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Thomas D Bird

Showing results (91-100 of 190) with videos related to

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American Journal of Human Genetics|July 13, 2004
Evidence for a novel late-onset Alzheimer disease locus on chromosome 19p13.2Ellen M Wijsman, E Warwick Daw, Change-En Yu, et al.
Annals of Neurology|March 19, 2011
Familial prion disease with Alzheimer disease-like tau pathology and clinical phenotypeSuman Jayadev, David Nochlin, Parvoneh Poorkaj, et al.
Neurology|March 22, 2022
Reader Response: Timing and Impact of Psychiatric, Cognitive, and Motor Abnormalities in Huntington DiseaseThomas D Bird, Herwig Lange, Travis Cruickshank, et al.
Movement Disorders Clinical Practice|January 24, 2020
Hyperphosphorylated Tau, Increased Adenylate Cyclase 5 (ADCY5) Immunoreactivity, but No Neuronal Loss in ADCY5-DyskinesiaDong-Hui Chen, Caitlin S Latimer, Min Spencer, et al.
Archives of Neurology|October 11, 2002
Familial dementia with lewy bodies: a clinical and neuropathological study of 2 familiesDebby W Tsuang, Aaron M Dalan, Charisma J Eugenio, et al.
Acta Neuropathologica Communications|November 24, 2020
Adult onset pan-neuronal human tau tubulin kinase 1 expression causes severe cerebellar neurodegeneration in micePamela McMillan, Jeanna Wheeler, Rachel E Gatlin, et al.
Plos One|April 12, 2011
Frequency of KCNC3 DNA variants as causes of spinocerebellar ataxia 13 (SCA13)Karla P Figueroa, Michael F Waters, Vartan Garibyan, et al.
American Journal of Human Genetics|September 26, 2002
Genomic rearrangements resulting in PLP1 deletion occur by nonhomologous end joining and cause different dysmyelinating phenotypes in males and femalesKen Inoue, Hitoshi Osaka, Virginia C Thurston, et al.
Neurology. Genetics|April 12, 2016
Novel mutations highlight the key role of the ankyrin repeat domain in TRPV4-mediated neuropathyJeremy M Sullivan, Christina M Zimanyi, William Aisenberg, et al.
Journal of Neurochemistry|September 27, 2003
Alteration in calcium channel properties is responsible for the neurotoxic action of a familial frontotemporal dementia tau mutationKatsutoshi Furukawa, Yue Wang, Pamela J Yao, et al.
Pageof 19

Showing results (91-100 of 190) with videos related to

Sort By:
Pageof 19
American Journal of Human Genetics|July 13, 2004
Evidence for a novel late-onset Alzheimer disease locus on chromosome 19p13.2Ellen M Wijsman, E Warwick Daw, Change-En Yu, et al.
Annals of Neurology|March 19, 2011
Familial prion disease with Alzheimer disease-like tau pathology and clinical phenotypeSuman Jayadev, David Nochlin, Parvoneh Poorkaj, et al.
Neurology|March 22, 2022
Reader Response: Timing and Impact of Psychiatric, Cognitive, and Motor Abnormalities in Huntington DiseaseThomas D Bird, Herwig Lange, Travis Cruickshank, et al.
Movement Disorders Clinical Practice|January 24, 2020
Hyperphosphorylated Tau, Increased Adenylate Cyclase 5 (ADCY5) Immunoreactivity, but No Neuronal Loss in ADCY5-DyskinesiaDong-Hui Chen, Caitlin S Latimer, Min Spencer, et al.
Archives of Neurology|October 11, 2002
Familial dementia with lewy bodies: a clinical and neuropathological study of 2 familiesDebby W Tsuang, Aaron M Dalan, Charisma J Eugenio, et al.
Acta Neuropathologica Communications|November 24, 2020
Adult onset pan-neuronal human tau tubulin kinase 1 expression causes severe cerebellar neurodegeneration in micePamela McMillan, Jeanna Wheeler, Rachel E Gatlin, et al.
Plos One|April 12, 2011
Frequency of KCNC3 DNA variants as causes of spinocerebellar ataxia 13 (SCA13)Karla P Figueroa, Michael F Waters, Vartan Garibyan, et al.
American Journal of Human Genetics|September 26, 2002
Genomic rearrangements resulting in PLP1 deletion occur by nonhomologous end joining and cause different dysmyelinating phenotypes in males and femalesKen Inoue, Hitoshi Osaka, Virginia C Thurston, et al.
Neurology. Genetics|April 12, 2016
Novel mutations highlight the key role of the ankyrin repeat domain in TRPV4-mediated neuropathyJeremy M Sullivan, Christina M Zimanyi, William Aisenberg, et al.
Journal of Neurochemistry|September 27, 2003
Alteration in calcium channel properties is responsible for the neurotoxic action of a familial frontotemporal dementia tau mutationKatsutoshi Furukawa, Yue Wang, Pamela J Yao, et al.
Pageof 19