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R Webster

Showing results (841-850 of 1,563) with videos related to

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Ophthalmology|June 18, 2023
Prognostication in Stargardt Disease Using Fundus Autofluorescence: Improving Patient CareMalena Daich Varela, Yannik Laich, Shaima Awadh Hashem, et al.
Journal of Medical Genetics|February 5, 2002
In vitro analysis of aminoglycoside therapy for the Arg120stop nonsense mutation in RP2 patientsC Grayson, J P Chapple, K R Willison, et al.
Australian Veterinary Journal|May 1, 1986
Melioidosis in intensive piggeries in south eastern QueenslandP J Ketterer, W R Webster, J Shield, et al.
Retina (Philadelphia, Pa.)|October 6, 2010
Nidek MP1 is able to detect subtle decline in function in inherited and age-related atrophic macular disease with stable visual acuityFred K Chen, Praveen J Patel, Andrew R Webster, et al.
Ethnicity & Health|June 19, 2004
Intended use of informal long-term care: the role of race and ethnicityElizabeth H Bradley, Leslie A Curry, Sarah A McGraw, et al.
JACC. Case Reports|September 19, 2024
Transcatheter Edge-to-Edge Repair in Complex Cyanotic Congenital Heart Disease With a Common Atrioventricular ValveStephanie J Connaire, Jessica R Webster, Michael J Mullen, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|March 30, 2023
Validation of a shortened MR imaging protocol for pediatric spinal pathologyW Wu, E Miller, J Hurteau-Miller, et al.
Neurosurgery|July 18, 2014
Spinal dural arteriovenous fistulas: how, when, and whyMatthew R Sanborn, R Webster Crowley, Timothy Uschold, et al.
Investigative Ophthalmology & Visual Science|December 28, 2013
Cone dystrophy with "supernormal" rod ERG: psychophysical testing shows comparable rod and cone temporal sensitivity losses with no gain in rod functionAndrew Stockman, G Bruce Henning, Michel Michaelides, et al.
Clinical Genetics|May 11, 2016
Advanced diagnostic genetic testing in inherited retinal disease: experience from a single tertiary referral centre in the UK National Health ServiceK N Khan, R Chana, N Ali, et al.
Pageof 157

Showing results (841-850 of 1,563) with videos related to

Sort By:
Pageof 157
Ophthalmology|June 18, 2023
Prognostication in Stargardt Disease Using Fundus Autofluorescence: Improving Patient CareMalena Daich Varela, Yannik Laich, Shaima Awadh Hashem, et al.
Journal of Medical Genetics|February 5, 2002
In vitro analysis of aminoglycoside therapy for the Arg120stop nonsense mutation in RP2 patientsC Grayson, J P Chapple, K R Willison, et al.
Australian Veterinary Journal|May 1, 1986
Melioidosis in intensive piggeries in south eastern QueenslandP J Ketterer, W R Webster, J Shield, et al.
Retina (Philadelphia, Pa.)|October 6, 2010
Nidek MP1 is able to detect subtle decline in function in inherited and age-related atrophic macular disease with stable visual acuityFred K Chen, Praveen J Patel, Andrew R Webster, et al.
Ethnicity & Health|June 19, 2004
Intended use of informal long-term care: the role of race and ethnicityElizabeth H Bradley, Leslie A Curry, Sarah A McGraw, et al.
JACC. Case Reports|September 19, 2024
Transcatheter Edge-to-Edge Repair in Complex Cyanotic Congenital Heart Disease With a Common Atrioventricular ValveStephanie J Connaire, Jessica R Webster, Michael J Mullen, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|March 30, 2023
Validation of a shortened MR imaging protocol for pediatric spinal pathologyW Wu, E Miller, J Hurteau-Miller, et al.
Neurosurgery|July 18, 2014
Spinal dural arteriovenous fistulas: how, when, and whyMatthew R Sanborn, R Webster Crowley, Timothy Uschold, et al.
Investigative Ophthalmology & Visual Science|December 28, 2013
Cone dystrophy with "supernormal" rod ERG: psychophysical testing shows comparable rod and cone temporal sensitivity losses with no gain in rod functionAndrew Stockman, G Bruce Henning, Michel Michaelides, et al.
Clinical Genetics|May 11, 2016
Advanced diagnostic genetic testing in inherited retinal disease: experience from a single tertiary referral centre in the UK National Health ServiceK N Khan, R Chana, N Ali, et al.
Pageof 157