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Journal of Clinical Medicine
|
December 11, 2022
Conjunctival Swabs Reveal Higher Detection Rate Compared to Schirmer Strips for SARS-CoV-2 RNA Detection in Tears of Hospitalized COVID-19 Patients
Luís Expedito Sabage, Young Joo Sun, Julian Wolf, et al.
American Journal of Ophthalmology Case Reports
|
April 11, 2020
Phenotypic variance in Calpain-5 retinal degeneration
Peter H Tang, Teja Chemudupati, Katherine J Wert, et al.
Investigative Ophthalmology & Visual Science
|
October 13, 2020
Retinal Manifestations of Mitochondrial Oxidative Phosphorylation Disorders
Jin Kyun Oh, Jose Ronaldo Lima de Carvalho, Yan Nuzbrokh, et al.
Molecular Genetics & Genomic Medicine
|
May 27, 2017
Structural modeling of a novel <i>SLC38A8</i> mutation that causes foveal hypoplasia
Marcus A Toral, Gabriel Velez, Katherine Boudreault, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)
|
April 13, 2011
Seroreactivity against aqueous-soluble and detergent-soluble retinal proteins in posterior uveitis
Audrey C Ko, Jason P Brinton, Vinit B Mahajan, et al.
Biofabrication
|
February 24, 2026
Implantable ocular therapeutic systems: an insight into their clinical potential in the long-term treatment of ocular diseases
Hyeonji Kim, Nae-Won Kang, Wen Hong, et al.
Diagnostics (Basel, Switzerland)
|
July 27, 2022
Predicting Systemic Health Features from Retinal Fundus Images Using Transfer-Learning-Based Artificial Intelligence Models
Nergis C Khan, Chandrashan Perera, Eliot R Dow, et al.
Nature Communications
|
February 26, 2022
Investigation of Cas9 antibodies in the human eye
Marcus A Toral, Carsten T Charlesworth, Benjamin Ng, et al.
Cold Spring Harbor Molecular Case Studies
|
December 15, 2019
Compound heterozygous novel frameshift variants in the <i>PROM1</i> gene result in Leber congenital amaurosis
Sara D Ragi, Jose Ronaldo Lima de Carvalho, Akemi J Tanaka, et al.
Orphanet Journal of Rare Diseases
|
August 3, 2019
Comparison of structural progression between ciliopathy and non-ciliopathy associated with autosomal recessive retinitis pigmentosa
Vitor K L Takahashi, Christine L Xu, Júlia T Takiuti, et al.
Page
of 26
Search research articles
Search
Showing results (151-160 of 259) with videos related to
Sort By:
Page
of 26
Journal of Clinical Medicine
|
December 11, 2022
Conjunctival Swabs Reveal Higher Detection Rate Compared to Schirmer Strips for SARS-CoV-2 RNA Detection in Tears of Hospitalized COVID-19 Patients
Luís Expedito Sabage, Young Joo Sun, Julian Wolf, et al.
American Journal of Ophthalmology Case Reports
|
April 11, 2020
Phenotypic variance in Calpain-5 retinal degeneration
Peter H Tang, Teja Chemudupati, Katherine J Wert, et al.
Investigative Ophthalmology & Visual Science
|
October 13, 2020
Retinal Manifestations of Mitochondrial Oxidative Phosphorylation Disorders
Jin Kyun Oh, Jose Ronaldo Lima de Carvalho, Yan Nuzbrokh, et al.
Molecular Genetics & Genomic Medicine
|
May 27, 2017
Structural modeling of a novel <i>SLC38A8</i> mutation that causes foveal hypoplasia
Marcus A Toral, Gabriel Velez, Katherine Boudreault, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)
|
April 13, 2011
Seroreactivity against aqueous-soluble and detergent-soluble retinal proteins in posterior uveitis
Audrey C Ko, Jason P Brinton, Vinit B Mahajan, et al.
Biofabrication
|
February 24, 2026
Implantable ocular therapeutic systems: an insight into their clinical potential in the long-term treatment of ocular diseases
Hyeonji Kim, Nae-Won Kang, Wen Hong, et al.
Diagnostics (Basel, Switzerland)
|
July 27, 2022
Predicting Systemic Health Features from Retinal Fundus Images Using Transfer-Learning-Based Artificial Intelligence Models
Nergis C Khan, Chandrashan Perera, Eliot R Dow, et al.
Nature Communications
|
February 26, 2022
Investigation of Cas9 antibodies in the human eye
Marcus A Toral, Carsten T Charlesworth, Benjamin Ng, et al.
Cold Spring Harbor Molecular Case Studies
|
December 15, 2019
Compound heterozygous novel frameshift variants in the <i>PROM1</i> gene result in Leber congenital amaurosis
Sara D Ragi, Jose Ronaldo Lima de Carvalho, Akemi J Tanaka, et al.
Orphanet Journal of Rare Diseases
|
August 3, 2019
Comparison of structural progression between ciliopathy and non-ciliopathy associated with autosomal recessive retinitis pigmentosa
Vitor K L Takahashi, Christine L Xu, Júlia T Takiuti, et al.
Page
of 26