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Michael D Geschwind

Showing results (81-90 of 140) with videos related to

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Neurology. Genetics|June 13, 2018
Neurodegeneration as the presenting symptom in 2 adults with xeroderma pigmentosum complementation group FNiraj M Shanbhag, Michael D Geschwind, John J DiGiovanna, et al.
Journal of Alzheimer'S Disease : JAD|October 8, 2016
Genetic Prion Disease Caused by PRNP Q160X Mutation Presenting with an Orbitofrontal Syndrome, Cyclic Diarrhea, and Peripheral NeuropathyJamie C Fong, Julio C Rojas, Jee Bang, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 20, 2006
Human prions and plasma lipoproteinsJiri G Safar, Holger Wille, Michael D Geschwind, et al.
JAMA Neurology|May 7, 2019
Association of Blood and Cerebrospinal Fluid Tau Level and Other Biomarkers With Survival Time in Sporadic Creutzfeldt-Jakob DiseaseAdam M Staffaroni, Abigail O Kramer, Megan Casey, et al.
Mbio|November 22, 2018
Prion Seeds Distribute throughout the Eyes of Sporadic Creutzfeldt-Jakob Disease PatientsChristina D Orrù, Katrin Soldau, Christian Cordano, et al.
Neurology. Genetics|April 10, 2018
Expanding the global prevalence of spinocerebellar ataxia type 42Kathie Ngo, Mamdouh Aker, Lauren E Petty, et al.
Neurology(R) Neuroimmunology & Neuroinflammation|February 8, 2020
Intrathecal B-cell activation in LGI1 antibody encephalitisKlaus Lehmann-Horn, Sarosh R Irani, Shengzhi Wang, et al.
Cell Reports|October 16, 2012
Induced pluripotent stem cell models of progranulin-deficient frontotemporal dementia uncover specific reversible neuronal defectsSandra Almeida, Zhijun Zhang, Giovanni Coppola, et al.
Neurology. Clinical Practice|July 3, 2015
Comparing CSF biomarkers and brain MRI in the diagnosis of sporadic Creutzfeldt-Jakob diseaseSven A Forner, Leonel T Takada, Brianne M Bettcher, et al.
JAMA Neurology|March 7, 2017
Precipitous Deterioration of Motor Function, Cognition, and BehaviorMireya Fernández-Fournier, David C Perry, Maria Carmela Tartaglia, et al.
Pageof 14

Showing results (81-90 of 140) with videos related to

Sort By:
Pageof 14
Neurology. Genetics|June 13, 2018
Neurodegeneration as the presenting symptom in 2 adults with xeroderma pigmentosum complementation group FNiraj M Shanbhag, Michael D Geschwind, John J DiGiovanna, et al.
Journal of Alzheimer'S Disease : JAD|October 8, 2016
Genetic Prion Disease Caused by PRNP Q160X Mutation Presenting with an Orbitofrontal Syndrome, Cyclic Diarrhea, and Peripheral NeuropathyJamie C Fong, Julio C Rojas, Jee Bang, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 20, 2006
Human prions and plasma lipoproteinsJiri G Safar, Holger Wille, Michael D Geschwind, et al.
JAMA Neurology|May 7, 2019
Association of Blood and Cerebrospinal Fluid Tau Level and Other Biomarkers With Survival Time in Sporadic Creutzfeldt-Jakob DiseaseAdam M Staffaroni, Abigail O Kramer, Megan Casey, et al.
Mbio|November 22, 2018
Prion Seeds Distribute throughout the Eyes of Sporadic Creutzfeldt-Jakob Disease PatientsChristina D Orrù, Katrin Soldau, Christian Cordano, et al.
Neurology. Genetics|April 10, 2018
Expanding the global prevalence of spinocerebellar ataxia type 42Kathie Ngo, Mamdouh Aker, Lauren E Petty, et al.
Neurology(R) Neuroimmunology & Neuroinflammation|February 8, 2020
Intrathecal B-cell activation in LGI1 antibody encephalitisKlaus Lehmann-Horn, Sarosh R Irani, Shengzhi Wang, et al.
Cell Reports|October 16, 2012
Induced pluripotent stem cell models of progranulin-deficient frontotemporal dementia uncover specific reversible neuronal defectsSandra Almeida, Zhijun Zhang, Giovanni Coppola, et al.
Neurology. Clinical Practice|July 3, 2015
Comparing CSF biomarkers and brain MRI in the diagnosis of sporadic Creutzfeldt-Jakob diseaseSven A Forner, Leonel T Takada, Brianne M Bettcher, et al.
JAMA Neurology|March 7, 2017
Precipitous Deterioration of Motor Function, Cognition, and BehaviorMireya Fernández-Fournier, David C Perry, Maria Carmela Tartaglia, et al.
Pageof 14