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D Geschwind

Showing results (81-90 of 170) with videos related to

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Annals of Neurology|June 20, 2025
Decoding the Clinical Features that Associate with Progression, Causes, and Outcomes in Patients with Suspected Rapidly Progressive DementiaYoav D Piura, Nihal Satyadev, Nick Corriveau-Lecavalier, et al.
Brain : a Journal of Neurology|September 28, 2016
A case cluster of variant Creutzfeldt-Jakob disease linked to the Kingdom of Saudi ArabiaMichael B Coulthart, Michael D Geschwind, Shireen Qureshi, et al.
Neurology|January 26, 2006
First symptom in sporadic Creutzfeldt-Jakob diseaseG D Rabinovici, P N Wang, J Levin, 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.
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.
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.
Neuroimage. Clinical|March 14, 2014
Application of quantitative DTI metrics in sporadic CJDE Caverzasi, R G Henry, P Vitali, 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.
Molecular Genetics and Metabolism|October 3, 2002
Human ARX gene: genomic characterization and expressionR Ohira, Y H Zhang, W Guo, et al.
Pageof 17

Showing results (81-90 of 170) with videos related to

Sort By:
Pageof 17
Annals of Neurology|June 20, 2025
Decoding the Clinical Features that Associate with Progression, Causes, and Outcomes in Patients with Suspected Rapidly Progressive DementiaYoav D Piura, Nihal Satyadev, Nick Corriveau-Lecavalier, et al.
Brain : a Journal of Neurology|September 28, 2016
A case cluster of variant Creutzfeldt-Jakob disease linked to the Kingdom of Saudi ArabiaMichael B Coulthart, Michael D Geschwind, Shireen Qureshi, et al.
Neurology|January 26, 2006
First symptom in sporadic Creutzfeldt-Jakob diseaseG D Rabinovici, P N Wang, J Levin, 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.
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.
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.
Neuroimage. Clinical|March 14, 2014
Application of quantitative DTI metrics in sporadic CJDE Caverzasi, R G Henry, P Vitali, 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.
Molecular Genetics and Metabolism|October 3, 2002
Human ARX gene: genomic characterization and expressionR Ohira, Y H Zhang, W Guo, et al.
Pageof 17