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G Jacobson

Showing results (301-310 of 677) with videos related to

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Experimental Eye Research|July 20, 2002
Spinocerebellar ataxia type 7 (SCA7) shows a cone-rod dystrophy phenotypeTomas S Aleman, Artur V Cideciyan, Nicholas J Volpe, et al.
BMC Ophthalmology|August 9, 2015
Outcome measure for the treatment of cone photoreceptor diseases: orientation to a scene with cone-only contrastAlejandro J Roman, Artur V Cideciyan, Rodrigo Matsui, et al.
Ebiomedicine|January 9, 2021
Childhood-onset genetic cone-rod photoreceptor diseases and underlying pathobiologyAlexandra V Garafalo, Rebecca Sheplock, Alexander Sumaroka, et al.
Journal of Sleep Research|May 19, 2024
Sleep health among US Navy afloat versus ashore personnel in the Millennium Cohort StudyIsabel G Jacobson, Judith Harbertson, Neika Sharifian, et al.
Investigative Ophthalmology & Visual Science|July 29, 2003
De novo mutation in the RP1 gene (Arg677ter) associated with retinitis pigmentosaSharon B Schwartz, Tomas S Aleman, Artur V Cideciyan, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|March 7, 2002
Novel mutation in the TIMP3 gene causes Sorsby fundus dystrophySamuel G Jacobson, Artur V Cideciyan, Jean Bennett, et al.
Investigative Ophthalmology & Visual Science|April 1, 1994
Phenotypes of stop codon and splice site rhodopsin mutations causing retinitis pigmentosaS G Jacobson, C M Kemp, A V Cideciyan, et al.
Primary Care Companion to the Journal of Clinical Psychiatry|July 4, 2007
The 3-year clinical and functional course of schizophrenia among individuals with and without diabetes at study entryHaya Ascher-Svanum, Baojin Zhu, Frank R Ernst, et al.
Journal of Diabetes|September 29, 2018
Concentrated insulins: History and critical reappraisalLutz Heinemann, John M Beals, James Malone, et al.
Experimental Eye Research|November 1, 1996
Preferential rod and cone photoreceptor abnormalities in heterozygotes with point mutations in the RDS geneS G Jacobson, A V Cideciyan, A M Maguire, et al.
Pageof 68

Showing results (301-310 of 677) with videos related to

Sort By:
Pageof 68
Experimental Eye Research|July 20, 2002
Spinocerebellar ataxia type 7 (SCA7) shows a cone-rod dystrophy phenotypeTomas S Aleman, Artur V Cideciyan, Nicholas J Volpe, et al.
BMC Ophthalmology|August 9, 2015
Outcome measure for the treatment of cone photoreceptor diseases: orientation to a scene with cone-only contrastAlejandro J Roman, Artur V Cideciyan, Rodrigo Matsui, et al.
Ebiomedicine|January 9, 2021
Childhood-onset genetic cone-rod photoreceptor diseases and underlying pathobiologyAlexandra V Garafalo, Rebecca Sheplock, Alexander Sumaroka, et al.
Journal of Sleep Research|May 19, 2024
Sleep health among US Navy afloat versus ashore personnel in the Millennium Cohort StudyIsabel G Jacobson, Judith Harbertson, Neika Sharifian, et al.
Investigative Ophthalmology & Visual Science|July 29, 2003
De novo mutation in the RP1 gene (Arg677ter) associated with retinitis pigmentosaSharon B Schwartz, Tomas S Aleman, Artur V Cideciyan, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|March 7, 2002
Novel mutation in the TIMP3 gene causes Sorsby fundus dystrophySamuel G Jacobson, Artur V Cideciyan, Jean Bennett, et al.
Investigative Ophthalmology & Visual Science|April 1, 1994
Phenotypes of stop codon and splice site rhodopsin mutations causing retinitis pigmentosaS G Jacobson, C M Kemp, A V Cideciyan, et al.
Primary Care Companion to the Journal of Clinical Psychiatry|July 4, 2007
The 3-year clinical and functional course of schizophrenia among individuals with and without diabetes at study entryHaya Ascher-Svanum, Baojin Zhu, Frank R Ernst, et al.
Journal of Diabetes|September 29, 2018
Concentrated insulins: History and critical reappraisalLutz Heinemann, John M Beals, James Malone, et al.
Experimental Eye Research|November 1, 1996
Preferential rod and cone photoreceptor abnormalities in heterozygotes with point mutations in the RDS geneS G Jacobson, A V Cideciyan, A M Maguire, et al.
Pageof 68