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Christian Hamel

Showing results (1-10 of 74) with videos related to

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Orphanet Journal of Rare Diseases|October 13, 2006
Retinitis pigmentosaChristian Hamel
European Journal of Human Genetics : EJHG|March 15, 2013
Clinical utility gene card for: Achromatopsia - update 2013Susanne Kohl, Christian Hamel
Ophthalmic Genetics|April 13, 2005
Novel mutations in MYO7A and USH2A in Usher syndromeCécilia Maubaret, Jean-Michel Griffoin, Bernard Arnaud, et al.
BMC Genetics|January 8, 2003
Identification of three novel OA1 gene mutations identified in three families misdiagnosed with congenital nystagmus and carrier status determination by real-time quantitative PCR assayValérie Faugère, Sylvie Tuffery-Giraud, Christian Hamel, et al.
Acta Ophthalmologica|November 3, 2016
Adaptive optics: a tool for screening hydroxychloroquine-induced maculopathy?Fanny Babeau, Timothé Busetto, Christian Hamel, et al.
European Journal of Anaesthesiology|October 5, 2011
Dantrolene for severe rhabdomyolysis in Staphylococcus aureus toxic shock syndromeHans F Ginz, Soledad Levano, Thierry Girard, et al.
Ophthalmic Research|July 12, 2017
Spatially Resolved Spectral Sensitivities as a Potential Read-out Parameter in Clinical Gene Therapeutic TrialsBirgit Lorenz, Erika Wegscheider, Christian Hamel, et al.
The Indian Journal of Surgery|September 23, 2011
Performance on a virtual reality angled laparoscope task correlates with spatial ability of traineesRachel Rosenthal, Christian Hamel, Daniel Oertli, et al.
Investigative Ophthalmology & Visual Science|July 19, 2012
Characterization of pupil responses to blue and red light stimuli in autosomal dominant retinitis pigmentosa due to NR2E3 mutationAki Kawasaki, Sylvain V Crippa, Randy Kardon, et al.
Scientific Reports|May 6, 2021
Quantification of the early pupillary dilation kinetic to assess rod and cone activityCorinne Kostic, Sylvain V Crippa, Lorette Leon, et al.
Pageof 8

Showing results (1-10 of 74) with videos related to

Sort By:
Pageof 8
Orphanet Journal of Rare Diseases|October 13, 2006
Retinitis pigmentosaChristian Hamel
European Journal of Human Genetics : EJHG|March 15, 2013
Clinical utility gene card for: Achromatopsia - update 2013Susanne Kohl, Christian Hamel
Ophthalmic Genetics|April 13, 2005
Novel mutations in MYO7A and USH2A in Usher syndromeCécilia Maubaret, Jean-Michel Griffoin, Bernard Arnaud, et al.
BMC Genetics|January 8, 2003
Identification of three novel OA1 gene mutations identified in three families misdiagnosed with congenital nystagmus and carrier status determination by real-time quantitative PCR assayValérie Faugère, Sylvie Tuffery-Giraud, Christian Hamel, et al.
Acta Ophthalmologica|November 3, 2016
Adaptive optics: a tool for screening hydroxychloroquine-induced maculopathy?Fanny Babeau, Timothé Busetto, Christian Hamel, et al.
European Journal of Anaesthesiology|October 5, 2011
Dantrolene for severe rhabdomyolysis in Staphylococcus aureus toxic shock syndromeHans F Ginz, Soledad Levano, Thierry Girard, et al.
Ophthalmic Research|July 12, 2017
Spatially Resolved Spectral Sensitivities as a Potential Read-out Parameter in Clinical Gene Therapeutic TrialsBirgit Lorenz, Erika Wegscheider, Christian Hamel, et al.
The Indian Journal of Surgery|September 23, 2011
Performance on a virtual reality angled laparoscope task correlates with spatial ability of traineesRachel Rosenthal, Christian Hamel, Daniel Oertli, et al.
Investigative Ophthalmology & Visual Science|July 19, 2012
Characterization of pupil responses to blue and red light stimuli in autosomal dominant retinitis pigmentosa due to NR2E3 mutationAki Kawasaki, Sylvain V Crippa, Randy Kardon, et al.
Scientific Reports|May 6, 2021
Quantification of the early pupillary dilation kinetic to assess rod and cone activityCorinne Kostic, Sylvain V Crippa, Lorette Leon, et al.
Pageof 8