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Orphanet Journal of Rare Diseases
|
October 13, 2006
Retinitis pigmentosa
Christian Hamel
European Journal of Human Genetics : EJHG
|
March 15, 2013
Clinical utility gene card for: Achromatopsia - update 2013
Susanne Kohl, Christian Hamel
Ophthalmic Genetics
|
April 13, 2005
Novel mutations in MYO7A and USH2A in Usher syndrome
Cécilia 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 assay
Valérie 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 syndrome
Hans 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 Trials
Birgit 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 trainees
Rachel 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 mutation
Aki 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 activity
Corinne Kostic, Sylvain V Crippa, Lorette Leon, et al.
Page
of 8
Search research articles
Search
Showing results (1-10 of 74) with videos related to
Sort By:
Page
of 8
Orphanet Journal of Rare Diseases
|
October 13, 2006
Retinitis pigmentosa
Christian Hamel
European Journal of Human Genetics : EJHG
|
March 15, 2013
Clinical utility gene card for: Achromatopsia - update 2013
Susanne Kohl, Christian Hamel
Ophthalmic Genetics
|
April 13, 2005
Novel mutations in MYO7A and USH2A in Usher syndrome
Cécilia 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 assay
Valérie 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 syndrome
Hans 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 Trials
Birgit 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 trainees
Rachel 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 mutation
Aki 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 activity
Corinne Kostic, Sylvain V Crippa, Lorette Leon, et al.
Page
of 8