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Michael D Geschwind

Showing results (61-70 of 140) with videos related to

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Acta Neuropathologica Communications|December 17, 2013
Genetic CJD with a novel E200G mutation in the prion protein gene and comparison with E200K mutation casesMee-Ohk Kim, Ignazio Cali, Abby Oehler, et al.
JAMA Neurology|February 13, 2013
Sporadic Jakob-Creutzfeldt disease presenting as primary progressive aphasiaDavid Y Johnson, Diana L Dunkelberger, Maya Henry, et al.
Medrxiv : the Preprint Server for Health Sciences|January 27, 2025
TRANSIENT ALTERATIONS IN THALAMO-CEREBELLAR FUNCTIONAL CONNECTIVITY IN PREMANIFEST HUNTINGTON'S DISEASEMelanie A Morrison, Jingwen Yao, Radhika Bhalerao, et al.
AJNR. American Journal of Neuroradiology|June 16, 2005
Diffusion-weighted and fluid-attenuated inversion recovery imaging in Creutzfeldt-Jakob disease: high sensitivity and specificity for diagnosisGeoffrey S Young, Michael D Geschwind, Nancy J Fischbein, et al.
Stem Cell Reports|May 15, 2026
PrP<sup>C</sup>-facilitated cell signaling activates phospholipase Cɣ1 and triggers an Arc/Arg3.1 response in mouse and iPSC-derived human neuronsDaniel Ojeda-Juarez, Gail Funk, Daniel B McClatchy, et al.
Frontiers in Immunology|June 30, 2026
Anti-mGluR5 encephalitis: distinctive clinical features and antibody patterns in the Chinese populationTianyu Gao, Xinjing Zhao, Chen Chen, et al.
Human Brain Mapping|June 6, 2022
Default Mode Network quantitative diffusion and resting-state functional magnetic resonance imaging correlates in sporadic Creutzfeldt-Jakob diseaseMatteo Paoletti, Eduardo Caverzasi, Maria Luisa Mandelli, et al.
Annals of Neurology|June 23, 2015
Modulation of Creutzfeldt-Jakob disease prion propagation by the A224V mutationJoel C Watts, Kurt Giles, Ana Serban, et al.
Neuropsychologia|April 22, 2017
Egocentric and allocentric visuospatial working memory in premotor Huntington's disease: A double dissociation with caudate and hippocampal volumesKatherine L Possin, Hosung Kim, Michael D Geschwind, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 3, 2005
Diagnosis of human prion diseaseJiri G Safar, Michael D Geschwind, Camille Deering, et al.
Pageof 14

Showing results (61-70 of 140) with videos related to

Sort By:
Pageof 14
Acta Neuropathologica Communications|December 17, 2013
Genetic CJD with a novel E200G mutation in the prion protein gene and comparison with E200K mutation casesMee-Ohk Kim, Ignazio Cali, Abby Oehler, et al.
JAMA Neurology|February 13, 2013
Sporadic Jakob-Creutzfeldt disease presenting as primary progressive aphasiaDavid Y Johnson, Diana L Dunkelberger, Maya Henry, et al.
Medrxiv : the Preprint Server for Health Sciences|January 27, 2025
TRANSIENT ALTERATIONS IN THALAMO-CEREBELLAR FUNCTIONAL CONNECTIVITY IN PREMANIFEST HUNTINGTON'S DISEASEMelanie A Morrison, Jingwen Yao, Radhika Bhalerao, et al.
AJNR. American Journal of Neuroradiology|June 16, 2005
Diffusion-weighted and fluid-attenuated inversion recovery imaging in Creutzfeldt-Jakob disease: high sensitivity and specificity for diagnosisGeoffrey S Young, Michael D Geschwind, Nancy J Fischbein, et al.
Stem Cell Reports|May 15, 2026
PrP<sup>C</sup>-facilitated cell signaling activates phospholipase Cɣ1 and triggers an Arc/Arg3.1 response in mouse and iPSC-derived human neuronsDaniel Ojeda-Juarez, Gail Funk, Daniel B McClatchy, et al.
Frontiers in Immunology|June 30, 2026
Anti-mGluR5 encephalitis: distinctive clinical features and antibody patterns in the Chinese populationTianyu Gao, Xinjing Zhao, Chen Chen, et al.
Human Brain Mapping|June 6, 2022
Default Mode Network quantitative diffusion and resting-state functional magnetic resonance imaging correlates in sporadic Creutzfeldt-Jakob diseaseMatteo Paoletti, Eduardo Caverzasi, Maria Luisa Mandelli, et al.
Annals of Neurology|June 23, 2015
Modulation of Creutzfeldt-Jakob disease prion propagation by the A224V mutationJoel C Watts, Kurt Giles, Ana Serban, et al.
Neuropsychologia|April 22, 2017
Egocentric and allocentric visuospatial working memory in premotor Huntington's disease: A double dissociation with caudate and hippocampal volumesKatherine L Possin, Hosung Kim, Michael D Geschwind, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 3, 2005
Diagnosis of human prion diseaseJiri G Safar, Michael D Geschwind, Camille Deering, et al.
Pageof 14