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Winston Lee

Showing results (91-100 of 124) with videos related to

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European Journal of Ophthalmology|September 15, 2020
A mutation in <i>CRX</i> causing pigmented paravenous retinochoroidal atrophyJin Kyun Oh, Yan Nuzbrokh, Winston Lee, et al.
Retinal Cases & Brief Reports|July 18, 2018
CHORIORETINAL CHANGES IN A GENETICALLY CONFIRMED CASE OF BOUCHER-NEUHÄUSER SYNDROMEBrittany B DeNaro, Elona Dhrami-Gavazi, David M Rubaltelli, et al.
Cold Spring Harbor Molecular Case Studies|June 1, 2018
Extremely hypomorphic and severe deep intronic variants in the <i>ABCA4</i> locus result in varying Stargardt disease phenotypesJana Zernant, Winston Lee, Takayuki Nagasaki, et al.
Human Molecular Genetics|April 28, 2021
Cis-acting modifiers in the ABCA4 locus contribute to the penetrance of the major disease-causing variant in Stargardt diseaseWinston Lee, Jana Zernant, Takayuki Nagasaki, et al.
Journal of Medical Genetics|April 28, 2017
Frequent hypomorphic alleles account for a significant fraction of ABCA4 disease and distinguish it from age-related macular degenerationJana Zernant, Winston Lee, Frederick T Collison, et al.
Investigative Ophthalmology & Visual Science|September 25, 2020
Quantitative Fundus Autofluorescence in HCQ RetinopathyVivienne C Greenstein, Jose Ronaldo Lima de Carvalho, Rait Parmann, et al.
American Journal of Clinical Pathology|September 18, 2024
Epstein-Barr virus-positive, primary cutaneous marginal zone lymphoma, with transformation: Case report and review of the literatureLori Soma, Liliana Crisan, Jack Reid, et al.
Leukemia Research|March 1, 2021
Hybrid chemotherapy regimen (FLAG-IDA-vincristine-prednisone) for acute leukemia with mixed-phenotype blastsJustin H Reid, Anthony J Perissinotti, Lydia L Benitez, et al.
Scientific Reports|September 13, 2017
Electroretinography Reveals Difference in Cone Function between Syndromic and Nonsyndromic USH2A PatientsJesse D Sengillo, Thiago Cabral, Kaspar Schuerch, et al.
Radiology. Imaging Cancer|November 14, 2025
Quantitative MRI Assessment of Bone Marrow Disease in Myelofibrosis: A Prospective StudyTanner H Robison, Annabel Levinson, Winston Lee, et al.
Pageof 13

Showing results (91-100 of 124) with videos related to

Sort By:
Pageof 13
European Journal of Ophthalmology|September 15, 2020
A mutation in <i>CRX</i> causing pigmented paravenous retinochoroidal atrophyJin Kyun Oh, Yan Nuzbrokh, Winston Lee, et al.
Retinal Cases & Brief Reports|July 18, 2018
CHORIORETINAL CHANGES IN A GENETICALLY CONFIRMED CASE OF BOUCHER-NEUHÄUSER SYNDROMEBrittany B DeNaro, Elona Dhrami-Gavazi, David M Rubaltelli, et al.
Cold Spring Harbor Molecular Case Studies|June 1, 2018
Extremely hypomorphic and severe deep intronic variants in the <i>ABCA4</i> locus result in varying Stargardt disease phenotypesJana Zernant, Winston Lee, Takayuki Nagasaki, et al.
Human Molecular Genetics|April 28, 2021
Cis-acting modifiers in the ABCA4 locus contribute to the penetrance of the major disease-causing variant in Stargardt diseaseWinston Lee, Jana Zernant, Takayuki Nagasaki, et al.
Journal of Medical Genetics|April 28, 2017
Frequent hypomorphic alleles account for a significant fraction of ABCA4 disease and distinguish it from age-related macular degenerationJana Zernant, Winston Lee, Frederick T Collison, et al.
Investigative Ophthalmology & Visual Science|September 25, 2020
Quantitative Fundus Autofluorescence in HCQ RetinopathyVivienne C Greenstein, Jose Ronaldo Lima de Carvalho, Rait Parmann, et al.
American Journal of Clinical Pathology|September 18, 2024
Epstein-Barr virus-positive, primary cutaneous marginal zone lymphoma, with transformation: Case report and review of the literatureLori Soma, Liliana Crisan, Jack Reid, et al.
Leukemia Research|March 1, 2021
Hybrid chemotherapy regimen (FLAG-IDA-vincristine-prednisone) for acute leukemia with mixed-phenotype blastsJustin H Reid, Anthony J Perissinotti, Lydia L Benitez, et al.
Scientific Reports|September 13, 2017
Electroretinography Reveals Difference in Cone Function between Syndromic and Nonsyndromic USH2A PatientsJesse D Sengillo, Thiago Cabral, Kaspar Schuerch, et al.
Radiology. Imaging Cancer|November 14, 2025
Quantitative MRI Assessment of Bone Marrow Disease in Myelofibrosis: A Prospective StudyTanner H Robison, Annabel Levinson, Winston Lee, et al.
Pageof 13