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P Leroy

Showing results (321-330 of 438) with videos related to

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Frontiers in Medicine|August 21, 2023
Paediatric cataract surgery with 27G vitrectomy instrumentation: the Ghent University Hospital ExperienceHwei Wuen Chan, Filip Van den Broeck, Axelle Cools, et al.
Experimental Eye Research|April 20, 2001
Spectrum of mutations in USH2A in British patients with Usher syndrome type IIB P Leroy, J A Aragon-Martin, M D Weston, et al.
Neurology|December 28, 2006
Muscle imaging in dominant core myopathies linked or unlinked to the ryanodine receptor 1 geneD Fischer, M Herasse, A Ferreiro, et al.
Journal of Clinical Medicine|July 9, 2022
Serum Calcification Propensity T50 Associates with Disease Severity in Patients with Pseudoxanthoma ElasticumLukas Nollet, Matthias Van Gils, Suzanne Fischer, et al.
Water Research|November 25, 2003
Measurement of glutathione in activated sludgesM A Dziurla, P Leroy, G W Strünkmann, et al.
Investigative Ophthalmology & Visual Science|November 30, 2000
RP1 protein truncating mutations predominate at the RP1 adRP locusA Payne, E Vithana, S Khaliq, et al.
Studies in Health Technology and Informatics|October 18, 2001
Doc'CISMEF: a search tool based on "encapsulated" MeSH thesaurusS J Darmoni, B Thirion, J P Leroy, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 21, 2012
Massively parallel sequencing for early molecular diagnosis in Leber congenital amaurosisFrauke Coppieters, Bram De Wilde, Steve Lefever, et al.
Investigative Ophthalmology & Visual Science|August 29, 2007
Pseudoxanthoma elasticum with generalized retinal dysfunction, a common finding?Isabelle Audo, Olivier M Vanakker, Alaric Smith, et al.
JIMD Reports|February 23, 2013
Questioning the Pathogenic Role of the GLA p.Ala143Thr "Mutation" in Fabry Disease: Implications for Screening Studies and ERTW Terryn, R Vanholder, D Hemelsoet, et al.
Pageof 44

Showing results (321-330 of 438) with videos related to

Sort By:
Pageof 44
Frontiers in Medicine|August 21, 2023
Paediatric cataract surgery with 27G vitrectomy instrumentation: the Ghent University Hospital ExperienceHwei Wuen Chan, Filip Van den Broeck, Axelle Cools, et al.
Experimental Eye Research|April 20, 2001
Spectrum of mutations in USH2A in British patients with Usher syndrome type IIB P Leroy, J A Aragon-Martin, M D Weston, et al.
Neurology|December 28, 2006
Muscle imaging in dominant core myopathies linked or unlinked to the ryanodine receptor 1 geneD Fischer, M Herasse, A Ferreiro, et al.
Journal of Clinical Medicine|July 9, 2022
Serum Calcification Propensity T50 Associates with Disease Severity in Patients with Pseudoxanthoma ElasticumLukas Nollet, Matthias Van Gils, Suzanne Fischer, et al.
Water Research|November 25, 2003
Measurement of glutathione in activated sludgesM A Dziurla, P Leroy, G W Strünkmann, et al.
Investigative Ophthalmology & Visual Science|November 30, 2000
RP1 protein truncating mutations predominate at the RP1 adRP locusA Payne, E Vithana, S Khaliq, et al.
Studies in Health Technology and Informatics|October 18, 2001
Doc'CISMEF: a search tool based on "encapsulated" MeSH thesaurusS J Darmoni, B Thirion, J P Leroy, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 21, 2012
Massively parallel sequencing for early molecular diagnosis in Leber congenital amaurosisFrauke Coppieters, Bram De Wilde, Steve Lefever, et al.
Investigative Ophthalmology & Visual Science|August 29, 2007
Pseudoxanthoma elasticum with generalized retinal dysfunction, a common finding?Isabelle Audo, Olivier M Vanakker, Alaric Smith, et al.
JIMD Reports|February 23, 2013
Questioning the Pathogenic Role of the GLA p.Ala143Thr "Mutation" in Fabry Disease: Implications for Screening Studies and ERTW Terryn, R Vanholder, D Hemelsoet, et al.
Pageof 44