Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

D Bird

Showing results (591-600 of 780) with videos related to

Pageof 78
Sort By:
Neurology|April 1, 1997
Chromosome 17 and hereditary dementia: linkage studies in three non-Alzheimer families and kindreds with late-onset FADT D Bird, E M Wijsman, D Nochlin, et al.
Archives of Physical Medicine and Rehabilitation|December 23, 1998
Neuropathic pain in Charcot-Marie-Tooth diseaseG T Carter, M P Jensen, B S Galer, et al.
Brain Pathology (Zurich, Switzerland)|July 16, 2008
Detergent-insoluble EAAC1/EAAT3 aberrantly accumulates in hippocampal neurons of Alzheimer's disease patientsKevin Duerson, Randall L Woltjer, Paramita Mookherjee, et al.
Parkinsonism & Related Disorders|July 2, 2022
Reduced gene dosage is a common mechanism of neuropathologies caused by ATP6AP2 splicing mutationsWilliam C Edelman, Kostantin Kiianitsa, Tuhin Virmani, et al.
Alcohol (Fayetteville, N.Y.)|June 29, 2012
Alcohol and epigenetic changes: summary of the 2011 Alcohol and Immunology Research Interest Group (AIRIG) meetingAnita Zahs, Brenda J Curtis, Thomas J Waldschmidt, et al.
Epilepsia|November 26, 2003
An Xp; Yq translocation causing a novel contiguous gene syndrome in brothers with generalized epilepsy, ichthyosis, and attention deficitsMichael J Doherty, Ian A Glass, Craig L Bennett, et al.
Life Sciences|July 1, 1985
The effects of a single acute dose of dexamethasone on monoamine and metabolite levels in rat brainA J Rothschild, P J Langlais, A F Schatzberg, et al.
American Journal of Human Genetics|September 1, 1995
Spinocerebellar ataxia type 1 and Machado-Joseph disease: incidence of CAG expansions among adult-onset ataxia patients from 311 families with dominant, recessive, or sporadic ataxiaL P Ranum, J K Lundgren, L J Schut, et al.
Acta Neuropathologica|September 4, 2025
Down syndrome and a presenilin 2 variant: dual genetic risk of Alzheimer's diseaseJordan Ogg, Nadia Postupna, Laura E Gibbons, et al.
Archives of Neurology|April 13, 2005
Presence of alanine-to-valine substitutions in myofibrillogenesis regulator 1 in paroxysmal nonkinesigenic dyskinesia: confirmation in 2 kindredsDong-Hui Chen, Mark Matsushita, Shirley Rainier, et al.
Pageof 78

Showing results (591-600 of 780) with videos related to

Sort By:
Pageof 78
Neurology|April 1, 1997
Chromosome 17 and hereditary dementia: linkage studies in three non-Alzheimer families and kindreds with late-onset FADT D Bird, E M Wijsman, D Nochlin, et al.
Archives of Physical Medicine and Rehabilitation|December 23, 1998
Neuropathic pain in Charcot-Marie-Tooth diseaseG T Carter, M P Jensen, B S Galer, et al.
Brain Pathology (Zurich, Switzerland)|July 16, 2008
Detergent-insoluble EAAC1/EAAT3 aberrantly accumulates in hippocampal neurons of Alzheimer's disease patientsKevin Duerson, Randall L Woltjer, Paramita Mookherjee, et al.
Parkinsonism & Related Disorders|July 2, 2022
Reduced gene dosage is a common mechanism of neuropathologies caused by ATP6AP2 splicing mutationsWilliam C Edelman, Kostantin Kiianitsa, Tuhin Virmani, et al.
Alcohol (Fayetteville, N.Y.)|June 29, 2012
Alcohol and epigenetic changes: summary of the 2011 Alcohol and Immunology Research Interest Group (AIRIG) meetingAnita Zahs, Brenda J Curtis, Thomas J Waldschmidt, et al.
Epilepsia|November 26, 2003
An Xp; Yq translocation causing a novel contiguous gene syndrome in brothers with generalized epilepsy, ichthyosis, and attention deficitsMichael J Doherty, Ian A Glass, Craig L Bennett, et al.
Life Sciences|July 1, 1985
The effects of a single acute dose of dexamethasone on monoamine and metabolite levels in rat brainA J Rothschild, P J Langlais, A F Schatzberg, et al.
American Journal of Human Genetics|September 1, 1995
Spinocerebellar ataxia type 1 and Machado-Joseph disease: incidence of CAG expansions among adult-onset ataxia patients from 311 families with dominant, recessive, or sporadic ataxiaL P Ranum, J K Lundgren, L J Schut, et al.
Acta Neuropathologica|September 4, 2025
Down syndrome and a presenilin 2 variant: dual genetic risk of Alzheimer's diseaseJordan Ogg, Nadia Postupna, Laura E Gibbons, et al.
Archives of Neurology|April 13, 2005
Presence of alanine-to-valine substitutions in myofibrillogenesis regulator 1 in paroxysmal nonkinesigenic dyskinesia: confirmation in 2 kindredsDong-Hui Chen, Mark Matsushita, Shirley Rainier, et al.
Pageof 78