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Alex V Levin

Showing results (101-110 of 231) with videos related to

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Current Opinion in Ophthalmology|August 11, 2018
New classification system for pediatric glaucoma: implications for clinical care and a research registryAvrey Thau, Maureen Lloyd, Sharon Freedman, et al.
Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus|January 17, 2012
Hypertensive retinopathy in a child caused by pheochromocytoma: identification after a failed school vision screeningMichael D Tibbetts, Richard Wise, Brian Forbes, et al.
Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus|February 29, 2012
The role of episcleral venous pressure in glaucoma associated with Sturge-Weber syndromeTiffany Shiau, Narendra Armogan, David B Yan, et al.
Ophthalmic Genetics|December 11, 2023
Mutations in <i>AGBL5</i> associated with Retinitis pigmentosaDiego I Paredes, Nicholas R Bello, Jenina E Capasso, et al.
Indian Journal of Ophthalmology|July 7, 2016
How genetics works? An illustrative case reportVikas Khetan, Mario Zanolli, Jenina Capasso, et al.
Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus|April 12, 2003
Hypotension and bradycardia in infants after the use of topical brimonidine and beta-blockersNils K Mungan, Thomas W Wilson, Ken K Nischal, et al.
Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus|September 19, 2025
Ophthalmic manifestations of Cousin syndromeManjushree Bhate, Venkatesh Pochaboina, Ravi Varma, et al.
International Journal of Pediatric Otorhinolaryngology|March 14, 2003
Nasal endoscopy in the treatment of congenital lacrimal sac mucocelesAlex V Levin, Tamara Wygnanski-Jaffe, Vito Forte, et al.
Ophthalmic Genetics|October 8, 2013
Autosomal-dominant Leber Congenital Amaurosis Caused by a Heterozygous CRX Mutation in a Father and SonKarthikeyan Arcot Sadagopan, Robert Battista, Rosanne B Keep, et al.
The Journal of Pediatrics|April 25, 2003
Nonophthalmologist accuracy in diagnosing retinal hemorrhages in the shaken baby syndromeYair Morad, Yuri M Kim, Marcellina Mian, et al.
Pageof 24

Showing results (101-110 of 231) with videos related to

Sort By:
Pageof 24
Current Opinion in Ophthalmology|August 11, 2018
New classification system for pediatric glaucoma: implications for clinical care and a research registryAvrey Thau, Maureen Lloyd, Sharon Freedman, et al.
Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus|January 17, 2012
Hypertensive retinopathy in a child caused by pheochromocytoma: identification after a failed school vision screeningMichael D Tibbetts, Richard Wise, Brian Forbes, et al.
Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus|February 29, 2012
The role of episcleral venous pressure in glaucoma associated with Sturge-Weber syndromeTiffany Shiau, Narendra Armogan, David B Yan, et al.
Ophthalmic Genetics|December 11, 2023
Mutations in <i>AGBL5</i> associated with Retinitis pigmentosaDiego I Paredes, Nicholas R Bello, Jenina E Capasso, et al.
Indian Journal of Ophthalmology|July 7, 2016
How genetics works? An illustrative case reportVikas Khetan, Mario Zanolli, Jenina Capasso, et al.
Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus|April 12, 2003
Hypotension and bradycardia in infants after the use of topical brimonidine and beta-blockersNils K Mungan, Thomas W Wilson, Ken K Nischal, et al.
Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus|September 19, 2025
Ophthalmic manifestations of Cousin syndromeManjushree Bhate, Venkatesh Pochaboina, Ravi Varma, et al.
International Journal of Pediatric Otorhinolaryngology|March 14, 2003
Nasal endoscopy in the treatment of congenital lacrimal sac mucocelesAlex V Levin, Tamara Wygnanski-Jaffe, Vito Forte, et al.
Ophthalmic Genetics|October 8, 2013
Autosomal-dominant Leber Congenital Amaurosis Caused by a Heterozygous CRX Mutation in a Father and SonKarthikeyan Arcot Sadagopan, Robert Battista, Rosanne B Keep, et al.
The Journal of Pediatrics|April 25, 2003
Nonophthalmologist accuracy in diagnosing retinal hemorrhages in the shaken baby syndromeYair Morad, Yuri M Kim, Marcellina Mian, et al.
Pageof 24