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D Bird

Showing results (631-640 of 780) with videos related to

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Archives of Neurology|March 15, 2006
Lewy body pathology in familial Alzheimer disease: evidence for disease- and mutation-specific pathologic phenotypeJames B Leverenz, Mark A Fishel, Elaine R Peskind, et al.
Human Genetics|January 24, 1998
Hereditary neuralgic amyotrophy: evidence for genetic homogeneity and mapping to chromosome 17q25J E Pellegrino, R A George, J Biegel, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|November 28, 2012
TOMM40 intron 6 poly-T length, age at onset, and neuropathology of AD in individuals with APOE ε3/ε3Ge Li, Lynn M Bekris, Lesley Leong, et al.
Archives of Neurology|July 12, 2012
Autosomal dominant familial dyskinesia and facial myokymia: single exome sequencing identifies a mutation in adenylyl cyclase 5Ying-Zhang Chen, Mark M Matsushita, Peggy Robertson, et al.
Chest|May 31, 2024
Quantifying Diaphragm Blood Flow With Contrast-Enhanced Ultrasound in HumansJordan D Bird, Megan L Lance, Ty R W Banser, et al.
Genetic Epidemiology|March 7, 2026
Variant Prioritization by Pedigree-Based HaplotypingRafael A Nafikov, Harkirat K Sohi, Alejandro Q Nato, et al.
Acta Neuropathologica|July 3, 2026
Mutation-specific neuropathologic signatures in MAPT-associated frontotemporal lobar degenerationMarika Bogdani, Vaishnavi S Jadhav, Brian C Kraemer, et al.
Journal of Alzheimer'S Disease : JAD|October 9, 2010
Heritability of different forms of memory in the Late Onset Alzheimer's Disease Family StudyRobert S Wilson, Sandra Barral, Joseph H Lee, et al.
Cell|January 15, 1993
DNA deletion associated with hereditary neuropathy with liability to pressure palsiesP F Chance, M K Alderson, K A Leppig, et al.
Annals of Neurology|August 12, 1999
Ataxin 1 and ataxin 3 in neuronal intranuclear inclusion diseaseA P Lieberman, J Q Trojanowski, D G Leonard, et al.
Pageof 78

Showing results (631-640 of 780) with videos related to

Sort By:
Pageof 78
Archives of Neurology|March 15, 2006
Lewy body pathology in familial Alzheimer disease: evidence for disease- and mutation-specific pathologic phenotypeJames B Leverenz, Mark A Fishel, Elaine R Peskind, et al.
Human Genetics|January 24, 1998
Hereditary neuralgic amyotrophy: evidence for genetic homogeneity and mapping to chromosome 17q25J E Pellegrino, R A George, J Biegel, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|November 28, 2012
TOMM40 intron 6 poly-T length, age at onset, and neuropathology of AD in individuals with APOE ε3/ε3Ge Li, Lynn M Bekris, Lesley Leong, et al.
Archives of Neurology|July 12, 2012
Autosomal dominant familial dyskinesia and facial myokymia: single exome sequencing identifies a mutation in adenylyl cyclase 5Ying-Zhang Chen, Mark M Matsushita, Peggy Robertson, et al.
Chest|May 31, 2024
Quantifying Diaphragm Blood Flow With Contrast-Enhanced Ultrasound in HumansJordan D Bird, Megan L Lance, Ty R W Banser, et al.
Genetic Epidemiology|March 7, 2026
Variant Prioritization by Pedigree-Based HaplotypingRafael A Nafikov, Harkirat K Sohi, Alejandro Q Nato, et al.
Acta Neuropathologica|July 3, 2026
Mutation-specific neuropathologic signatures in MAPT-associated frontotemporal lobar degenerationMarika Bogdani, Vaishnavi S Jadhav, Brian C Kraemer, et al.
Journal of Alzheimer'S Disease : JAD|October 9, 2010
Heritability of different forms of memory in the Late Onset Alzheimer's Disease Family StudyRobert S Wilson, Sandra Barral, Joseph H Lee, et al.
Cell|January 15, 1993
DNA deletion associated with hereditary neuropathy with liability to pressure palsiesP F Chance, M K Alderson, K A Leppig, et al.
Annals of Neurology|August 12, 1999
Ataxin 1 and ataxin 3 in neuronal intranuclear inclusion diseaseA P Lieberman, J Q Trojanowski, D G Leonard, et al.
Pageof 78