 X-linked retinitis pigmentosa.
(
- Contribution to journal › Article
-
Mark
Ocular phenotype analysis of a family with biallelic mutations in the BEST1 gene.
(
- Contribution to journal › Article
- 2012
-
Mark
A tapetal-like fundus reflex in a healthy male: evidence against a role in the pathophysiology of retinal degeneration?
(
- Contribution to journal › Article
-
Mark
Frequency, Genotype, and Clinical Spectrum of Best Vitelliform Macular Dystrophy: Data From a National Center in Denmark
(
- Contribution to journal › Article
- 2011
-
Mark
Clinical evaluation of two consanguineous families with homozygous mutations in BEST1
(
- Contribution to journal › Article
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Mark
Fundus Albipunctatus Associated with Compound Heterozygous Mutations in RPE65.
(
- Contribution to journal › Article
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Mark
Morphological and functional changes in multifocal vitelliform retinopathy and biallelic mutations in BEST1.
(
- Contribution to journal › Article
- 2010
-
Mark
Evaluation of Macular Structure and Function by OCT and Electrophysiology in Patients with Vitelliform Macular Dystrophy Due to Mutations in BEST1
(
- Contribution to journal › Article
-
Mark
RECOVERY OF RETINAL FUNCTION AFTER RECENT-ONSET RHEGMATOGENOUS RETINAL DETACHMENT IN RELATION TO TYPE OF SURGERY.
(
- Contribution to journal › Article
-
Mark
Improved retinal function after trabeculectomy in glaucoma patients.
(
- Contribution to journal › Article
-
Mark
LACK OF AUTOFLUORESCENCE IN FUNDUS ALBIPUNCTATUS ASSOCIATED WITH MUTATIONS IN RDH5.
(
- Contribution to journal › Article
- 2007
-
Mark
Retinal function after scleral buckling for recent onset rhegmatogenous retinal detachment: assessment with electroretinography and optical coherence tomography.
(
- Contribution to journal › Article
- 2006
-
Mark
Variant Phenotype of Best Vitelliform Macular Dystrophy Associated with Compound Heterozygous Mutations in VMD2.
(
- Contribution to journal › Article
-
Mark
Electrophysiology and optical coherence tomography in acquired and hereditary retinal disorders
2006)(
- Thesis › Doctoral thesis (compilation)
- 2005
-
Mark
Clinical phenotype in a Swedish family with a mutation in the IMPDH1 gene.
(
- Contribution to journal › Article
- 2004
-
Mark
Multifocal electroretinography and optical coherence tomography in two patients with solar retinopathy.
(
- Contribution to journal › Article
- 2003
-
Mark
Macular appearance by means of OCT and electrophysiology in members of two families with different mutations in RDS (the peripherin/RDS gene).
(
- Contribution to journal › Article
- 2002
-
Mark
Outcome of treatment of ruptured abdominal aortic aneurysms depending on the type of hospital.
(
- Contribution to journal › Article