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ABOUT JoVE

Overview Leadership Blog JoVE Help Center

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Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

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Testimonials Subscriptions Access Resources Library Advisory Board FAQ

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JoVE Journal Methods Collections JoVE Encyclopedia of Experiments Archive

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Raimondo Forte

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Ophthalmologica. Journal International D'Ophtalmologie. International Journal of Ophthalmology. Zeitschrift Fur Augenheilkunde|June 20, 2018

Choroidal Thickness in Birdshot Retinochoroiditis Over a 2-Year PeriodRaimondo Forte, Florent Aptel, Kim Thia-Soui-Tchong, et al.

Investigative Ophthalmology & Visual Science|August 11, 2012

Enhanced depth imaging optical coherence tomography in type 2 diabetesGiuseppe Querques, Rosangela Lattanzio, Lea Querques, et al.

Molecular Vision|May 3, 2014

Multimodal analysis of the progression of Best vitelliform macular dystrophyGiuseppe Querques, Jennyfer Zerbib, Anouk Georges, et al.

Molecular Cytogenetics|March 31, 2015

Phenotypic and genetic characterization of a family carrying two Xq21.1-21.3 interstitial deletions associated with syndromic hearing lossSandra Iossa, Valerio Costa, Virginia Corvino, et al.

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Search research articles

Showing results (61-70 of 64) with videos related to

Sort By:

Pageof 7

You have reached the last page of results.This site can display upto 64 results.

Ophthalmologica. Journal International D'Ophtalmologie. International Journal of Ophthalmology. Zeitschrift Fur Augenheilkunde|June 20, 2018

Choroidal Thickness in Birdshot Retinochoroiditis Over a 2-Year PeriodRaimondo Forte, Florent Aptel, Kim Thia-Soui-Tchong, et al.

Investigative Ophthalmology & Visual Science|August 11, 2012

Enhanced depth imaging optical coherence tomography in type 2 diabetesGiuseppe Querques, Rosangela Lattanzio, Lea Querques, et al.

Molecular Vision|May 3, 2014

Multimodal analysis of the progression of Best vitelliform macular dystrophyGiuseppe Querques, Jennyfer Zerbib, Anouk Georges, et al.

Molecular Cytogenetics|March 31, 2015

Phenotypic and genetic characterization of a family carrying two Xq21.1-21.3 interstitial deletions associated with syndromic hearing lossSandra Iossa, Valerio Costa, Virginia Corvino, et al.

Pageof 7