Search details
1.
Trial of Botulinum Toxin for Isolated or Essential Head Tremor.
N Engl J Med
; 389(19): 1753-1765, 2023 Nov 09.
Article
in English
| MEDLINE | ID: mdl-37937777
2.
Trial of Deferiprone in Parkinson's Disease.
N Engl J Med
; 387(22): 2045-2055, 2022 12 01.
Article
in English
| MEDLINE | ID: mdl-36449420
3.
Motivational and cognitive predictors of apathy after subthalamic nucleus stimulation in Parkinson's disease.
Brain
; 147(2): 472-485, 2024 Feb 01.
Article
in English
| MEDLINE | ID: mdl-37787488
4.
A Double-Blind, Randomized, Placebo-Controlled Trial of Bumetanide in Parkinson's Disease.
Mov Disord
; 39(3): 618-622, 2024 Mar.
Article
in English
| MEDLINE | ID: mdl-38291616
5.
Rare Missense Variants in KCNJ10 Are Associated with Paroxysmal Kinesigenic Dyskinesia.
Mov Disord
; 2024 Mar 04.
Article
in English
| MEDLINE | ID: mdl-38436103
6.
Intermediate repeat expansions of TBP and STUB1: Genetic modifier or pure digenic inheritance in spinocerebellar ataxias?
Genet Med
; 25(2): 100327, 2023 02.
Article
in English
| MEDLINE | ID: mdl-36422518
7.
Limbic Stimulation Drives Mania in STN-DBS in Parkinson Disease: A Prospective Study.
Ann Neurol
; 92(3): 411-417, 2022 09.
Article
in English
| MEDLINE | ID: mdl-35703252
8.
Natural History and Phenotypic Spectrum of GAA-FGF14 Sporadic Late-Onset Cerebellar Ataxia (SCA27B).
Mov Disord
; 38(10): 1950-1956, 2023 10.
Article
in English
| MEDLINE | ID: mdl-37470282
9.
Efficacy of Caffeine in ADCY5-Related Dyskinesia: A Retrospective Study.
Mov Disord
; 37(6): 1294-1298, 2022 06.
Article
in English
| MEDLINE | ID: mdl-35384065
10.
Highlighting the Dystonic Phenotype Related to GNAO1.
Mov Disord
; 37(7): 1547-1554, 2022 07.
Article
in English
| MEDLINE | ID: mdl-35722775
11.
Biallelic loss-of-function variations in PRDX3 cause cerebellar ataxia.
Brain
; 144(5): 1467-1481, 2021 06 22.
Article
in English
| MEDLINE | ID: mdl-33889951
12.
Quantification of Head Tremors in Medical Conditions: A Comparison of Analyses Using a 2D Video Camera and a 3D Wireless Inertial Motion Unit.
Sensors (Basel)
; 22(6)2022 Mar 19.
Article
in English
| MEDLINE | ID: mdl-35336555
13.
High rate of hypomorphic variants as the cause of inherited ataxia and related diseases: study of a cohort of 366 families.
Genet Med
; 23(11): 2160-2170, 2021 11.
Article
in English
| MEDLINE | ID: mdl-34234304
14.
Early-Onset Parkinsonism Is a Manifestation of the PPP2R5D p.E200K Mutation.
Ann Neurol
; 88(5): 1028-1033, 2020 11.
Article
in English
| MEDLINE | ID: mdl-32743835
15.
Characterization of Recessive Parkinson Disease in a Large Multicenter Study.
Ann Neurol
; 88(4): 843-850, 2020 10.
Article
in English
| MEDLINE | ID: mdl-33045815
16.
Fluoxetine for the Symptomatic Treatment of Multiple System Atrophy: The MSA-FLUO Trial.
Mov Disord
; 36(7): 1704-1711, 2021 07.
Article
in English
| MEDLINE | ID: mdl-33792958
17.
Impact of Subthalamic Deep Brain Stimulation on Impulse Control Disorders in Parkinson's Disease: A Prospective Study.
Mov Disord
; 36(3): 750-757, 2021 03.
Article
in English
| MEDLINE | ID: mdl-33022101
18.
Single-fiber studies for assigning pathogenicity of eight mitochondrial DNA variants associated with mitochondrial diseases.
Hum Mutat
; 41(8): 1394-1406, 2020 08.
Article
in English
| MEDLINE | ID: mdl-32419253
19.
Clinical, neuropathological, and genetic characterization of STUB1 variants in cerebellar ataxias: a frequent cause of predominant cognitive impairment.
Genet Med
; 22(11): 1851-1862, 2020 11.
Article
in English
| MEDLINE | ID: mdl-32713943
20.
Autosomal Recessive Cerebellar Ataxias With Elevated Alpha-Fetoprotein: Uncommon Diseases, Common Biomarker.
Mov Disord
; 35(12): 2139-2149, 2020 12.
Article
in English
| MEDLINE | ID: mdl-33044027