nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
A heterozygous deletion of PDGFB gene causes paroxysmal kinesigenic dyskinesia with primary familial brain calcification
|
Duan, Ruo-Nan |
|
|
92 |
C |
p. 83-87 |
artikel |
2 |
Anterior lead location predicts verbal fluency decline following STN-DBS in Parkinson's disease
|
Greif, Taylor R. |
|
|
92 |
C |
p. 36-40 |
artikel |
3 |
Apolipoprotein E ε4 is not associated with cognitive impairment in patients with idiopathic REM sleep behavior disorder
|
Sunwoo, Jun-Sang |
|
|
92 |
C |
p. 13-14 |
artikel |
4 |
Development of a cognitive composite for measuring change in progressive supranuclear palsy
|
Jaeger, Judith |
|
|
92 |
C |
p. 94-100 |
artikel |
5 |
DRPLA: An unusual disease or an underestimated cause of ataxia in Brazil?
|
Pinto, Wladimir Bocca Vieira de Rezende |
|
|
92 |
C |
p. 67-71 |
artikel |
6 |
Editorial Board
|
|
|
|
92 |
C |
p. i |
artikel |
7 |
Executive function and dopamine response in Parkinson's disease freezing of gait
|
Turner, Travis H. |
|
|
92 |
C |
p. 46-50 |
artikel |
8 |
How much time is needed in clinical practice to reach a diagnosis of clinically established Parkinson's disease?
|
Rossi, Malco |
|
|
92 |
C |
p. 53-58 |
artikel |
9 |
ΔHR/ΔWR derived from CPET; A novel predictor of ‘off’ symptom in Parkinson's disease
|
Yoshida, Kohsuke |
|
|
92 |
C |
p. 101-104 |
artikel |
10 |
Identical twins with progressive kyphoscoliosis and ophthalmoplegia
|
Emamikhah, Maziar |
|
|
92 |
C |
p. 119-122 |
artikel |
11 |
Identical twins with progressive kyphoscoliosis and ophthalmoplegia: Expert commentary
|
Vengoechea, J. |
|
|
92 |
C |
p. 123-124 |
artikel |
12 |
Increased functional connectivity in a population at risk of developing Parkinson's disease
|
Binder, Tobias |
|
|
92 |
C |
p. 1-6 |
artikel |
13 |
Increased neural motor activation and functional reorganization in patients with idiopathic rapid eye movement sleep behavior disorder
|
Brcina, Nikolina |
|
|
92 |
C |
p. 76-82 |
artikel |
14 |
Investigating ABCD1 mutations in a Taiwanese cohort with hereditary spastic paraplegia phenotype
|
Hsu, Shao-Lun |
|
|
92 |
C |
p. 7-12 |
artikel |
15 |
Low soluble amyloid-β 42 is associated with smaller brain volume in Parkinson's disease
|
Espay, Alberto J. |
|
|
92 |
C |
p. 15-21 |
artikel |
16 |
Navigating the open sea of commercial genetic testing in Parkinson's disease
|
Mata, Ignacio F. |
|
|
92 |
C |
p. 105-106 |
artikel |
17 |
Neuropsychological outcomes after thalamic deep brain stimulation for essential tremor
|
Dhima, Kaltra |
|
|
92 |
C |
p. 88-93 |
artikel |
18 |
North American survey on impact of the COVID-19 pandemic shutdown on DBS care
|
Siddiqui, Mustafa S. |
|
|
92 |
C |
p. 41-45 |
artikel |
19 |
Parkinson's disease-dementia in trans LRP10 and GBA variants: Response to deep brain stimulation
|
Neri, Marcella |
|
|
92 |
C |
p. 72-75 |
artikel |
20 |
Quadrupedal gait and cerebellar hypoplasia, the Uner Tan syndrome, caused by ITPR1 gene mutation
|
Raslan, Ivana Rocha |
|
|
92 |
C |
p. 33-35 |
artikel |
21 |
Spinocerebellar ataxias in Asia: Prevalence, phenotypes and management
|
van Prooije, Teije |
|
|
92 |
C |
p. 112-118 |
artikel |
22 |
The amplitude of low-frequency fluctuation predicts levodopa treatment response in patients with Parkinson's disease
|
Yang, Bowen |
|
|
92 |
C |
p. 26-32 |
artikel |
23 |
The commercial genetic testing landscape for Parkinson's disease
|
Cook, Lola |
|
|
92 |
C |
p. 107-111 |
artikel |
24 |
Validation and clinical value of the MANAGE-PD tool: A clinician-reported tool to identify Parkinson's disease patients inadequately controlled on oral medications
|
Antonini, Angelo |
|
|
92 |
C |
p. 59-66 |
artikel |
25 |
Visceral adipose tissue had a causal, independent role in lowering the risk of Parkinson's disease: A mendelian randomization study
|
Liu, Yaozhong |
|
|
92 |
C |
p. 51-52 |
artikel |
26 |
Visual dysfunction is associated with cognitive impairment in Parkinson's disease
|
Del Pino, Rocío |
|
|
92 |
C |
p. 22-25 |
artikel |