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Dive into the research topics where M. Busuioc is active.

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Featured researches published by M. Busuioc.


Investigative Ophthalmology & Visual Science | 2009

Lipofuscin and autofluorescence metrics in progressive STGD.

R. T. Smith; N.L. Gomes; G. Barile; M. Busuioc; Noah Lee; Andrew F. Laine

PURPOSE To evaluate Stargardt disease (STGD) progression and relative lipofuscin levels via autofluorescence image analysis. METHODS The relationship between focally increased autofluorescence (FIAF), geographic atrophy (GA) and focally decreased autofluorescence (FDAF) was analyzed in serial, registered autofluorescence (AF) scans of 10 patients with STGD (20 eyes, 40 scans; mean follow-up, 2.0 years) using automated techniques. RESULTS GA progressed uniformly in a transition zone with minimal FIAF. Only 4.3% of FIAF progressed to GA or FDAF, despite significant progression of GA (median 30%/year) and FDAF (mean, 29%/year). As a spatial predictor, the mean chance of FIAF for progression to FDAF was 4.3% +/- 4.4%, significantly less than that of random areas (6.7% +/- 4.0%, P = 0.029, Mann-Whitney test). In the seven eyes with GA, the mean chance of FIAF in the transition zone for transition to GA was 12% +/- 8.9%, significantly less than that of random areas (33% +/- 3.6%, P = 0.026, Mann-Whitney test). CONCLUSIONS Autofluorescent flecks and FIAF deposits with AF levels elevated above the initial macular background were less likely in the short term (2 years) to transform to GA and FDAF (AF levels below the final background) than random areas, suggesting additional mechanisms beyond direct lipofuscin toxicity. FIAF/FDAF levels were observed to fluctuate, with focal remodeling of FIAF and FDAF, or rarely, even transition of FDAF to FIAF. FDAF tended to develop, not coincident with, but adjacent to initial FIAF. Because AF identifies these characteristic biological markers so specifically, autofluorescence metrics merit consideration in the study of STGD.


Investigative Ophthalmology & Visual Science | 2006

Automating Drusen Analysis With User–Friendly Graphical Interfaces With and Without Artifact Correction

K. Uy; R. T. Smith; M. Busuioc; C. C. W. Klaver; D.D. G. Despriet


Investigative Ophthalmology & Visual Science | 2010

Controlled Field Entries versus Free Text in a Clinical/ Research Emr

M. Busuioc; R. T. Smith; Rando Allikmets; Noah Lee; Andrew F. Laine; Jianing Shi


Investigative Ophthalmology & Visual Science | 2010

Prospective Study of Reticular Pseudodrusen and Progression to Advanced Age-Related Macular Degeneration (AMD)

Nicole M. Pumariega; Mahsa A. Sohrab; Valerie Letien; M. Busuioc; R. T. Smith; Eric H. Souied


Investigative Ophthalmology & Visual Science | 2009

Perceptual Consequences of Macular Disease Evaluated Using a Model of V1

Jianing Shi; Jim Wielaard; M. Busuioc; R. T. Smith; Paul Sajda


Investigative Ophthalmology & Visual Science | 2009

Fractal Analysis of Age Related Macular Degeneration

E. Cheung; A. Jiminez; M. Busuioc; R. T. Smith


Investigative Ophthalmology & Visual Science | 2009

User Interactive Retinal Image Analysis: Realizing the Practical Digital Promise

M. Busuioc; R. T. Smith; R. P. Post; J. Chen; Noah Lee; Jianing Shi; Andrew F. Laine


Investigative Ophthalmology & Visual Science | 2008

Ontologies Used in a Clinical Database With Controlled Field Entries

M. Busuioc; R. T. Smith; Noah Lee


Investigative Ophthalmology & Visual Science | 2007

Database for Correlation of Demographic, Clinical Photo Documentation and Genetic Data

M. Busuioc; R. T. Smith; Noah Lee; Rando Allikmets


Investigative Ophthalmology & Visual Science | 2007

Autofluorescence and Geographic Atrophy

Terry J. Smith; M. Busuioc; Noah Lee; Andrew F. Laine; Steffen Schmitz-Valckenberg; Frank G. Holz

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