L. Gabriel

发表

ADAMTSL4, a secreted glycoprotein widely distributed in the eye, binds fibrillin-1 microfibrils and accelerates microfibril biogenesis.

Jason C. Ho, J. Hollyfield, E. Traboulsi, 2012, Investigative ophthalmology & visual science.

Safety and Efficacy of Moxifloxacin-Dexamethasone Eyedrops as Treatment for Bacterial Ocular Infection Associated with Bacterial Blepharitis

A. L. Höfling-Lima, C. Muccioli, D. Stroman, 2012, Advances in Therapy.

Deciphering the genetic architecture and ethnographic distribution of IRD in three ethnic populations by whole genome sequence analysis

K. Frazer, P. Sieving, Andrew Huynh, 2021, PLoS genetics.

Exome sequencing identifies NMNAT1 mutations as a cause of Leber congenital amaurosis

Renhua Wu, Yanhua Chen, Xin Yi, 2012, Nature Genetics.

Genetic analysis of 10 pedigrees with inherited retinal degeneration by exome sequencing and phenotype-genotype association.

G. Dagnelie, J. Duncan, J. Heckenlively, 2017, Physiological genomics.

Oculodentodigital dysplasia: new ocular findings and a novel connexin 43 mutation.

E. Traboulsi, E. Rockwood, A. Marcotty, 2011, Archives of ophthalmology.

Genetic Diagnostic Methods for Inherited Eye Diseases

E. Traboulsi, L. Gabriel, 2011, Middle East African journal of ophthalmology.

Intravitreal bevacizumab combined with infliximab in the treatment of choroidal neovascularization secondary to age-related macular degeneration: case report series.

M. Ávila, D. Isaac, L. Gabriel, 2013, Arquivos brasileiros de oftalmologia.

Comparative study of ophthalmological and serological manifestations and the therapeutic response of patients with isolated scleritis and scleritis associated with systemic diseases.

D. Freitas, V. Trevisani, J. M. Sousa, 2011, Arquivos brasileiros de oftalmologia.