Search details
1.
Clinical characteristics and pathophysiological properties of newly discovered LRRK2 variants associated with Parkinson's disease.
Neurobiol Dis
; 199: 106571, 2024 Jun 18.
Article
in English
| MEDLINE | ID: mdl-38901781
2.
Molecular genetics of Parkinson's disease: Contributions and global trends.
J Hum Genet
; 68(3): 125-130, 2023 Mar.
Article
in English
| MEDLINE | ID: mdl-35821405
3.
Analysis of LIN28A variants in patients with Parkinson's disease.
J Hum Genet
; 68(5): 329-331, 2023 May.
Article
in English
| MEDLINE | ID: mdl-36658347
4.
Long-Read Sequencing Resolves a Complex Structural Variant in PRKN Parkinson's Disease.
Mov Disord
; 38(12): 2249-2257, 2023 Dec.
Article
in English
| MEDLINE | ID: mdl-37926948
5.
Embracing Monogenic Parkinson's Disease: The MJFF Global Genetic PD Cohort.
Mov Disord
; 38(2): 286-303, 2023 02.
Article
in English
| MEDLINE | ID: mdl-36692014
6.
Motor neuron TDP-43 proteinopathy in progressive supranuclear palsy and corticobasal degeneration.
Brain
; 145(8): 2769-2784, 2022 08 27.
Article
in English
| MEDLINE | ID: mdl-35274674
7.
α-Synuclein V15A Variant in Familial Parkinson's Disease Exhibits a Weaker Lipid-Binding Property.
Mov Disord
; 37(10): 2075-2085, 2022 10.
Article
in English
| MEDLINE | ID: mdl-35894540
8.
Dairy Intake and Parkinson's Disease: A Mendelian Randomization Study.
Mov Disord
; 37(4): 857-864, 2022 04.
Article
in English
| MEDLINE | ID: mdl-34997937
9.
The Interaction between HLA-DRB1 and Smoking in Parkinson's Disease Revisited.
Mov Disord
; 37(9): 1929-1937, 2022 09.
Article
in English
| MEDLINE | ID: mdl-35810454
10.
Mutations in CHCHD2 cause α-synuclein aggregation.
Hum Mol Genet
; 28(23): 3895-3911, 2019 12 01.
Article
in English
| MEDLINE | ID: mdl-31600778
11.
Mitochondrial UQCRC1 mutations cause autosomal dominant parkinsonism with polyneuropathy.
Brain
; 143(11): 3352-3373, 2020 12 05.
Article
in English
| MEDLINE | ID: mdl-33141179
12.
Variants in saposin D domain of prosaposin gene linked to Parkinson's disease.
Brain
; 143(4): 1190-1205, 2020 04 01.
Article
in English
| MEDLINE | ID: mdl-32201884
13.
A Novel LRRK2 Variant p.G2294R in the WD40 Domain Identified in Familial Parkinson's Disease Affects LRRK2 Protein Levels.
Int J Mol Sci
; 22(7)2021 Apr 02.
Article
in English
| MEDLINE | ID: mdl-33918221
14.
Serial MRI alterations of pediatric patients with beta-propeller protein associated neurodegeneration (BPAN).
J Neuroradiol
; 48(2): 88-93, 2021 Mar.
Article
in English
| MEDLINE | ID: mdl-32335071
15.
Clinical characterization of patients with leucine-rich repeat kinase 2 genetic variants in Japan.
J Hum Genet
; 65(9): 771-781, 2020 Sep.
Article
in English
| MEDLINE | ID: mdl-32398759
16.
Arylsulfatase A, a genetic modifier of Parkinson's disease, is an α-synuclein chaperone.
Brain
; 142(9): 2845-2859, 2019 09 01.
Article
in English
| MEDLINE | ID: mdl-31312839
17.
Music Intervention Reduces Persistent Fibromyalgia Pain and Alters Functional Connectivity Between the Insula and Default Mode Network.
Pain Med
; 21(8): 1546-1552, 2020 08 01.
Article
in English
| MEDLINE | ID: mdl-32330259
18.
The E3 ligase synoviolin controls body weight and mitochondrial biogenesis through negative regulation of PGC-1ß.
EMBO J
; 34(8): 1042-55, 2015 Apr 15.
Article
in English
| MEDLINE | ID: mdl-25698262
19.
Investigation of 22q11.2 Deletion in Japanese Early-Onset Parkinsonism.
Mov Disord
; 39(3): 626-627, 2024 Mar.
Article
in English
| MEDLINE | ID: mdl-38146173
20.
Clinical heterogeneity of frontotemporal dementia and Parkinsonism linked to chromosome 17 caused by MAPT N279K mutation in relation to tau positron emission tomography features.
Mov Disord
; 34(4): 568-574, 2019 04.
Article
in English
| MEDLINE | ID: mdl-30773680