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Alex V Levin

Showing results (161-170 of 231) with videos related to

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Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus|September 21, 2016
Improving access to vision screening in urban Philadelphia elementary schoolsLisa A Hark, Eileen L Mayro, Judie Tran, et al.
American Journal of Medical Genetics. Part A|May 18, 2007
Cornelia de Lange syndrome: clinical review, diagnostic and scoring systems, and anticipatory guidanceAntonie D Kline, Ian D Krantz, Annemarie Sommer, et al.
Journal of Pediatric Ophthalmology and Strabismus|March 24, 2015
The Eagles Eye Mobile: assessing its ability to deliver eye care in a high-risk communityRizwan A Alvi, Leah Justason, Carter Liotta, et al.
Journal of Medical Genetics|May 14, 2013
No evidence for locus heterogeneity in Knobloch syndromeMohammed A Aldahmesh, Arif O Khan, Jawahir Y Mohamed, et al.
Ophthalmic Genetics|April 25, 2007
Attitudes regarding predictive testing for retinitis pigmentosaEedy Mezer, Riyana Babul-Hirji, Richard Wise, et al.
Ophthalmic Genetics|January 24, 2017
Spectral-domain optical coherence tomography findings in Alström syndromeGad Dotan, Vikas Khetan, Jan D Marshall, et al.
Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus|June 11, 2015
Peters anomaly in cri-du-chat syndromeWilliam C Hope, Jose A Cordovez, Jenina E Capasso, et al.
Retinal Cases & Brief Reports|June 26, 2026
Pathogenic Variants in HGSNAT associated with Autosomal Recessive Retinitis Pigmentosa without Overt Sanfilippo SyndromeLorena M Haefeli, Diego I Paredes, Celeste S Wyman, et al.
Child Abuse & Neglect|May 12, 2012
The role of prothrombotic factors in the ocular manifestations of abusive and non-abusive head trauma: a feasibility studyAnna Yu, Derek Stephens, Brian M Feldman, et al.
Molecular Vision|January 15, 2024
Protein modeling and in silico analysis to assess pathogenicity of <i>ABCA4</i> variants in patients with inherited retinal diseaseSenem Cevik, Nutsuchar Wangtiraumnuay, Kristof Van Schelvergem, et al.
Pageof 24

Showing results (161-170 of 231) with videos related to

Sort By:
Pageof 24
Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus|September 21, 2016
Improving access to vision screening in urban Philadelphia elementary schoolsLisa A Hark, Eileen L Mayro, Judie Tran, et al.
American Journal of Medical Genetics. Part A|May 18, 2007
Cornelia de Lange syndrome: clinical review, diagnostic and scoring systems, and anticipatory guidanceAntonie D Kline, Ian D Krantz, Annemarie Sommer, et al.
Journal of Pediatric Ophthalmology and Strabismus|March 24, 2015
The Eagles Eye Mobile: assessing its ability to deliver eye care in a high-risk communityRizwan A Alvi, Leah Justason, Carter Liotta, et al.
Journal of Medical Genetics|May 14, 2013
No evidence for locus heterogeneity in Knobloch syndromeMohammed A Aldahmesh, Arif O Khan, Jawahir Y Mohamed, et al.
Ophthalmic Genetics|April 25, 2007
Attitudes regarding predictive testing for retinitis pigmentosaEedy Mezer, Riyana Babul-Hirji, Richard Wise, et al.
Ophthalmic Genetics|January 24, 2017
Spectral-domain optical coherence tomography findings in Alström syndromeGad Dotan, Vikas Khetan, Jan D Marshall, et al.
Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus|June 11, 2015
Peters anomaly in cri-du-chat syndromeWilliam C Hope, Jose A Cordovez, Jenina E Capasso, et al.
Retinal Cases & Brief Reports|June 26, 2026
Pathogenic Variants in HGSNAT associated with Autosomal Recessive Retinitis Pigmentosa without Overt Sanfilippo SyndromeLorena M Haefeli, Diego I Paredes, Celeste S Wyman, et al.
Child Abuse & Neglect|May 12, 2012
The role of prothrombotic factors in the ocular manifestations of abusive and non-abusive head trauma: a feasibility studyAnna Yu, Derek Stephens, Brian M Feldman, et al.
Molecular Vision|January 15, 2024
Protein modeling and in silico analysis to assess pathogenicity of <i>ABCA4</i> variants in patients with inherited retinal diseaseSenem Cevik, Nutsuchar Wangtiraumnuay, Kristof Van Schelvergem, et al.
Pageof 24