Fouzia Studer
Strasbourg, France
Last Updated: 09/26/2026
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Found 9 publications
Response to comment on: Could internal limiting membrane peeling before Voretigen Neparvovec-ryzl subretinal injection prevent focal chorioretinal atrophy?
Journal: Heliyon
Published: September 12, 2024
Could internal limiting membrane peeling before Voretigen neparvovec-ryzl subretinal injection prevent focal chorioretinal atrophy?
Journal: Heliyon
Published: July 22, 2023
Comparative roadmaps of reprogramming and oncogenic transformation identify Bcl11b and Atoh8 as broad regulators of cellular plasticity.
Journal: Nature cell biology
Published: July 14, 2021
Atypical Retinal Phenotype in a Patient With Alström Syndrome and Biallelic Novel Pathogenic Variants in ALMS1, Including a de novo Variation.
Journal: Frontiers in genetics
Published: April 28, 2020
Proteasome subunit PSMC3 variants cause neurosensory syndrome combining deafness and cataract due to proteotoxic stress.
Journal: EMBO molecular medicine
Published: December 05, 2019
Synchrotron X-ray microbeams: A promising tool for drug-resistant epilepsy treatment.
Journal: Physica medica : PM : an international journal devoted to the applications of physics to medicine and biology : official journal of the Italian Association of Biomedical Physics (AIFB)
Published: January 08, 2015
Predominantly Cone-System Dysfunction as Rare Form of Retinal Degeneration in Patients With Molecularly Confirmed Bardet-Biedl Syndrome.
Journal: American journal of ophthalmology
Published: November 10, 2014
MSX2 Gene Duplication in a Patient with Eye Development Defects.
Journal: Ophthalmic genetics
Published: March 27, 2014
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Last Updated: 09/26/2026