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Ophthalmic Genetics|August 30, 2018
The uncommon occurrence of two common inherited disorders in a single patient: a mini case seriesFrancisca Zuazo, Alina V DumitrescuGenes|June 24, 2022
Biallelic Optic Atrophy 1 (<i>OPA1</i>) Related Disorder-Case Report and Literature ReviewBayan Al Othman, Jia Ern Ong, Alina V DumitrescuJournal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus|July 19, 2021
Clinical phenocopies of albinismAlina V Dumitrescu, Wanda L Pfeifer, Arlene V DrackOphthalmic Genetics|December 24, 2011
A family with branchio-oculo-facial syndrome with primarily ocular involvement associated with mutation of the TFAP2A geneAlina V Dumitrescu, Jeff M Milunsky, Susannah Q Longmuir, et al.Investigative Ophthalmology & Visual Science|August 25, 2012
Lack of immunoglobulins does not prevent C1q binding to RGC and does not alter the progression of experimental glaucomaQiong J Ding, Amy C Cook, Alina V Dumitrescu, et al.Experimental Eye Research|June 24, 2008
Disruption of the complement cascade delays retinal ganglion cell death following retinal ischemia-reperfusionMarkus H Kuehn, Chan Y Kim, Bing Jiang, et al.Canadian Journal of Ophthalmology. Journal Canadien D'Ophtalmologie|December 30, 2023
CACNA1F-related synaptic dysfunction: challenges diagnosing congenital stationary night blindness presenting without night blindnessAlina V Dumitrescu, Wanda L Pfeifer, Monica Arhens, et al.Frontiers in Ophthalmology|July 10, 2024
The long-term outcomes of the Anderson-Kestenbaum procedureJeffrey Kuziel, Hannah Pope, Aishwarya J Kothapalli, et al.Ophthalmology|June 14, 2011
Prevalence and characteristics of abnormal head posture in children with Down syndrome: a 20-year retrospective, descriptive reviewAlina V Dumitrescu, Daniela C Moga, Susannah Q Longmuir, et al.Biomolecules|February 25, 2022
Systemic Treatment with Pioglitazone Reverses Vision Loss in Preclinical Glaucoma ModelsHuilan Zeng, Alina V Dumitrescu, David Wadkins, et al.Pageof 3