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Thomas D Bird

Showing results (111-120 of 190) with videos related to

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Journal of Alzheimer'S Disease : JAD|August 18, 2006
Lewy body pathology in late-onset familial Alzheimer's disease: a clinicopathological case seriesDebby W Tsuang, Robert G Riekse, Kristina M Purganan, et al.
Human Molecular Genetics|December 23, 2006
Two sites in the MAPT region confer genetic risk for Guam ALS/PDC and dementiaPurnima Desai Sundar, Chang-En Yu, Weiva Sieh, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|July 7, 2007
Clinicopathological concordance and discordance in three monozygotic twin pairs with familial Alzheimer's diseaseKiri L Brickell, James B Leverenz, Ellen J Steinbart, et al.
Frontiers in Immunology|October 26, 2020
Triggering Receptor Expressed on Myeloid Cell 2 R47H Exacerbates Immune Response in Alzheimer's Disease BrainOlena Korvatska, Kostantin Kiianitsa, Alexander Ratushny, et al.
Acta Neuropathologica|June 30, 2009
Neuronal loss in Pelizaeus-Merzbacher disease differs in various mutations of the proteolipid protein 1Anders A F Sima, Christopher R Pierson, Randall L Woltjer, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|April 26, 2016
The discovery of LRRK2 p.R1441S, a novel mutation for Parkinson's disease, adds to the complexity of a mutational hotspotIgnacio F Mata, Marie Y Davis, Alexis N Lopez, et al.
Annals of Neurology|September 27, 2002
An R5L tau mutation in a subject with a progressive supranuclear palsy phenotypeParvoneh Poorkaj, Nancy A Muma, Victoria Zhukareva, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|December 13, 2016
The discovery of LRRK2 p.R1441S, a novel mutation for Parkinson's disease, adds to the complexity of a mutational hotspotIgnacio F Mata, Marie Y Davis, Alexis N Lopez, et al.
Archives of Neurology|March 12, 2008
Glucocerebrosidase gene mutations: a risk factor for Lewy body disordersIgnacio F Mata, Ali Samii, Seth H Schneer, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 7, 2022
Aβ and tau prions feature in the neuropathogenesis of Down syndromeCarlo Condello, Alison M Maxwell, Erika Castillo, et al.
Pageof 19

Showing results (111-120 of 190) with videos related to

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Pageof 19
Journal of Alzheimer'S Disease : JAD|August 18, 2006
Lewy body pathology in late-onset familial Alzheimer's disease: a clinicopathological case seriesDebby W Tsuang, Robert G Riekse, Kristina M Purganan, et al.
Human Molecular Genetics|December 23, 2006
Two sites in the MAPT region confer genetic risk for Guam ALS/PDC and dementiaPurnima Desai Sundar, Chang-En Yu, Weiva Sieh, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|July 7, 2007
Clinicopathological concordance and discordance in three monozygotic twin pairs with familial Alzheimer's diseaseKiri L Brickell, James B Leverenz, Ellen J Steinbart, et al.
Frontiers in Immunology|October 26, 2020
Triggering Receptor Expressed on Myeloid Cell 2 R47H Exacerbates Immune Response in Alzheimer's Disease BrainOlena Korvatska, Kostantin Kiianitsa, Alexander Ratushny, et al.
Acta Neuropathologica|June 30, 2009
Neuronal loss in Pelizaeus-Merzbacher disease differs in various mutations of the proteolipid protein 1Anders A F Sima, Christopher R Pierson, Randall L Woltjer, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|April 26, 2016
The discovery of LRRK2 p.R1441S, a novel mutation for Parkinson's disease, adds to the complexity of a mutational hotspotIgnacio F Mata, Marie Y Davis, Alexis N Lopez, et al.
Annals of Neurology|September 27, 2002
An R5L tau mutation in a subject with a progressive supranuclear palsy phenotypeParvoneh Poorkaj, Nancy A Muma, Victoria Zhukareva, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|December 13, 2016
The discovery of LRRK2 p.R1441S, a novel mutation for Parkinson's disease, adds to the complexity of a mutational hotspotIgnacio F Mata, Marie Y Davis, Alexis N Lopez, et al.
Archives of Neurology|March 12, 2008
Glucocerebrosidase gene mutations: a risk factor for Lewy body disordersIgnacio F Mata, Ali Samii, Seth H Schneer, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 7, 2022
Aβ and tau prions feature in the neuropathogenesis of Down syndromeCarlo Condello, Alison M Maxwell, Erika Castillo, et al.
Pageof 19