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Publications

Improved Diagnosis of Retinal Laser Injuries Using Near-Infrared Autofluorescence.

De Silva SR. et al, (2019), Am J Ophthalmol, 208, 87 - 93

Progression characteristics of ellipsoid zone loss in macular telangiectasia type 2.

Pauleikhoff D. et al, (2019), Acta Ophthalmol, 97, e998 - e1005

Genetic testing in patients with retinitis pigmentosa: Features of unsolved cases.

Birtel J. et al, (2019), Clin Exp Ophthalmol, 47, 779 - 786

An AAV Dual Vector Strategy Ameliorates the Stargardt Phenotype in AdultAbca4−/−Mice

McClements ME. et al, (2019), Human Gene Therapy, 30, 590 - 600

Dark-Adapted Two-Color Fundus-Controlled Perimetry in Macular Telangiectasia Type 2.

Heeren TFC. et al, (2019), Invest Ophthalmol Vis Sci, 60, 1760 - 1767

Retinal findings in carriers of monoallelic ABCC6 mutations.

Gliem M. et al, (2019), Br J Ophthalmol

Contrast sensitivity and visual acuity under low light conditions in macular telangiectasia type 2

Müller S. et al, (2019), British Journal of Ophthalmology, 103, 398 - 403

Near-Infrared Autofluorescence in Choroideremia: Anatomic and Functional Correlations

Birtel J. et al, (2019), American Journal of Ophthalmology, 199, 19 - 27

Retinal imaging including optical coherence tomography angiography for detecting active choroidal neovascularization in pseudoxanthoma elasticum

Birtel J. et al, (2019), Clinical & Experimental Ophthalmology, 47, 240 - 249

Right-angled vessels in macular telangiectasia type 2.

Tzaridis S. et al, (2019), Br J Ophthalmol

Estimating Retinal Sensitivity Using Optical Coherence Tomography With Deep-Learning Algorithms in Macular Telangiectasia Type 2.

Kihara Y. et al, (2019), JAMA Netw Open, 2

Electrophysiological verification of enhanced S-cone syndrome caused by a novel c.755T>C NR2E3 missense variant

Cehajic-Kapetanovic J. et al, (2019), Ophthalmic Genetics, 40, 29 - 33

Stereoscopic Vision in Macular Telangiectasia Type 2

Müller S. et al, (2019), Ophthalmologica, 241, 121 - 129

A Novel Achromatopsia Mouse Model Resulting From a Naturally Occurring Missense Change in Cngb3.

Hassall MM. et al, (2018), Invest Ophthalmol Vis Sci, 59, 6102 - 6110

Clinical and genetic characteristics of 251 consecutive patients with macular and cone/cone-rod dystrophy

Birtel J. et al, (2018), Scientific Reports, 8

Accessory heterozygous mutations in cone photoreceptor CNGA3 exacerbate CNG channel–associated retinopathy

Burkard M. et al, (2018), Journal of Clinical Investigation, 128, 5663 - 5675

Macular Pigment Distribution as Prognostic Marker for Disease Progression in Macular Telangiectasia Type 2

Müller S. et al, (2018), American Journal of Ophthalmology, 194, 163 - 169

Olfactory Dysfunction in Patients WithCNGB1-Associated Retinitis Pigmentosa

Charbel Issa P. et al, (2018), JAMA Ophthalmology, 136, 761 - 761

Next-generation sequencing identifies unexpected genotype-phenotype correlations in patients with retinitis pigmentosa.

Birtel J. et al, (2018), PLoS One, 13

The Progression of the Stargardt Disease Type 4 (ProgStar-4) Study: Design and Baseline Characteristics (ProgStar-4 Report No. 1)

Strauss RW. et al, (2018), Ophthalmic Research, 60, 185 - 194

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