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Investigative Ophthalmology & Visual Science
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May 12, 2017
Multifocal ERG Responses in Subjects With a History of Preterm Birth
Pablo Altschwager, Anne Moskowitz, Anne B Fulton, et al.
Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus
|
September 19, 2024
Intravenous fluorescein overdose in a child undergoing fluorescein angiography
Rhea W Teng, Michael T B Nguyen, David G Hunter, et al.
Seminars in Pediatric Neurology
|
September 25, 2017
Juvenile Macular Degenerations
Pablo Altschwager, Lucia Ambrosio, Emily A Swanson, et al.
Documenta Ophthalmologica. Advances in Ophthalmology
|
February 2, 2017
Progressive retinal degeneration in a girl with Knobloch syndrome who presented with signs of ocular albinism
Libe Gradstein, Ronald M Hansen, Gerald F Cox, et al.
Revista Medica De Chile
|
September 24, 2004
[Mechanical ventilation in patients with acute neurological disease: survival and functional outcome]
Enrique Norero, Pablo Altschwager, Carlos Romero, et al.
Ophthalmic Genetics
|
June 25, 2026
Absent cone function and stable ophthalmic features in a non-syndromic woman with pathogenic variants in <i>CEP290</i>
Samet Gulkas, Ines Fenniri, Hanna De Bruyn, et al.
American Journal of Ophthalmology
|
March 10, 2024
Characteristics of Eyes With CRB1-Associated EOSRD/LCA: Age-Related Changes
Jad Ayash, Russell L Woods, James D Akula, et al.
Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus
|
September 23, 2024
Characteristics, associations, and outcomes of children with posterior segment coloboma
Francisco Altamirano, Sandra Hoyek, Shravan V Savant, et al.
Documenta Ophthalmologica. Advances in Ophthalmology
|
May 10, 2022
The relation of the multifocal electroretinographic response to macular layer volume
Mariana I Fonseca, Alexandra Nouck-A-Nwal, Lucia Ambrosio, et al.
Ophthalmic Genetics
|
July 31, 2025
Novel structural variant in <i>CACNA1F</i> causing congenital stationary night blindness identified with whole genome sequencing
Mayra Martinez Sanchez, Nafiza Meher, Hanna DeBruyn, et al.
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of 2
Search research articles
Search
Showing results (1-10 of 12) with videos related to
Sort By:
Page
of 2
Investigative Ophthalmology & Visual Science
|
May 12, 2017
Multifocal ERG Responses in Subjects With a History of Preterm Birth
Pablo Altschwager, Anne Moskowitz, Anne B Fulton, et al.
Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus
|
September 19, 2024
Intravenous fluorescein overdose in a child undergoing fluorescein angiography
Rhea W Teng, Michael T B Nguyen, David G Hunter, et al.
Seminars in Pediatric Neurology
|
September 25, 2017
Juvenile Macular Degenerations
Pablo Altschwager, Lucia Ambrosio, Emily A Swanson, et al.
Documenta Ophthalmologica. Advances in Ophthalmology
|
February 2, 2017
Progressive retinal degeneration in a girl with Knobloch syndrome who presented with signs of ocular albinism
Libe Gradstein, Ronald M Hansen, Gerald F Cox, et al.
Revista Medica De Chile
|
September 24, 2004
[Mechanical ventilation in patients with acute neurological disease: survival and functional outcome]
Enrique Norero, Pablo Altschwager, Carlos Romero, et al.
Ophthalmic Genetics
|
June 25, 2026
Absent cone function and stable ophthalmic features in a non-syndromic woman with pathogenic variants in <i>CEP290</i>
Samet Gulkas, Ines Fenniri, Hanna De Bruyn, et al.
American Journal of Ophthalmology
|
March 10, 2024
Characteristics of Eyes With CRB1-Associated EOSRD/LCA: Age-Related Changes
Jad Ayash, Russell L Woods, James D Akula, et al.
Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus
|
September 23, 2024
Characteristics, associations, and outcomes of children with posterior segment coloboma
Francisco Altamirano, Sandra Hoyek, Shravan V Savant, et al.
Documenta Ophthalmologica. Advances in Ophthalmology
|
May 10, 2022
The relation of the multifocal electroretinographic response to macular layer volume
Mariana I Fonseca, Alexandra Nouck-A-Nwal, Lucia Ambrosio, et al.
Ophthalmic Genetics
|
July 31, 2025
Novel structural variant in <i>CACNA1F</i> causing congenital stationary night blindness identified with whole genome sequencing
Mayra Martinez Sanchez, Nafiza Meher, Hanna DeBruyn, et al.
Page
of 2