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Ophthalmic Genetics
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January 14, 2026
Reclassification of a novel <i>NR2E3</i> variant as likely pathogenic: a case report of autosomal recessive RP37 in siblings
Vincent Chen, Winston Lee, Eugene Yu-Chuan Kang, et al.
American Journal of Ophthalmology
|
July 19, 2015
Risk Factors Predictive of Endogenous Endophthalmitis Among Hospitalized Patients With Hematogenous Infections in the United States
Kuan-Jen Chen, An-Ning Chao, Tun-Lu Chen, et al.
Skeletal Muscle
|
December 2, 2016
Heme oxygenase and carbon monoxide protect from muscle dystrophy
Mun Chun Chan, Olivia Ziegler, Laura Liu, et al.
Retina (Philadelphia, Pa.)
|
January 31, 2020
ANATOMICAL AND FUNCTIONAL RESULTS OF INTRAVITREAL AFLIBERCEPT MONOTHERAPY FOR TYPE 1 RETINOPATHY OF PREMATURITY: One-Year Outcomes
Yen-Ting Chen, Laura Liu, Chi-Chun Lai, et al.
Cornea
|
December 19, 2006
Camphor-related self-inflicted keratoconjunctivitis complicating delusions of parasitosis
Gerald C S Lim, Yeong-Fong Chen, Laura Liu, et al.
Ophthalmic Genetics
|
May 7, 2021
A novel KCNV2 mutation in a patient taking hydroxychloroquine associated with cone dystrophy with supernormal rod response
Pei-Kang Liu, Joseph Ryu, Lung-Kun Yeh, et al.
Journal of Neurotrauma
|
April 23, 2011
Effects of age, gender, and socio-economic status on the incidence of spinal cord injury: an assessment using the eleven-year comprehensive nationwide database of Taiwan
Jau-Ching Wu, Yu-Chun Chen, Laura Liu, et al.
Neurology
|
March 2, 2012
Increased risk of stroke after spinal cord injury: a nationwide 4-year follow-up cohort study
Jau-Ching Wu, Yu-Chun Chen, Laura Liu, et al.
Retina (Philadelphia, Pa.)
|
February 12, 2024
LONGITUDINAL CHANGES IN CHOROIDAL THICKNESS IN CHILDREN WITH A HISTORY OF PREMATURITY: An 18-Month Prospective Cohort Study
Yung-Sung Lee, Laura Liu, Nan-Kai Wang, et al.
American Journal of Ophthalmology Case Reports
|
August 5, 2024
A <i>GUCY2D</i> variant associated cone-rod dystrophy with electronegative ERG: A case report and review
Pei-Liang Wu, Pei-Hsuan Lin, Winston Lee, et al.
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of 14
Search research articles
Search
Showing results (21-30 of 132) with videos related to
Sort By:
Page
of 14
Ophthalmic Genetics
|
January 14, 2026
Reclassification of a novel <i>NR2E3</i> variant as likely pathogenic: a case report of autosomal recessive RP37 in siblings
Vincent Chen, Winston Lee, Eugene Yu-Chuan Kang, et al.
American Journal of Ophthalmology
|
July 19, 2015
Risk Factors Predictive of Endogenous Endophthalmitis Among Hospitalized Patients With Hematogenous Infections in the United States
Kuan-Jen Chen, An-Ning Chao, Tun-Lu Chen, et al.
Skeletal Muscle
|
December 2, 2016
Heme oxygenase and carbon monoxide protect from muscle dystrophy
Mun Chun Chan, Olivia Ziegler, Laura Liu, et al.
Retina (Philadelphia, Pa.)
|
January 31, 2020
ANATOMICAL AND FUNCTIONAL RESULTS OF INTRAVITREAL AFLIBERCEPT MONOTHERAPY FOR TYPE 1 RETINOPATHY OF PREMATURITY: One-Year Outcomes
Yen-Ting Chen, Laura Liu, Chi-Chun Lai, et al.
Cornea
|
December 19, 2006
Camphor-related self-inflicted keratoconjunctivitis complicating delusions of parasitosis
Gerald C S Lim, Yeong-Fong Chen, Laura Liu, et al.
Ophthalmic Genetics
|
May 7, 2021
A novel KCNV2 mutation in a patient taking hydroxychloroquine associated with cone dystrophy with supernormal rod response
Pei-Kang Liu, Joseph Ryu, Lung-Kun Yeh, et al.
Journal of Neurotrauma
|
April 23, 2011
Effects of age, gender, and socio-economic status on the incidence of spinal cord injury: an assessment using the eleven-year comprehensive nationwide database of Taiwan
Jau-Ching Wu, Yu-Chun Chen, Laura Liu, et al.
Neurology
|
March 2, 2012
Increased risk of stroke after spinal cord injury: a nationwide 4-year follow-up cohort study
Jau-Ching Wu, Yu-Chun Chen, Laura Liu, et al.
Retina (Philadelphia, Pa.)
|
February 12, 2024
LONGITUDINAL CHANGES IN CHOROIDAL THICKNESS IN CHILDREN WITH A HISTORY OF PREMATURITY: An 18-Month Prospective Cohort Study
Yung-Sung Lee, Laura Liu, Nan-Kai Wang, et al.
American Journal of Ophthalmology Case Reports
|
August 5, 2024
A <i>GUCY2D</i> variant associated cone-rod dystrophy with electronegative ERG: A case report and review
Pei-Liang Wu, Pei-Hsuan Lin, Winston Lee, et al.
Page
of 14