Jacmine Pechmeja
Toulouse, 31300, France
Last Updated: 09/26/2026
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Found 14 publications
Structural Variant Disrupting the Expression of the Remote FOXC1 Gene in a Patient with Syndromic Complex Microphthalmia.
Journal: International journal of molecular sciences
Published: January 17, 2024
First evidence of SOX2 mutations in Peters' anomaly: Lessons from molecular screening of 95 patients.
Journal: Clinical genetics
Published: October 21, 2021
Pharmaceutical supply of human plasminogen replacement therapy for the treatment of ligneous conjunctivitis: Logistics for a university hospital
Journal: Journal francais d'ophtalmologie
Published: July 31, 2020
Long term outcomes of botulinum toxin injections in infantile esotropia
Journal: Journal francais d'ophtalmologie
Published: April 27, 2020
Identification of PITX3 mutations in individuals with various ocular developmental defects.
Journal: Ophthalmic genetics
Published: February 07, 2018
Spontaneous rupture of chorioretinal coloboma in an 8-year-old child is treated by temporal fascia graft.
Journal: Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus
Published: February 21, 2016
Immature retina evolution in a premature infant
Journal: Journal francais d'ophtalmologie
Published: September 17, 2015
Iris metastasis presenting as monocular diplopia
Journal: Journal francais d'ophtalmologie
Published: June 26, 2015
Persistent tunica vasculosa lentis
Journal: Journal francais d'ophtalmologie
Published: March 11, 2015
Intraoperative OCT of a Mittendorf dot with persistent hyaloid artery
Journal: Journal francais d'ophtalmologie
Published: March 11, 2015
Shaken baby syndrome: Retcam findings
Journal: Journal francais d'ophtalmologie
Published: July 29, 2014
Retinal astrocytoma in tuberous sclerosis: SD-OCT findings
Journal: Journal francais d'ophtalmologie
Published: February 25, 2014
Last Updated: 09/26/2026