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C Gardner

Showing results (651-660 of 708) with videos related to

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The Lancet. Neurology|August 13, 2022
Prognostic value of day-of-injury plasma GFAP and UCH-L1 concentrations for predicting functional recovery after traumatic brain injury in patients from the US TRACK-TBI cohort: an observational cohort studyFrederick K Korley, Sonia Jain, Xiaoying Sun, et al.
Neurology. Clinical Practice|September 4, 2015
Evaluating and treating neurobehavioral symptoms in professional American football players: Lessons from a case seriesRaquel C Gardner, Katherine L Possin, Christopher P Hess, et al.
Human Molecular Genetics|May 24, 2012
Deep intronic mutation in OFD1, identified by targeted genomic next-generation sequencing, causes a severe form of X-linked retinitis pigmentosa (RP23)Tom R Webb, David A Parfitt, Jessica C Gardner, et al.
Human Mutation|October 3, 2017
Missense variants in the X-linked gene PRPS1 cause retinal degeneration in femalesAlessia Fiorentino, Kaoru Fujinami, Gavin Arno, et al.
American Journal of Human Genetics|June 29, 2010
X-linked cone dystrophy caused by mutation of the red and green cone opsinsJessica C Gardner, Tom R Webb, Naheed Kanuga, et al.
Advances in Experimental Medicine and Biology|December 21, 2011
A novel missense mutation in both OPN1LW and OPN1MW cone opsin genes causes X-linked cone dystrophy (XLCOD5)Jessica C Gardner, Tom R Webb, Naheed Kanuga, et al.
Brain : a Journal of Neurology|May 14, 2019
Neuropathological correlates of structural and functional imaging biomarkers in 4-repeat tauopathiesSalvatore Spina, Jesse A Brown, Jersey Deng, et al.
Academic Emergency Medicine : Official Journal of the Society for Academic Emergency Medicine|February 19, 2025
Effect of blood alcohol on the diagnostic accuracy of glial fibrillary acidic protein and ubiquitin carboxy-terminal hydrolase L1 for traumatic intracranial hemorrhage: A TRACK-TBI studyMark Harris, John K Yue, Sonia Jain, et al.
American Journal of Human Genetics|February 17, 2001
Bone dysplasia sclerosteosis results from loss of the SOST gene product, a novel cystine knot-containing proteinM E Brunkow, J C Gardner, J Van Ness, et al.
Science Translational Medicine|November 13, 2015
Modeling pulmonary alveolar microlithiasis by epithelial deletion of the Npt2b sodium phosphate cotransporter reveals putative biomarkers and strategies for treatmentAtsushi Saito, Nikolaos M Nikolaidis, Hassane Amlal, et al.
Pageof 71

Showing results (651-660 of 708) with videos related to

Sort By:
Pageof 71
The Lancet. Neurology|August 13, 2022
Prognostic value of day-of-injury plasma GFAP and UCH-L1 concentrations for predicting functional recovery after traumatic brain injury in patients from the US TRACK-TBI cohort: an observational cohort studyFrederick K Korley, Sonia Jain, Xiaoying Sun, et al.
Neurology. Clinical Practice|September 4, 2015
Evaluating and treating neurobehavioral symptoms in professional American football players: Lessons from a case seriesRaquel C Gardner, Katherine L Possin, Christopher P Hess, et al.
Human Molecular Genetics|May 24, 2012
Deep intronic mutation in OFD1, identified by targeted genomic next-generation sequencing, causes a severe form of X-linked retinitis pigmentosa (RP23)Tom R Webb, David A Parfitt, Jessica C Gardner, et al.
Human Mutation|October 3, 2017
Missense variants in the X-linked gene PRPS1 cause retinal degeneration in femalesAlessia Fiorentino, Kaoru Fujinami, Gavin Arno, et al.
American Journal of Human Genetics|June 29, 2010
X-linked cone dystrophy caused by mutation of the red and green cone opsinsJessica C Gardner, Tom R Webb, Naheed Kanuga, et al.
Advances in Experimental Medicine and Biology|December 21, 2011
A novel missense mutation in both OPN1LW and OPN1MW cone opsin genes causes X-linked cone dystrophy (XLCOD5)Jessica C Gardner, Tom R Webb, Naheed Kanuga, et al.
Brain : a Journal of Neurology|May 14, 2019
Neuropathological correlates of structural and functional imaging biomarkers in 4-repeat tauopathiesSalvatore Spina, Jesse A Brown, Jersey Deng, et al.
Academic Emergency Medicine : Official Journal of the Society for Academic Emergency Medicine|February 19, 2025
Effect of blood alcohol on the diagnostic accuracy of glial fibrillary acidic protein and ubiquitin carboxy-terminal hydrolase L1 for traumatic intracranial hemorrhage: A TRACK-TBI studyMark Harris, John K Yue, Sonia Jain, et al.
American Journal of Human Genetics|February 17, 2001
Bone dysplasia sclerosteosis results from loss of the SOST gene product, a novel cystine knot-containing proteinM E Brunkow, J C Gardner, J Van Ness, et al.
Science Translational Medicine|November 13, 2015
Modeling pulmonary alveolar microlithiasis by epithelial deletion of the Npt2b sodium phosphate cotransporter reveals putative biomarkers and strategies for treatmentAtsushi Saito, Nikolaos M Nikolaidis, Hassane Amlal, et al.
Pageof 71