Tuy N. Brignol
Evry, France
Last Updated: 09/26/2026
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Found 13 publications
Reader response: Consensus-based care recommendations for adults with myotonic dystrophy type 1.
Journal: Neurology. Clinical practice
Published: November 22, 2019
What is the Ocular phenotype associated with a dystrophin deletion of exons 12-29?
Journal: Intractable & rare diseases research
Published: December 19, 2018
Cataract development associated with long-term glucocorticoid therapy in Duchenne muscular dystrophy patients.
Journal: Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus
Published: June 28, 2018
What is the ocular phenotype associated with a single exon 78 deletion in Duchenne muscular dystrophy?
Journal: Journal of human genetics
Published: May 04, 2018
Retinal involvement in type 1 myotonic dystrophy: Literature review and presentation of a project based on the DM-Scope
Journal: Journal francais d'ophtalmologie
Published: February 10, 2018
Neuromyelitis optica spectrum disorders positive for anti-AQP4 antibody associated with myasthenia gravis: A literature review
Journal: Journal francais d'ophtalmologie
Published: February 10, 2018
Finland: an ideally valued genetic heritage
Journal: Medecine sciences : M/S
Published: November 22, 2016
Literature review of the importance of retinal examination in two genetic neuromuscular diseases (DM1 and FSHD). Potential clinical applications
Journal: Journal francais d'ophtalmologie
Published: December 30, 2014
Ptosis in rare muscle and neuromuscular junction disorders: A literature review and diagnostic flowchart
Journal: Journal francais d'ophtalmologie
Published: August 08, 2014
Last Updated: 09/26/2026