Retinitis pigmentosa

per Hamel, Christian
Publicat 2006

Cone rod dystrophies

per Hamel Christian P
Publicat 2007-02-01

Cone rod dystrophies

per Hamel, Christian P
Publicat 2007

Clinical utility gene card for: Achromatopsia - update 2013

per Kohl, Susanne, Hamel, Christian
Publicat 2013

Clinical utility gene card for: achromatopsia

per Kohl, Susanne, Hamel, Christian P
Publicat 2011

Clinical utility gene card for: blue cone monochromatism

per Kohl, Susanne, Hamel, Christian P
Publicat 2011

Identification of three novel OA1 gene mutations identified in three families misdiagnosed with congenital nystagmus and carrier status determination by real-time quantitative PCR...

per Hamel Christian, Claustres Mireille, Tuffery-Giraud Sylvie, Faugère Valérie
Publicat 2003-01-01

Identification of three novel OA1 gene mutations identified in three families misdiagnosed with congenital nystagmus and carrier status determination by real-time quantitative PCR...

per Faugère, Valérie, Tuffery-Giraud, Sylvie, Hamel, Christian, Claustres, Mireille
Publicat 2003

Gene structure and chromosomal localization of mouse Opa1 : its exclusion from the Bst locus

per Delettre, Cécile, Lenaers, Guy, Belenguer, Pascale, Hamel, Christian P
Publicat 2003

Performance on a Virtual Reality Angled Laparoscope Task Correlates with Spatial Ability of Trainees

per Rosenthal, Rachel, Hamel, Christian, Oertli, Daniel, Demartines, Nicolas, Gantert, Walter A.
Publicat 2010

Fatty acid transport protein 1 regulates retinoid metabolism and photoreceptor development in mouse retina

per Cubizolle, Aurélie, Guillou, Laurent, Mollereau, Bertrand, Hamel, Christian P., Brabet, Philippe
Publicat a PLoS One (2017)

Quantification of the early pupillary dilation kinetic to assess rod and cone activity

per Kostic, Corinne, Crippa, Sylvain V., Leon, Lorette, Hamel, Christian, Meunier, Isabelle, Kawasaki, Aki
Publicat a Sci Rep (2021)

Impairment of Visual Function and Retinal ER Stress Activation in Wfs1-Deficient Mice

per Bonnet Wersinger, Delphine, Benkafadar, Nesrine, Jagodzinska, Jolanta, Hamel, Christian, Tanizawa, Yukio, Lenaers, Guy, Delettre, Cécile
Publicat 2014

A novel mutation of AFG3L2 might cause dominant optic atrophy in patients with mild intellectual disability

per Charif, Majida, Roubertie, Agathe, Salime, Sara, Mamouni, Sonia, Goizet, Cyril, Hamel, Christian P., Lenaers, Guy
Publicat a Front Genet (2015)

Optical Coherence Tomography: Imaging Mouse Retinal Ganglion Cells In Vivo

per Jagodzinska, Jolanta, Sarzi, Emmanuelle, Cavalier, Mélanie, Seveno, Marie, Baecker, Volker, Hamel, Christian, Péquignot, Marie, Delettre, Cecile
Publicat a J Vis Exp (2017)

The future of patient safety: Surgical trainees accept virtual reality as a new training tool

per Rosenthal, Rachel, Gantert, Walter A, Hamel, Christian, Metzger, Jürg, Kocher, Thomas, Vogelbach, Peter, Demartines, Nicolas, Hahnloser, Dieter
Publicat 2008

Dominant optic atrophy

per Lenaers, Guy, Hamel, Christian, Delettre, Cécile, Amati-Bonneau, Patrizia, Procaccio, Vincent, Bonneau, Dominique, Reynier, Pascal, Milea, Dan
Publicat 2012

Homozygosity mapping in autosomal recessive retinitis pigmentosa families detects novel mutations

per Bocquet, Béatrice, Marzouka, Nour al Dain, Hebrard, Maxime, Manes, Gaël, Sénéchal, Audrey, Meunier, Isabelle, Hamel, Christian P.
Publicat 2013

A Truncated Form of Rod Photoreceptor PDE6 β-Subunit Causes Autosomal Dominant Congenital Stationary Night Blindness by Interfering with the Inhibitory Activity of the γ-Subunit

per Manes, Gaël, Cheguru, Pallavi, Majumder, Anurima, Bocquet, Béatrice, Sénéchal, Audrey, Artemyev, Nikolai O., Hamel, Christian P., Brabet, Philippe
Publicat 2014

Genome Editing in Patient iPSCs Corrects the Most Prevalent USH2A Mutations and Reveals Intriguing Mutant mRNA Expression Profiles

per Sanjurjo-Soriano, Carla, Erkilic, Nejla, Baux, David, Mamaeva, Daria, Hamel, Christian P., Meunier, Isabelle, Roux, Anne-Françoise, Kalatzis, Vasiliki
Publicat a Mol Ther Methods Clin Dev (2019)