Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

A Rutherford

Showing results (501-510 of 518) with videos related to

Pageof 52
Sort By:
American Journal of Human Genetics|October 23, 2012
A mutation in PNPT1, encoding mitochondrial-RNA-import protein PNPase, causes hereditary hearing lossSimon von Ameln, Geng Wang, Redouane Boulouiz, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 8, 2018
Identifying the deficiencies of current diagnostic criteria for neurofibromatosis 2 using databases of 2777 individuals with molecular testingD Gareth Evans, Andrew T King, Naomi L Bowers, et al.
Journal of Neurosurgery|March 18, 2023
Intraoperative diagnosis of facial schwannomas: a multicenter summation of clinical experience, preoperative avoidance, and intraoperative management protocolDaniel Lewis, Cathal John Hannan, Aaron R Plitt, et al.
Imaging Neuroscience (Cambridge, Mass.)|August 13, 2025
The developing Human Connectome Project fetal functional MRI release: Methods and data structuresVyacheslav R Karolis, Lucilio Cordero-Grande, Anthony N Price, et al.
Neuroimage|August 22, 2021
Preterm birth alters the development of cortical microstructure and morphology at term-equivalent ageRalica Dimitrova, Maximilian Pietsch, Judit Ciarrusta, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|October 19, 2013
English consensus protocol evaluating candidacy for auditory brainstem and cochlear implantation in neurofibromatosis type 2James R Tysome, Patrick R Axon, Neil P Donnelly, et al.
Neuro-Oncology Advances|April 13, 2023
Radiation treatment of benign tumors in NF2-related-schwannomatosis: A national study of 266 irradiated patients showing a significant increase in malignancy/malignant progressionD Gareth Evans, Dorothy Halliday, Rupert Obholzer, et al.
Stroke|October 27, 2022
Risk Factors for Perioperative Brain Lesions in Infants With Congenital Heart Disease: A European CollaborationAlexandra F Bonthrone, Raymond Stegeman, Maria Feldmann, et al.
Nature Microbiology|March 13, 2026
Epitope-focused discovery of SARS-CoV-2 antibodies that potently neutralize Omicron variantsSeth J Zost, Naveenchandra Suryadevara, Lauren E Williamson, et al.
Cerebral Cortex (New York, N.Y. : 1991)|April 6, 2021
Phenotyping the Preterm Brain: Characterizing Individual Deviations From Normative Volumetric Development in Two Large Infant CohortsRalica Dimitrova, Sophie Arulkumaran, Olivia Carney, et al.
Pageof 52

Showing results (501-510 of 518) with videos related to

Sort By:
Pageof 52
American Journal of Human Genetics|October 23, 2012
A mutation in PNPT1, encoding mitochondrial-RNA-import protein PNPase, causes hereditary hearing lossSimon von Ameln, Geng Wang, Redouane Boulouiz, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 8, 2018
Identifying the deficiencies of current diagnostic criteria for neurofibromatosis 2 using databases of 2777 individuals with molecular testingD Gareth Evans, Andrew T King, Naomi L Bowers, et al.
Journal of Neurosurgery|March 18, 2023
Intraoperative diagnosis of facial schwannomas: a multicenter summation of clinical experience, preoperative avoidance, and intraoperative management protocolDaniel Lewis, Cathal John Hannan, Aaron R Plitt, et al.
Imaging Neuroscience (Cambridge, Mass.)|August 13, 2025
The developing Human Connectome Project fetal functional MRI release: Methods and data structuresVyacheslav R Karolis, Lucilio Cordero-Grande, Anthony N Price, et al.
Neuroimage|August 22, 2021
Preterm birth alters the development of cortical microstructure and morphology at term-equivalent ageRalica Dimitrova, Maximilian Pietsch, Judit Ciarrusta, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|October 19, 2013
English consensus protocol evaluating candidacy for auditory brainstem and cochlear implantation in neurofibromatosis type 2James R Tysome, Patrick R Axon, Neil P Donnelly, et al.
Neuro-Oncology Advances|April 13, 2023
Radiation treatment of benign tumors in NF2-related-schwannomatosis: A national study of 266 irradiated patients showing a significant increase in malignancy/malignant progressionD Gareth Evans, Dorothy Halliday, Rupert Obholzer, et al.
Stroke|October 27, 2022
Risk Factors for Perioperative Brain Lesions in Infants With Congenital Heart Disease: A European CollaborationAlexandra F Bonthrone, Raymond Stegeman, Maria Feldmann, et al.
Nature Microbiology|March 13, 2026
Epitope-focused discovery of SARS-CoV-2 antibodies that potently neutralize Omicron variantsSeth J Zost, Naveenchandra Suryadevara, Lauren E Williamson, et al.
Cerebral Cortex (New York, N.Y. : 1991)|April 6, 2021
Phenotyping the Preterm Brain: Characterizing Individual Deviations From Normative Volumetric Development in Two Large Infant CohortsRalica Dimitrova, Sophie Arulkumaran, Olivia Carney, et al.
Pageof 52