User profiles for "author:Roberto Pineda"
Roberto PinedaMassachusetts Eye and Ear Infirmary, Harvard Medical School Verified email at meei.harvard.edu Cited by 5063 |
Cataract in the adult eye preferred practice pattern®
Preferred Practice Pattern® guidelines are developed by the Academy's H. Dunbar Hoskins
Jr., MD Center for Quality Eye Care without any external financial support. Authors and …
Jr., MD Center for Quality Eye Care without any external financial support. Authors and …
[HTML][HTML] The evolution of corneal and refractive surgery with the femtosecond laser
A Aristeidou, EV Taniguchi, M Tsatsos, R Muller… - Eye and Vision, 2015 - Springer
The use of femtosecond lasers has created an evolution in modern corneal and refractive
surgery. With accuracy, safety, and repeatability, eye surgeons can utilize the femtosecond …
surgery. With accuracy, safety, and repeatability, eye surgeons can utilize the femtosecond …
Monkeypox virus and ophthalmology—a primer on the 2022 monkeypox outbreak and monkeypox-related ophthalmic disease
AR Kaufman, J Chodosh, R Pineda - JAMA ophthalmology, 2023 - jamanetwork.com
Importance An ongoing global monkeypox virus outbreak in 2022 includes the US and other
nonendemic countries. Monkeypox ophthalmic manifestations may present to the …
nonendemic countries. Monkeypox ophthalmic manifestations may present to the …
[HTML][HTML] Brillouin optical microscopy for corneal biomechanics
Purpose.: The mechanical properties of corneal tissue are linked to prevalent ocular
diseases and therapeutic procedures. Brillouin microscopy is a novel optical technology that …
diseases and therapeutic procedures. Brillouin microscopy is a novel optical technology that …
[HTML][HTML] Brillouin microscopy of collagen crosslinking: noncontact depth-dependent analysis of corneal elastic modulus
G Scarcelli, S Kling, E Quijano… - … & visual science, 2013 - iovs.arvojournals.org
Purpose.: Corneal collagen crosslinking (CXL) is designed to halt the progression of
keratoconus and corneal ectasia by inducing corneal stiffening. However, it currently is …
keratoconus and corneal ectasia by inducing corneal stiffening. However, it currently is …
Topical bevacizumab in the treatment of corneal neovascularization: results of a prospective, open-label, noncomparative study
MH Dastjerdi, KM Al-Arfaj, N Nallasamy… - Archives of …, 2009 - jamanetwork.com
Objective To study the safety and efficacy of topical bevacizumab in the treatment of corneal
neovascularization (NV). Design In a prospective, open-label, noncomparative study, 10 …
neovascularization (NV). Design In a prospective, open-label, noncomparative study, 10 …
[HTML][HTML] Biomechanical characterization of keratoconus corneas ex vivo with Brillouin microscopy
G Scarcelli, S Besner, R Pineda… - … ophthalmology & visual …, 2014 - iovs.arvojournals.org
Purpose.: Loss of corneal strength is a central feature of keratoconus progression. However,
it is currently difficult to measure corneal mechanical changes noninvasively. The objective …
it is currently difficult to measure corneal mechanical changes noninvasively. The objective …
Photocrosslinking of Silk Fibroin Using Riboflavin for Ocular Prostheses.
MB Applegate, BP Partlow, J Coburn… - … (Deerfield Beach, Fla …, 2016 - europepmc.org
A novel method to photocrosslink silk fibroin protein is reported, using riboflavin (vitamin B2)
as a photoinitiator and the mechanism of crosslinking is determined. Exposure of riboflavin …
as a photoinitiator and the mechanism of crosslinking is determined. Exposure of riboflavin …
In vivo biomechanical mapping of normal and keratoconus corneas
G Scarcelli, S Besner, R Pineda, P Kalout… - JAMA …, 2015 - jamanetwork.com
Methods| The study recruited 6 volunteers with normal corneas (mean [SD] age, 37 [15]
years) and 5 patients with advanced keratoconus (mean [SD] age, 43 [7] years). All …
years) and 5 patients with advanced keratoconus (mean [SD] age, 43 [7] years). All …
[HTML][HTML] Alzheimer's disease amyloid-β links lens and brain pathology in down syndrome
Down syndrome (DS, trisomy 21) is the most common chromosomal disorder and the
leading genetic cause of intellectual disability in humans. In DS, triplication of chromosome …
leading genetic cause of intellectual disability in humans. In DS, triplication of chromosome …