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Jennifer A Thompson

Showing results (111-120 of 141) with videos related to

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Acta Neurologica Scandinavica|July 31, 2018
Effects of multidisciplinary therapy on physical function in Huntington's diseaseTravis M Cruickshank, Alvaro P Reyes, Luis E Penailillo, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|November 18, 2018
Clinical and molecular characterization of non-syndromic retinal dystrophy due to c.175G>A mutation in ceroid lipofuscinosis neuronal 3 (CLN3)Fred K Chen, Xiao Zhang, Jonathan Eintracht, et al.
Ophthalmology Science|October 17, 2022
Atrophy Expansion Rates in Stargardt Disease Using Ultra-Widefield Fundus AutofluorescenceRachael C Heath Jeffery, Jennifer A Thompson, Johnny Lo, et al.
Retina (Philadelphia, Pa.)|March 28, 2022
SIBLING CONCORDANCE IN SYMPTOM ONSET AND ATROPHY GROWTH RATES IN STARGARDT DISEASE USING ULTRA-WIDEFIELD FUNDUS AUTOFLUORESCENCERachael C Heath Jeffery, Jennifer A Thompson, Johnny Lo, et al.
Antiviral Therapy|October 13, 2017
HIV-1 viral load and resistance in genital secretions in patients taking protease-inhibitor-based second-line therapy in AfricaAnne Hoppe, Marina Giuliano, Abbas Lugemwa, et al.
Stem Cell Research|January 11, 2021
Generation of two induced pluripotent stem cell lines from a patient with recessive inherited retinal disease caused by compound heterozygous mutations in SNRNP200Dan Zhang, Samuel McLenachan, Shang-Chih Chen, et al.
Scientific Reports|October 6, 2020
Deep learning segmentation of hyperautofluorescent fleck lesions in Stargardt diseaseJason Charng, Di Xiao, Maryam Mehdizadeh, et al.
Pediatric Research|July 4, 2018
The lifelong impact of fetal growth restriction on cardiac developmentEmily P Masoumy, Alexandra A Sawyer, Suash Sharma, et al.
Ophthalmic Genetics|September 4, 2024
Expanding the genotypic and phenotypic spectra with a novel variant in the ciliopathy gene, <i>CFAP410</i>, associated with selective cone degenerationGrace A Borchert, Morag E Shanks, Jennifer Whitfield, et al.
Ophthalmology Science|January 15, 2025
Longitudinal Assessment of Structural and Functional Changes in Rod-cone Dystrophy: A 10-year Follow-up StudyAlexis Ceecee Britten-Jones, Chi D Luu, Jasleen K Jolly, et al.
Pageof 15

Showing results (111-120 of 141) with videos related to

Sort By:
Pageof 15
Acta Neurologica Scandinavica|July 31, 2018
Effects of multidisciplinary therapy on physical function in Huntington's diseaseTravis M Cruickshank, Alvaro P Reyes, Luis E Penailillo, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|November 18, 2018
Clinical and molecular characterization of non-syndromic retinal dystrophy due to c.175G>A mutation in ceroid lipofuscinosis neuronal 3 (CLN3)Fred K Chen, Xiao Zhang, Jonathan Eintracht, et al.
Ophthalmology Science|October 17, 2022
Atrophy Expansion Rates in Stargardt Disease Using Ultra-Widefield Fundus AutofluorescenceRachael C Heath Jeffery, Jennifer A Thompson, Johnny Lo, et al.
Retina (Philadelphia, Pa.)|March 28, 2022
SIBLING CONCORDANCE IN SYMPTOM ONSET AND ATROPHY GROWTH RATES IN STARGARDT DISEASE USING ULTRA-WIDEFIELD FUNDUS AUTOFLUORESCENCERachael C Heath Jeffery, Jennifer A Thompson, Johnny Lo, et al.
Antiviral Therapy|October 13, 2017
HIV-1 viral load and resistance in genital secretions in patients taking protease-inhibitor-based second-line therapy in AfricaAnne Hoppe, Marina Giuliano, Abbas Lugemwa, et al.
Stem Cell Research|January 11, 2021
Generation of two induced pluripotent stem cell lines from a patient with recessive inherited retinal disease caused by compound heterozygous mutations in SNRNP200Dan Zhang, Samuel McLenachan, Shang-Chih Chen, et al.
Scientific Reports|October 6, 2020
Deep learning segmentation of hyperautofluorescent fleck lesions in Stargardt diseaseJason Charng, Di Xiao, Maryam Mehdizadeh, et al.
Pediatric Research|July 4, 2018
The lifelong impact of fetal growth restriction on cardiac developmentEmily P Masoumy, Alexandra A Sawyer, Suash Sharma, et al.
Ophthalmic Genetics|September 4, 2024
Expanding the genotypic and phenotypic spectra with a novel variant in the ciliopathy gene, <i>CFAP410</i>, associated with selective cone degenerationGrace A Borchert, Morag E Shanks, Jennifer Whitfield, et al.
Ophthalmology Science|January 15, 2025
Longitudinal Assessment of Structural and Functional Changes in Rod-cone Dystrophy: A 10-year Follow-up StudyAlexis Ceecee Britten-Jones, Chi D Luu, Jasleen K Jolly, et al.
Pageof 15