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X
Soto-Beasley, Alexandra I.
65  Ergebnisse:
Personensuche X
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1

Systematic rare variant analyses identify RAB32 as a suscep..:

Hop, Paul J. ; Lai, Dongbing ; Keagle, Pamela J....
Nature Genetics.  , 2024
Link: https://doi.org/10.1038/..
 
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2

MAPT H2 haplotype and risk of Pick's disease in the Pick's ..:

Valentino, Rebecca R ; Scotton, William J ; Roemer, Shanu F...
The Lancet Neurology.  23 (2024)  5 - p. 487-499 , 2024
Link: https://doi.org/10.1016/..
 
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3

Case report of a patient with unclassified tauopathy with m..:

Koga, Shunsuke ; Metrick II, Michael A. ; Golbe, Lawrence I....
Acta Neuropathologica Communications.  11 (2023)  1 - p. , 2023
Link: https://doi.org/10.1186/..
 
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4

PTPA variants are rare in early-onset and familial Parkinso..:

Dulski, Jarosław ; Soto-Beasley, Alexandra I ; Uitti, Ryan J..
Brain.  146 (2023)  12 - p. e125-e127 , 2023
Link: https://doi.org/10.1093/..
 
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5

Publisher Correction to: Diffuse argyrophilic grain disease..:

Koga, Shunsuke ; Murakami, Aya ; Soto-Beasley, Alexandra I....
Acta Neuropathologica Communications.  11 (2023)  1 - p. , 2023
Link: https://doi.org/10.1186/..
 
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6

Diffuse argyrophilic grain disease with TDP-43 proteinopath..:

Koga, Shunsuke ; Murakami, Aya ; Soto-Beasley, Alexandra I....
Acta Neuropathologica Communications.  11 (2023)  1 - p. , 2023
Link: https://doi.org/10.1186/..
 
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7

Cathepsin B p.Gly284Val Variant in Parkinson's Disease Path..:

Milanowski, Lukasz M. ; Hou, Xu ; Bredenberg, Jenny M....
International Journal of Molecular Sciences.  23 (2022)  13 - p. 7086 , 2022
Link: https://doi.org/10.3390/..
 
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8

Mitochondrial genomic variation in dementia with Lewy bodie..:

Valentino, Rebecca R. ; Ramnarine, Chloe ; Heckman, Michael G....
Acta Neuropathologica Communications.  10 (2022)  1 - p. , 2022
Link: https://doi.org/10.1186/..
 
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9

Dancing Feet Dyskinesia in a Patient with GBA-PD:

Olszewska, Diana A. ; McCarthy, Allan ; Soto-Beasley, Alexandra I....
Journal of Movement Disorders.  15 (2022)  1 - p. 83-85 , 2022
Link: https://doi.org/10.14802..
 
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10

Systematic Functional Analysis of PINK1 and PRKN Coding Var..:

Broadway, Benjamin J. ; Boneski, Paige K. ; Bredenberg, Jenny M....
Cells.  11 (2022)  15 - p. 2426 , 2022
Link: https://doi.org/10.3390/..
 
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11

Frequency of spinocerebellar ataxia mutations in patients w..:

Wernick, Anna I. ; Walton, Ronald L. ; Soto-Beasley, Alexandra I....
Clinical Autonomic Research.  31 (2021)  1 - p. 117-125 , 2021
Link: https://doi.org/10.1007/..
 
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12

Association of Mitochondrial DNA Genomic Variation With Ris..:

Valentino, Rebecca R. ; Heckman, Michael G. ; Johnson, Patrick W....
Neurology.  96 (2021)  13 - p. , 2021
Link: https://doi.org/10.1212/..
 
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13

PARKIN, PINK1, and DJ1 analysis in early-onset Parkinson's ..:

Olszewska, Diana A. ; McCarthy, Allan ; Soto-Beasley, Alexandra I....
Irish Journal of Medical Science (1971 -).  191 (2021)  2 - p. 901-907 , 2021
Link: https://doi.org/10.1007/..
 
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14

Fine-mapping of the non-coding variation driving the Caucas..:

Heckman, Michael G. ; Labbé, Catherine ; Kolicheski, Ana L....
Parkinsonism & Related Disorders.  83 (2021)  - p. 22-30 , 2021
Link: https://doi.org/10.1016/..
 
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15

Early-Onset Parkinson Disease Screening in Patients From Ni..:

Milanowski, Lukasz M. ; Oshinaike, Olajumoke ; Broadway, Benjamin J....
Frontiers in Neurology.  11 (2021)  - p. , 2021
Link: https://doi.org/10.3389/..
 
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