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P Leroy

Showing results (301-310 of 438) with videos related to

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Retina (Philadelphia, Pa.)|August 21, 2024
DIAGNOSTIC YIELD OF AN INHERITED RETINAL DISEASE GENE PANEL IN RETINOPATHY OF UNKNOWN ORIGINStéphane Abramowicz, Audrey Meunier, Laurence Postelmans, et al.
The Journal of Pathology|February 13, 2001
The detection of Tel-TrkC chimeric transcripts is more specific than TrkC immunoreactivity for the diagnosis of congenital fibrosarcomaP Dubus, J M Coindre, A Groppi, et al.
Journal of Biomedical Nanotechnology|June 16, 2016
Elaboration of Sterically Stabilized Liposomes for S-Nitrosoglutathione Targeting to MacrophagesR Diab, A S Virriat, C Ronzani, et al.
Plos One|January 27, 2026
The socioeconomic impact of inherited retinal dystrophies (IRDs) in Belgium: A cost-of-illness studyIne Vandersmissen, Janice Geers, Tom Denee, et al.
Stem Cell Research|May 30, 2025
Generation of two iPSC lines (UGENTi003 and UGENTi004) from patients with intermediate rod-cone dystrophy carrying the c.[-123C>T;701G>A];[806_810del] variants in the RDH12 geneM Bouckaert, F Van Den Broeck, M Ghazvini, et al.
Human Mutation|December 25, 2007
Novel clinico-molecular insights in pseudoxanthoma elasticum provide an efficient molecular screening method and a comprehensive diagnostic flowchartOlivier M Vanakker, Bart P Leroy, Paul Coucke, et al.
Ophthalmology Science|March 19, 2026
Expert Consensus on Characteristics, Etiology, and Management of Chorioretinal Atrophy in Patients Treated with Voretigene NeparvovecM Dominik Fischer, Isabelle Audo, David Gaucher, et al.
Clinical Genetics|April 10, 2020
VEGFA variants as prognostic markers for the retinopathy in pseudoxanthoma elasticumEva Y G De Vilder, Mohammad J Hosen, Ludovic Martin, et al.
Revue De Pneumologie Clinique|February 25, 2014
[Lung cancer, how to deal with critical situations?]F Scotté, P Leroy, S Hans, et al.
Human Molecular Genetics|April 2, 2014
Abnormal retinal development associated with FRMD7 mutationsMervyn G Thomas, Moira Crosier, Susan Lindsay, et al.
Pageof 44

Showing results (301-310 of 438) with videos related to

Sort By:
Pageof 44
Retina (Philadelphia, Pa.)|August 21, 2024
DIAGNOSTIC YIELD OF AN INHERITED RETINAL DISEASE GENE PANEL IN RETINOPATHY OF UNKNOWN ORIGINStéphane Abramowicz, Audrey Meunier, Laurence Postelmans, et al.
The Journal of Pathology|February 13, 2001
The detection of Tel-TrkC chimeric transcripts is more specific than TrkC immunoreactivity for the diagnosis of congenital fibrosarcomaP Dubus, J M Coindre, A Groppi, et al.
Journal of Biomedical Nanotechnology|June 16, 2016
Elaboration of Sterically Stabilized Liposomes for S-Nitrosoglutathione Targeting to MacrophagesR Diab, A S Virriat, C Ronzani, et al.
Plos One|January 27, 2026
The socioeconomic impact of inherited retinal dystrophies (IRDs) in Belgium: A cost-of-illness studyIne Vandersmissen, Janice Geers, Tom Denee, et al.
Stem Cell Research|May 30, 2025
Generation of two iPSC lines (UGENTi003 and UGENTi004) from patients with intermediate rod-cone dystrophy carrying the c.[-123C>T;701G>A];[806_810del] variants in the RDH12 geneM Bouckaert, F Van Den Broeck, M Ghazvini, et al.
Human Mutation|December 25, 2007
Novel clinico-molecular insights in pseudoxanthoma elasticum provide an efficient molecular screening method and a comprehensive diagnostic flowchartOlivier M Vanakker, Bart P Leroy, Paul Coucke, et al.
Ophthalmology Science|March 19, 2026
Expert Consensus on Characteristics, Etiology, and Management of Chorioretinal Atrophy in Patients Treated with Voretigene NeparvovecM Dominik Fischer, Isabelle Audo, David Gaucher, et al.
Clinical Genetics|April 10, 2020
VEGFA variants as prognostic markers for the retinopathy in pseudoxanthoma elasticumEva Y G De Vilder, Mohammad J Hosen, Ludovic Martin, et al.
Revue De Pneumologie Clinique|February 25, 2014
[Lung cancer, how to deal with critical situations?]F Scotté, P Leroy, S Hans, et al.
Human Molecular Genetics|April 2, 2014
Abnormal retinal development associated with FRMD7 mutationsMervyn G Thomas, Moira Crosier, Susan Lindsay, et al.
Pageof 44