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Showing results (471-480 of 523) with videos related to

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Brain : a Journal of Neurology|April 7, 2007
Pathophysiology of REM sleep behaviour disorder and relevance to neurodegenerative diseaseB F Boeve, M H Silber, C B Saper, et al.
Brain : a Journal of Neurology|July 5, 2013
Dissecting phenotypic traits linked to human resilience to Alzheimer's pathologyBeatriz G Perez-Nievas, Thor D Stein, Hwan-Ching Tai, et al.
American Journal of Medical Genetics. Part A|November 20, 2018
Extension of the mutational and clinical spectrum of SOX2 related disorders: Description of six new cases and a novel association with suprasellar teratomaPatrick R Blackburn, Oscar F Chacon-Camacho, Xilma R Ortiz-González, et al.
Human Molecular Genetics|August 30, 2008
Common variation in the miR-659 binding-site of GRN is a major risk factor for TDP43-positive frontotemporal dementiaRosa Rademakers, Jason L Eriksen, Matt Baker, et al.
Neurobiology of Disease|October 19, 2018
Distinct cytokine profiles in human brains resilient to Alzheimer's pathologyIsabel Barroeta-Espar, Laura D Weinstock, Beatriz G Perez-Nievas, et al.
Neurology|October 11, 2013
MRI and pathology of REM sleep behavior disorder in dementia with Lewy bodiesMelissa E Murray, Tanis J Ferman, Bradley F Boeve, et al.
Annals of Neurology|December 4, 2020
Lewy Body Disease is a Contributor to Logopenic Progressive Aphasia PhenotypeMarina Buciuc, Jennifer L Whitwell, Koji Kasanuki, et al.
Acta Neuropathologica|May 7, 2015
Whole-genome sequencing reveals important role for TBK1 and OPTN mutations in frontotemporal lobar degeneration without motor neuron diseaseCyril Pottier, Kevin F Bieniek, NiCole Finch, et al.
Neurobiology of Aging|October 24, 2007
Prominent phenotypic variability associated with mutations in ProgranulinBrendan J Kelley, Wael Haidar, Bradley F Boeve, et al.
Nature Genetics|May 3, 2011
Mutations in DNMT1 cause hereditary sensory neuropathy with dementia and hearing lossChristopher J Klein, Maria-Victoria Botuyan, Yanhong Wu, et al.
Pageof 53

Showing results (471-480 of 523) with videos related to

Sort By:
Pageof 53
Brain : a Journal of Neurology|April 7, 2007
Pathophysiology of REM sleep behaviour disorder and relevance to neurodegenerative diseaseB F Boeve, M H Silber, C B Saper, et al.
Brain : a Journal of Neurology|July 5, 2013
Dissecting phenotypic traits linked to human resilience to Alzheimer's pathologyBeatriz G Perez-Nievas, Thor D Stein, Hwan-Ching Tai, et al.
American Journal of Medical Genetics. Part A|November 20, 2018
Extension of the mutational and clinical spectrum of SOX2 related disorders: Description of six new cases and a novel association with suprasellar teratomaPatrick R Blackburn, Oscar F Chacon-Camacho, Xilma R Ortiz-González, et al.
Human Molecular Genetics|August 30, 2008
Common variation in the miR-659 binding-site of GRN is a major risk factor for TDP43-positive frontotemporal dementiaRosa Rademakers, Jason L Eriksen, Matt Baker, et al.
Neurobiology of Disease|October 19, 2018
Distinct cytokine profiles in human brains resilient to Alzheimer's pathologyIsabel Barroeta-Espar, Laura D Weinstock, Beatriz G Perez-Nievas, et al.
Neurology|October 11, 2013
MRI and pathology of REM sleep behavior disorder in dementia with Lewy bodiesMelissa E Murray, Tanis J Ferman, Bradley F Boeve, et al.
Annals of Neurology|December 4, 2020
Lewy Body Disease is a Contributor to Logopenic Progressive Aphasia PhenotypeMarina Buciuc, Jennifer L Whitwell, Koji Kasanuki, et al.
Acta Neuropathologica|May 7, 2015
Whole-genome sequencing reveals important role for TBK1 and OPTN mutations in frontotemporal lobar degeneration without motor neuron diseaseCyril Pottier, Kevin F Bieniek, NiCole Finch, et al.
Neurobiology of Aging|October 24, 2007
Prominent phenotypic variability associated with mutations in ProgranulinBrendan J Kelley, Wael Haidar, Bradley F Boeve, et al.
Nature Genetics|May 3, 2011
Mutations in DNMT1 cause hereditary sensory neuropathy with dementia and hearing lossChristopher J Klein, Maria-Victoria Botuyan, Yanhong Wu, et al.
Pageof 53