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Showing results (1221-1230 of 1,711) with videos related to
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American Journal of Ophthalmology
|
September 7, 2015
Retinal Architecture in RGS9- and R9AP-Associated Retinal Dysfunction (Bradyopsia)
Rupert W Strauss, Adam M Dubis, Robert F Cooper, et al.
The Journal of Surgical Research
|
March 20, 2023
Telehealth Follow-Up After Inguinal Hernia Repair in Veterans
Danielle Abbitt, Kevin Choy, Rose Castle, et al.
Investigative Ophthalmology & Visual Science
|
August 10, 2022
Dominant Cone Rod Dystrophy, Previously Assigned to a Missense Variant in RIMS1, Is Fully Explained by Co-Inheritance of a Dominant Allele of PROM1
Maria Pilar Martin-Gutierrez, Elena R Schiff, Genevieve Wright, et al.
Plos One
|
November 13, 2015
Analysis of the Optimal Duration of Behavioral Observations Based on an Automated Continuous Monitoring System in Tree Swallows (Tachycineta bicolor): Is One Hour Good Enough?
Ádám Z Lendvai, Çağlar Akçay, Jenny Q Ouyang, et al.
American Journal of Physiology. Regulatory, Integrative and Comparative Physiology
|
June 7, 2003
Differential mechanisms for regulation of the stress response across latitudinal gradients
C W Breuner, M Orchinik, T P Hahn, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)
|
November 16, 2001
Autosomal dominant cone-rod dystrophy with mutations in the guanylate cyclase 2D gene encoding retinal guanylate cyclase-1
S M Downes, A M Payne, R E Kelsell, et al.
Journal of Pediatric Surgery
|
December 6, 2001
Novel use of an established agent: Topotecan is anti-angiogenic in experimental Wilms tumor
S Z Soffer, E Kim, J T Moore, et al.
Investigative Ophthalmology & Visual Science
|
November 1, 2011
Autosomal dominant retinitis pigmentosa with intrafamilial variability and incomplete penetrance in two families carrying mutations in PRPF8
Cécilia G Maubaret, Veronika Vaclavik, Rajarshi Mukhopadhyay, et al.
American Journal of Human Genetics
|
April 1, 1994
Further refinement of the location for autosomal dominant retinitis pigmentosa on chromosome 7p (RP9)
C F Inglehearn, T J Keen, M al-Maghtheh, et al.
Mitochondrion
|
July 22, 2017
The pattern of retinal ganglion cell dysfunction in Leber hereditary optic neuropathy
A Majander, A G Robson, C João, et al.
Page
of 172
Search research articles
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Showing results (1221-1230 of 1,711) with videos related to
Sort By:
Page
of 172
American Journal of Ophthalmology
|
September 7, 2015
Retinal Architecture in RGS9- and R9AP-Associated Retinal Dysfunction (Bradyopsia)
Rupert W Strauss, Adam M Dubis, Robert F Cooper, et al.
The Journal of Surgical Research
|
March 20, 2023
Telehealth Follow-Up After Inguinal Hernia Repair in Veterans
Danielle Abbitt, Kevin Choy, Rose Castle, et al.
Investigative Ophthalmology & Visual Science
|
August 10, 2022
Dominant Cone Rod Dystrophy, Previously Assigned to a Missense Variant in RIMS1, Is Fully Explained by Co-Inheritance of a Dominant Allele of PROM1
Maria Pilar Martin-Gutierrez, Elena R Schiff, Genevieve Wright, et al.
Plos One
|
November 13, 2015
Analysis of the Optimal Duration of Behavioral Observations Based on an Automated Continuous Monitoring System in Tree Swallows (Tachycineta bicolor): Is One Hour Good Enough?
Ádám Z Lendvai, Çağlar Akçay, Jenny Q Ouyang, et al.
American Journal of Physiology. Regulatory, Integrative and Comparative Physiology
|
June 7, 2003
Differential mechanisms for regulation of the stress response across latitudinal gradients
C W Breuner, M Orchinik, T P Hahn, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)
|
November 16, 2001
Autosomal dominant cone-rod dystrophy with mutations in the guanylate cyclase 2D gene encoding retinal guanylate cyclase-1
S M Downes, A M Payne, R E Kelsell, et al.
Journal of Pediatric Surgery
|
December 6, 2001
Novel use of an established agent: Topotecan is anti-angiogenic in experimental Wilms tumor
S Z Soffer, E Kim, J T Moore, et al.
Investigative Ophthalmology & Visual Science
|
November 1, 2011
Autosomal dominant retinitis pigmentosa with intrafamilial variability and incomplete penetrance in two families carrying mutations in PRPF8
Cécilia G Maubaret, Veronika Vaclavik, Rajarshi Mukhopadhyay, et al.
American Journal of Human Genetics
|
April 1, 1994
Further refinement of the location for autosomal dominant retinitis pigmentosa on chromosome 7p (RP9)
C F Inglehearn, T J Keen, M al-Maghtheh, et al.
Mitochondrion
|
July 22, 2017
The pattern of retinal ganglion cell dysfunction in Leber hereditary optic neuropathy
A Majander, A G Robson, C João, et al.
Page
of 172