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Showing results (471-480 of 486) with videos related to

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European Journal of Human Genetics : EJHG|July 7, 2019
Expansion of B4GALT7 linkeropathy phenotype to include perinatal lethal skeletal dysplasiaTheresa Mihalic Mosher, Deborah A Zygmunt, Daniel C Koboldt, et al.
The British Journal of Ophthalmology|October 31, 2019
Qualitative evaluation of neuroretinal rim and retinal nerve fibre layer on optical coherence tomography to detect glaucomatous damageZhichao Wu, Jayme R Vianna, Alexandre S C Reis, et al.
American Journal of Ophthalmology|April 13, 2020
Detection of Progression With 10-2 Standard Automated Perimetry: Development and Validation of an Event-Based AlgorithmCarlos Gustavo De Moraes, Jayter Silva Paula, Dana M Blumberg, et al.
Academic Radiology|February 24, 2024
A Novel Design-Thinking, Hospital Innovation Core Certificate Curriculum for Radiologists and Trainees: Creation, Implementation, and Multiyear ResultsDavid S Liu, Mercy H Mazurek, David C Whitehead, et al.
Plos One|October 17, 2019
Concordance between gene expression in peripheral whole blood and colonic tissue in children with inflammatory bowel diseaseNathan P Palmer, Jocelyn A Silvester, Jessica J Lee, et al.
Anatomical Sciences Education|December 19, 2017
Impact and educational outcomes of a small group self-directed teaching strategy in a clinical neuroscience curriculumThomas I Nathaniel, Jordan C Gainey, Jessica A Williams, et al.
Ophthalmology. Glaucoma|April 13, 2021
Variability and Power to Detect Progression of Different Visual Field PatternsFernanda N Susanna, Bruna Melchior, Jayter S Paula, et al.
Investigative Ophthalmology & Visual Science|June 6, 2013
The pupil light reflex in Leber's hereditary optic neuropathy: evidence for preservation of melanopsin-expressing retinal ganglion cellsAna Laura A Moura, Balázs V Nagy, Chiara La Morgia, et al.
Journal of Neuropathology and Experimental Neurology|April 9, 2014
Clinical, pathologic, and mutational spectrum of dystroglycanopathy caused by LARGE mutationsKatherine G Meilleur, Kristen Zukosky, Livija Medne, et al.
Molecular Therapy. Methods & Clinical Development|August 4, 2018
An Isolated Limb Infusion Method Allows for Broad Distribution of rAAVrh74.MCK.<i>GALGT2</i> to Leg Skeletal Muscles in the Rhesus MacaqueRui Xu, Ying Jia, Deborah A Zygmunt, et al.
Pageof 49

Showing results (471-480 of 486) with videos related to

Sort By:
Pageof 49
European Journal of Human Genetics : EJHG|July 7, 2019
Expansion of B4GALT7 linkeropathy phenotype to include perinatal lethal skeletal dysplasiaTheresa Mihalic Mosher, Deborah A Zygmunt, Daniel C Koboldt, et al.
The British Journal of Ophthalmology|October 31, 2019
Qualitative evaluation of neuroretinal rim and retinal nerve fibre layer on optical coherence tomography to detect glaucomatous damageZhichao Wu, Jayme R Vianna, Alexandre S C Reis, et al.
American Journal of Ophthalmology|April 13, 2020
Detection of Progression With 10-2 Standard Automated Perimetry: Development and Validation of an Event-Based AlgorithmCarlos Gustavo De Moraes, Jayter Silva Paula, Dana M Blumberg, et al.
Academic Radiology|February 24, 2024
A Novel Design-Thinking, Hospital Innovation Core Certificate Curriculum for Radiologists and Trainees: Creation, Implementation, and Multiyear ResultsDavid S Liu, Mercy H Mazurek, David C Whitehead, et al.
Plos One|October 17, 2019
Concordance between gene expression in peripheral whole blood and colonic tissue in children with inflammatory bowel diseaseNathan P Palmer, Jocelyn A Silvester, Jessica J Lee, et al.
Anatomical Sciences Education|December 19, 2017
Impact and educational outcomes of a small group self-directed teaching strategy in a clinical neuroscience curriculumThomas I Nathaniel, Jordan C Gainey, Jessica A Williams, et al.
Ophthalmology. Glaucoma|April 13, 2021
Variability and Power to Detect Progression of Different Visual Field PatternsFernanda N Susanna, Bruna Melchior, Jayter S Paula, et al.
Investigative Ophthalmology & Visual Science|June 6, 2013
The pupil light reflex in Leber's hereditary optic neuropathy: evidence for preservation of melanopsin-expressing retinal ganglion cellsAna Laura A Moura, Balázs V Nagy, Chiara La Morgia, et al.
Journal of Neuropathology and Experimental Neurology|April 9, 2014
Clinical, pathologic, and mutational spectrum of dystroglycanopathy caused by LARGE mutationsKatherine G Meilleur, Kristen Zukosky, Livija Medne, et al.
Molecular Therapy. Methods & Clinical Development|August 4, 2018
An Isolated Limb Infusion Method Allows for Broad Distribution of rAAVrh74.MCK.<i>GALGT2</i> to Leg Skeletal Muscles in the Rhesus MacaqueRui Xu, Ying Jia, Deborah A Zygmunt, et al.
Pageof 49