Publications associées à Optométrie

3-Dimensional magnetic resonance imaging of the freely moving human eye

Jérôme Yerly, João Pedro Forjaco Jorge, Lorenzo Di Sopra, Josefina Adriana Maria Bastiaansen, Silvio Ionta, Benedetta Franceschiello, David Zeugin

Eye motion is a major confound for magnetic resonance imaging (MRI) in neuroscience or ophthalmology. Currently, solutions toward eye stabilisation include participants fixating or administration of paralytics/anaesthetics. We developed a novel MRI protoco ...

PERGAMON-ELSEVIER SCIENCE LTD2020

Ocular Structures Segmentation from Multi-sequences MRI Using 3D Unet with Fully Connected CRFs

Meritxell Bach Cuadra, Raphael Sznitman, Alessia Pica

The use of 3D Magnetic Resonance Imaging (MRI) has attracted growing attention for the purpose of diagnosis and treatment planning of intraocular ocular cancers. Precise segmentation of such tumors are highly important to characterize tumors, their progres ...

SPRINGER INTERNATIONAL PUBLISHING AG2018

Towards the Use of Social Interaction Conventions as Prior for Gaze Model Adaptation

Jean-Marc Odobez, Rémy Alain Siegfried, Yu Yu

Gaze is an important non-verbal cue involved in many facets of social interactions like communication, attentiveness or attitudes. Nevertheless, extracting gaze directions visually and remotely usually suffers large errors because of low resolution images, ...

ACM2017

Identifying mutations in Tunisian families with retinal dystrophy

Imen Habibi

Retinal dystrophies (RD) are a rare genetic disorder with high genetic heterogeneity. This study aimed at identifying disease-causing variants in fifteen consanguineous Tunisian families. Full ophthalmic examination was performed. Index patients were subje ...

Nature Research2016

Novel ADAM9 homozygous mutation in a consanguineous Egyptian family with severe cone-rod dystrophy and cataract

Tatiana Favez

Objective To genetically and phenotypically describe a new ADAM9 homozygous mutation in a consanguineous family from Egypt with autosomal recessive cone-rod dystrophy (arCRD), anterior polar and posterior subcapsular cataract. Design, setting and participa ...

Bmj Publishing Group2014

Dental Phenotype in Jalili Syndrome Due to a c.1312 dupC Homozygous Mutation in the CNNM4 Gene

Jalili syndrome denotes a recessively inherited combination of an eye disease (cone-rod dystrophy) and a dental disorder (amelogenesis imperfecta), which is caused by mutations in the CNNM4 gene. Whereas the ophthalmic consequences of these mutations have ...

Public Library of Science2013

Clinical and genetic investigation of a large Tunisian family with complete achromatopsia: identification of a new nonsense mutation in GNAT2 gene

Farah Ouechtati

Complete achromatopsia is a rare autosomal recessive disease associated with CNGA3, CNGB3, GNAT2 and PDE6C mutations. This retinal disorder is characterized by complete loss of color discrimination due to the absence or alteration of the cones function. Th ...

2011

Hes1 regulates corneal development and the function of corneal epithelial stem/progenitor cells

Yann Barrandon

Hes1, a major target gene in Notch signaling, regulates the fate and differentiation of various cell types in many developmental systems. To gain a novel insight into the role of Hes1 in corneal tissue, we performed gain-of-function and loss-of-function st ...

2008