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Showing results (661-670 of 780) with videos related to

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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.
American Journal of Human Genetics|April 1, 1996
Gender difference in apolipoprotein E-associated risk for familial Alzheimer disease: a possible clue to the higher incidence of Alzheimer disease in womenH Payami, S Zareparsi, K R Montee, 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.
Neurology|May 23, 2008
Late-onset hereditary axonal neuropathiesC L Bennett, V H Lawson, K L Brickell, et al.
Neurology|December 17, 1998
Incidence of dominant spinocerebellar and Friedreich triplet repeats among 361 ataxia familiesM L Moseley, K A Benzow, L J Schut, et al.
Brain : a Journal of Neurology|September 1, 1999
The impact of different presenilin 1 andpresenilin 2 mutations on amyloid deposition, neurofibrillary changes and neuronal loss in the familial Alzheimer's disease brain: evidence for other phenotype-modifying factorsT Gómez-Isla, W B Growdon, M J McNamara, 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|June 1, 1997
Presenilin-1 protein expression in familial and sporadic Alzheimer's diseaseA I Levey, C J Heilman, J J Lah, 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.
Pageof 78

Showing results (661-670 of 780) with videos related to

Sort By:
Pageof 78
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.
American Journal of Human Genetics|April 1, 1996
Gender difference in apolipoprotein E-associated risk for familial Alzheimer disease: a possible clue to the higher incidence of Alzheimer disease in womenH Payami, S Zareparsi, K R Montee, 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.
Neurology|May 23, 2008
Late-onset hereditary axonal neuropathiesC L Bennett, V H Lawson, K L Brickell, et al.
Neurology|December 17, 1998
Incidence of dominant spinocerebellar and Friedreich triplet repeats among 361 ataxia familiesM L Moseley, K A Benzow, L J Schut, et al.
Brain : a Journal of Neurology|September 1, 1999
The impact of different presenilin 1 andpresenilin 2 mutations on amyloid deposition, neurofibrillary changes and neuronal loss in the familial Alzheimer's disease brain: evidence for other phenotype-modifying factorsT Gómez-Isla, W B Growdon, M J McNamara, 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|June 1, 1997
Presenilin-1 protein expression in familial and sporadic Alzheimer's diseaseA I Levey, C J Heilman, J J Lah, 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.
Pageof 78