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Thomas D Bird

Showing results (41-50 of 190) with videos related to

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American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|August 4, 2011
Genome scan of age-at-onset in the NIMH Alzheimer disease sample uncovers multiple loci, along with evidence of both genetic and sample heterogeneityYoonha Choi, Elizabeth E Marchani, Thomas D Bird, et al.
American Journal of Medical Genetics. Part A|November 2, 2017
Novel pregnancy-triggered episodes of CAPOS syndromeIrene J Chang, Margaret P Adam, Suman Jayadev, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|December 10, 2016
ADCY5-related dyskinesia: Comments on characteristic manifestations and variant-associated severityWendy H Raskind, Jennifer R Friedman, Emmanuel Roze, et al.
Journal of Huntington'S Disease|February 27, 2018
A Genetic Study of Psychosis in Huntington's Disease: Evidence for the Involvement of Glutamate Signaling PathwaysDebby W Tsuang, Tiffany A Greenwood, Suman Jayadev, et al.
American Journal of Medical Genetics|May 7, 2002
Autosomal dominant sensory/motor neuropathy with Ataxia (SMNA): Linkage to chromosome 7q22-q32Zoran Brkanac, Magali Fernandez, Mark Matsushita, et al.
Cerebellum (London, England)|September 10, 2017
Psychosis in Spinocerebellar Ataxias: a Case Series and Study of Tyrosine Hydroxylase in Substantia NigraKatherine W Turk, Margaret E Flanagan, Samuel Josephson, et al.
Brain : a Journal of Neurology|August 11, 2022
Aberrant splicing of PSEN2, but not PSEN1, in individuals with sporadic Alzheimer's diseaseMeredith M Course, Kathryn Gudsnuk, C Dirk Keene, et al.
Journal of the Neurological Sciences|October 23, 2012
The unique co-occurrence of spinocerebellar ataxia type 10 (SCA10) and Huntington diseaseRichard H Roxburgh, Corrie O Smith, Jung G Lim, et al.
Archives of Clinical Neuropsychology : the Official Journal of the National Academy of Neuropsychologists|April 24, 2021
Familial Idiopathic Basal Ganglia Calcification: A Father-Son Dyad Demonstrate Heterogeneity of Presentation and Disease ProgressionEvan Zahniser, Thomas D Bird, Dong-Hui Chen, et al.
Archives of Neurology|March 12, 2008
Conjugal Alzheimer disease: risk in children when both parents have Alzheimer diseaseSuman Jayadev, Ellen J Steinbart, Yueh-Yun Chi, et al.
Pageof 19

Showing results (41-50 of 190) with videos related to

Sort By:
Pageof 19
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|August 4, 2011
Genome scan of age-at-onset in the NIMH Alzheimer disease sample uncovers multiple loci, along with evidence of both genetic and sample heterogeneityYoonha Choi, Elizabeth E Marchani, Thomas D Bird, et al.
American Journal of Medical Genetics. Part A|November 2, 2017
Novel pregnancy-triggered episodes of CAPOS syndromeIrene J Chang, Margaret P Adam, Suman Jayadev, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|December 10, 2016
ADCY5-related dyskinesia: Comments on characteristic manifestations and variant-associated severityWendy H Raskind, Jennifer R Friedman, Emmanuel Roze, et al.
Journal of Huntington'S Disease|February 27, 2018
A Genetic Study of Psychosis in Huntington's Disease: Evidence for the Involvement of Glutamate Signaling PathwaysDebby W Tsuang, Tiffany A Greenwood, Suman Jayadev, et al.
American Journal of Medical Genetics|May 7, 2002
Autosomal dominant sensory/motor neuropathy with Ataxia (SMNA): Linkage to chromosome 7q22-q32Zoran Brkanac, Magali Fernandez, Mark Matsushita, et al.
Cerebellum (London, England)|September 10, 2017
Psychosis in Spinocerebellar Ataxias: a Case Series and Study of Tyrosine Hydroxylase in Substantia NigraKatherine W Turk, Margaret E Flanagan, Samuel Josephson, et al.
Brain : a Journal of Neurology|August 11, 2022
Aberrant splicing of PSEN2, but not PSEN1, in individuals with sporadic Alzheimer's diseaseMeredith M Course, Kathryn Gudsnuk, C Dirk Keene, et al.
Journal of the Neurological Sciences|October 23, 2012
The unique co-occurrence of spinocerebellar ataxia type 10 (SCA10) and Huntington diseaseRichard H Roxburgh, Corrie O Smith, Jung G Lim, et al.
Archives of Clinical Neuropsychology : the Official Journal of the National Academy of Neuropsychologists|April 24, 2021
Familial Idiopathic Basal Ganglia Calcification: A Father-Son Dyad Demonstrate Heterogeneity of Presentation and Disease ProgressionEvan Zahniser, Thomas D Bird, Dong-Hui Chen, et al.
Archives of Neurology|March 12, 2008
Conjugal Alzheimer disease: risk in children when both parents have Alzheimer diseaseSuman Jayadev, Ellen J Steinbart, Yueh-Yun Chi, et al.
Pageof 19