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Andrew B Singleton

Showing results (151-160 of 397) with videos related to

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Movement Disorders : Official Journal of the Movement Disorder Society|August 2, 2025
A CGG Repeat Expansion in CSNK1E Associated with Progressive Myoclonic Epilepsy with Incomplete PenetranceFulya Akçimen, Pilar Alvarez Jerez, Ulviyya Guliyeva, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|June 29, 2024
Long-Read Sequencing Unravels the Complexity of Structural Variants in PRKN in Two Individuals with Early-Onset Parkinson's DiseaseGuillaume Cogan, Kensuke Daida, Kimberley J Billingsley, et al.
Plos Genetics|March 14, 2009
Measures of autozygosity in decline: globalization, urbanization, and its implications for medical geneticsMichael A Nalls, Javier Simon-Sanchez, J Raphael Gibbs, et al.
Nature Genetics|November 27, 2007
Mutations in TTBK2, encoding a kinase implicated in tau phosphorylation, segregate with spinocerebellar ataxia type 11Henry Houlden, Janel Johnson, Christopher Gardner-Thorpe, et al.
Medrxiv : the Preprint Server for Health Sciences|December 11, 2023
The non-coding <i>GBA1</i> rs3115534 variant is associated with REM sleep behavior disorder in NigeriansOluwadamilola O Ojo, Sara Bandres-Ciga, Mary B Makarious, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|February 23, 2024
GBA1 rs3115534 Is Associated with REM Sleep Behavior Disorder in Parkinson's Disease in NigeriansOluwadamilola Omolara Ojo, Sara Bandres-Ciga, Mary B Makarious, et al.
Medrxiv : the Preprint Server for Health Sciences|May 15, 2024
Long-read sequencing unravels the complexity of structural variants in <i>PRKN</i> in two individuals with early-onset Parkinson's diseaseGuillaume Cogan, Kensuke Daida, Kimberley J Billingsley, et al.
Frontiers in Neurology|December 1, 2015
Plasma 24-metabolite Panel Predicts Preclinical Transition to Clinical Stages of Alzheimer's DiseaseMassimo S Fiandaca, Xiaogang Zhong, Amrita K Cheema, et al.
Neuroscience Letters|November 22, 2005
The human prion gene M129V polymorphism is not associated with idiopathic Parkinson's disease in three distinct populationsSonja W Scholz, Georgia Xiromerisiou, Hon C Fung, et al.
Human Molecular Genetics|September 17, 2014
Genome-wide admixture and association study of serum iron, ferritin, transferrin saturation and total iron binding capacity in African AmericansJin Li, Leslie A Lange, Qing Duan, et al.
Pageof 40

Showing results (151-160 of 397) with videos related to

Sort By:
Pageof 40
Movement Disorders : Official Journal of the Movement Disorder Society|August 2, 2025
A CGG Repeat Expansion in CSNK1E Associated with Progressive Myoclonic Epilepsy with Incomplete PenetranceFulya Akçimen, Pilar Alvarez Jerez, Ulviyya Guliyeva, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|June 29, 2024
Long-Read Sequencing Unravels the Complexity of Structural Variants in PRKN in Two Individuals with Early-Onset Parkinson's DiseaseGuillaume Cogan, Kensuke Daida, Kimberley J Billingsley, et al.
Plos Genetics|March 14, 2009
Measures of autozygosity in decline: globalization, urbanization, and its implications for medical geneticsMichael A Nalls, Javier Simon-Sanchez, J Raphael Gibbs, et al.
Nature Genetics|November 27, 2007
Mutations in TTBK2, encoding a kinase implicated in tau phosphorylation, segregate with spinocerebellar ataxia type 11Henry Houlden, Janel Johnson, Christopher Gardner-Thorpe, et al.
Medrxiv : the Preprint Server for Health Sciences|December 11, 2023
The non-coding <i>GBA1</i> rs3115534 variant is associated with REM sleep behavior disorder in NigeriansOluwadamilola O Ojo, Sara Bandres-Ciga, Mary B Makarious, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|February 23, 2024
GBA1 rs3115534 Is Associated with REM Sleep Behavior Disorder in Parkinson's Disease in NigeriansOluwadamilola Omolara Ojo, Sara Bandres-Ciga, Mary B Makarious, et al.
Medrxiv : the Preprint Server for Health Sciences|May 15, 2024
Long-read sequencing unravels the complexity of structural variants in <i>PRKN</i> in two individuals with early-onset Parkinson's diseaseGuillaume Cogan, Kensuke Daida, Kimberley J Billingsley, et al.
Frontiers in Neurology|December 1, 2015
Plasma 24-metabolite Panel Predicts Preclinical Transition to Clinical Stages of Alzheimer's DiseaseMassimo S Fiandaca, Xiaogang Zhong, Amrita K Cheema, et al.
Neuroscience Letters|November 22, 2005
The human prion gene M129V polymorphism is not associated with idiopathic Parkinson's disease in three distinct populationsSonja W Scholz, Georgia Xiromerisiou, Hon C Fung, et al.
Human Molecular Genetics|September 17, 2014
Genome-wide admixture and association study of serum iron, ferritin, transferrin saturation and total iron binding capacity in African AmericansJin Li, Leslie A Lange, Qing Duan, et al.
Pageof 40