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Peter Charbel Issa

Showing results (171-180 of 231) with videos related to

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Clinical & Experimental Ophthalmology|September 1, 2018
Retinal imaging including optical coherence tomography angiography for detecting active choroidal neovascularization in pseudoxanthoma elasticumJohannes Birtel, Moritz Lindner, Divyansh K Mishra, et al.
Human Genetics|December 16, 2006
A novel gene for Usher syndrome type 2: mutations in the long isoform of whirlin are associated with retinitis pigmentosa and sensorineural hearing lossInga Ebermann, Hendrik P N Scholl, Peter Charbel Issa, et al.
Retina (Philadelphia, Pa.)|June 10, 2008
Abnormal macular pigment distribution in type 2 idiopathic macular telangiectasiaHans-Martin Helb, Peter Charbel Issa, Rob L P VAN DER Veen, et al.
Progress in Retinal and Eye Research|December 11, 2012
Macular telangiectasia type 2Peter Charbel Issa, Mark C Gillies, Emily Y Chew, et al.
Investigative Ophthalmology & Visual Science|April 2, 2010
Tracking progression with spectral-domain optical coherence tomography in geographic atrophy caused by age-related macular degenerationMonika Fleckenstein, Steffen Schmitz-Valckenberg, Christine Adrion, et al.
Klinische Monatsblatter Fur Augenheilkunde|January 26, 2025
[N-Acetylcysteine (NAC) for Retinitis pigmentosa]Kristina Pfau, Josep Callizo, Petra Rossouw, et al.
Human Mutation|February 16, 2007
Truncating mutation of the DFNB59 gene causes cochlear hearing impairment and central vestibular dysfunctionInga Ebermann, Martin Walger, Hendrik P N Scholl, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 29, 2022
Impaired glutamylation of RPGR<sup>ORF15</sup> underlies the cone-dominated phenotype associated with truncating distal ORF15 variantsJasmina Cehajic-Kapetanovic, Cristina Martinez-Fernandez de la Camara, Johannes Birtel, et al.
Ophthalmology|December 10, 2013
The spectrum of ocular alterations in patients with β-thalassemia syndromes suggests a pathology similar to pseudoxanthoma elasticumGiulio Barteselli, Laura Dell'arti, Robert P Finger, et al.
American Journal of Ophthalmology|March 29, 2021
Fundus Autofluorescence Imaging in Macular Telangiectasia Type 2: MacTel Study Report Number 9Laurenz Pauleikhoff, Tjebo F C Heeren, Martin Gliem, et al.
Pageof 24

Showing results (171-180 of 231) with videos related to

Sort By:
Pageof 24
Clinical & Experimental Ophthalmology|September 1, 2018
Retinal imaging including optical coherence tomography angiography for detecting active choroidal neovascularization in pseudoxanthoma elasticumJohannes Birtel, Moritz Lindner, Divyansh K Mishra, et al.
Human Genetics|December 16, 2006
A novel gene for Usher syndrome type 2: mutations in the long isoform of whirlin are associated with retinitis pigmentosa and sensorineural hearing lossInga Ebermann, Hendrik P N Scholl, Peter Charbel Issa, et al.
Retina (Philadelphia, Pa.)|June 10, 2008
Abnormal macular pigment distribution in type 2 idiopathic macular telangiectasiaHans-Martin Helb, Peter Charbel Issa, Rob L P VAN DER Veen, et al.
Progress in Retinal and Eye Research|December 11, 2012
Macular telangiectasia type 2Peter Charbel Issa, Mark C Gillies, Emily Y Chew, et al.
Investigative Ophthalmology & Visual Science|April 2, 2010
Tracking progression with spectral-domain optical coherence tomography in geographic atrophy caused by age-related macular degenerationMonika Fleckenstein, Steffen Schmitz-Valckenberg, Christine Adrion, et al.
Klinische Monatsblatter Fur Augenheilkunde|January 26, 2025
[N-Acetylcysteine (NAC) for Retinitis pigmentosa]Kristina Pfau, Josep Callizo, Petra Rossouw, et al.
Human Mutation|February 16, 2007
Truncating mutation of the DFNB59 gene causes cochlear hearing impairment and central vestibular dysfunctionInga Ebermann, Martin Walger, Hendrik P N Scholl, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 29, 2022
Impaired glutamylation of RPGR<sup>ORF15</sup> underlies the cone-dominated phenotype associated with truncating distal ORF15 variantsJasmina Cehajic-Kapetanovic, Cristina Martinez-Fernandez de la Camara, Johannes Birtel, et al.
Ophthalmology|December 10, 2013
The spectrum of ocular alterations in patients with β-thalassemia syndromes suggests a pathology similar to pseudoxanthoma elasticumGiulio Barteselli, Laura Dell'arti, Robert P Finger, et al.
American Journal of Ophthalmology|March 29, 2021
Fundus Autofluorescence Imaging in Macular Telangiectasia Type 2: MacTel Study Report Number 9Laurenz Pauleikhoff, Tjebo F C Heeren, Martin Gliem, et al.
Pageof 24