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Philipp Herrmann

Showing results (51-60 of 95) with videos related to

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Retina (Philadelphia, Pa.)|September 15, 2025
Frequency of misdiagnoses and associated risk factors in Macular Telangiectasia Type 2Kristin Raming, Jose Luis Rodriguez Garcia, Nele Steffens, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|July 21, 2021
Analysis of imaging biomarkers and retinal nerve fiber layer thickness in RPGR-associated retinitis pigmentosaTheresa H Birtel, Johannes Birtel, Kristina Hess, et al.
Investigative Ophthalmology & Visual Science|August 16, 2019
Quantification of Retinal and Choriocapillaris Perfusion in Different Stages of Macular Telangiectasia Type 2Simone Tzaridis, Maximilian W M Wintergerst, Clarissa Mai, et al.
Ophthalmologica. Journal International D'Ophtalmologie. International Journal of Ophthalmology. Zeitschrift Fur Augenheilkunde|December 11, 2025
Chorioretinal Atrophy after Voretigene Neparvovec Therapy in <italic>RPE65</italic> Mutation-Associated Inherited Retinal Disease: Longitudinal Characterization in Multimodal ImagingSandrine H Sassen, Marlene Sassmannshausen, Josua Sassen, et al.
Retina (Philadelphia, Pa.)|December 5, 2019
DARK ADAPTATION IN MACULAR TELANGIECTASIA TYPE 2Simone Tzaridis, Kristina Hess, Tjebo F C Heeren, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|December 22, 2019
Aflibercept for choroidal neovascularizations secondary to pseudoxanthoma elasticum: a prospective studyMartin Gliem, Johannes Birtel, Philipp Herrmann, et al.
Pediatric Nephrology (Berlin, Germany)|October 19, 2022
The retinal phenotype in primary hyperoxaluria type 2 and 3Johannes Birtel, Roselie M Diederen, Philipp Herrmann, et al.
Genes|October 29, 2025
Mutation of the Thyroid Hormone Receptor Beta Gene (<i>THRB</i>) Causes Vitelliform Macular Dystrophy with High Intrafamilial VariabilityElisa A Mahler, Lars C Moeller, Katharina Wall, et al.
JAMA Ophthalmology|August 9, 2019
Acute Retinopathy in Pseudoxanthoma ElasticumMartin Gliem, Johannes Birtel, Philipp L Müller, et al.
The British Journal of Ophthalmology|March 31, 2021
North Carolina macular dystrophy shows a particular drusen phenotype and atrophy progressionJohannes Birtel, Martin Gliem, Philipp Herrmann, et al.
Pageof 10

Showing results (51-60 of 95) with videos related to

Sort By:
Pageof 10
Retina (Philadelphia, Pa.)|September 15, 2025
Frequency of misdiagnoses and associated risk factors in Macular Telangiectasia Type 2Kristin Raming, Jose Luis Rodriguez Garcia, Nele Steffens, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|July 21, 2021
Analysis of imaging biomarkers and retinal nerve fiber layer thickness in RPGR-associated retinitis pigmentosaTheresa H Birtel, Johannes Birtel, Kristina Hess, et al.
Investigative Ophthalmology & Visual Science|August 16, 2019
Quantification of Retinal and Choriocapillaris Perfusion in Different Stages of Macular Telangiectasia Type 2Simone Tzaridis, Maximilian W M Wintergerst, Clarissa Mai, et al.
Ophthalmologica. Journal International D'Ophtalmologie. International Journal of Ophthalmology. Zeitschrift Fur Augenheilkunde|December 11, 2025
Chorioretinal Atrophy after Voretigene Neparvovec Therapy in <italic>RPE65</italic> Mutation-Associated Inherited Retinal Disease: Longitudinal Characterization in Multimodal ImagingSandrine H Sassen, Marlene Sassmannshausen, Josua Sassen, et al.
Retina (Philadelphia, Pa.)|December 5, 2019
DARK ADAPTATION IN MACULAR TELANGIECTASIA TYPE 2Simone Tzaridis, Kristina Hess, Tjebo F C Heeren, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|December 22, 2019
Aflibercept for choroidal neovascularizations secondary to pseudoxanthoma elasticum: a prospective studyMartin Gliem, Johannes Birtel, Philipp Herrmann, et al.
Pediatric Nephrology (Berlin, Germany)|October 19, 2022
The retinal phenotype in primary hyperoxaluria type 2 and 3Johannes Birtel, Roselie M Diederen, Philipp Herrmann, et al.
Genes|October 29, 2025
Mutation of the Thyroid Hormone Receptor Beta Gene (<i>THRB</i>) Causes Vitelliform Macular Dystrophy with High Intrafamilial VariabilityElisa A Mahler, Lars C Moeller, Katharina Wall, et al.
JAMA Ophthalmology|August 9, 2019
Acute Retinopathy in Pseudoxanthoma ElasticumMartin Gliem, Johannes Birtel, Philipp L Müller, et al.
The British Journal of Ophthalmology|March 31, 2021
North Carolina macular dystrophy shows a particular drusen phenotype and atrophy progressionJohannes Birtel, Martin Gliem, Philipp Herrmann, et al.
Pageof 10